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Volumn 12, Issue 1, 2014, Pages 47-72

Organogels as matrices for controlled drug delivery: A review on the current state

Author keywords

Biocompatibility; Biopolymers; Controlled drug delivery; Organogelators; Organogels

Indexed keywords

ACTIVE INGREDIENTS; CHARACTERIZATION TECHNIQUES; IN-SITU FORMING; LIPOPHILIC CONSTITUENTS; NASAL ROUTES; ORGANOGEL FORMATION; ORGANOGELATORS; ORGANOGELS;

EID: 84881321345     PISSN: 1539445X     EISSN: 15394468     Source Type: Journal    
DOI: 10.1080/1539445X.2012.756016     Document Type: Review
Times cited : (114)

References (336)
  • 1
    • 0343885104 scopus 로고
    • The problem of gel structure
    • Alexander. J., Ed.
    • Lloyd, J. (1926) The problem of gel structure. In Colloid Chemistry; Alexander. J., Ed.; 1:767-782.
    • (1926) Colloid Chemistry , vol.1 , pp. 767-782
    • Lloyd, J.1
  • 2
    • 84881348473 scopus 로고
    • Polymer gels: Fundamentals and biomedical applications
    • Derossi, D., et al., Eds.; Plenum Press: New York
    • Levon, K. (1992) Polymer gels: Fundamentals and biomedical applications. In Polymers for Advanced Technologies, Vol. 3, Derossi, D., et al., Eds.; Plenum Press: New York.
    • (1992) Polymers for Advanced Technologies , vol.3
    • Levon, K.1
  • 3
    • 28144462471 scopus 로고    scopus 로고
    • Organogels in drug delivery
    • Murdan, S. (2005) Organogels in drug delivery. Expert Opinion on Drug Delivery 2(3):489-505.
    • (2005) Expert Opinion on Drug Delivery , vol.2 , Issue.3 , pp. 489-505
    • Murdan, S.1
  • 4
    • 0033640318 scopus 로고    scopus 로고
    • N-Alkanes gel and many other organic liquids
    • Abdallah, D.J., and Weiss, R.G. (1999) n-Alkanes gel and many other organic liquids. Langmuir 16(2):352-355.
    • (1999) Langmuir , vol.16 , Issue.2 , pp. 352-355
    • Abdallah, D.J.1    Weiss, R.G.2
  • 5
    • 77953807285 scopus 로고    scopus 로고
    • Tyrosine-based rivastigmine-loaded organogels in the treatment of Alzheimer's disease
    • Bastiat, G., et al. (2010) Tyrosine-based rivastigmine-loaded organogels in the treatment of Alzheimer's disease. Biomaterials 31(23):6031-6038.
    • (2010) Biomaterials , vol.31 , Issue.23 , pp. 6031-6038
    • Bastiat, G.1
  • 6
    • 0042904456 scopus 로고    scopus 로고
    • Dynamics in thermoreversible polymer gels
    • Bohidar, B.H. (2001) Dynamics in thermoreversible polymer gels. Curr. Sci. 80(8):1008.
    • (2001) Curr. Sci , vol.80 , Issue.8 , pp. 1008
    • Bohidar, B.H.1
  • 7
    • 47249132847 scopus 로고    scopus 로고
    • Crops: A green approach toward self-assembled soft materials
    • Vemula, P.K., and John, G. (2008) Crops: A green approach toward self-assembled soft materials. Acct Chem. Res. 41(6):769-782.
    • (2008) Acct Chem. Res , vol.41 , Issue.6 , pp. 769-782
    • Vemula, P.K.1    John, G.2
  • 8
    • 0027847854 scopus 로고
    • Towards a phenomenological definition of the term gel
    • Almdal, K., et al. (1993) Towards a phenomenological definition of the term gel. Polym. Gels Network 1(1):5-17.
    • (1993) Polym. Gels Network , vol.1 , Issue.1 , pp. 5-17
    • Almdal, K.1
  • 9
    • 38349188632 scopus 로고    scopus 로고
    • Organogels and their use in drug delivery - A review
    • Vintiloiu, A., and Leroux, J. C. (2008) Organogels and their use in drug delivery - A review. J. Control. Rel. 125(3):179-192.
    • (2008) J. Control. Rel. , vol.125 , Issue.3 , pp. 179-192
    • Vintiloiu, A.1    Leroux, J.C.2
  • 10
    • 69249216455 scopus 로고    scopus 로고
    • A novel reverse wormlike micelle from a lecithin/sucrose fatty acid ester/oil system
    • Hashizaki, K., Taguchi, H. and Saito, Y. (2009) A novel reverse wormlike micelle from a lecithin/sucrose fatty acid ester/oil system. Coll. Polym. Sci. 287(9):1099-1105.
    • (2009) Coll. Polym. Sci , vol.287 , Issue.9 , pp. 1099-1105
    • Hashizaki, K.1    Taguchi, H.2    Saito, Y.3
  • 11
    • 33644788245 scopus 로고    scopus 로고
    • Lecithin organogels as a potential phospholipid-structured system for topical drug delivery: A review
    • Kumar, R., and Katare, O. P. (2005) Lecithin organogels as a potential phospholipid-structured system for topical drug delivery: a review. AAPS Pharm. Sci. Tech. 6(298):E298.
    • (2005) AAPS Pharm. Sci. Tech. , vol.6 , Issue.298
    • Kumar, R.1    Katare, O.P.2
  • 12
    • 33947161453 scopus 로고    scopus 로고
    • Structuring edible oil with lecithin and sorbitan tri-stearate
    • Pernetti, M., et al. (2006) Structuring edible oil with lecithin and sorbitan tri-stearate. Food Hydrocolloids 21(5-6):855-861.
    • (2006) Food Hydrocolloids , vol.21 , Issue.5-6 , pp. 855-861
    • Pernetti, M.1
  • 13
    • 78249287386 scopus 로고    scopus 로고
    • Microemulsion-based organogels containing inorganic nanoparticles
    • Trickett, K., et al. (2010) Microemulsion-based organogels containing inorganic nanoparticles. Soft Matter 6(6):1291-1296.
    • (2010) Soft Matter , vol.6 , Issue.6 , pp. 1291-1296
    • Trickett, K.1
  • 14
    • 34547873740 scopus 로고    scopus 로고
    • Gelatin-stabilised microemulsion-based organogels facilitates percutaneous penetration of Cyclosporin A in Vitro and dermal pharmacokinetics in Vivo
    • Liu, H., et al. (2007) Gelatin-stabilised microemulsion-based organogels facilitates percutaneous penetration of Cyclosporin A In Vitro and dermal pharmacokinetics In Vivo. J. Pharm. Sci. 96(11):3000-3009.
    • (2007) J. Pharm. Sci , vol.96 , Issue.11 , pp. 3000-3009
    • Liu, H.1
  • 15
    • 77955614043 scopus 로고    scopus 로고
    • Water-in-ionic liquid microemulsion-based organogels as novel matrices for enzyme immobilization
    • Pavlidis, I.V., Tzafestas, K., and Stamatis, H. (2010) Water-in-ionic liquid microemulsion-based organogels as novel matrices for enzyme immobilization. Biotechnol. J. 5(8):805-812.
    • (2010) Biotechnol. J. , vol.5 , Issue.8 , pp. 805-812
    • Pavlidis, I.V.1    Tzafestas, K.2    Stamatis, H.3
  • 16
    • 84881328577 scopus 로고
    • Characterization of microemulsion-based organo-gels
    • Corti, V.M., and Mallamace, F., Eds.; Springer: Berlin/Heidelberg
    • Atkinson, P., et al. (1991) Characterization of microemulsion-based organo-gels. In Trends in Colloid and Interface Science, Corti, V.M., and Mallamace, F., Eds.; Springer: Berlin/Heidelberg. pp. 129-132.
    • (1991) Trends in Colloid and Interface Science , pp. 129-132
    • Atkinson, P.1
  • 17
    • 77949568536 scopus 로고    scopus 로고
    • Microemulsion-based organogels as matrices for lipase immobilization
    • Zoumpanioti, M., Stamatis, H., and Xenakis, A. (2010) Microemulsion-based organogels as matrices for lipase immobilization. Biotechnol. Adv. 28(3):395-406.
    • (2010) Biotechnol. Adv. , vol.28 , Issue.3 , pp. 395-406
    • Zoumpanioti, M.1    Stamatis, H.2    Xenakis, A.3
  • 18
    • 8344265263 scopus 로고    scopus 로고
    • Structure-property correlation of a new family of organogelators based on organic salts and their selective gelation of oil from oil/water mixtures
    • Trivedi, D.R., et al. (2004) Structure-property correlation of a new family of organogelators based on organic salts and their selective gelation of oil from oil/water mixtures. Chem. - A Eur. J. 10(21):5311-5322.
    • (2004) Chem. - A Eur. J , vol.10 , Issue.21 , pp. 5311-5322
    • Trivedi, D.R.1
  • 19
    • 0033640318 scopus 로고    scopus 로고
    • N-Alkanes Gel n-Alkanes (and Many Other Organic Liquids)
    • Abdallah, D.J., andWeiss, R. G. (1999) n-Alkanes Gel n-Alkanes (and Many Other Organic Liquids). Langmuir 16(2):352-355.
    • (1999) Langmuir , vol.16 , Issue.2 , pp. 352-355
    • Abdallah, D.J.1    Weiss, R.G.2
  • 20
    • 34548621881 scopus 로고    scopus 로고
    • Crystal network for edible oil organogels: Possibilities and limitations of the fatty acid and fatty alcohol systems
    • Schaink, H.M., et al. (2007) Crystal network for edible oil organogels: Possibilities and limitations of the fatty acid and fatty alcohol systems. Food Res. Int. 40(9):1185-1193.
    • (2007) Food Res. Int , vol.40 , Issue.9 , pp. 1185-1193
    • Schaink, H.M.1
  • 21
    • 0001629673 scopus 로고    scopus 로고
    • Low molecular mass gelators of organic liquids and the properties of their gels
    • Terech, P., and Weiss, R.G. (1997) Low molecular mass gelators of organic liquids and the properties of their gels. Chem. Rev. 97(8):3133-3160.
    • (1997) Chem. Rev , vol.97 , Issue.8 , pp. 3133-3160
    • Terech, P.1    Weiss, R.G.2
  • 22
    • 0000296080 scopus 로고
    • Chiral mesophases of 12-hydroxyoctadecanoic acid in jelly and in the solid state I. A new type of lyotropic mesophase in jelly with organic solvents
    • Tachibana, T., Mori, T., and Hori, K. (1980) Chiral mesophases of 12-hydroxyoctadecanoic acid in jelly and in the solid state. I. A new type of lyotropic mesophase in jelly with organic solvents. Bull. Chem. Soc. Jap. 53(6):1714-1719.
    • (1980) Bull. Chem. Soc. Jap. , vol.53 , Issue.6 , pp. 1714-1719
    • Tachibana, T.1    Mori, T.2    Hori, K.3
  • 23
    • 17144441749 scopus 로고    scopus 로고
    • Lecithin organogel: A micellar system with unique properties
    • Shchipunov, Y.A. (2001) Lecithin organogel: A micellar system with unique properties. Colloid Surfaces A 183-185:541-554.
    • (2001) Colloid Surfaces A , vol.183-185 , pp. 541-554
    • Shchipunov, Y.A.1
  • 24
    • 0036305824 scopus 로고    scopus 로고
    • Bioavailability of transdermal methimazole in a pluronic lecithin organogel (PLO) in healthy cats
    • Hoffman, S.B., Yoder, A.R., and Trepanier, L.A. (2002) Bioavailability of transdermal methimazole in a pluronic lecithin organogel (PLO) in healthy cats. J. Vet. Pharm. Therap. 25(3):189-193.
    • (2002) J. Vet. Pharm. Therap , vol.25 , Issue.3 , pp. 189-193
    • Hoffman, S.B.1    Yoder, A.R.2    Trepanier, L.A.3
  • 25
    • 33745655854 scopus 로고    scopus 로고
    • In-vitro transcutaneous delivery of ketoprofen and polyunsaturated fatty acids from a pluronic lecithin organogel vehicle containing fish oil
    • Richards, H., et al. (2006) In-vitro transcutaneous delivery of ketoprofen and polyunsaturated fatty acids from a pluronic lecithin organogel vehicle containing fish oil. J. Pharm. Pharmacol. 58(7):903-908.
    • (2006) J. Pharm. Pharmacol , vol.58 , Issue.7 , pp. 903-908
    • Richards, H.1
  • 26
    • 0038050761 scopus 로고    scopus 로고
    • Comparison of serum dexamethasone concentrations in cats after oral or transdermal administration using Pluronic Lecithin Organogel (PLO): A pilot study
    • Willis-Goulet, H.S., et al. (2003) Comparison of serum dexamethasone concentrations in cats after oral or transdermal administration using Pluronic Lecithin Organogel (PLO): A pilot study. Vet. Derm. 14(2):83-89.
    • (2003) Vet. Derm , vol.14 , Issue.2 , pp. 83-89
    • Willis-Goulet, H.S.1
  • 27
    • 0033053206 scopus 로고    scopus 로고
    • Novel sorbitan monostearate organogels
    • Murdan, S., Gregoriadis, G., and Florence, T.F. (1999) Novel sorbitan monostearate organogels. J. Pharm. Sci. 88(6):608-614.
    • (1999) J. Pharm. Sci , vol.88 , Issue.6 , pp. 608-614
    • Murdan, S.1    Gregoriadis, G.2    Florence, T.F.3
  • 28
    • 15544384141 scopus 로고    scopus 로고
    • Relative bioavailability of ketoprofen 20% in a poloxamer-lecithin organogel
    • Dowling, T., et al. (2004) Relative bioavailability of ketoprofen 20% in a poloxamer-lecithin organogel. Am. J. Health-Syst. Pharm. 61(23):2541-2544.
    • (2004) Am. J. Health-Syst. Pharm , vol.61 , Issue.23 , pp. 2541-2544
    • Dowling, T.1
  • 29
    • 57249094221 scopus 로고    scopus 로고
    • Fibrils of γ-Oryzanol + ß-Sitosterol in edible oil organogels
    • Bot, A., Den, A.R., and Roijers, E. (2008) Fibrils of γ-Oryzanol + ß-Sitosterol in edible oil organogels. J. America.n Oil Chem. Soc. 85(12):1127-1134.
    • (2008) J. America.n Oil Chem. Soc , vol.85 , Issue.12 , pp. 1127-1134
    • Bot, A.1    Den, A.R.2    Roijers, E.3
  • 30
    • 0142030988 scopus 로고    scopus 로고
    • A new urea gelator: Incorporation of intra- and intermolecular hydrogen bonding for stable 1D self-assembly
    • Yabuuchi, K., Marfo-Owusu, E., and Kato, T. (2003) A new urea gelator: Incorporation of intra- and intermolecular hydrogen bonding for stable 1D self-assembly. Org. Biomol. Chem. (1):3464-3469.
    • (2003) Org. Biomol. Chem. , Issue.1 , pp. 3464-3469
    • Yabuuchi, K.1    Marfo-Owusu, E.2    Kato, T.3
  • 31
    • 27744446202 scopus 로고    scopus 로고
    • First report on the efficacy of l-alanine-based in situ-forming implants for the long-term parenteral delivery of drugs
    • Plourde, F., et al. (2005) First report on the efficacy of l-alanine-based in situ-forming implants for the long-term parenteral delivery of drugs. J. Control. Release 108(2-3):433-441.
    • (2005) J. Control. Release , vol.108 , Issue.2-3 , pp. 433-441
    • Plourde, F.1
  • 32
    • 20444462461 scopus 로고    scopus 로고
    • Characterization and biocompatibility of organogels based on l-alanine for parenteral drug delivery implants
    • Motulsky, A., et al. (2005) Characterization and biocompatibility of organogels based on l-alanine for parenteral drug delivery implants. Biomaterials 26(31):6242-6253.
    • (2005) Biomaterials , vol.26 , Issue.31 , pp. 6242-6253
    • Motulsky, A.1
  • 33
    • 33748355395 scopus 로고    scopus 로고
    • Molecular organogels. Soft matter comprised of low-molecular-mass organic gelators and organic liquids†
    • George, M., and Weiss, R.G. (2006) Molecular organogels. Soft matter comprised of low-molecular-mass organic gelators and organic liquids†. Accts Chem. Res. 39(8):489-497.
    • (2006) Accts Chem. Res , vol.39 , Issue.8 , pp. 489-497
    • George, M.1    Weiss, R.G.2
  • 34
    • 0001006207 scopus 로고    scopus 로고
    • Structural study of cholesteryl anthraquinone-2-carboxylate (CAQ) Physical organogels by neutron and X-ray small angle scattering
    • Terech, P., Ostuni, E., and Weiss, R. G. (1996) Structural study of cholesteryl anthraquinone-2-carboxylate (CAQ) Physical organogels by neutron and X-ray small angle scattering. J. Phys. Chem. 100(9):3759-3766.
    • (1996) J. Phys. Chem , vol.100 , Issue.9 , pp. 3759-3766
    • Terech, P.1    Ostuni, E.2    Weiss, R.G.3
  • 35
    • 52049089435 scopus 로고    scopus 로고
    • Supramolecular gels based on organic diacid monoamides of cholesteryl glycinate
    • Liu, K., et al. (2008) Supramolecular gels based on organic diacid monoamides of cholesteryl glycinate. J. Colloid Interface Sci. 327(1):233-242.
    • (2008) J. Colloid Interface Sci , vol.327 , Issue.1 , pp. 233-242
    • Liu, K.1
  • 36
    • 34548292857 scopus 로고    scopus 로고
    • An air-stable organometallic low-molecularmass gelator: Synthesis, aggregation, and catalytic application of a palladium pincer complex
    • Tu, T., et al. (2007) An air-stable organometallic low-molecularmass gelator: Synthesis, aggregation, and catalytic application of a palladium pincer complex. Angew. Chem. Int. Ed. 46(33):6368-6371.
    • (2007) Angew. Chem. Int. Ed , vol.46 , Issue.33 , pp. 6368-6371
    • Tu, T.1
  • 37
    • 64749094559 scopus 로고    scopus 로고
    • Novel organometallic gelators with enhanced amphiphilic character: Structure-property correlations, principles for design, and diversity of gelation
    • Gansäuer, A., et al. (2009) Novel organometallic gelators with enhanced amphiphilic character: Structure-property correlations, principles for design, and diversity of gelation. Organometallics 28(5):1377-1382.
    • (2009) Organometallics , vol.28 , Issue.5 , pp. 1377-1382
    • Gansäuer, A.1
  • 38
    • 33747151964 scopus 로고    scopus 로고
    • Amino Acid derivatives of cholesterol as "latent" organogelators with hydrogen chloride as a protonation reagent
    • Li, Y., et al. (2006) Amino Acid derivatives of cholesterol as "latent" organogelators with hydrogen chloride as a protonation reagent. Langmuir 22(16):7016-7020.
    • (2006) Langmuir , vol.22 , Issue.16 , pp. 7016-7020
    • Li, Y.1
  • 39
    • 0034977488 scopus 로고    scopus 로고
    • N-cholyl amino acid alkyl esters - A novel class of organogelators
    • Willemen, Hendra M., et al. (2001) N-cholyl amino acid alkyl esters - A novel class of organogelators. Eur. J. Organ. Chem. (12):2329-2335.
    • (2001) Eur. J. Organ. Chem. , Issue.12 , pp. 2329-2335
    • Willemen Hendra, M.1
  • 40
    • 79958830034 scopus 로고    scopus 로고
    • Bile acid alkylamide derivatives as low molecular weight organogelators: Systematic gelation studies and qualitative structural analysis of the systems
    • Löfman, M., et al. (2011) Bile acid alkylamide derivatives as low molecular weight organogelators: Systematic gelation studies and qualitative structural analysis of the systems. J. Colloid Interface Sci. 360(2):633-644.
    • (2011) J. Colloid Interface Sci. , vol.360 , Issue.2 , pp. 633-644
    • Löfman, M.1
  • 41
    • 84881349076 scopus 로고    scopus 로고
    • Pyrene appended bile acid conjugates: Synthesis and a structure-gelation property study
    • Bhat, S., et al. (2011) Pyrene appended bile acid conjugates: Synthesis and a structure-gelation property study. J. Chem. Sci. 2011:1-13.
    • (2011) J. Chem. Sci. , vol.2011 , pp. 1-13
    • Bhat, S.1
  • 42
    • 0042159829 scopus 로고    scopus 로고
    • New gemini organogelators linked by oxalyl amide: Organogel formation and their thermal stabilities
    • Suzuki, M., et al. (2003) New gemini organogelators linked by oxalyl amide: organogel formation and their thermal stabilities. Tetrahedron Lett. 44(36):6841-6843.
    • (2003) Tetrahedron Lett , vol.44 , Issue.36 , pp. 6841-6843
    • Suzuki, M.1
  • 43
    • 0345377476 scopus 로고    scopus 로고
    • L-Lysine based gemini organogelators: Their organogelation properties and thermally stable organogels
    • Suzuki, M., et al. (2003) l-Lysine based gemini organogelators: their organogelation properties and thermally stable organogels. Org. Biomol. Chem. 1(22):4124-4131.
    • (2003) Org. Biomol. Chem , vol.1 , Issue.22 , pp. 4124-4131
    • Suzuki, M.1
  • 44
    • 9644254429 scopus 로고    scopus 로고
    • A family of strong low-molecular-weight organogelators based on aminoacid derivatives
    • Brosse, N., Barth, D., and Jamart-Grégoire, B. (2004) A family of strong low-molecular-weight organogelators based on aminoacid derivatives. Tetrahedron Lett. 45(52):9521-9524.
    • (2004) Tetrahedron Lett , vol.45 , Issue.52 , pp. 9521-9524
    • Brosse, N.1    Barth, D.2    Jamart-Grégoire, B.3
  • 45
    • 79959791712 scopus 로고    scopus 로고
    • Gelation mechanism and microstructure of organogels formed with l-Valine dihydrazide derivatives
    • Wang, C., et al. (2011) Gelation mechanism and microstructure of organogels formed with l-Valine dihydrazide derivatives. Colloids Surfaces A 384(1-3):490-495.
    • (2011) Colloids Surfaces A , vol.384 , Issue.1-3 , pp. 490-495
    • Wang, C.1
  • 46
    • 0025880664 scopus 로고
    • Lecithin organogels as matrix for the transdermal transport of drugs
    • Willimann, H.-L., and Luisi, P.L. (1991) Lecithin organogels as matrix for the transdermal transport of drugs. Biochem. Biophys. Res. Comm. 177(3):897-900.
    • (1991) Biochem. Biophys. Res. Comm , vol.177 , Issue.3 , pp. 897-900
    • Willimann, H.-L.1    Luisi, P.L.2
  • 47
    • 0001751101 scopus 로고    scopus 로고
    • Sugar-integrated gelators of organic fluids on their versatility as building-blocks and diversity in superstructures
    • Yoza, K., et al. (1998) Sugar-integrated gelators of organic fluids on their versatility as building-blocks and diversity in superstructures. Chem. Commun. 1998:907-908.
    • (1998) Chem. Commun , vol.1998 , pp. 907-908
    • Yoza, K.1
  • 48
    • 77749249660 scopus 로고    scopus 로고
    • Tuning the helicity of self-assembled structure of a sugar-based organogelator by the proper choice of cooling rate
    • Cui, J., et al. (2009) Tuning the Helicity of Self-Assembled Structure of a Sugar-Based Organogelator by the Proper Choice of Cooling Rate. Langmuir 26(5):3615-3622.
    • (2009) Langmuir , vol.26 , Issue.5 , pp. 3615-3622
    • Cui, J.1
  • 49
    • 85047697114 scopus 로고    scopus 로고
    • Synthesis and self-assembling properties of polymerizable organogelators
    • Wang, G., and Hamilton, A.D. (2002) Synthesis and Self-Assembling Properties of Polymerizable Organogelators. Chem. - A Eur. J. 8(8):1954-1961.
    • (2002) Chem. - A Eur. J , vol.8 , Issue.8 , pp. 1954-1961
    • Wang, G.1    Hamilton, A.D.2
  • 50
    • 0034275888 scopus 로고    scopus 로고
    • Organogels and low molecular mass organic gelators
    • Abdallah, D.J., and Weiss, G.R. (2000) Organogels and low molecular mass organic gelators. Adv. Mater. 12(17):1237-1247.
    • (2000) Adv. Mater , vol.12 , Issue.17 , pp. 1237-1247
    • Abdallah, D.J.1    Weiss, G.R.2
  • 51
    • 19944369098 scopus 로고    scopus 로고
    • Urea and thiourea derivatives as low molecular-mass organogelators
    • George, M., et al. (2005) Urea and Thiourea Derivatives as Low Molecular-Mass Organogelators. Chem. - A Eur. J. 11(11): 3243-3254.
    • (2005) Chem. - A Eur. J , vol.11 , Issue.11 , pp. 3243-3254
    • George, M.1
  • 52
    • 79951880762 scopus 로고    scopus 로고
    • Amino acid based low-molecular-weight tris(bis-amido) organogelators
    • Samai, S., Dey, J., and Biradha, K. (2011) Amino acid based low-molecular-weight tris(bis-amido) organogelators. Soft Matter 7(5):2121-2126.
    • (2011) Soft Matter , vol.7 , Issue.5 , pp. 2121-2126
    • Samai, S.1    Dey, J.2    Biradha, K.3
  • 53
    • 53849083475 scopus 로고    scopus 로고
    • Dipeptide-based low-molecular-weight efficient organogelators and their application in water purification
    • Debnath, S., et al. (2008) Dipeptide-Based Low-Molecular-Weight Efficient Organogelators and Their Application in Water Purification. Chem. - A Eur. J. 14(23):6870-6881.
    • (2008) Chem. - A Eur. J , vol.14 , Issue.23 , pp. 6870-6881
    • Debnath, S.1
  • 54
    • 78649869599 scopus 로고    scopus 로고
    • Synthetically accessible, tunable, low-molecular-weight oligopeptide organogelators
    • Lagadec, C., and Smith, D. K. (2011) Synthetically accessible, tunable, low-molecular-weight oligopeptide organogelators. Chem. Comm. 47(1):340-342.
    • (2011) Chem. Comm. , vol.47 , Issue.1 , pp. 340-342
    • Lagadec, C.1    Smith, D.K.2
  • 55
    • 77949488205 scopus 로고    scopus 로고
    • Low molecular mass organogelator based gel electrolyte gelated by a quaternary ammonium halide salt for quasi-solid-state dye-sensitized solar cells
    • Huo, Z., et al. (2010) Low molecular mass organogelator based gel electrolyte gelated by a quaternary ammonium halide salt for quasi-solid-state dye-sensitized solar cells. J. Power Source 195(13):4384-4390.
    • (2010) J. Power Source , vol.195 , Issue.13 , pp. 4384-4390
    • Huo, Z.1
  • 56
    • 0035801383 scopus 로고    scopus 로고
    • Rational design of low molecular mass organogelators: Toward a library of functional N-Acyl-1,ω-amino acid derivatives
    • Mieden-Gundert, G., et al. (2001) Rational design of low molecular mass organogelators: toward a library of functional N-Acyl-1,ω-amino acid derivatives. Angew. Chem. Int. Ed. 40(17):3164-3166.
    • (2001) Angew. Chem. Int. Ed , vol.40 , Issue.17 , pp. 3164-3166
    • Mieden-Gundert, G.1
  • 57
    • 0037453609 scopus 로고    scopus 로고
    • Structural aspects of the gelation process observed with low molecular mass organogelators
    • Lescanne, M., et al. (2003) Structural aspects of the gelation process observed with low molecular mass organogelators. Langmuir 19(6):2013-2020.
    • (2003) Langmuir , vol.19 , Issue.6 , pp. 2013-2020
    • Lescanne, M.1
  • 58
    • 0041429596 scopus 로고    scopus 로고
    • N-alkyl perfluoroalkanamides as low molecular-mass organogelators
    • George, M., et al. (2003) N-alkyl perfluoroalkanamides as low molecular-mass organogelators. J. Am. Chem. Soc. 125(34):10275-10283.
    • (2003) J. Am. Chem. Soc , vol.125 , Issue.34 , pp. 10275-10283
    • George, M.1
  • 59
    • 31444431757 scopus 로고    scopus 로고
    • A family of low-molecular-weight organogelators based on long chain substituted benzoic acid hydrazides
    • Tan, C., et al. (2006) A family of low-molecular-weight organogelators based on long chain substituted benzoic acid hydrazides. J. Molecul. Liquid 124(1-3):32-36.
    • (2006) J. Molecul. Liquid , vol.124 , Issue.1-3 , pp. 32-36
    • Tan, C.1
  • 60
    • 18544369759 scopus 로고    scopus 로고
    • Low molecular weight organogels based on long-chain carbamates
    • Moniruzzaman, M., and Sundararajan, P.R. (2005) Low molecular weight organogels based on long-chain carbamates. Langmuir 21(9):3802-3807.
    • (2005) Langmuir , vol.21 , Issue.9 , pp. 3802-3807
    • Moniruzzaman, M.1    Sundararajan, P.R.2
  • 61
    • 33745704829 scopus 로고    scopus 로고
    • Chirality effects in self assembled fibrillar networks
    • Brizard, A., Oda, R., and Hue, I. (2005) Chirality effects in self assembled fibrillar networks. Curr. Chem. 2005(256):167-218.
    • (2005) Curr. Chem , vol.2005 , Issue.256 , pp. 167-218
    • Brizard, A.1    Oda, R.2    Hue, I.3
  • 62
    • 79961139174 scopus 로고    scopus 로고
    • Influence of chirality on the modes of self-assembly of 12-hydroxystearic acid in molecular gels of mineral oil
    • Grahame, D.A.S., et al. (2011) Influence of chirality on the modes of self-assembly of 12-hydroxystearic acid in molecular gels of mineral oil. Soft Matter 7:7359-7365.
    • (2011) Soft Matter , vol.7 , pp. 7359-7365
    • Grahame, D.A.S.1
  • 63
    • 50649083259 scopus 로고    scopus 로고
    • Cyclic voltammetry investigation of diffusion of ferrocene within propylene carbonate organogel formed by gelator
    • Feng, G., et al. (2008) Cyclic voltammetry investigation of diffusion of ferrocene within propylene carbonate organogel formed by gelator. Electrochim. Acta 53(28):8253-8257.
    • (2008) Electrochim. Acta , vol.53 , Issue.28 , pp. 8253-8257
    • Feng, G.1
  • 64
    • 68149091655 scopus 로고    scopus 로고
    • Balancing hydrogen bonding and van der Waals interactions in cyclohexane-based bisamide and bisurea organogelators†
    • Zweep, N., et al. (2009) Balancing hydrogen bonding and van der Waals interactions in cyclohexane-based bisamide and bisurea organogelators†. Langmuir 25(15):8802-8809.
    • (2009) Langmuir , vol.25 , Issue.15 , pp. 8802-8809
    • Zweep, N.1
  • 65
    • 0033925894 scopus 로고    scopus 로고
    • Organogelators for making porous solgel derived silica at two different length scales
    • Clavier, G.M., et al. (2000) Organogelators for making porous solgel derived silica at two different length scales. J. Mater. Chem. 10(7):1725-1730.
    • (2000) J. Mater. Chem , vol.10 , Issue.7 , pp. 1725-1730
    • Clavier, G.M.1
  • 66
    • 80053600157 scopus 로고    scopus 로고
    • Low molecular mass gelators of organic liquids
    • Maity, G.C. (2007) Low Molecular Mass Gelators of Organic Liquids. J. Phys. Sci. 11:156-171.
    • (2007) J. Phys. Sci , vol.11 , pp. 156-171
    • Maity, G.C.1
  • 67
    • 34250681006 scopus 로고    scopus 로고
    • Rheometry of an androstanol steroid derivative paramagnetic organogel. Methodology for a comparison with a fatty acid organogel
    • Terech, P., and Friol, S. (2007) Rheometry of an androstanol steroid derivative paramagnetic organogel. Methodology for a comparison with a fatty acid organogel. Tetrahedron 63(31):7366-7374.
    • (2007) Tetrahedron , vol.63 , Issue.31 , pp. 7366-7374
    • Terech, P.1    Friol, S.2
  • 68
    • 33845230896 scopus 로고    scopus 로고
    • Distinct kinetic pathways generate organogel networks with contrasting fractality and thixotropic properties
    • Huang, X., et al. (2006) Distinct kinetic pathways generate organogel networks with contrasting fractality and thixotropic properties. J. Am. Chem. Soc. 128(47):15341-15352.
    • (2006) J. Am. Chem. Soc , vol.128 , Issue.47 , pp. 15341-15352
    • Huang, X.1
  • 69
    • 76749143687 scopus 로고    scopus 로고
    • Selfassembly of a silylated steroid-based organogelator and its use as template for the in situ sol-gel polymerization of tetraethyl orthosilicate
    • Edelsztein, V.C., Burton, G., and Di Chenna, P.H. (2010) Selfassembly of a silylated steroid-based organogelator and its use as template for the in situ sol-gel polymerization of tetraethyl orthosilicate. Tetrahedron 66(12):2162-2167.
    • (2010) Tetrahedron , vol.66 , Issue.12 , pp. 2162-2167
    • Edelsztein, V.C.1    Burton, G.2    Di Chenna, P.H.3
  • 70
    • 39849093496 scopus 로고    scopus 로고
    • Inorganic and hybrid nanofibrous materials templated with organogelators†
    • Llusar, M., and Sanchez, C. (2008) Inorganic and Hybrid Nanofibrous Materials Templated with Organogelators†. Chem.Mater. 20(3):782-820.
    • (2008) Chem. Mater , vol.20 , Issue.3 , pp. 782-820
    • Llusar, M.1    Sanchez, C.2
  • 71
    • 84891997829 scopus 로고    scopus 로고
    • Safin gels with amphiphilic molecules
    • Weiss, R.G., and Terech, P., Eds.; Springer: Netherlands
    • Oda, R. (2006) Safin gels with amphiphilic molecules. In Molecular Gels, Weiss, R.G., and Terech, P., Eds.; Springer: Netherlands. pp. 577-609.
    • (2006) Molecular Gels , pp. 577-609
    • Oda, R.1
  • 72
    • 0035850534 scopus 로고    scopus 로고
    • Helical ribbon aggregate composed of a crownappended cholesterol derivative which acts as an amphiphilic gelator of organic solvents and as a template for chiral silica transcription
    • Jung, J.H., et al. (2001) Helical ribbon aggregate composed of a crownappended cholesterol derivative which acts as an amphiphilic gelator of organic solvents and as a template for chiral silica transcription. J. Am. Chem. Soc. 123(36):8785-8789.
    • (2001) J. Am. Chem. Soc , vol.123 , Issue.36 , pp. 8785-8789
    • Jung, J.H.1
  • 73
    • 4544362830 scopus 로고    scopus 로고
    • Rearrangement of the aggregation of the gelator during sol-gel transcription of a dimeric cholesterol-based viologen derivative into fibrous silica
    • Xue, P., et al. (2004) Rearrangement of the aggregation of the gelator during sol-gel transcription of a dimeric cholesterol-based viologen derivative into fibrous silica. Chem. Mater. 16(19):3702-3707.
    • (2004) Chem. Mater , vol.16 , Issue.19 , pp. 3702-3707
    • Xue, P.1
  • 74
    • 33947411437 scopus 로고    scopus 로고
    • Color-tunable, aggregation-induced emission of a butterfly-shaped molecule comprising a pyran skeleton and two cholesteryl wings
    • Tong, H., et al. (2007) Color-tunable, aggregation-induced emission of a butterfly-shaped molecule comprising a pyran skeleton and two cholesteryl wings. J. Phys. Chem. B 111(8):2000-2007.
    • (2007) J. Phys. Chem. B , vol.111 , Issue.8 , pp. 2000-2007
    • Tong, H.1
  • 75
    • 84881349264 scopus 로고    scopus 로고
    • Cholesterol-based gelators
    • Springer: Berlin/Heidelberg
    • Žinic, M., Vögtle, F., and Fages, F. (2005) Cholesterol-based gelators. In Low Molecular Mass Gelator; Springer: Berlin/Heidelberg. pp. 833-836.
    • (2005) Low Molecular Mass Gelator , pp. 833-836
    • Žinic, M.1    Vögtle, F.2    Fages, F.3
  • 76
    • 0000335313 scopus 로고    scopus 로고
    • Physical gelation of organic fluids by anthraquinone-steroid-based molecules. Structural features influencing the properties of gels
    • Mukkamala, R., and Weiss, R.G. (1996) Physical gelation of organic fluids by anthraquinone-steroid-based molecules. structural features influencing the properties of gels. Langmuir 12(6):1474-1482.
    • (1996) Langmuir , vol.12 , Issue.6 , pp. 1474-1482
    • Mukkamala, R.1    Weiss, R.G.2
  • 77
    • 77952880034 scopus 로고    scopus 로고
    • Preparation of novel organometallic derivatives of cholesterol and their gel-formation properties
    • He, P., et al. (2010) Preparation of novel organometallic derivatives of cholesterol and their gel-formation properties. Colloid Surface A 362(1-3):127-134.
    • (2010) Colloid Surface A , vol.362 , Issue.1-3 , pp. 127-134
    • He, P.1
  • 78
    • 78651365759 scopus 로고    scopus 로고
    • Photoinduced reversible gel-sol transitions of dicholesterol-linked azobenzene derivatives through breaking and reforming of van der Waals interactions
    • Wu, Y., et al. (2011) Photoinduced reversible gel-sol transitions of dicholesterol-linked azobenzene derivatives through breaking and reforming of van der Waals interactions. Soft Matter 7(2): 716-721.
    • (2011) Soft Matter , vol.7 , Issue.2 , pp. 716-721
    • Wu, Y.1
  • 79
    • 42249095839 scopus 로고    scopus 로고
    • New dicholesteryl-based gelators: Chirality and spacer length effect
    • Peng, J., et al. (2008) New dicholesteryl-based gelators: Chirality and spacer length effect. Langmuir 24(7):2992-3000.
    • (2008) Langmuir , vol.24 , Issue.7 , pp. 2992-3000
    • Peng, J.1
  • 80
    • 16244393064 scopus 로고    scopus 로고
    • Kinetics of 5a-cholestan-3ß-yl n-(2-naphthyl)carbamate/n-alkane organogel formation and its influence on the fibrillar networks
    • Huang, X., et al. (2005) Kinetics of 5a-cholestan-3ß-yl n-(2-naphthyl)carbamate/n-alkane organogel formation and its influence on the fibrillar networks. J. Am. Chem. Soc. 127(12):4336-4344.
    • (2005) J. Am. Chem. Soc , vol.127 , Issue.12 , pp. 4336-4344
    • Huang, X.1
  • 81
    • 41649109761 scopus 로고    scopus 로고
    • An easy access to an organometallic low molecular weight gelator: A crystal engineering approach
    • Sahoo, P., et al. (2008) An easy access to an organometallic low molecular weight gelator: a crystal engineering approach. Tetrahedron Lett. 49(19):3052-3055.
    • (2008) Tetrahedron Lett , vol.49 , Issue.19 , pp. 3052-3055
    • Sahoo, P.1
  • 82
    • 65349116520 scopus 로고    scopus 로고
    • Towards a general organogelator: Combining a versatile scaffold and an efficient linking process
    • Ghini, G., et al. (2009) Towards a general organogelator: combining a versatile scaffold and an efficient linking process. Soft Matter 5(9):1863-1869.
    • (2009) Soft Matter , vol.5 , Issue.9 , pp. 1863-1869
    • Ghini, G.1
  • 83
    • 79955811379 scopus 로고    scopus 로고
    • Ferrocene based organometallic gelators: A supramolecular synthon approach
    • Sahoo, P., et al. (2011) Ferrocene based organometallic gelators: a supramolecular synthon approach. Soft Matter 7(7):3634-3641.
    • (2011) Soft Matter , vol.7 , Issue.7 , pp. 3634-3641
    • Sahoo, P.1
  • 84
    • 34250849815 scopus 로고    scopus 로고
    • A tailored organometallic gelator with enhanced amphiphilic character and structural diversity of gelation
    • Klawonn, T., et al. (2007) A tailored organometallic gelator with enhanced amphiphilic character and structural diversity of gelation. Chem. Comm. 2007(19):1894-1895.
    • (2007) Chem. Comm , vol.2007 , Issue.19 , pp. 1894-1895
    • Klawonn, T.1
  • 85
    • 0037519741 scopus 로고    scopus 로고
    • Organometallic amphiphiles: Novel mechanisms for redox chemical control of aggregation behavior
    • Muñoz, S., and Gokel, G.W. (1996) Organometallic amphiphiles: novel mechanisms for redox chemical control of aggregation behavior. Inorgan. Chim. Acta 250(1-2):59-67.
    • (1996) Inorgan. Chim. Acta , vol.250 , Issue.1-2 , pp. 59-67
    • Muñoz, S.1    Gokel, G.W.2
  • 86
    • 33748432575 scopus 로고    scopus 로고
    • Understanding the mechanism of gelation and stimuli-responsive nature of a class of metallo-supramolecular gels
    • Weng, W., et al. (2006) Understanding the mechanism of gelation and stimuli-responsive nature of a class of metallo-supramolecular gels. J. Am. Chem. Soc. 128(35):11663-11672.
    • (2006) J. Am. Chem. Soc , vol.128 , Issue.35 , pp. 11663-11672
    • Weng, W.1
  • 87
    • 33847682608 scopus 로고    scopus 로고
    • Reversible switching of the sol-gel transition with ultrasound in rhodium(I) and iridium(I) coordination networks
    • Paulusse, J.M.J., van Beek, D.J.M., and Sijbesma, R.P. (2007) Reversible Switching of the sol-gel transition with ultrasound in rhodium(I) and iridium(I) coordination networks. J. Am. Chem. Soc. 129(8):2392-2397.
    • (2007) J. Am. Chem. Soc. , vol.129 , Issue.8 , pp. 2392-2397
    • Paulusse, J.M.J.1    Van Beek, D.J.M.2    Sijbesma, R.P.3
  • 88
    • 54949097379 scopus 로고    scopus 로고
    • An organometallic super-gelator with multiplestimulus responsive properties
    • Liu, J., et al. (2008) An organometallic super-gelator with multiplestimulus responsive properties. Adv. Mater. 20(13):2508-2511.
    • (2008) Adv. Mater , vol.20 , Issue.13 , pp. 2508-2511
    • Liu, J.1
  • 89
    • 8844252315 scopus 로고    scopus 로고
    • Bile acid amidoalcohols: Simple organogelators
    • Valkonen, A., et al. (2004) Bile acid amidoalcohols: simple organogelators. Biosensor Bioelectron. 20(6):1233-1241.
    • (2004) Biosensor Bioelectron , vol.20 , Issue.6 , pp. 1233-1241
    • Valkonen, A.1
  • 90
    • 77955363594 scopus 로고    scopus 로고
    • Bile acid-amino acid ester conjugates: Gelation, structural properties, and thermoreversible solid to solid phase transition
    • Noponen, V., et al. (2010) Bile acid-amino acid ester conjugates: gelation, structural properties, and thermoreversible solid to solid phase transition. Soft Matter 6(16):3789-3796.
    • (2010) Soft Matter , vol.6 , Issue.16 , pp. 3789-3796
    • Noponen, V.1
  • 91
    • 79960288575 scopus 로고    scopus 로고
    • Design, synthesis and stimuli responsive gelation of novel stigmasterol-amino acid conjugates
    • et al
    • Svobodová, H., et al. (2011) Design, synthesis and stimuli responsive gelation of novel stigmasterol-amino acid conjugates. J. Colloid Interface Sci. 361(2):587-593.et al
    • (2011) J. Colloid Interface Sci. , vol.361 , Issue.2 , pp. 587-593
    • Svobodová, H.1
  • 92
    • 79954458005 scopus 로고    scopus 로고
    • Synthesis and gelation behaviors of five new dimeric cholesteryl derivatives
    • Liu, K., et al. (2011) Synthesis and gelation behaviors of five new dimeric cholesteryl derivatives. Sci. China Chem. 54(3):475-482.
    • (2011) Sci. China Chem. , vol.54 , Issue.3 , pp. 475-482
    • Liu, K.1
  • 93
    • 34047145929 scopus 로고    scopus 로고
    • Synthesis and gelation behavior of cholesteryl glycinate anthraquinone-2-carboxylamide and cholesteryl glycinate 9,10-dimethyloxyl anthracene-2-carboxylamide
    • Li, Y.G., et al. (2006) Synthesis and gelation behavior of cholesteryl glycinate anthraquinone-2-carboxylamide and cholesteryl glycinate 9,10-dimethyloxyl anthracene-2-carboxylamide. J. Chin. Chem. Soc. 53(2):359-366.
    • (2006) J. Chin. Chem. Soc , vol.53 , Issue.2 , pp. 359-366
    • Li, Y.G.1
  • 94
    • 70349108847 scopus 로고    scopus 로고
    • Role of capping ligands on the nanoparticles in the modulation of properties of a hybrid matrix of nanoparticles in a 2D film and in a supramolecular organogel
    • Pal, A., Srivastava, A., and Bhattacharya, S. (2009) Role of capping ligands on the nanoparticles in the modulation of properties of a hybrid matrix of nanoparticles in a 2D film and in a supramolecular organogel. Chem.-Eur. J. 15(36):9169-9182.
    • (2009) Chem.-Eur. J , vol.15 , Issue.36 , pp. 9169-9182
    • Pal, A.1    Srivastava, A.2    Bhattacharya, S.3
  • 95
    • 0033531638 scopus 로고    scopus 로고
    • First donor-acceptor interaction promoted gelation of organic fluids
    • Maitra, U., et al. (1999) First donor-acceptor interaction promoted gelation of organic fluids. Chem. Comm. 1999(7):595-596.
    • (1999) Chem. Comm , vol.1999 , Issue.7 , pp. 595-596
    • Maitra, U.1
  • 96
    • 35348853418 scopus 로고    scopus 로고
    • Simple esters of cholic acid as potent organogelators: Direct imaging of the collapse of SAFINs
    • Nonappa, and Maitra, U. Simple esters of cholic acid as potent organogelators: direct imaging of the collapse of SAFINs. Soft Matter 3(11):1428-1433.
    • Soft Matter , vol.3 , Issue.11 , pp. 1428-1433
    • Nonappa1    Maitra, U.2
  • 97
    • 74049157759 scopus 로고    scopus 로고
    • Novel deoxycholic acid alkylamide-phenylurea-derived organogelators
    • Koivukorpi, J., and Kolehmainen, E. (2010) Novel deoxycholic acid alkylamide-phenylurea-derived organogelators. Tetrahedron Lett. 51(8):1199-1201.
    • (2010) Tetrahedron Lett. , vol.51 , Issue.8 , pp. 1199-1201
    • Koivukorpi, J.1    Kolehmainen, E.2
  • 98
    • 0037126107 scopus 로고    scopus 로고
    • Alkyl derivatives of cholic acid as organogelators: One-component and two-component gels†
    • Willemen, H.M., et al. (2002) Alkyl derivatives of cholic acid as organogelators: One-component and two-component gels†. Langmuir 18(19):7102-7106.
    • (2002) Langmuir , vol.18 , Issue.19 , pp. 7102-7106
    • Willemen, H.M.1
  • 99
    • 79851509887 scopus 로고    scopus 로고
    • Structuring in [beta]-sitosterol + [gamma]-oryzanol-based emulsion gels during various stages of a temperature cycle
    • Bot, A., et al. (2011) Structuring in [beta]-sitosterol + [gamma]-oryzanol-based emulsion gels during various stages of a temperature cycle. Food Hydrocolloid 25(4):639-646.
    • (2011) Food Hydrocolloid , vol.25 , Issue.4 , pp. 639-646
    • Bot, A.1
  • 100
    • 33745934852 scopus 로고    scopus 로고
    • Structuring of edible oils by mixtures of γ-oryzanol with ß-sitosterol or related phytosterols
    • Bot, A., and Agterof, W. (2006) Structuring of edible oils by mixtures of γ-oryzanol with ß-sitosterol or related phytosterols. J. Am. Oil Chem. Soc. 83(6):513-521.
    • (2006) J. Am. Oil Chem. Soc , vol.83 , Issue.6 , pp. 513-521
    • Bot, A.1    Agterof, W.2
  • 101
    • 70450257684 scopus 로고    scopus 로고
    • Effect of sterol type on structure of tubules in sterol + γ-oryzanol-based organogels
    • Bot, A., et al. (2009) Effect of Sterol Type on Structure of Tubules in Sterol + γ-Oryzanol-Based Organogels. Food Biophys. 4(4):266-272.
    • (2009) Food Biophys , vol.4 , Issue.4 , pp. 266-272
    • Bot, A.1
  • 102
    • 78651082562 scopus 로고    scopus 로고
    • Effect of water on self-assembled tubules in ß-sitosterol + γ-oryzanol-based organogels
    • Ruud den, A., and et al. (2010) Effect of water on self-assembled tubules in ß-sitosterol + γ-oryzanol-based organogels. J. Physics: Confer. Ser. 247(1):012025.
    • (2010) J. Physics: Confer. Ser. , vol.247 , Issue.1 , pp. 012025
    • Ruud Den, A.1
  • 103
    • 67349140897 scopus 로고    scopus 로고
    • Novel structuring strategies for unsaturated fats - Meeting the zero-trans, zero-saturated fat challenge: A review
    • Rogers, M.A. (2009) Novel structuring strategies for unsaturated fats - Meeting the zero-trans, zero-saturated fat challenge: A review. Food Res. Int. 42(7):747-753.
    • (2009) Food Res. Int , vol.42 , Issue.7 , pp. 747-753
    • Rogers, M.A.1
  • 105
    • 79955537181 scopus 로고    scopus 로고
    • Amino acids as rawmaterial for biocompatible surfactants
    • Pinazo, A., et al. (2011) Amino acids as rawmaterial for biocompatible surfactants. Indust. Eng. Chem. Res. 50(9):4805-4817.
    • (2011) Indust. Eng. Chem. Res. , vol.50 , Issue.9 , pp. 4805-4817
    • Pinazo, A.1
  • 106
    • 74249111179 scopus 로고    scopus 로고
    • Two-component organogelators based on two l-amino acids: Effect of combination of l-lysine with various l-amino acids on organogelation behavior†
    • Suzuki, M., Saito, H., and Hanabusa, K. (2009) Two-component organogelators based on two l-amino acids: Effect of combination of l-lysine with various l-amino acids on organogelation behavior†. Langmuir 25(15):8579-8585.
    • (2009) Langmuir , vol.25 , Issue.15 , pp. 8579-8585
    • Suzuki, M.1    Saito, H.2    Hanabusa, K.3
  • 107
    • 85055290836 scopus 로고    scopus 로고
    • Lysine-based surfactants
    • Pons, R., et al. (2010) Lysine-based surfactants. Colloid Biotechnol. 152:125-138.
    • (2010) Colloid Biotechnol. , vol.152 , pp. 125-138
    • Pons, R.1
  • 108
    • 47049126859 scopus 로고    scopus 로고
    • Stable organogels derived from triazines functionalized with chiral a-amino acid derivatives
    • Maffezzoni, R., and Zanda, M. (2008) Stable organogels derived from triazines functionalized with chiral a-amino acid derivatives. Tetrahedron Lett. 49(35):5129-5132.
    • (2008) Tetrahedron Lett , vol.49 , Issue.35 , pp. 5129-5132
    • Maffezzoni, R.1    Zanda, M.2
  • 109
    • 0031270032 scopus 로고    scopus 로고
    • Excellent gelators for organic fluids: Simple bolaform amides derived from amino acids
    • Hanabusa, K., et al. (1997) Excellent gelators for organic fluids: Simple bolaform amides derived from amino acids. Adv. Mater. 9(14):1095-1097.
    • (1997) Adv. Mater , vol.9 , Issue.14 , pp. 1095-1097
    • Hanabusa, K.1
  • 110
    • 18744389779 scopus 로고    scopus 로고
    • Novel low-molecular-weight gelators based on azobenzene containing L-amino acids
    • Inoue, D., et al. (2005) Novel low-molecular-weight gelators based on azobenzene containing L-amino acids. Bull. Chem. Soc. Jap. 78(4):721-726.
    • (2005) Bull. Chem. Soc. Jap , vol.78 , Issue.4 , pp. 721-726
    • Inoue, D.1
  • 111
    • 0001754299 scopus 로고    scopus 로고
    • Easy preparation and useful character of organogel electrolytes based on low molecular weight gelator
    • Hanabusa, K., et al. (1999) Easy preparation and useful character of organogel electrolytes based on low molecular weight gelator. Chem. Mater. 11(3):649-655.
    • (1999) Chem. Mater , vol.11 , Issue.3 , pp. 649-655
    • Hanabusa, K.1
  • 112
    • 28144443018 scopus 로고    scopus 로고
    • Novel dumbbell-form low-molecular-weight gelators based on L-lysine: Their hydrogelation and organogelation properties
    • Suzuki, M., et al. (2005) Novel dumbbell-form low-molecular-weight gelators based on L-lysine: Their hydrogelation and organogelation properties. New J. Chem. 29(11):1439-1444.
    • (2005) New J. Chem , vol.29 , Issue.11 , pp. 1439-1444
    • Suzuki, M.1
  • 113
    • 1542511354 scopus 로고    scopus 로고
    • In situ-forming pharmaceutical organogels based on the self-assembly of L-alanine derivatives
    • Couffin-Hoarau, A.-C., et al. (2004) In situ-forming pharmaceutical organogels based on the self-assembly of L-alanine derivatives. Pharm. Res. 21(3):454-457.
    • (2004) Pharm. Res , vol.21 , Issue.3 , pp. 454-457
    • Couffin-Hoarau, A.-C.1
  • 114
    • 34250612645 scopus 로고    scopus 로고
    • Molecular mechanism of physical gelation of hydrocarbons by fatty acid amides of natural amino acids
    • Pal, A., Ghosh, Y.K., and Bhattacharya, S. (2007) Molecular mechanism of physical gelation of hydrocarbons by fatty acid amides of natural amino acids. Tetrahedron 63(31):7334-7348.
    • (2007) Tetrahedron , vol.63 , Issue.31 , pp. 7334-7348
    • Pal, A.1    Ghosh, Y.K.2    Bhattacharya, S.3
  • 115
    • 15944419195 scopus 로고    scopus 로고
    • New low-molecular weight gelators based on l-valine and l-isoleucine with various terminal groups
    • Suzuki, M., et al. (2005) New low-molecular weight gelators based on l-valine and l-isoleucine with various terminal groups. Tetrahedron Lett. 46(16):2741-2745.
    • (2005) Tetrahedron Lett , vol.46 , Issue.16 , pp. 2741-2745
    • Suzuki, M.1
  • 116
    • 76049091622 scopus 로고    scopus 로고
    • Birefringent physical gels of N-(4-n-alkyloxybenzoyl)-l-alanine amphiphiles in organic solvents: The role of hydrogen-bonding
    • Patra, T., Pal, A., and Dey, J. (2010) Birefringent physical gels of N-(4-n-alkyloxybenzoyl)-l-alanine amphiphiles in organic solvents: The role of hydrogen-bonding. J. Colloid Interface Sci. 344(1):10-20.
    • (2010) J. Colloid Interface Sci. , vol.344 , Issue.1 , pp. 10-20
    • Patra, T.1    Pal, A.2    Dey, J.3
  • 117
    • 38849145815 scopus 로고    scopus 로고
    • Synthesis, self-assembling properties, and atom transfer radical polymerization of an alkylated l-phenylalanine-derived monomeric organogel from silica: A new approach to prepare packing materials for high-performance liquid chromatography
    • Rahman, M.M., et al. (2008) Synthesis, self-assembling properties, and atom transfer radical polymerization of an alkylated l-phenylalanine-derived monomeric organogel from silica: A new approach to prepare packing materials for high-performance liquid chromatography. Chem.-Eur. J. 14(4):1312-1321.
    • (2008) Chem.-Eur. J , vol.14 , Issue.4 , pp. 1312-1321
    • Rahman, M.M.1
  • 118
    • 0037126096 scopus 로고    scopus 로고
    • Chirality control of self-assembling organogels from a lipophilic l-glutamide derivative with metal chlorides†
    • Ihara, H., et al. (2002) Chirality Control of Self-Assembling Organogels from a Lipophilic l-Glutamide Derivative with Metal Chlorides†. Langmuir 18(19):7120-7123.
    • (2002) Langmuir , vol.18 , Issue.19 , pp. 7120-7123
    • Ihara, H.1
  • 119
    • 78751521978 scopus 로고    scopus 로고
    • Towards racemizable chiral organogelators
    • Lin, J.B., et al. (2010) Towards racemizable chiral organogelators. Beilstein J. Organ. Chem. 6:960.
    • (2010) Beilstein J. Organ. Chem. , vol.6 , pp. 960
    • Lin, J.B.1
  • 120
    • 0036306204 scopus 로고    scopus 로고
    • Metal ion-induced chirality and morphology control of self-assembling organogels from L-glutamic acid-derived lipids
    • Takafuji, M., et al. (2002) Metal ion-induced chirality and morphology control of self-assembling organogels from L-glutamic acid-derived lipids. Chem. Lett. 31(5):548-549.
    • (2002) Chem. Lett , vol.31 , Issue.5 , pp. 548-549
    • Takafuji, M.1
  • 121
    • 45749138027 scopus 로고    scopus 로고
    • Pentapeptide based organogels: The role of adjacently located phenylalanine residues in gel formation
    • Banerjee, A., Palui, G., and Banerjee, A. (2008) Pentapeptide based organogels: the role of adjacently located phenylalanine residues in gel formation. Soft Matter 4(7):1430-1437.
    • (2008) Soft Matter , vol.4 , Issue.7 , pp. 1430-1437
    • Banerjee, A.1    Palui, G.2    Banerjee, A.3
  • 122
    • 80053217126 scopus 로고    scopus 로고
    • Pyrene-containing peptide-based fluorescent organogels: Inclusion of graphene into the organogel
    • n.p
    • Adhikari, B., Nanda, J., and Banerjee, A. (2011) Pyrene-containing peptide-based fluorescent organogels: Inclusion of graphene into the organogel. Chem.-Eur. J. 2011:n.p.
    • (2011) Chem.-Eur. J. , vol.2011
    • Adhikari, B.1    Nanda, J.2    Banerjee, A.3
  • 123
    • 33846363551 scopus 로고    scopus 로고
    • Color-tunable fluorescent organogels: Columnar self-assembly of pyrene-containing oligo(glutamic acid)s†
    • Kamikawa, Y., and Kato, T. (2006) Color-tunable fluorescent organogels: Columnar self-assembly of pyrene-containing oligo(glutamic acid)s†. Langmuir 23(1):274-278.
    • (2006) Langmuir , vol.23 , Issue.1 , pp. 274-278
    • Kamikawa, Y.1    Kato, T.2
  • 124
    • 4344599409 scopus 로고    scopus 로고
    • Two-component dendritic gel: Effect of spacer chain length on the supramolecular chiral assembly
    • Hirst, A.R., et al. (2004) Two-component dendritic gel: Effect of spacer chain length on the supramolecular chiral assembly. Langmuir 20(17):7070-7077.
    • (2004) Langmuir , vol.20 , Issue.17 , pp. 7070-7077
    • Hirst, A.R.1
  • 125
    • 36348956841 scopus 로고    scopus 로고
    • Organogelators from self-assembling peptide based dendrimers: Structural and morphological features
    • Palui, G., et al. (2008) Organogelators from self-assembling peptide based dendrimers: structural and morphological features. Tetrahedron 64(1):175-185.
    • (2008) Tetrahedron , vol.64 , Issue.1 , pp. 175-185
    • Palui, G.1
  • 126
    • 34547129103 scopus 로고    scopus 로고
    • Glycine and l-glutamic acid-based dendritic gelators
    • Li, W.-S., et al. (2007) Glycine and l-glutamic acid-based dendritic gelators. Tetrahedron 63(36):8794-8800.
    • (2007) Tetrahedron , vol.63 , Issue.36 , pp. 8794-8800
    • Li, W.-S.1
  • 127
    • 47749113713 scopus 로고    scopus 로고
    • Self-assembly of amino-acid-based dendrons: Organogels and lyotropic and thermotropic liquid crystals
    • Kuang, G.-C., et al. (2008) Self-assembly of amino-acid-based dendrons: Organogels and lyotropic and thermotropic liquid crystals. Chem. Mater. 20(13):4173-4175.
    • (2008) Chem. Mater , vol.20 , Issue.13 , pp. 4173-4175
    • Kuang, G.-C.1
  • 128
    • 30344483618 scopus 로고    scopus 로고
    • Architecture of a biocompatible supramolecular material by supersaturation-driven fabrication of its fiber network
    • Li, J.-L., et al. (2005) Architecture of a biocompatible supramolecular material by supersaturation-driven fabrication of its fiber network. J. Phys. Chem. B 109(51):24231-24235.
    • (2005) J. Phys. Chem. B , vol.109 , Issue.51 , pp. 24231-24235
    • Li, J.-L.1
  • 129
    • 34548625325 scopus 로고    scopus 로고
    • Structuring of edible oils by alternatives to crystalline fat
    • Pernetti, M., et al. (2007) Structuring of edible oils by alternatives to crystalline fat. Curr. Opin. Colloid Interface Sci. 12(4-5):221-231.
    • (2007) Curr. Opin. Colloid Interface Sci , vol.12 , Issue.4-5 , pp. 221-231
    • Pernetti, M.1
  • 130
    • 1942541468 scopus 로고    scopus 로고
    • Structuring of edible oils by long-chain FA, fatty alcohols, and their mixtures
    • Gandolfo, F., Bot, A., and Flöter, E. (2004) Structuring of edible oils by long-chain FA, fatty alcohols, and their mixtures. J. Am. Oil Chem. Soc. 81(1):1-6.
    • (2004) J. Am. Oil Chem. Soc , vol.81 , Issue.1 , pp. 1-6
    • Gandolfo, F.1    Bot, A.2    Flöter, E.3
  • 131
    • 0026686254 scopus 로고
    • Chlorophyll a dimer photoreactions in lecithin organogels
    • Agostiano, A., Monica, M.D., and Mallardi, A. (1992) Chlorophyll a dimer photoreactions in lecithin organogels. J. Photochem. Photobiol. B 13(3-4):241-251.
    • (1992) J. Photochem. Photobiol. B , vol.13 , Issue.3-4 , pp. 241-251
    • Agostiano, A.1    Monica, M.D.2    Mallardi, A.3
  • 132
    • 78651485569 scopus 로고    scopus 로고
    • Preparation and evaluation of tubular micelles of pluronic lecithin organogel for transdermal delivery of sumatriptan
    • Agrawal, V., et al. (2010) Preparation and evaluation of tubular micelles of pluronic lecithin organogel for transdermal delivery of sumatriptan. AAPS PharmSciTech 11(4):1718-1725.
    • (2010) AAPS PharmSciTech , vol.11 , Issue.4 , pp. 1718-1725
    • Agrawal, V.1
  • 133
    • 67749092910 scopus 로고    scopus 로고
    • Organogel-based emulsion systems, microstructural features and impact on in vitro digestion
    • Duffy, N., et al. (2009) Organogel-based emulsion systems, microstructural features and impact on in vitro digestion. J. Am. Oil Chem. Soc. 86(8):733-741.
    • (2009) J. Am. Oil Chem. Soc , vol.86 , Issue.8 , pp. 733-741
    • Duffy, N.1
  • 134
    • 0030607105 scopus 로고    scopus 로고
    • Phase behaviour of lecithin - Water - alcohol - Triacylglycerol mixtures
    • Leser, M.E., van Evert, W.C., and Agterol, W.J.M. (1996) Phase behaviour of lecithin - water - alcohol - triacylglycerol mixtures. Colloid Surface A 116(3):293-308.
    • (1996) Colloid Surface A , vol.116 , Issue.3 , pp. 293-308
    • Leser, M.E.1    Van Evert, W.C.2    Agterol, W.J.M.3
  • 135
    • 18044400211 scopus 로고    scopus 로고
    • Lecithin organogels containing poly(ethylene glycol) monolaurate
    • Khromova, Y.L., Shumilina, E.V., and Shchipunov, Y.A. (2001) Lecithin organogels containing poly(ethylene glycol) monolaurate. Colloid J. 63(2):242-247.
    • (2001) Colloid J , vol.63 , Issue.2 , pp. 242-247
    • Khromova, Y.L.1    Shumilina, E.V.2    Shchipunov, Y.A.3
  • 136
    • 8644234167 scopus 로고    scopus 로고
    • Rheological analysis of the structural properties effecting the percutaneous absorption and stability in pharmaceutical organogels
    • Pénzes, T., Csóka, I., and Erös, I. (2004) Rheological analysis of the structural properties effecting the percutaneous absorption and stability in pharmaceutical organogels. Rheolog. Acta 43(5): 457-463.
    • (2004) Rheolog. Acta , vol.43 , Issue.5 , pp. 457-463
    • Pénzes, T.1    Csóka, I.2    Erös, I.3
  • 137
    • 20644443889 scopus 로고    scopus 로고
    • Topical absorption of piroxicam from organogels-in vitro and in vivo correlations
    • Pénzes, T., et al. (2005) Topical absorption of piroxicam from organogels-in vitro and in vivo correlations. Int. J. Pharm. 298(1):47-54.
    • (2005) Int. J. Pharm , vol.298 , Issue.1 , pp. 47-54
    • Pénzes, T.1
  • 138
    • 58249125095 scopus 로고    scopus 로고
    • Macroscopic properties and microstructure of HSA based organogels: Sensitivity to polar additives
    • Burkhardt, M., Kinzel, S., and Gradzielski, M. (2009) Macroscopic properties and microstructure of HSA based organogels: Sensitivity to polar additives. J. Colloid Interface Sci. 331(2):514-521.
    • (2009) J. Colloid Interface Sci , vol.331 , Issue.2 , pp. 514-521
    • Burkhardt, M.1    Kinzel, S.2    Gradzielski, M.3
  • 139
    • 0033050184 scopus 로고    scopus 로고
    • Water-in-sorbitan monostearate organogels (water-in-oil gels
    • Murdan, S., et al. (1999) Water-in-sorbitan monostearate organogels (water-in-oil gels). J. Pharm. Sci. 88(6):615-619.
    • (1999) J. Pharm. Sci , vol.88 , Issue.6 , pp. 615-619
    • Murdan, S.1
  • 140
    • 0032963524 scopus 로고    scopus 로고
    • Interaction of a nonionic surfactant-based organogel with aqueous media
    • Murdan, S., Gregoriadis, G., and Florence, A.T. (1999) Interaction of a nonionic surfactant-based organogel with aqueous media. Int. J. Pharm. 180(2):211-214.
    • (1999) Int. J. Pharm , vol.180 , Issue.2 , pp. 211-214
    • Murdan, S.1    Gregoriadis, G.2    Florence, A.T.3
  • 141
    • 84866270951 scopus 로고    scopus 로고
    • Gelation of hexadecane with span 60: A potential organogel-based controlled release system
    • Murdan, S., Gregoriadis, G.; and Florence, A.T. (1996) Gelation of hexadecane with span 60: A potential organogel-based controlled release system. Eur. J. Pharm. Sci. 4, Supplement 1(0):S158.
    • (1996) Eur. J. Pharm. Sci. , vol.4 , Issue.SUPPL. 1
    • Murdan, S.1    Gregoriadis, G.2    Florence, A.T.3
  • 142
    • 45749103299 scopus 로고    scopus 로고
    • Engineering the oil binding capacity and crystallinity of self-assembled fibrillar networks of 12-hydroxystearic acid in edible oils
    • Rogers, M.A., Wright, A.J., and Marangoni, A.G. (2008) Engineering the oil binding capacity and crystallinity of self-assembled fibrillar networks of 12-hydroxystearic acid in edible oils. Soft Matter 4:1483-1490.
    • (2008) Soft Matter , vol.4 , pp. 1483-1490
    • Rogers, M.A.1    Wright, A.J.2    Marangoni, A.G.3
  • 143
    • 68149141550 scopus 로고    scopus 로고
    • Robust organogels from nitrogen-containing derivatives of (r)-12-hydroxystearic acid as gelators: Comparisons with gels from stearic acid derivatives†
    • Mallia, V.A., et al. (2009) Robust organogels from nitrogen-containing derivatives of (r)-12-hydroxystearic acid as gelators: Comparisons with gels from stearic acid derivatives†. Langmuir 25(15):8615-8625.
    • (2009) Langmuir , vol.25 , Issue.15 , pp. 8615-8625
    • Mallia, V.A.1
  • 144
    • 34447125714 scopus 로고    scopus 로고
    • Sorbitan ester organogels for transdermal delivery of sumatriptan
    • Upadhyay, K.K., et al. (2007) Sorbitan ester organogels for transdermal delivery of sumatriptan. Drug Dev. Ind. Pharm. 33(6):617-625.
    • (2007) Drug Dev. Ind. Pharm , vol.33 , Issue.6 , pp. 617-625
    • Upadhyay, K.K.1
  • 145
    • 31544457106 scopus 로고    scopus 로고
    • Amphiphilogels as drug carriers: Effects of drug incorporation on the gel and on the active drug
    • Jibry, N., Sarwar, T., and Murdan, S. (2006) Amphiphilogels as drug carriers: effects of drug incorporation on the gel and on the active drug. J. Pharm. Pharmacol. 58(2):187-194.
    • (2006) J. Pharm. Pharmacol , vol.58 , Issue.2 , pp. 187-194
    • Jibry, N.1    Sarwar, T.2    Murdan, S.3
  • 146
    • 6344292470 scopus 로고    scopus 로고
    • Amphiphilogels for drug delivery: Formulation and characterization
    • Jibry, N., Heenan, R.K., and Murdan, S. (2004) Amphiphilogels for drug delivery: Formulation and characterization. Pharm. Res. 21(10):1852-1861.
    • (2004) Pharm. Res , vol.21 , Issue.10 , pp. 1852-1861
    • Jibry, N.1    Heenan, R.K.2    Murdan, S.3
  • 147
    • 0033166266 scopus 로고    scopus 로고
    • Sorbitan monostearate/polysorbate 20 organogels containing niosomes: A delivery vehicle for antigens?
    • Murdan, S., Gregoriadis, G., and Florence, A.T. (1999) Sorbitan monostearate/polysorbate 20 organogels containing niosomes: a delivery vehicle for antigens? Eur. J. Pharm. Sci. 8(3):177-186.
    • (1999) Eur. J. Pharm. Sci , vol.8 , Issue.3 , pp. 177-186
    • Murdan, S.1    Gregoriadis, G.2    Florence, A.T.3
  • 148
    • 35648947918 scopus 로고    scopus 로고
    • Thermal and textural properties of organogels developed by candelilla wax in safflower oil
    • Toro-Vazquez, J., et al. (2007) Thermal and textural properties of organogels developed by candelilla wax in safflower oil. J. Am. Oil Chem. Soc. 84(11):989-1000.
    • (2007) J. Am. Oil Chem. Soc , vol.84 , Issue.11 , pp. 989-1000
    • Toro-Vazquez, J.1
  • 149
    • 67749090784 scopus 로고    scopus 로고
    • Rheological properties of candelilla wax and dotriacontane organogels measured with a true-gap system
    • Morales-Rueda, J.A., et al. (2009) Rheological properties of candelilla wax and dotriacontane organogels measured with a true-gap system. J. Am. Oil Chem. Soc. 86(8):765-772.
    • (2009) J. Am. Oil Chem. Soc , vol.86 , Issue.8 , pp. 765-772
    • Morales-Rueda, J.A.1
  • 150
    • 3242724820 scopus 로고    scopus 로고
    • Anandamide is an endogenous inhibitor for the migration of tumor cells and T lymphocytes
    • Joseph, J., et al. (2004) Anandamide is an endogenous inhibitor for the migration of tumor cells and T lymphocytes. Cancer Immunol. Immunother. 53(8):723-728.
    • (2004) Cancer Immunol. Immunother , vol.53 , Issue.8 , pp. 723-728
    • Joseph, J.1
  • 151
    • 0035211628 scopus 로고    scopus 로고
    • Effect of oleamide on sleep and its relationship to blood pressure, body temperature, and locomotor activity in rats
    • Huitron-Resendiz, S., et al. (2001) Effect of oleamide on sleep and its relationship to blood pressure, body temperature, and locomotor activity in rats. Exper. Neurol. 172(1):235-243.
    • (2001) Exper. Neurol , vol.172 , Issue.1 , pp. 235-243
    • Huitron-Resendiz, S.1
  • 152
    • 77955649293 scopus 로고    scopus 로고
    • Towards a multidisciplinary approach to structuring in reduced saturated fat-based systems - A review
    • Wassell, P., et al. (2010) Towards a multidisciplinary approach to structuring in reduced saturated fat-based systems - a review. Int. J. Food Sci. Technol. 45(4):642-655.
    • (2010) Int. J. Food Sci. Technol. , vol.45 , Issue.4 , pp. 642-655
    • Wassell, P.1
  • 153
    • 33646451957 scopus 로고    scopus 로고
    • Crystal or low molecularmass organogel based on sugar-derived chiral pyrano[2,3-b]naphtho[1,2-e]pyrans
    • Ghosh, R., et al. (2006) Crystal or low molecularmass organogel based on sugar-derived chiral pyrano[2,3-b]naphtho[1,2-e]pyrans. Organ. Lett. 8(6):1061-1064.
    • (2006) Organ. Lett. , vol.8 , Issue.6 , pp. 1061-1064
    • Ghosh, R.1
  • 155
    • 77957751838 scopus 로고    scopus 로고
    • Tailor-made chiral pyranopyrans based on glucose and galactose and studies on self-assembly of some crystals and low molecular weight organogel (LMOG)
    • Roy, S., et al. (2010) Tailor-made chiral pyranopyrans based on glucose and galactose and studies on self-assembly of some crystals and low molecular weight organogel (LMOG). Tetrahedron 66(44):8512-8521.
    • (2010) Tetrahedron , vol.66 , Issue.44 , pp. 8512-8521
    • Roy, S.1
  • 156
    • 0035848884 scopus 로고    scopus 로고
    • Further evidence for the gelation ability-structure correlation in sugar-based gelators
    • Gronwald, O., et al. (2001) Further evidence for the gelation ability-structure correlation in sugar-based gelators. Carbohyd. Res. 331(3):307-318.
    • (2001) Carbohyd. Res , vol.331 , Issue.3 , pp. 307-318
    • Gronwald, O.1
  • 157
    • 78751471581 scopus 로고    scopus 로고
    • Formation and characterization of inclusion complexes of alkyne functionalized poly(e-caprolactone) with ß-cyclodextrin. Pseudo-polyrotaxane-based supramolecular organogels
    • Jazkewitsch, O., and Ritter, H. (2010) Formation and characterization of inclusion complexes of alkyne functionalized poly(e-caprolactone) with ß-cyclodextrin. Pseudo-polyrotaxane-based supramolecular organogels. Macromolecules 44(2):375-382.
    • (2010) Macromolecules , vol.44 , Issue.2 , pp. 375-382
    • Jazkewitsch, O.1    Ritter, H.2
  • 158
    • 78650245443 scopus 로고    scopus 로고
    • Heat-set supramolecular organogels composed of ß-cyclodextrin and substituted aniline in N,N-dimethylformamide
    • Zhao,W., et al. (2011) Heat-set supramolecular organogels composed of ß-cyclodextrin and substituted aniline in N,N-dimethylformamide. Colloid. Surface A 374(1-3):115-120.
    • (2011) Colloid. Surface A , vol.374 , Issue.1-3 , pp. 115-120
    • Zhao, W.1
  • 159
    • 0035932672 scopus 로고    scopus 로고
    • Morphological characteristics of 1,3:2,4-dibenzylidene sorbitol/poly(propylene glycol) organogels
    • Mercurio, D.J., and Spontak, R.J. (2001) Morphological characteristics of 1,3:2,4-dibenzylidene sorbitol/poly(propylene glycol) organogels. J. Phys. Chem. B 105(11):2091-2098.
    • (2001) J. Phys. Chem. B , vol.105 , Issue.11 , pp. 2091-2098
    • Mercurio, D.J.1    Spontak, R.J.2
  • 160
    • 0242321073 scopus 로고    scopus 로고
    • Physical organogels composed of amphiphilic block copolymers and 1,3:2,4-dibenzylidene-D-sorbitol
    • Wilder, E.A., Hall, C.K., and Spontak, R.J. (2003) Physical organogels composed of amphiphilic block copolymers and 1,3:2,4-dibenzylidene-D-sorbitol. J. Colloid Interface Sci. 267(2):509-518.
    • (2003) J. Colloid Interface Sci. , vol.267 , Issue.2 , pp. 509-518
    • Wilder, E.A.1    Hall, C.K.2    Spontak, R.J.3
  • 161
    • 0036274287 scopus 로고    scopus 로고
    • Gelators for organic liquids based on self-assembly: A new facet of supramolecular and combinatorial chemistry
    • Gronwald, O., Snip, E., and Shinkai, S. (2002) Gelators for organic liquids based on self-assembly: a new facet of supramolecular and combinatorial chemistry. Curr. Opin. Colloid Interface Sci. 7(1-2): 148-156.
    • (2002) Curr. Opin. Colloid Interface Sci , vol.7 , Issue.1-2 , pp. 148-156
    • Gronwald, O.1    Snip, E.2    Shinkai, S.3
  • 162
    • 84856911964 scopus 로고    scopus 로고
    • Soft optical devices from self-healing gels formed by oil and sugar-based organogelators
    • 2011
    • Vidyasagar, A., Handore, K., and Sureshan, K.M. (2011) Soft optical devices from self-healing gels formed by oil and sugar-based organogelators. Angew. Chem. 2011. 123(35):8171-8174.
    • (2011) Angew. Chem. , vol.123 , Issue.35 , pp. 8171-8174
    • Vidyasagar, A.1    Handore, K.2    Sureshan, K.M.3
  • 163
    • 0001590801 scopus 로고    scopus 로고
    • Lecithin organogels with n-alkyl-D-glucosides and n-alkly-D- lactobionamide
    • Shchipunov, Y.A., Shumilina, E., and Hoffmann, H. (1998) Lecithin organogels with n-alkyl-D-glucosides and n-alkly-D-lactobionamide. Colloid Polym Sci. 276(4):368-372.
    • (1998) Colloid Polym Sci , vol.276 , Issue.4 , pp. 368-372
    • Shchipunov, Y.A.1    Shumilina, E.2    Hoffmann, H.3
  • 165
    • 2942661346 scopus 로고    scopus 로고
    • Supramolecular assemblies of nucleoside phosphocholine amphiphiles
    • Moreau, L., et al. (2004) Supramolecular assemblies of nucleoside phosphocholine amphiphiles. J. Am. Chem. Soc. 126(24):7533-7539.
    • (2004) J. Am. Chem. Soc , vol.126 , Issue.24 , pp. 7533-7539
    • Moreau, L.1
  • 166
    • 0043023446 scopus 로고    scopus 로고
    • [60]Fullerenemotivated organogel formation in a porphyrin derivative bearing programmed hydrogen-bonding sites
    • Shirakawa, M., Fujita, N., and Shinkai, S. (2003) [60]Fullerenemotivated organogel formation in a porphyrin derivative bearing programmed hydrogen-bonding sites. J. Am. Chem. Soc. 125(33):9902-9903.
    • (2003) J. Am. Chem. Soc. , vol.125 , Issue.33 , pp. 9902-9903
    • Shirakawa, M.1    Fujita, N.2    Shinkai, S.3
  • 168
    • 16244391781 scopus 로고    scopus 로고
    • A stable single piece of unimolecularly p-stacked porphyrin aggregate in a thixotropic low molecular weight gel: A one-dimensional molecular template for polydiacetylene wiring up to several tens of micrometers in length
    • Shirakawa, M., Fujita, N., and Shinkai, S. (2005) A stable single piece of unimolecularly p-stacked porphyrin aggregate in a thixotropic low molecular weight gel: A one-dimensional molecular template for polydiacetylene wiring up to several tens of micrometers in length. J. Am. Chem. Soc. 127(12):4164-4165.
    • (2005) J. Am. Chem. Soc , vol.127 , Issue.12 , pp. 4164-4165
    • Shirakawa, M.1    Fujita, N.2    Shinkai, S.3
  • 169
    • 18244377970 scopus 로고    scopus 로고
    • Gelation of a highly fluorescent ureafunctionalized perylene bisimide dye
    • Würthner, F., et al. (2005) Gelation of a highly fluorescent ureafunctionalized perylene bisimide dye. Organ. Lett. 7(6):967-970.
    • (2005) Organ. Lett , vol.7 , Issue.6 , pp. 967-970
    • Würthner, F.1
  • 170
    • 0037872197 scopus 로고    scopus 로고
    • Hydrogen-bond-assisted control of h versus j aggregation mode of porphyrins stacks in an organogel system
    • Shirakawa, M., et al. (2003) Hydrogen-bond-assisted control of h versus j aggregation mode of porphyrins stacks in an organogel system. J. Organ. Chem. 68(13):5037-5044.
    • (2003) J. Organ. Chem , vol.68 , Issue.13 , pp. 5037-5044
    • Shirakawa, M.1
  • 171
    • 34548782358 scopus 로고    scopus 로고
    • P-Organogels of selfassembled p-phenylenevinylenes: Soft materials with distinct size, shape, and functions
    • Ajayaghosh, A., and Praveen, V.K. (2007) p-Organogels of selfassembled p-phenylenevinylenes: Soft materials with distinct size, shape, and functions. Acct. Chem. Res. 40(8):644-656.
    • (2007) Acct. Chem. Res , vol.40 , Issue.8 , pp. 644-656
    • Ajayaghosh, A.1    Praveen, V.K.2
  • 172
    • 0034600775 scopus 로고    scopus 로고
    • New functional materials based on self assembling organogels: From serendipity towards design
    • van Esch, J.H., and Feringa, B.L. (2000) New functional materials based on self assembling organogels: from serendipity towards design. Angew. Chem. Int. Ed. 39(13):2263-2266.
    • (2000) Angew. Chem. Int. Ed , vol.39 , Issue.13 , pp. 2263-2266
    • Van Esch, J.H.1    Feringa, B.L.2
  • 173
    • 33745637738 scopus 로고    scopus 로고
    • Poly(dimethylsiloxane)-based polymer organogelators with L-lysine derivatives as a organogelation-causing segment
    • Suzuki, M., et al. (2006) Poly(dimethylsiloxane)-based polymer organogelators with L-lysine derivatives as a organogelation-causing segment. J. Polym. Sci. A 44(12):3817-3824.
    • (2006) J. Polym. Sci. A , vol.44 , Issue.12 , pp. 3817-3824
    • Suzuki, M.1
  • 174
    • 38349137695 scopus 로고    scopus 로고
    • Polymer thermoreversible gels from organogelators enabled by [']click' chemistry
    • Díaz, D.D., et al. (2008) Polymer thermoreversible gels from organogelators enabled by [']click' chemistry. Tetrahedron Lett. 49(8):1340-1343.
    • (2008) Tetrahedron Lett , vol.49 , Issue.8 , pp. 1340-1343
    • Díaz, D.D.1
  • 175
    • 35349015189 scopus 로고    scopus 로고
    • Organogelation by polymer organogelators with a l-lysine derivative: Formation of a three-dimensional network consisting of supramolecular and conventional polymers
    • Suzuki, M., et al. (2007) Organogelation by polymer organogelators with a l-lysine derivative: Formation of a three-dimensional network consisting of supramolecular and conventional polymers. Chem.-Eur. J. 13(29):8193-8200.
    • (2007) Chem.-Eur. J , vol.13 , Issue.29 , pp. 8193-8200
    • Suzuki, M.1
  • 176
    • 0025216424 scopus 로고
    • Plastibase: A new base for patch testing of metal antigens
    • Bajaj, A.K., Gupta, S.C., and Chatterjee, A.K. (1990) Plastibase: A new base for patch testing of metal antigens. Int. J. Dermatol. 29(1):73-73.
    • (1990) Int. J. Dermatol , vol.29 , Issue.1 , pp. 73-73
    • Bajaj, A.K.1    Gupta, S.C.2    Chatterjee, A.K.3
  • 177
    • 75749123150 scopus 로고    scopus 로고
    • Polymer organogelators that make supramolecular organogels through physical cross-linking and self-assembly
    • Suzuki, M., and Hanabusa, K. (2010) Polymer organogelators that make supramolecular organogels through physical cross-linking and self-assembly. Chem. Soc. Rev. 13(2):455-463.
    • (2010) Chem. Soc. Rev. , vol.13 , Issue.2 , pp. 455-463
    • Suzuki, M.1    Hanabusa, K.2
  • 178
    • 0032490112 scopus 로고    scopus 로고
    • Dynamics of polar solvation in lecithin/water/cyclohexane reverse micelles
    • Willard, D.M., Riter, R.E., and Levinger, N.E. (1998) Dynamics of polar solvation in lecithin/water/cyclohexane reverse micelles. J. Am. Chem. Soc. 120(17):4151-4160.
    • (1998) J. Am. Chem. Soc , vol.120 , Issue.17 , pp. 4151-4160
    • Willard, D.M.1    Riter, R.E.2    Levinger, N.E.3
  • 179
    • 0025332444 scopus 로고
    • Phospholipid-based reverse micelles
    • Walde, P., et al. (1990) Phospholipid-based reverse micelles. Chem. Physic. Lipid 53(4):265-288.
    • (1990) Chem. Physic. Lipid , vol.53 , Issue.4 , pp. 265-288
    • Walde, P.1
  • 180
    • 27744570717 scopus 로고    scopus 로고
    • Production of soybean phosphatidylcholinechitosan nanovesicles by reverse phase evaporation: A step by step study
    • Mertins, O., et al., Production of soybean phosphatidylcholinechitosan nanovesicles by reverse phase evaporation: a step by step study. Chemistry and Physics of Lipids, 2005. 138(1-2): p. 29-37.
    • (2005) Chemistry and Physics of Lipids , vol.138 , Issue.1-2 , pp. 29-37
    • Mertins, O.1
  • 181
    • 0035202251 scopus 로고    scopus 로고
    • Rheology and structure of worm-like micelles
    • Walker, L.M. (2001) Rheology and structure of worm-like micelles. Curr. Opin. Colloid Interface Sci. 6(5-6):451-456.
    • (2001) Curr. Opin. Colloid Interface Sci , vol.6 , Issue.5-6 , pp. 451-456
    • Walker, L.M.1
  • 182
    • 12144255194 scopus 로고    scopus 로고
    • Biocompatible lecithin organogels: Structure and phase equilibria
    • Angelico, R., et al. (2004) Biocompatible lecithin organogels: Structure and phase equilibria. Langmuir 21(1):140-148.
    • (2004) Langmuir , vol.21 , Issue.1 , pp. 140-148
    • Angelico, R.1
  • 183
    • 26644471536 scopus 로고    scopus 로고
    • Self-organizing structures of lecithin
    • Yurii, A.S. (1997) Self-organizing structures of lecithin. Russ. Chem. Rev. 66(4):301.
    • (1997) Russ. Chem. Rev , vol.66 , Issue.4 , pp. 301
    • Yurii, A.S.1
  • 184
    • 0029390078 scopus 로고
    • Lecithin bridging by hydrogen bonds in the organogel
    • Shchipunov, Y.A., and Shumilina, E.V. (1995) Lecithin bridging by hydrogen bonds in the organogel. Mater. Sci. Eng. C 3(1):43-50.
    • (1995) Mater. Sci. Eng. C , vol.3 , Issue.1 , pp. 43-50
    • Shchipunov, Y.A.1    Shumilina, E.V.2
  • 186
    • 0031146846 scopus 로고    scopus 로고
    • Effect of lecithin on organogel formation of 12-hydroxystearic acid
    • Tamura, T., and Ichikawa, M. (1997) Effect of lecithin on organogel formation of 12-hydroxystearic acid. J. Am. Oil Chem. Soc. 74(5):491-495.
    • (1997) J. Am. Oil Chem. Soc , vol.74 , Issue.5 , pp. 491-495
    • Tamura, T.1    Ichikawa, M.2
  • 187
    • 0028521711 scopus 로고
    • Organogels and aerogels of racemic and chiral 12-hydroxyoctadecanoic acid
    • Terech, P., et al. (1994) Organogels and aerogels of racemic and chiral 12-hydroxyoctadecanoic acid. Langmuir 10(10):3406-3418.
    • (1994) Langmuir , vol.10 , Issue.10 , pp. 3406-3418
    • Terech, P.1
  • 188
    • 57049152906 scopus 로고    scopus 로고
    • Nanostructuring fiber morphology and solvent inclusions in 12-hydroxystearic acid/canola oil organogels
    • Rogers, M.A., Wright, A.J., and Marangoni, A.G. (2009) Nanostructuring fiber morphology and solvent inclusions in 12-hydroxystearic acid/canola oil organogels. Curr. Opin. Colloid Interface Sci. 14(1):33-42.
    • (2009) Curr. Opin. Colloid Interface Sci , vol.14 , Issue.1 , pp. 33-42
    • Rogers, M.A.1    Wright, A.J.2    Marangoni, A.G.3
  • 189
    • 0034188189 scopus 로고    scopus 로고
    • Rheological properties and structural correlations in molecular organogels
    • Terech, P., et al. (2000) Rheological Properties and structural correlations in molecular organogels. Langmuir 16(10):4485-4494.
    • (2000) Langmuir , vol.16 , Issue.10 , pp. 4485-4494
    • Terech, P.1
  • 190
    • 61549095783 scopus 로고    scopus 로고
    • Non-isothermal nucleation and crystallization of 12-hydroxystearic acid in vegetable oils
    • Rogers,M.A., andMarangoni, A.G. (2008) Non-isothermal nucleation and crystallization of 12-hydroxystearic acid in vegetable oils. Cryst. Growth Des. 8(12):4596-4601.
    • (2008) Cryst. Growth des , vol.8 , Issue.12 , pp. 4596-4601
    • Rogers, M.A.1    Marangoni, A.G.2
  • 191
    • 34250765515 scopus 로고    scopus 로고
    • Molecular organogels of the sodium salt of (R)-12-hydroxystearic acid and their templated syntheses of inorganic oxides
    • Huang, X., and Weiss, R.G. (2007) Molecular organogels of the sodium salt of (R)-12-hydroxystearic acid and their templated syntheses of inorganic oxides. Tetrahedron 63(31):7375-7385.
    • (2007) Tetrahedron , vol.63 , Issue.31 , pp. 7375-7385
    • Huang, X.1    Weiss, R.G.2
  • 192
    • 34748826190 scopus 로고    scopus 로고
    • A novel cryo-SEM technique for imaging vegetable oil based organogels
    • Rogers, M., et al. (2007) A novel cryo-SEM technique for imaging vegetable oil based organogels. J. Am. Oil Chem. Soc. 84(10):899-906.
    • (2007) J. Am. Oil Chem. Soc , vol.84 , Issue.10 , pp. 899-906
    • Rogers, M.1
  • 193
    • 23144459616 scopus 로고    scopus 로고
    • Effect of organogel components on in vitro nasal delivery of propranolol hydrochloride
    • Pisal, et al. (2004) Effect of organogel components on in vitro nasal delivery of propranolol hydrochloride. AAPS PharmSciTech 5(4):92-100.
    • (2004) AAPS PharmSciTech , vol.5 , Issue.4 , pp. 92-100
    • Pisal1
  • 194
    • 0033058716 scopus 로고    scopus 로고
    • Inverse toroidal vesicles: Precursors of tubules in sorbitan monostearate organogels
    • Murdan, S., Gregoriadis, G., and Florence, A.T. (1999) Inverse toroidal vesicles: Precursors of tubules in sorbitan monostearate organogels. Int. J. Pharm. 183(1):47-49.
    • (1999) Int. J. Pharm , vol.183 , Issue.1 , pp. 47-49
    • Murdan, S.1    Gregoriadis, G.2    Florence, A.T.3
  • 195
    • 33847016423 scopus 로고    scopus 로고
    • Amphiphilic gels as a potential carrier for topical drug delivery
    • Prasad, V., Kumar, N., and Mishra, P.R. (2007) Amphiphilic gels as a potential carrier for topical drug delivery. Drug Deliv. 14(2):75-85.
    • (2007) Drug Deliv , vol.14 , Issue.2 , pp. 75-85
    • Prasad, V.1    Kumar, N.2    Mishra, P.R.3
  • 196
    • 84881327395 scopus 로고
    • Fluid and solid fibers made of lipid molecular bilayers
    • Fuhrhop, J.H., and Helfrich, W. (1993) Fluid and solid fibers made of lipid molecular bilayers. ChemInform 93(4):1562-1582.
    • (1993) ChemInform , vol.93 , Issue.4 , pp. 1562-1582
    • Fuhrhop, J.H.1    Helfrich, W.2
  • 197
    • 46749110028 scopus 로고    scopus 로고
    • Influence of the gelator structure and solvent on the organisation and chirality of self-assembling fibrillar networks
    • Pham, Q.N., et al. (2008) Influence of the gelator structure and solvent on the organisation and chirality of self-assembling fibrillar networks. New J. Chem. 32(7):1131-1139.
    • (2008) New J. Chem , vol.32 , Issue.7 , pp. 1131-1139
    • Pham, Q.N.1
  • 198
    • 3242683774 scopus 로고    scopus 로고
    • Visible-lightharvesting organogel composed of cholesterol-based perylene derivatives
    • Sugiyasu, K., Fujita, N., and Shinkai, S. (2004) Visible-lightharvesting organogel composed of cholesterol-based perylene derivatives. Angew. Chem. Int. Ed. 43(10):1229-1233.
    • (2004) Angew. Chem. Int. Ed , vol.43 , Issue.10 , pp. 1229-1233
    • Sugiyasu, K.1    Fujita, N.2    Shinkai, S.3
  • 199
    • 1642580683 scopus 로고    scopus 로고
    • Strong fluorescence emission induced by supramolecular assembly and gelation: Luminescent organogel from nonemissive oxadiazole-based benzene-1,3,5-tricarboxamide gelator
    • Ryu, S.Y., et al. (2004) Strong fluorescence emission induced by supramolecular assembly and gelation: luminescent organogel from nonemissive oxadiazole-based benzene-1,3,5-tricarboxamide gelator. Chem. Comm. 2004(1):70-71.
    • (2004) Chem. Comm. , vol.2004 , Issue.1 , pp. 70-71
    • Ryu, S.Y.1
  • 200
    • 4143131026 scopus 로고    scopus 로고
    • Strongly fluorescent organogel system comprising fibrillar self-assembly of a trifluoromethyl-based cyanostilbene derivative
    • An, B.-K., et al. (2004) Strongly fluorescent organogel system comprising fibrillar self-assembly of a trifluoromethyl-based cyanostilbene derivative. J. Am. Chem. Soc. 126(33):10232-10233.
    • (2004) J. Am. Chem. Soc , vol.126 , Issue.33 , pp. 10232-10233
    • An, B.-K.1
  • 201
    • 0001134912 scopus 로고
    • Thermal and light control of the sol-gel phase transition in cholesterol-based organic gels. Novel helical aggregation modes as detected by circular dichroism and electron microscopic observation
    • Murata, K., et al. (1994) Thermal and light control of the sol-gel phase transition in cholesterol-based organic gels. Novel helical aggregation modes as detected by circular dichroism and electron microscopic observation. J. Am. Chem. Soc. 116(15):6664-6676.
    • (1994) J. Am. Chem. Soc , vol.116 , Issue.15 , pp. 6664-6676
    • Murata, K.1
  • 202
    • 33748323086 scopus 로고    scopus 로고
    • Structural variations in a family of orthodialkoxyarenes organogelators
    • Terech, P., et al. (2006) Structural variations in a family of orthodialkoxyarenes organogelators. J. Colloid Interface Sci. 302(2): 633-642.
    • (2006) J. Colloid Interface Sci , vol.302 , Issue.2 , pp. 633-642
    • Terech, P.1
  • 203
    • 0037126095 scopus 로고    scopus 로고
    • Flow-Induced alignment of fiberlike supramolecular self-assemblies during organogel formation with various low molecular mass organogelator-solvent systems†
    • Lescanne, M., et al. (2002) Flow-Induced alignment of fiberlike supramolecular self-assemblies during organogel formation with various low molecular mass organogelator-solvent systems†. Langmuir 18(19):7151-7153.
    • (2002) Langmuir , vol.18 , Issue.19 , pp. 7151-7153
    • Lescanne, M.1
  • 204
    • 0031633738 scopus 로고    scopus 로고
    • A dynamic study of onion phases under shear flow: Size changes
    • Panizza, P., et al. (1998) A dynamic study of onion phases under shear flow: size changes. Eur. Physical J. B 4(1):65-74.
    • (1998) Eur. Physical J. B , vol.4 , Issue.1 , pp. 65-74
    • Panizza, P.1
  • 205
    • 0000497342 scopus 로고    scopus 로고
    • Influence of shear on lyotropic lamellar phases with different membrane defects
    • Zipfel, J., et al. (1999) Influence of shear on lyotropic lamellar phases with different membrane defects. J. Phys. Chem. B 103(15):2841-2849.
    • (1999) J. Phys. Chem. B , vol.103 , Issue.15 , pp. 2841-2849
    • Zipfel, J.1
  • 206
    • 1642616996 scopus 로고    scopus 로고
    • Shear-induced states of orientation of the lamellar phase of C12E4/water
    • Müller, S., et al. (1999) Shear-induced states of orientation of the lamellar phase of C12E4/water. Langmuir 15(22):7558-7564.
    • (1999) Langmuir , vol.15 , Issue.22 , pp. 7558-7564
    • Müller, S.1
  • 207
    • 20544437818 scopus 로고    scopus 로고
    • Effect of an organogelator on the properties of dental composites
    • Wilder, E.A., et al. (2005) Effect of an organogelator on the properties of dental composites. Chem. Mater. 17(11):2946-2952.
    • (2005) Chem. Mater , vol.17 , Issue.11 , pp. 2946-2952
    • Wilder, E.A.1
  • 208
    • 0001145484 scopus 로고    scopus 로고
    • Self-organization of 3,4,5-tris(octyloxy)benzamide in solution and embedding of the aggregates into methacrylate resins
    • Beginn, U., Sheiko, S., and Möller, M. (2000) Self-organization of 3,4,5-tris(octyloxy)benzamide in solution and embedding of the aggregates into methacrylate resins. Macromolecul. Chem. Phys. 201(10):1008-1015.
    • (2000) Macromolecul. Chem. Phys. , vol.201 , Issue.10 , pp. 1008-1015
    • Beginn, U.1    Sheiko, S.2    Möller, M.3
  • 209
    • 0003079980 scopus 로고    scopus 로고
    • Polymerized gels and 'reverse aerogels' from methyl methacrylate or styrene and tetraoctadecylammonium bromide as gelator
    • Gu, W., et al. (1997) Polymerized gels and 'reverse aerogels' from methyl methacrylate or styrene and tetraoctadecylammonium bromide as gelator. Chem. Comm. 1997(6):543-544.
    • (1997) Chem. Comm , vol.1997 , Issue.6 , pp. 543-544
    • Gu, W.1
  • 210
    • 0034272229 scopus 로고    scopus 로고
    • Polymerization of a diacetylene dicholesteryl ester having two urethanes in organic gel states
    • Tamaoki, N., et al. (2000) Polymerization of a diacetylene dicholesteryl ester having two urethanes in organic gel states. Langmuir 16(19):7545-7547.
    • (2000) Langmuir , vol.16 , Issue.19 , pp. 7545-7547
    • Tamaoki, N.1
  • 211
    • 33745442411 scopus 로고    scopus 로고
    • Synthesis and self-assembling properties of diacetylene-containing glycolipids
    • Nie, X., and Wang, G. (2006) Synthesis and self-assembling properties of diacetylene-containing glycolipids. J. Organ. Chem. 71(13):4734-4741.
    • (2006) J. Organ. Chem , vol.71 , Issue.13 , pp. 4734-4741
    • Nie, X.1    Wang, G.2
  • 212
    • 0033279443 scopus 로고    scopus 로고
    • Synthesis and properties of chiral self-assembling lamellar polydiacetylene systems with very-long-range order
    • Wang, G., and Hollingsworth, R.I. (1999) Synthesis and properties of chiral self-assembling lamellar polydiacetylene systems with very-long-range order. Langmuir 15(9):3062-3069.
    • (1999) Langmuir , vol.15 , Issue.9 , pp. 3062-3069
    • Wang, G.1    Hollingsworth, R.I.2
  • 213
    • 0031343505 scopus 로고    scopus 로고
    • Remarkable stabilization of selfassembled organogels by polymerization
    • de Loos, M., et al. (1997) Remarkable stabilization of selfassembled organogels by polymerization. J. Am. Chem. Soc. 119(51):12675-12676.
    • (1997) J. Am. Chem. Soc , vol.119 , Issue.51 , pp. 12675-12676
    • De Loos, M.1
  • 214
    • 52649181581 scopus 로고    scopus 로고
    • Embedding nanofibers in a polymer matrix by polymerization of organogels comprising heterobifunctional organogelators and monomeric solvents
    • Kang, S.H., et al. (2008) Embedding nanofibers in a polymer matrix by polymerization of organogels comprising heterobifunctional organogelators and monomeric solvents. Chem. Mater. 20(17):5532-5540.
    • (2008) Chem. Mater , vol.20 , Issue.17 , pp. 5532-5540
    • Kang, S.H.1
  • 215
    • 0033579611 scopus 로고    scopus 로고
    • Remarkably simple small organogelators: Din-alkoxy-benzene derivatives
    • Clavier, G., et al. (1999) Remarkably simple small organogelators: Din-alkoxy-benzene derivatives. Tetrahedron Lett. 40(51):9021-9024.
    • (1999) Tetrahedron Lett , vol.40 , Issue.51 , pp. 9021-9024
    • Clavier, G.1
  • 216
    • 77955830991 scopus 로고    scopus 로고
    • Spectroscopic, microscopic and first rheological investigations in charge-transfer interaction induced organogels
    • Das, R.K., et al. (2010) Spectroscopic, microscopic and first rheological investigations in charge-transfer interaction induced organogels. J. Mater. Chem. 20(34):7227-7235.
    • (2010) J. Mater. Chem. , vol.20 , Issue.34 , pp. 7227-7235
    • Das, R.K.1
  • 217
    • 2342564469 scopus 로고    scopus 로고
    • Synthesis of dendritic polyaniline nanofibers in a surfactant gel
    • Li, G., and Zhang, Z. (2004) Synthesis of dendritic polyaniline nanofibers in a surfactant gel. Macromolecules 37(8):2683-2685.
    • (2004) Macromolecules , vol.37 , Issue.8 , pp. 2683-2685
    • Li, G.1    Zhang, Z.2
  • 218
    • 10444270956 scopus 로고    scopus 로고
    • Novel CuS nanofibers using organogel as a template: Controlled by binding sites
    • Xue, P., et al. (2004) Novel CuS nanofibers using organogel as a template: Controlled by binding sites. Langmuir 20(25):11234-11239.
    • (2004) Langmuir , vol.20 , Issue.25 , pp. 11234-11239
    • Xue, P.1
  • 219
    • 26444587278 scopus 로고    scopus 로고
    • Use of a self-assembling organogel as a reverse template in the preparation of imprinted porous polymer films
    • Tan, G., et al. (2005) Use of a self-assembling organogel as a reverse template in the preparation of imprinted porous polymer films. Langmuir 21(20):9322-9326.
    • (2005) Langmuir , vol.21 , Issue.20 , pp. 9322-9326
    • Tan, G.1
  • 220
    • 0036117829 scopus 로고    scopus 로고
    • Creation of novel helical ribbon and doublelayered nanotube tio2 structures using an organogel template
    • Jung, J.H., et al. (2002) Creation of novel helical ribbon and doublelayered nanotube tio2 structures using an organogel template. Chem. Mater. 14(4):1445-1447.
    • (2002) Chem. Mater , vol.14 , Issue.4 , pp. 1445-1447
    • Jung, J.H.1
  • 221
    • 33845572649 scopus 로고    scopus 로고
    • Template synthesized molecularly imprinted polymer nanotube membranes for chemical separations
    • Wang, H.-J., et al. (2006) Template synthesized molecularly imprinted polymer nanotube membranes for chemical separations. J. Am. Chem. Soc. 128(50):15954-15955.
    • (2006) J. Am. Chem. Soc , vol.128 , Issue.50 , pp. 15954-15955
    • Wang, H.-J.1
  • 222
    • 34247108090 scopus 로고    scopus 로고
    • Formation of helical mesopores in organic polymer matrices
    • Simon, F.-X., et al. (2007) Formation of helical mesopores in organic polymer matrices. J. Am. Chem. Soc. 129(13):3788-3789.
    • (2007) J. Am. Chem. Soc , vol.129 , Issue.13 , pp. 3788-3789
    • Simon, F.-X.1
  • 223
    • 0034709419 scopus 로고    scopus 로고
    • Creation of both right-handed and left-handed silica structures by sol-gel transcription of organogel fibers comprised of chiral diaminocyclohexane derivatives
    • Jung, J.H., et al. (2000) Creation of both right-handed and left-handed silica structures by sol-gel transcription of organogel fibers comprised of chiral diaminocyclohexane derivatives. J. Am. Chem. Soc. 122(20):5008-5009.
    • (2000) J. Am. Chem. Soc , vol.122 , Issue.20 , pp. 5008-5009
    • Jung, J.H.1
  • 224
    • 0000044790 scopus 로고
    • Microemulsions and organogels: Properties and novel applications
    • Rees, G.D., and Robinson, B.H. (1993) Microemulsions and organogels: Properties and novel applications. Adv. Mater. 5(9):608-619.
    • (1993) Adv. Mater , vol.5 , Issue.9 , pp. 608-619
    • Rees, G.D.1    Robinson, B.H.2
  • 225
    • 0000373763 scopus 로고
    • Structure and stability of microemulsionbased organo-gels
    • Atkinson, P.J., et al. (1991) Structure and stability of microemulsionbased organo-gels. J. Chem. Soc. Faraday Trans. 87(20):3389-3397.
    • (1991) J. Chem. Soc. Faraday Trans , vol.87 , Issue.20 , pp. 3389-3397
    • Atkinson, P.J.1
  • 226
    • 0031033717 scopus 로고    scopus 로고
    • Biocatalysis using gelatin microemulsionbased organogels containing immobilized Chromobacterium viscosum lipase
    • Jenta, T.R.J., et al. (1997) Biocatalysis using gelatin microemulsionbased organogels containing immobilized Chromobacterium viscosum lipase. Biotechnol. Bioeng. 53(2):121-131.
    • (1997) Biotechnol. Bioeng , vol.53 , Issue.2 , pp. 121-131
    • Jenta, T.R.J.1
  • 227
    • 0028823532 scopus 로고
    • Preparativescale kinetic resolutions catalysed by microbial lipases immobilised in AOT-stabilized microemulsion-based organogels: Cryoenzymology as a tool for improving enantioselectivity
    • Rees, G.D., Robinson, B.H., and Stephenson, G.R. (1995) Preparativescale kinetic resolutions catalysed by microbial lipases immobilised in AOT-stabilized microemulsion-based organogels: cryoenzymology as a tool for improving enantioselectivity. Biochim. Biophys. Acta 1259(1):73-81.
    • (1995) Biochim. Biophys. Acta , vol.1259 , Issue.1 , pp. 73-81
    • Rees, G.D.1    Robinson, B.H.2    Stephenson, G.R.3
  • 228
    • 0442279173 scopus 로고    scopus 로고
    • Rhizopus delemar lipase in microemulsion-based organogels: Reactivity and rate-limiting study
    • Nagayama, K., et al. (2003) Rhizopus delemar lipase in microemulsion-based organogels: Reactivity and rate-limiting study. Biocatal. Biotransform. 21(6):321-324.
    • (2003) Biocatal. Biotransform , vol.21 , Issue.6 , pp. 321-324
    • Nagayama, K.1
  • 229
    • 37449013321 scopus 로고    scopus 로고
    • Candida rugosa lipase immobilized in Triton-X100 microemulsion based organogels (MBGs) for ester synthesis
    • Dave, R., and Madamwar, D. (2008) Candida rugosa lipase immobilized in Triton-X100 microemulsion based organogels (MBGs) for ester synthesis. Proc. Biochem. 43(1):70-75.
    • (2008) Proc. Biochem , vol.43 , Issue.1 , pp. 70-75
    • Dave, R.1    Madamwar, D.2
  • 230
    • 20144369211 scopus 로고    scopus 로고
    • Enhanced activity of Mucor javanicus lipase in polyoxyethylene sorbitan trioleate containing microemulsion-based organogels
    • Nagayama, K., and Imai, M. (2005) Enhanced activity of Mucor javanicus lipase in polyoxyethylene sorbitan trioleate containing microemulsion-based organogels. J. Molecul. Catal. B 34(1-6):44-50.
    • (2005) J. Molecul. Catal. B , vol.34 , Issue.1-6 , pp. 44-50
    • Nagayama, K.1    Imai, M.2
  • 231
    • 0036883486 scopus 로고    scopus 로고
    • Fatty acid esterification catalyzed by Candida rugosa lipase in lecithin microemulsion-based organogels
    • Nagayama, K., Yamasaki, N., and Imai, M. (2002) Fatty acid esterification catalyzed by Candida rugosa lipase in lecithin microemulsion-based organogels. Biochem. Eng. J. 12(3):231-236.
    • (2002) Biochem. Eng. J , vol.12 , Issue.3 , pp. 231-236
    • Nagayama, K.1    Yamasaki, N.2    Imai, M.3
  • 232
    • 27444442189 scopus 로고    scopus 로고
    • Biocatalysis using lipase encapsulated in microemulsion-based organogels in supercritical carbon dioxide
    • Blattner, C., et al. (2006) Biocatalysis using lipase encapsulated in microemulsion-based organogels in supercritical carbon dioxide. J. Supercrit. Fluid. 36(3):182-193.
    • (2006) J. Supercrit. Fluid , vol.36 , Issue.3 , pp. 182-193
    • Blattner, C.1
  • 233
    • 0025753453 scopus 로고
    • Reverse enzyme synthesis in microemulsionbased organo-gels
    • Rees, G.D., et al. (1991) Reverse enzyme synthesis in microemulsionbased organo-gels. Biochim. Biophys. Acta 1073(3):493-501.
    • (1991) Biochim. Biophys. Acta , vol.1073 , Issue.3 , pp. 493-501
    • Rees, G.D.1
  • 234
    • 0036788038 scopus 로고    scopus 로고
    • Activity and stability studies of mucor miehei lipase immobilized in novel microemulsion-based organogels
    • Delimitsou, C., et al. (2002) Activity and stability studies of mucor miehei lipase immobilized in novel microemulsion-based organogels. Biocatal. Biotransform. 20(5):319-327.
    • (2002) Biocatal. Biotransform , vol.20 , Issue.5 , pp. 319-327
    • Delimitsou, C.1
  • 235
    • 0033515889 scopus 로고    scopus 로고
    • Biocatalysis using microemulsion-based polymer gels containing lipase
    • Stamatis, H., and Xenakis, A. (1999) Biocatalysis using microemulsion-based polymer gels containing lipase. J. Molecul. Catal. B 6(4):399-406.
    • (1999) J. Molecul. Catal. B , vol.6 , Issue.4 , pp. 399-406
    • Stamatis, H.1    Xenakis, A.2
  • 236
    • 0034435069 scopus 로고    scopus 로고
    • Microemulsion-based organogels containing lipase: Application in the synthesis of esters
    • Pastou, A., Stamatis, H., and Xenakis, A. (2000) Microemulsion-based organogels containing lipase: application in the synthesis of esters. Trends Colloid Interface Sci. XIV 115:192-195.
    • (2000) Trends Colloid Interface Sci. XIV , vol.115 , pp. 192-195
    • Pastou, A.1    Stamatis, H.2    Xenakis, A.3
  • 237
    • 3242883328 scopus 로고    scopus 로고
    • Lipase factor (LF) as a characterization parameter to explain the catalytic activity of crude lipases from Candida rugosa, free or immobilized in microemulsion-based organogels
    • de María, P.D.N., et al. (2004) Lipase factor (LF) as a characterization parameter to explain the catalytic activity of crude lipases from Candida rugosa, free or immobilized in microemulsion-based organogels. Enzyme Microb. Tech. 35(4):277-283.
    • (2004) Enzyme Microb. Tech , vol.35 , Issue.4 , pp. 277-283
    • De María, P.D.N.1
  • 238
    • 0028559002 scopus 로고
    • Enantioselective esterification of 2-methylbutyric acid catalyzed via lipase immobilized in microemulsion-based organogels
    • Uemasu, I., and Hinze, W.L. (1994) Enantioselective esterification of 2-methylbutyric acid catalyzed via lipase immobilized in microemulsion-based organogels. Chirality 6(8):649-653.
    • (1994) Chirality , vol.6 , Issue.8 , pp. 649-653
    • Uemasu, I.1    Hinze, W.L.2
  • 239
    • 49749116769 scopus 로고    scopus 로고
    • Esterification reactions catalyzed by lipases immobilized in organogels: Effect of temperature and substrate diffusion
    • Zoumpanioti, M., et al. (2008) Esterification reactions catalyzed by lipases immobilized in organogels: effect of temperature and substrate diffusion. Biotechnol. Lett. 30(9):1627-1631.
    • (2008) Biotechnol. Lett , vol.30 , Issue.9 , pp. 1627-1631
    • Zoumpanioti, M.1
  • 240
    • 0031554438 scopus 로고    scopus 로고
    • Kinetic studies of Chromobacterium viscosum lipase in AOT water in oil microemulsions and gelatin microemulsionbased organogels
    • Jenta, T.R.J., et al. Kinetic studies of Chromobacterium viscosum lipase in AOT water in oil microemulsions and gelatin microemulsionbased organogels. Biotechnol. Bioeng. 54(5):416-427.
    • Biotechnol. Bioeng , vol.54 , Issue.5 , pp. 416-427
    • Jenta, T.R.J.1
  • 241
    • 0026471803 scopus 로고
    • Enzyme-catalyzed esterifications in microemulsion-based organo gels
    • Nascimento, M. d.G., et al. (1992) Enzyme-catalyzed esterifications in microemulsion-based organo gels. Tetrahedron Lett. 33(40):5891-5894.
    • (1992) Tetrahedron Lett , vol.33 , Issue.40 , pp. 5891-5894
    • Nascimento, M.D.G.1
  • 242
    • 28944453689 scopus 로고    scopus 로고
    • The novel hexadecyltrimethylammonium bromide (CTAB) based organogel as reactor for ester synthesis by entrapped Candida rugosa lipase
    • Lopez, F., et al. (2006) The novel hexadecyltrimethylammonium bromide (CTAB) based organogel as reactor for ester synthesis by entrapped Candida rugosa lipase. Proc. Biochem. 41(1): 114-119.
    • (2006) Proc. Biochem , vol.41 , Issue.1 , pp. 114-119
    • Lopez, F.1
  • 243
    • 4344603866 scopus 로고    scopus 로고
    • Entrapment of enzyme in water-restricted microenvironment for enzyme-mediated catalysis under microemulsion-based organogels
    • Madamwar, D., and Thakar, A. (2004) Entrapment of enzyme in water-restricted microenvironment for enzyme-mediated catalysis under microemulsion-based organogels. Appl. Biochem. Biotechnol. 118(1):361-369.
    • (2004) Appl. Biochem. Biotechnol , vol.118 , Issue.1 , pp. 361-369
    • Madamwar, D.1    Thakar, A.2
  • 244
    • 34249331354 scopus 로고    scopus 로고
    • Novel approach for the synthesis of ethyl isovalerate using surfactant coated Candida rugosa lipase immobilized in microemulsion based organogels
    • Dandavate, V., and Madamwar, D. (2007) Novel approach for the synthesis of ethyl isovalerate using surfactant coated Candida rugosa lipase immobilized in microemulsion based organogels. Enzyme Microb. Technol. 41(3):265-270.
    • (2007) Enzyme Microb. Technol , vol.41 , Issue.3 , pp. 265-270
    • Dandavate, V.1    Madamwar, D.2
  • 245
    • 33646524708 scopus 로고    scopus 로고
    • Rheological properties and microstructures of gelatin-containing microemulsion-based organogels
    • Zhao, X.Y., et al. (2006) Rheological properties and microstructures of gelatin-containing microemulsion-based organogels. Colloid. Surface A 281(1-3):67-73.
    • (2006) Colloid. Surface A , vol.281 , Issue.1-3 , pp. 67-73
    • Zhao, X.Y.1
  • 246
    • 33749544413 scopus 로고    scopus 로고
    • Topical delivery of aceclofenac from lecithin organogels: Preformulation study
    • Shaikh, I.M., et al. (2006) Topical delivery of aceclofenac from lecithin organogels: preformulation study. Curr. Drug Deliv. 3(4):417-427.
    • (2006) Curr. Drug Deliv , vol.3 , Issue.4 , pp. 417-427
    • Shaikh, I.M.1
  • 247
    • 66749138214 scopus 로고    scopus 로고
    • Formulation and evaluation of lecithin organogel for topical delivery of fluconazole
    • Jadhav, K.R., Kadam, V.J., and Pisal, S.S. (2009) Formulation and evaluation of lecithin organogel for topical delivery of fluconazole. Curr. Drug Deliv. 6(2):174-183.
    • (2009) Curr. Drug Deliv , vol.6 , Issue.2 , pp. 174-183
    • Jadhav, K.R.1    Kadam, V.J.2    Pisal, S.S.3
  • 248
    • 0001229488 scopus 로고    scopus 로고
    • Thermoreversible organogels from alkane gelators with one heteroatom
    • Abdallah, D.J., Lu, L., and Weiss, R.G. (1999) Thermoreversible organogels from alkane gelators with one heteroatom. Chem. Mater. 11(10):2907-2911.
    • (1999) Chem. Mater , vol.11 , Issue.10 , pp. 2907-2911
    • Abdallah, D.J.1    Lu, L.2    Weiss, R.G.3
  • 249
    • 0034378510 scopus 로고    scopus 로고
    • The quest for the simplest possible organogelators and some properties of their organogels
    • Abdallah, D.J., andWeiss, R.G. (2000) The quest for the simplest possible organogelators and some properties of their organogels. J. Brazil. Chem. Soc. 11:209-218.
    • (2000) J. Brazil. Chem. Soc , vol.11 , pp. 209-218
    • Abdallah, D.J.1    Weiss, R.G.2
  • 250
    • 61849096275 scopus 로고    scopus 로고
    • Aceclofenac organogels: In vitro and in vivo characterization
    • Shaikh, I.M., et al. Aceclofenac organogels: In vitro and in vivo characterization. Curr. Drug Deliv. 6:1-7.
    • Curr. Drug Deliv , vol.6 , pp. 1-7
    • Shaikh, I.M.1
  • 251
    • 0029879096 scopus 로고    scopus 로고
    • Non ionic surfactant based organogels incorporating niosomes
    • Murdan, S., Gregoriadis, G., and Florence, A. (1996) Non ionic surfactant based organogels incorporating niosomes. STP Pharm. Sci. 6(1):44-48.
    • (1996) STP Pharm. Sci , vol.6 , Issue.1 , pp. 44-48
    • Murdan, S.1    Gregoriadis, G.2    Florence, A.3
  • 252
    • 34250680948 scopus 로고    scopus 로고
    • Time, temperature, and concentration dependence of ricinelaidic acid-canola oil organogelation
    • Wright, A., and Marangoni, A. (2007) Time, temperature, and concentration dependence of ricinelaidic acid-canola oil organogelation. J. Am. Oil Chem. Soc. 84(1):3-9.
    • (2007) J. Am. Oil Chem. Soc , vol.84 , Issue.1 , pp. 3-9
    • Wright, A.1    Marangoni, A.2
  • 253
    • 33745967248 scopus 로고    scopus 로고
    • Formation, structure, and rheological properties of ricinelaidic acid-vegetable oil organogels
    • Wright, A., and Marangoni, A. (2006) Formation, structure, and rheological properties of ricinelaidic acid-vegetable oil organogels. J. Am. Oil Chem. Soc. 83(6):497-503.
    • (2006) J. Am. Oil Chem. Soc , vol.83 , Issue.6 , pp. 497-503
    • Wright, A.1    Marangoni, A.2
  • 254
    • 55849083089 scopus 로고    scopus 로고
    • Crystalline stability of self-assembled fibrillar networks of 12-hydroxystearic acid in edible oils
    • Rogers, M.A., Wright, A.J., and Marangoni, A.G. (2008) Crystalline stability of self-assembled fibrillar networks of 12-hydroxystearic acid in edible oils. Food Res. Int. 41(10):1026-1034.
    • (2008) Food Res. Int , vol.41 , Issue.10 , pp. 1026-1034
    • Rogers, M.A.1    Wright, A.J.2    Marangoni, A.G.3
  • 255
    • 70049093299 scopus 로고    scopus 로고
    • Potential food applications of edible oil organogels
    • Hughes, N.E., et al. (2009) Potential food applications of edible oil organogels. Trends Food Sci. Technol. 20(10):470-480.
    • (2009) Trends Food Sci. Technol , vol.20 , Issue.10 , pp. 470-480
    • Hughes, N.E.1
  • 256
    • 79960612043 scopus 로고    scopus 로고
    • The effect of shearing in the thermomechanical properties of candelilla wax and candelilla wax-tripalmitin organogels
    • Chopin-Doroteo, M., et al. (2011) The effect of shearing in the thermomechanical properties of candelilla wax and candelilla wax-tripalmitin organogels. Food Biophys. 6(3):359-376.
    • (2011) Food Biophys. , vol.6 , Issue.3 , pp. 359-376
    • Chopin-Doroteo, M.1
  • 257
    • 0034299183 scopus 로고    scopus 로고
    • Hexatriacontane organogels. The first determination of the conformation and molecular packing of a low-molecular-mass organogelator in its gelled state
    • Abdallah, D.J., Sirchio, S.A., and Weiss, R.G. (2000) Hexatriacontane organogels. The first determination of the conformation and molecular packing of a low-molecular-mass organogelator in its gelled state. Langmuir 16(20):7558-7561.
    • (2000) Langmuir , vol.16 , Issue.20 , pp. 7558-7561
    • Abdallah, D.J.1    Sirchio, S.A.2    Weiss, R.G.3
  • 258
    • 77954536068 scopus 로고    scopus 로고
    • Shear nanostructuring of monoglyceride organogels
    • Da Pieve, S., et al. (2010) Shear nanostructuring of monoglyceride organogels. Food Biophys. 5(3):211-217.
    • (2010) Food Biophys , vol.5 , Issue.3 , pp. 211-217
    • Da Pieve, S.1
  • 259
    • 76249093278 scopus 로고    scopus 로고
    • Organogels from different self-assembling new dendritic peptides: Morphology, reheology, and structural investigations
    • Palui, G., et al. (2009) Organogels from different self-assembling new dendritic peptides: morphology, reheology, and structural investigations. J. Phys. Chem. B 114(3):1249-1256.
    • (2009) J. Phys. Chem. B , vol.114 , Issue.3 , pp. 1249-1256
    • Palui, G.1
  • 260
    • 0035279941 scopus 로고    scopus 로고
    • TEM and SEM observations of super-structures constructed in organogel systems from a combination of boronic-acid-appended bola-amphiphiles with chiral diols
    • Kazuya, K. and et al. (2001) TEM and SEM observations of super-structures constructed in organogel systems from a combination of boronic-acid-appended bola-amphiphiles with chiral diols. Nanotechnology 12(1):25.
    • (2001) Nanotechnology , vol.12 , Issue.1 , pp. 25
    • Kazuya, K.1
  • 262
    • 0022082545 scopus 로고
    • Small angle neutron scattering study of steroidal gels
    • Terech, P., Volino, F., and Ramasseul, R. (1985) Small angle neutron scattering study of steroidal gels. J. Phys-Paris 46(6): 895-903.
    • (1985) J. Phys-Paris , vol.46 , Issue.6 , pp. 895-903
    • Terech, P.1    Volino, F.2    Ramasseul, R.3
  • 263
    • 68149117585 scopus 로고    scopus 로고
    • Hybrid thermoreversible gels from covalent polymers and organogels
    • Dasgupta, D., et al. (2009) Hybrid thermoreversible gels from covalent polymers and organogels. Langmuir 25(15):8593-8598.
    • (2009) Langmuir , vol.25 , Issue.15 , pp. 8593-8598
    • Dasgupta, D.1
  • 264
    • 33748453521 scopus 로고    scopus 로고
    • Polymer thermoreversible gels vs organogels
    • Guenet, J.M. (2006) Polymer thermoreversible gels vs organogels. Macromol. Symp. 241(1):45-50.
    • (2006) Macromol. Symp , vol.241 , Issue.1 , pp. 45-50
    • Guenet, J.M.1
  • 265
    • 0028282274 scopus 로고
    • Polymer-like lecithin reverse micelles. 1. A light scattering study
    • Schurtenberger, P., and Cavaco, C. (1994) Polymer-like lecithin reverse micelles. 1. A light scattering study. Langmuir 10(1):100-108.
    • (1994) Langmuir , vol.10 , Issue.1 , pp. 100-108
    • Schurtenberger, P.1    Cavaco, C.2
  • 266
    • 77950791102 scopus 로고    scopus 로고
    • Self-sorting chiral organogels from a long chain carbamate of 1-benzyl-pyrrolidine-3,4-diol
    • Cicchi, S., et al. (2010) Self-sorting chiral organogels from a long chain carbamate of 1-benzyl-pyrrolidine-3,4-diol. Soft Matter 6(8):1655-1661.
    • (2010) Soft Matter , vol.6 , Issue.8 , pp. 1655-1661
    • Cicchi, S.1
  • 267
    • 77957897975 scopus 로고    scopus 로고
    • Supramolecular chirality in organogels: A detailed spectroscopic, morphological, and rheological investigation of gels (and xerogels) derived from alkyl pyrenyl urethanes
    • Das, R.K., et al. (2010) Supramolecular chirality in organogels: A detailed spectroscopic, morphological, and rheological investigation of gels (and xerogels) derived from alkyl pyrenyl urethanes. Langmuir 26(20):16141-16149.
    • (2010) Langmuir , vol.26 , Issue.20 , pp. 16141-16149
    • Das, R.K.1
  • 268
    • 33751156126 scopus 로고
    • Structures of organogels based upon cholesteryl 4-(2-anthryloxy) butanoate, a highly efficient luminescing gelator: Neutron and X-ray small-angle scattering investigations
    • Terech, P., Furman, I., andWeiss, R.G. (1995) Structures of organogels based upon cholesteryl 4-(2-anthryloxy)butanoate, a highly efficient luminescing gelator: Neutron and X-ray small-angle scattering investigations. J. Phys. Chem. 99(23):9558-9566.
    • (1995) J. Phys. Chem , vol.99 , Issue.23 , pp. 9558-9566
    • Terech, P.1    Furman, I.2    Weiss, R.G.3
  • 269
    • 0034811666 scopus 로고    scopus 로고
    • Microstructure determination of aot + phenol organogels utilizing small-angle X-ray scattering and atomic force microscopy
    • Simmons, B.A., et al. (2001) Microstructure determination of aot + phenol organogels utilizing small-angle X-ray scattering and atomic force microscopy. J. Am. Chem. Soc. 123(10):2414-2421.
    • (2001) J. Am. Chem. Soc , vol.123 , Issue.10 , pp. 2414-2421
    • Simmons, B.A.1
  • 270
    • 0000850227 scopus 로고    scopus 로고
    • Multinuclear NMR investigation of phosphatidylcholine organogels†
    • Capitani, D., et al. (1996) Multinuclear NMR investigation of phosphatidylcholine organogels†. J. Phys. Chem. 100(37):15211-15217.
    • (1996) J. Phys. Chem , vol.100 , Issue.37 , pp. 15211-15217
    • Capitani, D.1
  • 271
    • 0032781940 scopus 로고    scopus 로고
    • The fluidity of hydrocarbon regions in organogels, studied by NMR: Basic translational and rotational diffusion measurements
    • Hermansson, M. (1999) The fluidity of hydrocarbon regions in organogels, studied by NMR: Basic translational and rotational diffusion measurements. Colloid Surface A 154(3):303-309.
    • (1999) Colloid Surface A , vol.154 , Issue.3 , pp. 303-309
    • Hermansson, M.1
  • 272
    • 0011719744 scopus 로고    scopus 로고
    • A spontaneous phase transition from reverse micelles to organogels due to surfactant interactions with specific benzenediols
    • Tata, M., et al. (1997) A spontaneous phase transition from reverse micelles to organogels due to surfactant interactions with specific benzenediols. J. Molecul. Liquid 72(1-3):121-135.
    • (1997) J. Molecul. Liquid , vol.72 , Issue.1-3 , pp. 121-135
    • Tata, M.1
  • 273
    • 0000417007 scopus 로고
    • Lecithin organogels: Rheological properties of polymer-like micelles formed in the presence of water
    • Shchipunov, Y.A. (1995) Lecithin organogels: rheological properties of polymer-like micelles formed in the presence of water. Colloid J. 57:556-560.
    • (1995) Colloid J , vol.57 , pp. 556-560
    • Shchipunov, Y.A.1
  • 274
    • 79960425314 scopus 로고    scopus 로고
    • Structure and dynamics of hydrogels and organogels: An NMR spectroscopy approach
    • Shapiro, Y.E. (2011) Structure and dynamics of hydrogels and organogels: An NMR spectroscopy approach. Prog. Polym. Sci. 36(9):1184-1253.
    • (2011) Prog. Polym. Sci. , vol.36 , Issue.9 , pp. 1184-1253
    • Shapiro, Y.E.1
  • 276
    • 79958034967 scopus 로고    scopus 로고
    • Rheology of oleogels based on sorbitan and glyceryl monostearates and vegetable oils for lubricating applications
    • Sánchez, R., et al., (2011) Rheology of oleogels based on sorbitan and glyceryl monostearates and vegetable oils for lubricating applications. Grasas y Aceites, 62(3):328-336.
    • (2011) Grasas y Aceites , vol.62 , Issue.3 , pp. 328-336
    • Sánchez, R.1
  • 277
    • 84859580982 scopus 로고    scopus 로고
    • Properties of topically applied organogels: Rheology and in vitro drug release
    • Yang, Y., et al. (2008) Properties of topically applied organogels: Rheology and in vitro drug release. Asian J. Pharm. Sci. 3(4):175-183.
    • (2008) Asian J. Pharm. Sci , vol.3 , Issue.4 , pp. 175-183
    • Yang, Y.1
  • 278
    • 0022694827 scopus 로고
    • Analysis of linear viscoelasticity of a crosslinking polymer at the gel point
    • Winter, H.H., and Chambon, F. (1986) Analysis of linear viscoelasticity of a crosslinking polymer at the gel point. J. Rheol. 30(2):367-382.
    • (1986) J. Rheol , vol.30 , Issue.2 , pp. 367-382
    • Winter, H.H.1    Chambon, F.2
  • 280
    • 0032181870 scopus 로고    scopus 로고
    • Growth, branching, and local ordering of lecithin polymer-like micelles
    • Shchipunov, Y.A., and Hoffmann, H. (1998) Growth, branching, and local ordering of lecithin polymer-like micelles. Langmuir 14(22):6350-6360.
    • (1998) Langmuir , vol.14 , Issue.22 , pp. 6350-6360
    • Shchipunov, Y.A.1    Hoffmann, H.2
  • 281
    • 0033668449 scopus 로고    scopus 로고
    • Thinning and thickening effects induced by shearing in lecithin solutions of polymer-like micelles
    • Shchipunov, Y.A., and Hoffmann, H. (2000) Thinning and thickening effects induced by shearing in lecithin solutions of polymer-like micelles. Rheol. Acta 39(6):542-553.
    • (2000) Rheol. Acta , vol.39 , Issue.6 , pp. 542-553
    • Shchipunov, Y.A.1    Hoffmann, H.2
  • 282
    • 0034499691 scopus 로고    scopus 로고
    • Lecithin organogel as a binary blend of monodisperse polymer-like micelles
    • Mezzasalma, S.A., Koper, G.J.M., and Shchipunov, Y.A. (2000) Lecithin organogel as a binary blend of monodisperse polymer-like micelles. Langmuir 16(26):10564-10565.
    • (2000) Langmuir , vol.16 , Issue.26 , pp. 10564-10565
    • Mezzasalma, S.A.1    Koper, G.J.M.2    Shchipunov, Y.A.3
  • 283
    • 0001148049 scopus 로고
    • Structural and dynamic properties of polymer-like reverse micelles
    • Schurtenberger, P. (1990) Structural and dynamic properties of polymer-like reverse micelles. J. Phys. Chem. 94(9):3695-3701.
    • (1990) J. Phys. Chem , vol.94 , Issue.9 , pp. 3695-3701
    • Schurtenberger, P.1
  • 284
    • 33845279354 scopus 로고
    • Organogels from lecithins
    • Scartazzini, R., and Luisi, P.L. (1988) Organogels from lecithins. J. Phys. Chem. 92:829-833.
    • (1988) J. Phys. Chem , vol.92 , pp. 829-833
    • Scartazzini, R.1    Luisi, P.L.2
  • 285
    • 0033204477 scopus 로고    scopus 로고
    • Indicative evidence for coexistence of long and short polymer-like micelles in lecithin organogel from rheological studies
    • Shchipunov, Y.A., and Hoffmann, H. (1999) Indicative evidence for coexistence of long and short polymer-like micelles in lecithin organogel from rheological studies. Langmuir 15(21): 7108-7110.
    • (1999) Langmuir , vol.15 , Issue.21 , pp. 7108-7110
    • Shchipunov, Y.A.1    Hoffmann, H.2
  • 286
    • 0033102581 scopus 로고    scopus 로고
    • The branching of reversed polymerlike micelles of lecithin by sugar-containing surfactants
    • Shchipunov, Y.A., et al. (1999) The branching of reversed polymerlike micelles of lecithin by sugar-containing surfactants. J. Colloid Interface Sci. 211(1):81-88.
    • (1999) J. Colloid Interface Sci , vol.211 , Issue.1 , pp. 81-88
    • Shchipunov, Y.A.1
  • 288
    • 44449172374 scopus 로고    scopus 로고
    • Physicochemical effects of terpenes on organogel for transdermal drug delivery
    • Lim, P.F.C., et al. (2008) Physicochemical effects of terpenes on organogel for transdermal drug delivery. Int. J. Pharm. 358(1-2):102-107.
    • (2008) Int. J. Pharm , vol.358 , Issue.1-2 , pp. 102-107
    • Lim, P.F.C.1
  • 289
    • 70849118820 scopus 로고    scopus 로고
    • Physical properties of rice bran wax in bulk and organogels
    • Dassanayake, L., et al. (2009) Physical properties of rice bran wax in bulk and organogels. J. Am. Oil Chem. Soc. 86(12):1163-1173.
    • (2009) J. Am. Oil Chem. Soc , vol.86 , Issue.12 , pp. 1163-1173
    • Dassanayake, L.1
  • 290
    • 70350361240 scopus 로고    scopus 로고
    • Host-guest interactions of 5-fluorouracil in supramolecular organogels
    • Wang, H., et al. (2009) Host-guest interactions of 5-fluorouracil in supramolecular organogels. Eur. J. Pharm. Biopharm. 73(3): 357-360.
    • (2009) Eur. J. Pharm. Biopharm , vol.73 , Issue.3 , pp. 357-360
    • Wang, H.1
  • 291
    • 0038335390 scopus 로고    scopus 로고
    • Mechanism of solvent entrapment within organogel structure
    • Markovic, N., Ginic-Markovic, M., and Dutta, N.K. (2003) Mechanism of solvent entrapment within organogel structure. Polym. Int. 52(7):1095-1107.
    • (2003) Polym. Int , vol.52 , Issue.7 , pp. 1095-1107
    • Markovic, N.1    Ginic-Markovic, M.2    Dutta, N.K.3
  • 292
    • 52649128687 scopus 로고    scopus 로고
    • Confinement effects on the self-assembly of 1,3:2,4-di-p- methylbenzylidene sorbitol based organogel
    • Chen, W., et al. (2008) Confinement effects on the self-assembly of 1,3:2,4-di-p-methylbenzylidene sorbitol based organogel. Langmuir 24(18):10432-10436.
    • (2008) Langmuir , vol.24 , Issue.18 , pp. 10432-10436
    • Chen, W.1
  • 294
    • 0027070867 scopus 로고
    • Lecithin organogel as matrix for transdermal transport of drugs
    • Willimann, H., et al. (1992) Lecithin organogel as matrix for transdermal transport of drugs. J. Pharm. Sci. 81(9):871-874.
    • (1992) J. Pharm. Sci , vol.81 , Issue.9 , pp. 871-874
    • Willimann, H.1
  • 295
    • 0031050471 scopus 로고    scopus 로고
    • Interaction of a lecithin microemulsion gel with human stratum corneum and its effect on transdermal transport
    • Dreher, F., et al. (1997) Interaction of a lecithin microemulsion gel with human stratum corneum and its effect on transdermal transport. J. Control. Release 45(2):131-140.
    • (1997) J. Control. Release , vol.45 , Issue.2 , pp. 131-140
    • Dreher, F.1
  • 296
    • 33947643606 scopus 로고    scopus 로고
    • Preparation and characterization of polyvinyl alcohol-gelatin hydrogel membranes for biomedical applications
    • Pal, K., Banthia, A.K., and Majumdar, D.K. (2007) Preparation and characterization of polyvinyl alcohol-gelatin hydrogel membranes for biomedical applications. AAPS PharmSciTech 8(1):142-146.
    • (2007) AAPS PharmSciTech , vol.8 , Issue.1 , pp. 142-146
    • Pal, K.1    Banthia, A.K.2    Majumdar, D.K.3
  • 297
    • 34447515812 scopus 로고    scopus 로고
    • A thermostable and long-term-stable ionicliquid-based gel electrolyte for efficient dye-sensitized solar cells
    • Chen, Z., et al. (2007) A thermostable and long-term-stable ionicliquid-based gel electrolyte for efficient dye-sensitized solar cells. Chem. Phys. Chem. 8(9):1293-1297.
    • (2007) Chem. Phys. Chem , vol.8 , Issue.9 , pp. 1293-1297
    • Chen, Z.1
  • 298
    • 23444460408 scopus 로고    scopus 로고
    • Novel gels and their dispersions-oral drug delivery systems for ciclosporin
    • Murdan, S., Andrýsek, T., and Son, D. (2005) Novel gels and their dispersions-oral drug delivery systems for ciclosporin. Int. J. Pharm. 300(1-2):113-124.
    • (2005) Int. J. Pharm , vol.300 , Issue.1-2 , pp. 113-124
    • Murdan, S.1    Andrýsek, T.2    Son, D.3
  • 299
    • 0034661919 scopus 로고    scopus 로고
    • On the measurement of phase transition temperatures in physical molecular organogels
    • Terech, P., Rossat, C., and Volino, F. (2000) On the measurement of phase transition temperatures in physical molecular organogels. J. Colloid Interface Sci. 227(2):363-370.
    • (2000) J. Colloid Interface Sci , vol.227 , Issue.2 , pp. 363-370
    • Terech, P.1    Rossat, C.2    Volino, F.3
  • 300
    • 77950838096 scopus 로고    scopus 로고
    • Organogels of Lignin-derived stable metabolic intermediate, 2-pyrone-4, 6-dicarboxylic acid (PDC), bearing cholesteryl groups
    • Michinobu, T., et al. (2010) Organogels of Lignin-derived stable metabolic intermediate, 2-pyrone-4, 6-dicarboxylic acid (PDC), bearing cholesteryl groups. Chem. Lett. 39(4):400-401.
    • (2010) Chem. Lett. , vol.39 , Issue.4 , pp. 400-401
    • Michinobu, T.1
  • 301
    • 0034315811 scopus 로고    scopus 로고
    • Rheology and thermotropic properties of Bis-urea-based organogels in various primary alcohols
    • Brinksma, J., et al. (2000) Rheology and thermotropic properties of Bis-urea-based organogels in various primary alcohols. Langmuir 16(24):9249-9255.
    • (2000) Langmuir , vol.16 , Issue.24 , pp. 9249-9255
    • Brinksma, J.1
  • 302
    • 33748453521 scopus 로고    scopus 로고
    • Microfibrillar networks: Polymer thermoreversible gels vs organogels
    • Guenet, J.-M. (2006) Microfibrillar networks: Polymer thermoreversible gels vs organogels. Macromol. Symp. 241(1):45-50.
    • (2006) Macromol. Symp. , vol.241 , Issue.1 , pp. 45-50
    • Guenet, J.-M.1
  • 303
    • 79651468920 scopus 로고    scopus 로고
    • The influence of concentration and temperature on the formation of -oryzanol+ -sitosterol tubules in edible oil organogels
    • Sawalha, H., et al. (2011) The influence of concentration and temperature on the formation of -oryzanol+ -sitosterol tubules in edible oil organogels. Food Biophys. 6(1):1-6.
    • (2011) Food Biophys. , vol.6 , Issue.1 , pp. 1-6
    • Sawalha, H.1
  • 304
    • 41549163918 scopus 로고    scopus 로고
    • Development of pH sensitive polyacrylamide grafted pectin hydrogel for controlled drug delivery system
    • Sutar, P.B., et al. (2008) Development of pH sensitive polyacrylamide grafted pectin hydrogel for controlled drug delivery system. J. Mater. Sci. 19(6):2247-2253.
    • (2008) J. Mater. Sci , vol.19 , Issue.6 , pp. 2247-2253
    • Sutar, P.B.1
  • 305
    • 37249087433 scopus 로고    scopus 로고
    • Development of porous ultra high molecular weight polyethylene scaffolds for the fabrication of orbital implant
    • Pal, K., Bag, S., and Pal, S. (2008) Development of porous ultra high molecular weight polyethylene scaffolds for the fabrication of orbital implant. J. Porous Mater. 15(1):53-59.
    • (2008) J. Porous Mater , vol.15 , Issue.1 , pp. 53-59
    • Pal, K.1    Bag, S.2    Pal, S.3
  • 306
    • 0036812998 scopus 로고    scopus 로고
    • Transdermal delivery of nicardipine: An approach to in vitro permeation enhancement
    • Aboofazeli, R., Zia, H., and Needham, T.E. (2002) Transdermal delivery of nicardipine: An approach to in vitro permeation enhancement. Drug Deliv. 9(4):239-247.
    • (2002) Drug Deliv , vol.9 , Issue.4 , pp. 239-247
    • Aboofazeli, R.1    Zia, H.2    Needham, T.E.3
  • 307
    • 0036851496 scopus 로고    scopus 로고
    • Influence of microemulsions on cutaneous drug delivery
    • Kreilgaard, M. (2002) Influence of microemulsions on cutaneous drug delivery. Adv. Drug Deliv. Rev. 54(Supplement 1):S77-S98.
    • (2002) Adv. Drug Deliv. Rev. , vol.54 , Issue.SUPPL. 1
    • Kreilgaard, M.1
  • 308
    • 27144456260 scopus 로고    scopus 로고
    • Pharmaceutical development and clinical effectiveness of a novel gel technology for transdermal drug delivery
    • Alberti, I., et al. (2005) Pharmaceutical development and clinical effectiveness of a novel gel technology for transdermal drug delivery. Exp. Opin. Drug Deliv. 2(5):935-950.
    • (2005) Exp. Opin. Drug Deliv , vol.2 , Issue.5 , pp. 935-950
    • Alberti, I.1
  • 309
    • 0023103368 scopus 로고
    • Transdermal drug delivery and cutaneous metabolism
    • Guy, R.H., Hadgraft, J., and Bucks, D.A.W. (1987) Transdermal drug delivery and cutaneous metabolism. Xenobiotica 17(3):325-343.
    • (1987) Xenobiotica , vol.17 , Issue.3 , pp. 325-343
    • Guy, R.H.1    Hadgraft, J.2    Bucks, D.A.W.3
  • 310
    • 1642382619 scopus 로고    scopus 로고
    • Preparation and characterization of reverse micelle based organogels of piroxicam
    • Agrawal, G.P., et al. (2004) Preparation and characterization of reverse micelle based organogels of piroxicam. Pharmazie 59(3):191-193.
    • (2004) Pharmazie , vol.59 , Issue.3 , pp. 191-193
    • Agrawal, G.P.1
  • 311
    • 84881353687 scopus 로고    scopus 로고
    • Study and description of hydrogels and organogels as vehicles for cosmetic active ingredients
    • Morales, M.E., et al. (2010) Study and description of hydrogels and organogels as vehicles for cosmetic active ingredients. Int. J. Cosmetic Sci. 32(4):314-314.
    • (2010) Int. J. Cosmetic Sci. , vol.32 , Issue.4 , pp. 314-314
    • Morales, M.E.1
  • 312
    • 0037436962 scopus 로고    scopus 로고
    • In vitro and in vivo evaluations of the efficacy and safety of skin permeation enhancers using flurbiprofen as a model drug
    • Fang, Y., Hwang, T.L., and Fang, C.L (2003) In vitro and in vivo evaluations of the efficacy and safety of skin permeation enhancers using flurbiprofen as a model drug. Int. J. Pharm. 255:153-166.
    • (2003) Int. J. Pharm , vol.255 , pp. 153-166
    • Fang, Y.1    Hwang, T.L.2    Fang, C.L.3
  • 314
    • 33644620075 scopus 로고    scopus 로고
    • Limonene GP1/PG organogel as a vehicle in transdermal delivery of haloperidol
    • Lim, P.F.C., et al. (2006) Limonene GP1/PG organogel as a vehicle in transdermal delivery of haloperidol. Int. J. Pharm. 311(1-2):157-164.
    • (2006) Int. J. Pharm , vol.311 , Issue.1-2 , pp. 157-164
    • Lim, P.F.C.1
  • 315
    • 23744450852 scopus 로고    scopus 로고
    • SMGA gels for the skin permeation of haloperidol
    • Kang, L., et al. (2005) SMGA gels for the skin permeation of haloperidol. J. Control. Release 106(1-2):88-98.
    • (2005) J. Control. Release , vol.106 , Issue.1-2 , pp. 88-98
    • Kang, L.1
  • 317
    • 84878901409 scopus 로고    scopus 로고
    • Invitro release study of sodium salicylate from lecithin based phospholipid microemulsions
    • Aboofazeli, R., Mortazavi, A.S., and Khoshnevis, P. (2003) Invitro release study of sodium salicylate from lecithin based phospholipid microemulsions. Iranian J. Pharm. Res. 2(2):95-101.
    • (2003) Iranian J. Pharm. Res , vol.2 , Issue.2 , pp. 95-101
    • Aboofazeli, R.1    Mortazavi, A.S.2    Khoshnevis, P.3
  • 318
    • 0030596510 scopus 로고    scopus 로고
    • Skin permeation of indomethacin from gel formed by fatty-acid ester and phospholipid
    • Fujii, M., et al. (1996) Skin permeation of indomethacin from gel formed by fatty-acid ester and phospholipid. Int. J. Pharm. 137(1):117-124.
    • (1996) Int. J. Pharm , vol.137 , Issue.1 , pp. 117-124
    • Fujii, M.1
  • 319
    • 0028291096 scopus 로고
    • Organogel-based system for transdermal delivery of propranolol
    • Bhatnagar, S., and Vyas, S.P. (1994) Organogel-based system for transdermal delivery of propranolol. J. Microencapsulat. 11(4):431-438.
    • (1994) J. Microencapsulat , vol.11 , Issue.4 , pp. 431-438
    • Bhatnagar, S.1    Vyas, S.P.2
  • 320
    • 0032783044 scopus 로고    scopus 로고
    • Gelatinstabilized microemulsion-based organogels: Rheology and application in iontophoretic transdermal drug delivery
    • Kantaria, S., Rees, G.D., and Lawrence, M.J. (1999) Gelatinstabilized microemulsion-based organogels: rheology and application in iontophoretic transdermal drug delivery. J. Control. Release 60(2-3):355-365.
    • (1999) J. Control. Release , vol.60 , Issue.2-3 , pp. 355-365
    • Kantaria, S.1    Rees, G.D.2    Lawrence, M.J.3
  • 321
    • 1842869254 scopus 로고    scopus 로고
    • Formulation of electrically conducting microemulsion-based organogels
    • Kantaria, S., Rees, G.D., and Lawrence, M.J. (2003) Formulation of electrically conducting microemulsion-based organogels. Int. J. Pharm. 250(1):65-83.
    • (2003) Int. J. Pharm , vol.250 , Issue.1 , pp. 65-83
    • Kantaria, S.1    Rees, G.D.2    Lawrence, M.J.3
  • 323
    • 70350348905 scopus 로고    scopus 로고
    • Formulation and optimization of microemulsion-based organogels containing propranolol hydrochloride using experimental design methods
    • Hadidi, N., Nazari, N., and Aboofazeli, R. (2009) Formulation and optimization of microemulsion-based organogels containing propranolol hydrochloride using experimental design methods. DARU J. Pharm Sci. 17(3):217-224.
    • (2009) DARU J. Pharm Sci , vol.17 , Issue.3 , pp. 217-224
    • Hadidi, N.1    Nazari, N.2    Aboofazeli, R.3
  • 324
    • 58149252072 scopus 로고    scopus 로고
    • Colloidal soft matter as drug delivery system
    • Bonacucina, G., et al. (2009) Colloidal soft matter as drug delivery system. J. Pharm. Sci. 98(1):1-42.
    • (2009) J. Pharm. Sci , vol.98 , Issue.1 , pp. 1-42
    • Bonacucina, G.1
  • 325
    • 73649084412 scopus 로고    scopus 로고
    • Preparation of thermosensitive polymeric organogels and their drug release behaviors
    • Tokuyama, H., and Kato, Y. (2010) Preparation of thermosensitive polymeric organogels and their drug release behaviors. Eur. Polym. J. 46(2):277-282.
    • (2010) Eur. Polym. J. , vol.46 , Issue.2 , pp. 277-282
    • Tokuyama, H.1    Kato, Y.2
  • 326
    • 35348988755 scopus 로고    scopus 로고
    • An examination of the rheological and mucoadhesive properties of poly(acrylic acid) organogels designed as platforms for local drug delivery to the oral cavity
    • Jones, D.S., et al. (2007) An examination of the rheological and mucoadhesive properties of poly(acrylic acid) organogels designed as platforms for local drug delivery to the oral cavity. J. Pharm. Sci. 96(10):2632-2646.
    • (2007) J. Pharm. Sci , vol.96 , Issue.10 , pp. 2632-2646
    • Jones, D.S.1
  • 327
    • 39749147636 scopus 로고    scopus 로고
    • Physicochemical characterization of bioactive polyacrylic acid organogels as potential antimicrobial implants for the buccal cavity
    • Jones, D.S., et al. (2008) Physicochemical characterization of bioactive polyacrylic acid organogels as potential antimicrobial implants for the buccal cavity. Biomacromolecules 9(2):624-633.
    • (2008) Biomacromolecules , vol.9 , Issue.2 , pp. 624-633
    • Jones, D.S.1
  • 328
    • 76549089037 scopus 로고    scopus 로고
    • Characterization of organogel as a novel oral controlled release formulation for lipophilic compounds
    • Iwanaga, K., et al. (2010) Characterization of organogel as a novel oral controlled release formulation for lipophilic compounds. Int. J. Pharm. 388(1-2):123-128.
    • (2010) Int. J. Pharm. , vol.388 , Issue.1-2 , pp. 123-128
    • Iwanaga, K.1
  • 329
    • 78149371273 scopus 로고    scopus 로고
    • Self-assembled l-alanine derivative organogel as in situ drug delivery implant: Characterization, biodegradability, and biocompatibility
    • Wang, K., et al. (2010) Self-assembled l-alanine derivative organogel as in situ drug delivery implant: characterization, biodegradability, and biocompatibility. Drug Develop. Ind. Pharm. 36(12): 1511-1521.
    • (2010) Drug Develop. Ind. Pharm. , vol.36 , Issue.12 , pp. 1511-1521
    • Wang, K.1
  • 330
    • 33845945920 scopus 로고    scopus 로고
    • Biodegradable injectable in situ depotforming drug delivery systems
    • Chitkara, D., et al. (2006) Biodegradable injectable in situ depotforming drug delivery systems. Macromol. Biosci. 6(12):977-990.
    • (2006) Macromol. Biosci , vol.6 , Issue.12 , pp. 977-990
    • Chitkara, D.1
  • 331
    • 0037161339 scopus 로고    scopus 로고
    • Biodegradable injectable in situ forming drug delivery systems
    • Hatefi, A., and Amsden, B. (2002) Biodegradable injectable in situ forming drug delivery systems. J. Control. Release 80(1-3): 9-28.
    • (2002) J. Control. Release , vol.80 , Issue.1-3 , pp. 9-28
    • Hatefi, A.1    Amsden, B.2
  • 332
    • 0029009390 scopus 로고
    • Controlled release of contraceptive steroids from biodegradable and injectable gel formulations: In vivo evaluation
    • Gao, Z., et al. (1995) Controlled release of contraceptive steroids from biodegradable and injectable gel formulations: In vivo evaluation. Pharm. Res. 12(6):864-868.
    • (1995) Pharm. Res , vol.12 , Issue.6 , pp. 864-868
    • Gao, Z.1
  • 333
    • 0029010726 scopus 로고
    • Controlled release of a contraceptive steroid from biodegradable and injectable gel formulations: In vitro evaluation
    • Gao, Z.H., et al. (1995) Controlled release of a contraceptive steroid from biodegradable and injectable gel formulations: in vitro evaluation. Pharm. Res. 12(6):857-863.
    • (1995) Pharm. Res , vol.12 , Issue.6 , pp. 857-863
    • Gao, Z.H.1
  • 334
    • 67149125598 scopus 로고    scopus 로고
    • Pharmaceutical organogels prepared from aromatic amino acid derivatives
    • Bastiat, G., and Leroux, J.-C. (2009) Pharmaceutical organogels prepared from aromatic amino acid derivatives. J. Mater. Chem. 19(23):3867-3877.
    • (2009) J. Mater. Chem , vol.19 , Issue.23 , pp. 3867-3877
    • Bastiat, G.1    Leroux, J.-C.2
  • 335
    • 0025947549 scopus 로고
    • Preparation and evaluation of eudragit gels. I: Eudragit organogels containing drugs as rectal sustained-release preparations
    • Goto, S., et al. (1991) Preparation and evaluation of eudragit gels. I: Eudragit organogels containing drugs as rectal sustained-release preparations. J. Pharm. Sci. 80(10):958-961.
    • (1991) J. Pharm. Sci. , vol.80 , Issue.10 , pp. 958-961
    • Goto, S.1
  • 336
    • 0026779334 scopus 로고
    • Preparation and evaluation of Eudragit gels. III: Rectal gel preparations for sustained release of pentoxifylline
    • Kim, N.S., et al. (1992) Preparation and evaluation of Eudragit gels. III: Rectal gel preparations for sustained release of pentoxifylline. J. Pharm. Sci. 81(6):537-540.
    • (1992) J. Pharm. Sci , vol.81 , Issue.6 , pp. 537-540
    • Kim, N.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.