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Volumn 17, Issue 11-12, 2012, Pages 608-614

Auto-associative amphiphilic polysaccharides as drug delivery systems

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOSE; CHITOSAN; DEXTRAN; DRUG CARRIER; HEPARIN; HYALURONIC ACID; NANOPARTICLE; POLYSACCHARIDE; PULLULAN;

EID: 84861588489     PISSN: 13596446     EISSN: 18785832     Source Type: Journal    
DOI: 10.1016/j.drudis.2012.01.016     Document Type: Review
Times cited : (97)

References (72)
  • 1
    • 55749108851 scopus 로고    scopus 로고
    • Polysaccharides-based nanoparticles as drug delivery systems
    • Z. Liu Polysaccharides-based nanoparticles as drug delivery systems Adv. Drug Deliv. Rev. 60 2008 1650 1662
    • (2008) Adv. Drug Deliv. Rev. , vol.60 , pp. 1650-1662
    • Liu, Z.1
  • 2
    • 34147178396 scopus 로고    scopus 로고
    • Polysaccharide hydrogels for modified release formulations
    • T. Coviello Polysaccharide hydrogels for modified release formulations J. Control. Release 119 2007 5 24
    • (2007) J. Control. Release , vol.119 , pp. 5-24
    • Coviello, T.1
  • 3
    • 63949086707 scopus 로고    scopus 로고
    • Methods for the preparation and manufacturing of polymeric nanoparticles
    • C. Vauthier, and K. Bouchemal Methods for the preparation and manufacturing of polymeric nanoparticles Pharm. Res. 26 2009 1025 1058
    • (2009) Pharm. Res. , vol.26 , pp. 1025-1058
    • Vauthier, C.1    Bouchemal, K.2
  • 4
    • 16644398458 scopus 로고    scopus 로고
    • Preparation and characterization of N-acetylchitosan, N-propionylchitosan and N-butyrylchitosan microspheres for controlled release of 6-mercaptourine
    • F-L. Mi Preparation and characterization of N-acetylchitosan, N-propionylchitosan and N-butyrylchitosan microspheres for controlled release of 6-mercaptourine Carbohydr. Polym. 60 2005 219 227
    • (2005) Carbohydr. Polym. , vol.60 , pp. 219-227
    • Mi, F.-L.1
  • 5
    • 0034829845 scopus 로고    scopus 로고
    • Controls on polymer molecular weight may be used to control the size of palmitoyl glycol chitosan polymeric vesicles
    • W. Wang Controls on polymer molecular weight may be used to control the size of palmitoyl glycol chitosan polymeric vesicles Langmuir 17 2001 631 636
    • (2001) Langmuir , vol.17 , pp. 631-636
    • Wang, W.1
  • 6
    • 34447337302 scopus 로고    scopus 로고
    • Preparation, characterization and pharmacokinetics of N-palmitoyl chitosan anchoched docetaxel liposomes
    • G. Liang Preparation, characterization and pharmacokinetics of N-palmitoyl chitosan anchoched docetaxel liposomes J. Pharm. Pharmacol. 59 2007 661 667
    • (2007) J. Pharm. Pharmacol. , vol.59 , pp. 661-667
    • Liang, G.1
  • 7
    • 0033635385 scopus 로고    scopus 로고
    • Niosomes and polymeric chitosan based vesicles bearing transferrin and glucose ligands for drug targeting
    • C. Dufes Niosomes and polymeric chitosan based vesicles bearing transferrin and glucose ligands for drug targeting Pharm. Res. 17 2000 1250 1258
    • (2000) Pharm. Res. , vol.17 , pp. 1250-1258
    • Dufes, C.1
  • 8
    • 0346094228 scopus 로고    scopus 로고
    • Structure and interactions in covalently and ionically crosslinked chitosan hydrogels for biomedical applications
    • J. Berger Structure and interactions in covalently and ionically crosslinked chitosan hydrogels for biomedical applications Eur. J. Pharm. Biopharm. 57 2004 19 34
    • (2004) Eur. J. Pharm. Biopharm. , vol.57 , pp. 19-34
    • Berger, J.1
  • 9
    • 0037409924 scopus 로고    scopus 로고
    • Implantable applications of chitin and chitosan
    • E. Khor, and L.Y. Lim Implantable applications of chitin and chitosan Biomaterials 24 2003 2339 2349
    • (2003) Biomaterials , vol.24 , pp. 2339-2349
    • Khor, E.1    Lim, L.Y.2
  • 10
    • 0034672873 scopus 로고    scopus 로고
    • Application of chitosan-based polysaccharide biomaterials in cartilage tissue engineering: A review
    • J.K.F. Suh, and H.W.T. Matthew Application of chitosan-based polysaccharide biomaterials in cartilage tissue engineering: a review Biomaterials 21 2000 2589 2598
    • (2000) Biomaterials , vol.21 , pp. 2589-2598
    • Suh, J.K.F.1    Matthew, H.W.T.2
  • 11
    • 1842484779 scopus 로고    scopus 로고
    • Designing materials for biology and medicine
    • R. Langer, and D.A. Tirrell Designing materials for biology and medicine Nature 428 2004 487 492
    • (2004) Nature , vol.428 , pp. 487-492
    • Langer, R.1    Tirrell, D.A.2
  • 12
    • 55149123559 scopus 로고    scopus 로고
    • Chitosan derivatives obtained by chemical modifications for biomedical and environmental applications
    • N.M. Alvarez, and J.F. Mano Chitosan derivatives obtained by chemical modifications for biomedical and environmental applications Int. J. Biol. Macromol. 43 2008 401 414
    • (2008) Int. J. Biol. Macromol. , vol.43 , pp. 401-414
    • Alvarez, N.M.1    Mano, J.F.2
  • 13
    • 63349092889 scopus 로고    scopus 로고
    • Chitosan: An option for development of essential oil delivery systems for oral cavity care?
    • A.S. Pedro Chitosan: an option for development of essential oil delivery systems for oral cavity care? Carbohydr. Polym. 76 2009 501 508
    • (2009) Carbohydr. Polym. , vol.76 , pp. 501-508
    • Pedro, A.S.1
  • 14
    • 0035849686 scopus 로고    scopus 로고
    • Competitive sorption of platinum and palladium on chitosan derivatives
    • E. Guibal Competitive sorption of platinum and palladium on chitosan derivatives Int. J. Biol. Macromol. 28 2001 401 408
    • (2001) Int. J. Biol. Macromol. , vol.28 , pp. 401-408
    • Guibal, E.1
  • 15
    • 0035121789 scopus 로고    scopus 로고
    • Adsorption of Cu (II) and Cr (VI) ions by chitosan: Kinetics and equilibrium studies
    • R. Schmuhl Adsorption of Cu (II) and Cr (VI) ions by chitosan: kinetics and equilibrium studies Water SA 27 2001 1 7
    • (2001) Water SA , vol.27 , pp. 1-7
    • Schmuhl, R.1
  • 16
    • 0033015577 scopus 로고    scopus 로고
    • Food applications of chitin and chitosans
    • F. Shahidi Food applications of chitin and chitosans Trends Food Sci. Technol. 10 1999 37 51
    • (1999) Trends Food Sci. Technol. , vol.10 , pp. 37-51
    • Shahidi, F.1
  • 17
    • 0009365216 scopus 로고    scopus 로고
    • A review of chitin and chitosan application
    • N.V. Majeti, and R. Kumar A review of chitin and chitosan application React. Funct. Polym. 46 2000 1 27
    • (2000) React. Funct. Polym. , vol.46 , pp. 1-27
    • Majeti, N.V.1    Kumar, R.2
  • 18
    • 0031599367 scopus 로고    scopus 로고
    • Chemistry and application of chitin and chitosan
    • K. Kurita Chemistry and application of chitin and chitosan Polym. Degrad. Stab. 59 1998 117 120
    • (1998) Polym. Degrad. Stab. , vol.59 , pp. 117-120
    • Kurita, K.1
  • 20
    • 48449087776 scopus 로고    scopus 로고
    • Why is chitosan mucoadhesive?
    • I.A. Sogias Why is chitosan mucoadhesive? Biomacromolecules 9 2008 1837 1842
    • (2008) Biomacromolecules , vol.9 , pp. 1837-1842
    • Sogias, I.A.1
  • 21
    • 0025912761 scopus 로고
    • Evaluation of mucoadhesive polymers in ocular drug delivery. I. Viscous solutions
    • N.M. Davies Evaluation of mucoadhesive polymers in ocular drug delivery. I. Viscous solutions Pharm. Res. 8 1991 1039 1043
    • (1991) Pharm. Res. , vol.8 , pp. 1039-1043
    • Davies, N.M.1
  • 22
    • 0345257221 scopus 로고    scopus 로고
    • Chitosan as antimicrobial agent: Applications and mode of action
    • E.I. Rabea Chitosan as antimicrobial agent: applications and mode of action Biomacromolecules 4 2003 1457 1465
    • (2003) Biomacromolecules , vol.4 , pp. 1457-1465
    • Rabea, E.I.1
  • 23
    • 33749470766 scopus 로고    scopus 로고
    • Aggregation of hydrophobically modified chitosan in solution and at the air-water interface
    • Y-Y. Li Aggregation of hydrophobically modified chitosan in solution and at the air-water interface J. Appl. Polym. Sci. 102 2006 1968 1973
    • (2006) J. Appl. Polym. Sci. , vol.102 , pp. 1968-1973
    • Li, Y.-Y.1
  • 24
    • 0242352525 scopus 로고    scopus 로고
    • N-acylated chitosan: Hydrophobic matrices for controlled drug release
    • C. Le Tien N-acylated chitosan: hydrophobic matrices for controlled drug release J. Control. Release 93 2003 1 13
    • (2003) J. Control. Release , vol.93 , pp. 1-13
    • Le Tien, C.1
  • 25
    • 0032509928 scopus 로고    scopus 로고
    • Preparation of chitosan self-aggregates as a gene delivery system
    • K.Y. Lee Preparation of chitosan self-aggregates as a gene delivery system J. Control. Release 51 1998 213 220
    • (1998) J. Control. Release , vol.51 , pp. 213-220
    • Lee, K.Y.1
  • 26
    • 33745346800 scopus 로고    scopus 로고
    • Shell cross-linked stearic acid grafted chitosan oligosaccharide self-aggregated micelles for controlled release of paclitaxel
    • F-Q. Hu Shell cross-linked stearic acid grafted chitosan oligosaccharide self-aggregated micelles for controlled release of paclitaxel Colloid Surf. B 50 2006 97 103
    • (2006) Colloid Surf. B , vol.50 , pp. 97-103
    • Hu, F.-Q.1
  • 27
    • 28444488033 scopus 로고    scopus 로고
    • Self-assembled nanoparticles based on linoleic-acid modified chitosan: Stability and adsorption of trypsin
    • C-G. Liu Self-assembled nanoparticles based on linoleic-acid modified chitosan: stability and adsorption of trypsin Carbohydr. Polym. 62 2005 293 298
    • (2005) Carbohydr. Polym. , vol.62 , pp. 293-298
    • Liu, C.-G.1
  • 28
    • 67449168133 scopus 로고    scopus 로고
    • Preparation, characterization, and antibacterial activity of oleic acid-grafted chitosan oligosaccharide nanoparticles
    • L. Huang Preparation, characterization, and antibacterial activity of oleic acid-grafted chitosan oligosaccharide nanoparticles Front. Biol. China 4 2009 321 327
    • (2009) Front. Biol. China , vol.4 , pp. 321-327
    • Huang, L.1
  • 29
    • 62749167820 scopus 로고    scopus 로고
    • SPION-loaded chitosan-linoleic acid nanoparticles to target hepatocytes
    • C-M. Lee SPION-loaded chitosan-linoleic acid nanoparticles to target hepatocytes Int. J. Pharm. 371 2009 163 169
    • (2009) Int. J. Pharm. , vol.371 , pp. 163-169
    • Lee, C.-M.1
  • 30
    • 0031673162 scopus 로고    scopus 로고
    • Structural determination and interior polarity of self-aggregates prepared from deoxycholic acid-modified chitosan in water
    • K.Y. Lee Structural determination and interior polarity of self-aggregates prepared from deoxycholic acid-modified chitosan in water Macromolecules 31 1998 378 383
    • (1998) Macromolecules , vol.31 , pp. 378-383
    • Lee, K.Y.1
  • 31
    • 0029395304 scopus 로고
    • Blood compatibility and biodegradability of partially N-acylated chitosan derivatives
    • K.Y. Lee Blood compatibility and biodegradability of partially N-acylated chitosan derivatives Biomaterials 16 1995 1211 1216
    • (1995) Biomaterials , vol.16 , pp. 1211-1216
    • Lee, K.Y.1
  • 32
    • 23044438554 scopus 로고    scopus 로고
    • Synthesis of chitosan-based polymeric surfactants and their adsorption properties for heavy metals and fatty acids
    • M.Y. Lee Synthesis of chitosan-based polymeric surfactants and their adsorption properties for heavy metals and fatty acids Int. J. Biol. Macromol. 36 2005 152 158
    • (2005) Int. J. Biol. Macromol. , vol.36 , pp. 152-158
    • Lee, M.Y.1
  • 33
    • 43049175030 scopus 로고    scopus 로고
    • Chitosan-modifications and applications: Opportunities galore
    • V.K. Mourya, and N.N. Inamdar Chitosan-modifications and applications: opportunities galore React. Funct. Polym. 68 2008 1013 1051
    • (2008) React. Funct. Polym. , vol.68 , pp. 1013-1051
    • Mourya, V.K.1    Inamdar, N.N.2
  • 34
    • 0016943565 scopus 로고
    • Selective N-acylation of chitosan
    • S. Hirano Selective N-acylation of chitosan Carbohydr. Res. 47 1976 315 320
    • (1976) Carbohydr. Res. , vol.47 , pp. 315-320
    • Hirano, S.1
  • 35
  • 36
    • 33750445973 scopus 로고    scopus 로고
    • Preparation of polymeric micelles based on chitosan bearing a small amount of highly hydrophobic groups
    • G.-B. Jiang, and D. Quan Preparation of polymeric micelles based on chitosan bearing a small amount of highly hydrophobic groups Carbohydr. Polym. 66 2006 514 520
    • (2006) Carbohydr. Polym. , vol.66 , pp. 514-520
    • Jiang, G.-B.1    Quan, D.2
  • 37
    • 0036567944 scopus 로고    scopus 로고
    • Novel N-saturated-fatty-acyl derivatives of chitosan soluble in water and in aqueous acid and alkaline solutions
    • S. Hirano Novel N-saturated-fatty-acyl derivatives of chitosan soluble in water and in aqueous acid and alkaline solutions Carbohydr. Polym. 48 2002 203 207
    • (2002) Carbohydr. Polym. , vol.48 , pp. 203-207
    • Hirano, S.1
  • 38
    • 0030309474 scopus 로고    scopus 로고
    • Chitin biotechnology applications
    • S. Hirano Chitin biotechnology applications Biotechnol. Annu. Rev. 2 1996 237 258
    • (1996) Biotechnol. Annu. Rev. , vol.2 , pp. 237-258
    • Hirano, S.1
  • 39
    • 33646370758 scopus 로고    scopus 로고
    • Novel polymer micelles prepared from chitosan grafted hydrophobic palmitoyl groups for drug delivery
    • G-B. Jiang Novel polymer micelles prepared from chitosan grafted hydrophobic palmitoyl groups for drug delivery Mol. Pharm. 3 2006 152 160
    • (2006) Mol. Pharm. , vol.3 , pp. 152-160
    • Jiang, G.-B.1
  • 40
    • 0032411620 scopus 로고    scopus 로고
    • Development of novel chitosan derivates as micellar carriers of taxol
    • A. Miwa development of novel chitosan derivates as micellar carriers of taxol Pharm. Res. 15 1998 1844 1850
    • (1998) Pharm. Res. , vol.15 , pp. 1844-1850
    • Miwa, A.1
  • 41
    • 0344082860 scopus 로고    scopus 로고
    • Physicochemical characteristics of self-assembled nanoparticles based on glycol chitosan bearing 5β-cholanic acid
    • K.Y. Lee Physicochemical characteristics of self-assembled nanoparticles based on glycol chitosan bearing 5β-cholanic acid Langmuir 19 1998 10188 10193
    • (1998) Langmuir , vol.19 , pp. 10188-10193
    • Lee, K.Y.1
  • 42
    • 84861587026 scopus 로고    scopus 로고
    • Preparation and characterization of self-assembled nanoparticles based on linolenic-acid modified chitosan
    • C. Liu Preparation and characterization of self-assembled nanoparticles based on linolenic-acid modified chitosan J. Ocean Univ. China 4 2005 234 239
    • (2005) J. Ocean Univ. China , vol.4 , pp. 234-239
    • Liu, C.1
  • 43
    • 33847111064 scopus 로고    scopus 로고
    • Self-assembled nanoparticles based on linoleic-acid modified carboxymethyl-chitosan as carrier of adriamycin (ADR)
    • C. Liu Self-assembled nanoparticles based on linoleic-acid modified carboxymethyl-chitosan as carrier of adriamycin (ADR) Curr. Appl. Phys. 7 2007 125 129
    • (2007) Curr. Appl. Phys. , vol.7 , pp. 125-129
    • Liu, C.1
  • 44
    • 39549108475 scopus 로고    scopus 로고
    • Core-modified chitosan-based polymeric micelles for controlled release of doxorubicin
    • Y-Q. Ye Core-modified chitosan-based polymeric micelles for controlled release of doxorubicin Int. J. Pharm. 352 2008 294 301
    • (2008) Int. J. Pharm. , vol.352 , pp. 294-301
    • Ye, Y.-Q.1
  • 45
    • 0038746780 scopus 로고    scopus 로고
    • O/W Emulsification for the self-aggregation and nanoparticle formation of linoleic acid-modified chitosan in the aqueous system
    • X-G. Chen O/W Emulsification for the self-aggregation and nanoparticle formation of linoleic acid-modified chitosan in the aqueous system J. Agric. Food Chem. 51 2003 3135 3139
    • (2003) J. Agric. Food Chem. , vol.51 , pp. 3135-3139
    • Chen, X.-G.1
  • 46
    • 21644481747 scopus 로고    scopus 로고
    • Self-assembled nanoparticles of bile acid-modified glycol chitosans and their applications for cancer therapy
    • K. Kim Self-assembled nanoparticles of bile acid-modified glycol chitosans and their applications for cancer therapy Macromol. Res. 13 2005 167 175
    • (2005) Macromol. Res. , vol.13 , pp. 167-175
    • Kim, K.1
  • 47
    • 33344466821 scopus 로고    scopus 로고
    • Hydrophobically modified glycol chitosan nanoparticles as carriers for paclitaxel
    • J-H. Kim Hydrophobically modified glycol chitosan nanoparticles as carriers for paclitaxel J. Control. Release 111 2006 228 234
    • (2006) J. Control. Release , vol.111 , pp. 228-234
    • Kim, J.-H.1
  • 48
    • 67349170344 scopus 로고    scopus 로고
    • Potential of amphiphilically modified low molecular weight chitosan as a novel carrier for hydrophobic anticancer drug: Synthesis, characterization, micellization and cytotoxicity evaluation
    • Y. Zhang Potential of amphiphilically modified low molecular weight chitosan as a novel carrier for hydrophobic anticancer drug: synthesis, characterization, micellization and cytotoxicity evaluation Carbohydr. Polym. 77 2009 231 238
    • (2009) Carbohydr. Polym. , vol.77 , pp. 231-238
    • Zhang, Y.1
  • 49
    • 0033638749 scopus 로고    scopus 로고
    • Self-aggregates of deoxycholic acid-modified chitosan as a novel carrier of adriamycin
    • K.Y. Lee Self-aggregates of deoxycholic acid-modified chitosan as a novel carrier of adriamycin Colloid. Polym. Sci. 278 2000 1216 1219
    • (2000) Colloid. Polym. Sci. , vol.278 , pp. 1216-1219
    • Lee, K.Y.1
  • 50
    • 23944522293 scopus 로고    scopus 로고
    • Complex formation between plasmid DNA and self-aggregates of deoxycholic acid-modified chitosan
    • K.Y. Lee Complex formation between plasmid DNA and self-aggregates of deoxycholic acid-modified chitosan Polymer 46 2005 8107 8112
    • (2005) Polymer , vol.46 , pp. 8107-8112
    • Lee, K.Y.1
  • 51
    • 0036847898 scopus 로고    scopus 로고
    • Physically cross-linked chitosan hydrogels as topical vehicles for hydrophilic drugs
    • T. Cerchiara Physically cross-linked chitosan hydrogels as topical vehicles for hydrophilic drugs J. Pharm. Pharmacol. 54 2002 1453 1459
    • (2002) J. Pharm. Pharmacol. , vol.54 , pp. 1453-1459
    • Cerchiara, T.1
  • 52
    • 0037161322 scopus 로고    scopus 로고
    • The release of model macromolecules may be controlled by the hydrophobicity of palmitoyl glycol chitosan hydrogels
    • L. Martin The release of model macromolecules may be controlled by the hydrophobicity of palmitoyl glycol chitosan hydrogels J. Control. Release 80 2002 87 100
    • (2002) J. Control. Release , vol.80 , pp. 87-100
    • Martin, L.1
  • 53
    • 0033204185 scopus 로고    scopus 로고
    • Aggregation in water of dextran hydrophobically modified with bile acids
    • M. Nichifor Aggregation in water of dextran hydrophobically modified with bile acids Macromolecules 32 1999 7078 7085
    • (1999) Macromolecules , vol.32 , pp. 7078-7085
    • Nichifor, M.1
  • 54
    • 9044223277 scopus 로고    scopus 로고
    • Cationic facial amphiphiles: A promising class of transfection agents
    • S. Walker Cationic facial amphiphiles: a promising class of transfection agents Proc. Natl. Acad. Sci. U.S.A. 93 1996 1585 1590
    • (1996) Proc. Natl. Acad. Sci. U.S.A. , vol.93 , pp. 1585-1590
    • Walker, S.1
  • 55
    • 0000878905 scopus 로고
    • Radikalisch polymerisierbare gallensäuren in monoschichten, mizellen and vesikeln
    • M. Alheim, and M.L. Hallensleben Radikalisch polymerisierbare gallensäuren in monoschichten, mizellen and vesikeln Makromol. Chem. 193 1992 779 797
    • (1992) Makromol. Chem. , vol.193 , pp. 779-797
    • Alheim, M.1    Hallensleben, M.L.2
  • 56
    • 84986808811 scopus 로고
    • Preparation of new polymers from bile acid derivatives
    • J.K. Denike, and X.X. Zhu Preparation of new polymers from bile acid derivatives Macromol. Rapid Commun. 15 1994 459 465
    • (1994) Macromol. Rapid Commun. , vol.15 , pp. 459-465
    • Denike, J.K.1    Zhu, X.X.2
  • 57
    • 68949213642 scopus 로고    scopus 로고
    • Microcalorimetric investigation on the formation of supramolecular nanoassemblies of associative polymers loaded with gadolinium chelate derivatives
    • M. Othman Microcalorimetric investigation on the formation of supramolecular nanoassemblies of associative polymers loaded with gadolinium chelate derivatives Int. J. Pharm. 379 2009 218 225
    • (2009) Int. J. Pharm. , vol.379 , pp. 218-225
    • Othman, M.1
  • 58
    • 78650717373 scopus 로고    scopus 로고
    • A comprehensive study of the spontaneous formation of nanoassemblies in water by a Lock-and-Key interaction between two associative polymers
    • M. Othman A comprehensive study of the spontaneous formation of nanoassemblies in water by a Lock-and-Key interaction between two associative polymers J. Colloid Interface Sci. 354 2011 517 527
    • (2011) J. Colloid Interface Sci. , vol.354 , pp. 517-527
    • Othman, M.1
  • 59
    • 65249113763 scopus 로고    scopus 로고
    • Cyclodextrin and polysaccharide-based nanogels: Entrapment of two hydrophobic molecules, benzophenone and tamoxifen
    • S. Daoud-Mahammed Cyclodextrin and polysaccharide-based nanogels: entrapment of two hydrophobic molecules, benzophenone and tamoxifen Biomacromolecules 10 2009 547 554
    • (2009) Biomacromolecules , vol.10 , pp. 547-554
    • Daoud-Mahammed, S.1
  • 60
    • 84855725559 scopus 로고    scopus 로고
    • Efficient loading and controlled release of benzophenone-3 entrapped into self-assembling nanogels
    • S. Daoud-Mahammed Efficient loading and controlled release of benzophenone-3 entrapped into self-assembling nanogels Curr. Nanosci. 6 2010 1 12
    • (2010) Curr. Nanosci. , vol.6 , pp. 1-12
    • Daoud-Mahammed, S.1
  • 61
    • 70350759653 scopus 로고    scopus 로고
    • A comprehensive study on the inclusion mechanism of benzophenone into supramolecular nanoassemblies prepared using two water-soluble associative polymers
    • K. Bouchemal A comprehensive study on the inclusion mechanism of benzophenone into supramolecular nanoassemblies prepared using two water-soluble associative polymers J. Therm. Anal. Calorim. 98 2009 57 64
    • (2009) J. Therm. Anal. Calorim. , vol.98 , pp. 57-64
    • Bouchemal, K.1
  • 62
    • 0031869863 scopus 로고    scopus 로고
    • Hyaluronic acid-modified bioadhesive liposomes as local drug depots: Effects of cellular and fluid dynamics on liposome retention at target sites
    • N. Yerushalmi Hyaluronic acid-modified bioadhesive liposomes as local drug depots: effects of cellular and fluid dynamics on liposome retention at target sites Arch. Biochem. Biophys. 349 1998 21 26
    • (1998) Arch. Biochem. Biophys. , vol.349 , pp. 21-26
    • Yerushalmi, N.1
  • 63
    • 68249105200 scopus 로고    scopus 로고
    • Lipoplexes targeting the CD44 hyaluronic acid receptor for efficient transfection of breast cancer cells
    • C. Surace Lipoplexes targeting the CD44 hyaluronic acid receptor for efficient transfection of breast cancer cells Mol. Pharm. 6 2009 1062 1073
    • (2009) Mol. Pharm. , vol.6 , pp. 1062-1073
    • Surace, C.1
  • 64
    • 0035866799 scopus 로고    scopus 로고
    • Liposome-encapsulated doxorubicin targeted to CD44: A strategy to kill CD44-overexpressing tumor cells
    • R.E. Eliaz, and F.C. Szoka Liposome-encapsulated doxorubicin targeted to CD44: a strategy to kill CD44-overexpressing tumor cells Cancer Res. 61 2001 2592 2601
    • (2001) Cancer Res. , vol.61 , pp. 2592-2601
    • Eliaz, R.E.1    Szoka, F.C.2
  • 65
    • 0027911260 scopus 로고
    • Self-aggregates of hydrophobized polysaccharides in water. Formation and characteristics of nanoparticles
    • K. Akiyoshi Self-aggregates of hydrophobized polysaccharides in water. Formation and characteristics of nanoparticles Macromolecules 26 1993 3062 3068
    • (1993) Macromolecules , vol.26 , pp. 3062-3068
    • Akiyoshi, K.1
  • 66
    • 0030103931 scopus 로고    scopus 로고
    • Supramolecular assembly of hydrophobized polysaccharides
    • K. Akiyoshi Supramolecular assembly of hydrophobized polysaccharides Supramol. Sci. 3 1996 157 163
    • (1996) Supramol. Sci. , vol.3 , pp. 157-163
    • Akiyoshi, K.1
  • 67
    • 0031079237 scopus 로고    scopus 로고
    • Microscopic structure and thermoresponsiveness of a hydrogel nanoparticle by self-assembly of a hydrophobized polysaccharide
    • K. Akiyoshi Microscopic structure and thermoresponsiveness of a hydrogel nanoparticle by self-assembly of a hydrophobized polysaccharide Macromolecules 30 1997 857 861
    • (1997) Macromolecules , vol.30 , pp. 857-861
    • Akiyoshi, K.1
  • 68
    • 0033750128 scopus 로고    scopus 로고
    • Controlled association of amphiphilic polymers in water: Thermosensitive nanoparticles formed by self-assembly of hydrophobically modified pullulans and poly(N-isopropylacrylamides)
    • K. Akiyoshi Controlled association of amphiphilic polymers in water: thermosensitive nanoparticles formed by self-assembly of hydrophobically modified pullulans and poly(N-isopropylacrylamides) Macromolecules 33 2000 3244 3249
    • (2000) Macromolecules , vol.33 , pp. 3244-3249
    • Akiyoshi, K.1
  • 69
    • 0037076619 scopus 로고    scopus 로고
    • Hierarchical self-assembly of hydrophobically modified pullulan in water: Gelation by networks of nanoparticles
    • K. Kuruda Hierarchical self-assembly of hydrophobically modified pullulan in water: gelation by networks of nanoparticles Langmuir 18 2002 3780 3786
    • (2002) Langmuir , vol.18 , pp. 3780-3786
    • Kuruda, K.1
  • 70
    • 14044276825 scopus 로고    scopus 로고
    • Utilization of amylose-lipid complexes as molecular nanocapsules for conjugated linoleic acid
    • I. Lalush Utilization of amylose-lipid complexes as molecular nanocapsules for conjugated linoleic acid Biomacromolecules 6 2005 121 130
    • (2005) Biomacromolecules , vol.6 , pp. 121-130
    • Lalush, I.1
  • 71
    • 0028968326 scopus 로고
    • Some factors determining the thermal properties of amylose inclusion complexes with fatty acids
    • J. Karkalas Some factors determining the thermal properties of amylose inclusion complexes with fatty acids Carbohydr. Res. 268 1995 233 247
    • (1995) Carbohydr. Res. , vol.268 , pp. 233-247
    • Karkalas, J.1
  • 72
    • 11144247937 scopus 로고    scopus 로고
    • Preparation and characterization of self-assembled nanoparticles of heparin-deoxycholic acid conjugates
    • K. Park Preparation and characterization of self-assembled nanoparticles of heparin-deoxycholic acid conjugates Langmuir 20 2004 11726 11731
    • (2004) Langmuir , vol.20 , pp. 11726-11731
    • Park, K.1


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