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Volumn 8, Issue 11, 2011, Pages 1501-1519

Solid dispersions, Part I: Recent evolutions and future opportunities in manufacturing methods for dissolution rate enhancement of poorly water-soluble drugs

Author keywords

Cyclodextrins complexation; Kneading; Poorly water soluble drugs; Solid dispersions; Solubility enhancement; Solvent evaporation; Spray drying; Wet milling

Indexed keywords

ACECLOFENAC; ALBENDAZOLE; APREPITANT; CARBAMAZEPINE; CARVEDILOL; CILOSTAZOL; CYCLOSPORIN A; DANAZOL; FENOFIBRATE; FUROSEMIDE; GLICLAZIDE; HESPERETIN; HYDROXYPROPYLMETHYLCELLULOSE; INDOMETACIN; ITRACONAZOLE; MACROGOL 6000; MEGESTROL; MEGESTROL ACETATE; MELOXICAM; NARINGENIN; NICARDIPINE; NORFLOXACIN; OMEPRAZOLE; RAPAMYCIN; SILICON DIOXIDE; SIMVASTATIN; SOLVENT; TELMISARTAN; TRANILAST; TRICOL; UNCLASSIFIED DRUG; UNINDEXED DRUG; VALACICLOVIR; VOCIFLON;

EID: 80054796578     PISSN: 17425247     EISSN: 17447593     Source Type: Journal    
DOI: 10.1517/17425247.2011.618181     Document Type: Review
Times cited : (169)

References (91)
  • 1
    • 0028948839 scopus 로고
    • A theoretical basis for a biopharmaceutic drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability
    • Amidon GL, Lennernas H, Shah VP, et al. A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res 1995;12:413-20
    • (1995) Pharm Res , vol.12 , pp. 413-20
    • Amidon, G.L.1    Lennernas, H.2    Shah, V.P.3
  • 2
    • 0036742053 scopus 로고    scopus 로고
    • Poor aqueous solubility-an industry wide problem in drug delivery
    • Lipinski C. Poor aqueous solubility-an industry wide problem in drug delivery. Am Pharm Rev 2002;5:82-5
    • (2002) Am Pharm Rev , vol.5 , pp. 82-5
    • Lipinski, C.1
  • 3
    • 0035292910 scopus 로고    scopus 로고
    • Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract
    • Horter D, Dressman JB. Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract. Adv Drug Deliv Rev 2001;46:75-87
    • (2001) Adv Drug Deliv Rev , vol.46 , pp. 75-87
    • Horter, D.1    Dressman, J.B.2
  • 4
    • 0033460251 scopus 로고    scopus 로고
    • The effect of dry mixing on the apparent solubility of hydrophobic, sparingly soluble drugs
    • DOI 10.1016/S0928-0987(99)00043-3, PII S0928098799000433
    • Mosharraf M, Nystrom C. The effect of dry mixing on the apparent solubility of hydrophobic, sparingly soluble drugs. Eur J Pharm Sci 1999;9:145-56 (Pubitemid 30012071)
    • (1999) European Journal of Pharmaceutical Sciences , vol.9 , Issue.2 , pp. 145-156
    • Mosharraf, M.1    Nystrom, C.2
  • 6
    • 0015124656 scopus 로고
    • Pharmaceutical applications of solid dispersion systems
    • Chiou WL, Riegelman S. Pharmaceutical applications of solid dispersion systems. J Pharm Sci 1971;60:1281-302
    • (1971) J Pharm Sci , vol.60 , pp. 1281-302
    • Chiou, W.L.1    Riegelman, S.2
  • 7
    • 36549042006 scopus 로고    scopus 로고
    • Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs
    • DOI 10.1016/j.drudis.2007.09.005, PII S1359644607003753
    • Vasconcelos T, Sarmento B, Costa P. Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs. Drug Discov Today 2007;12:1068-75 (Pubitemid 350186132)
    • (2007) Drug Discovery Today , vol.12 , Issue.23-24 , pp. 1068-1075
    • Vasconcelos, T.1    Sarmento, B.2    Costa, P.3
  • 8
    • 34548049483 scopus 로고    scopus 로고
    • Nanosizing - Oral formulation development and biopharmaceutical evaluation
    • DOI 10.1016/j.addr.2007.05.003, PII S0169409X0700083X
    • Kesisoglu F, Panmai S, Wu Y. Nanosizing-oral formulation development and biopharmaceutical evaluation. Adv Drug Deliv Rev 2007;59:631-44 (Pubitemid 47285408)
    • (2007) Advanced Drug Delivery Reviews , vol.59 , Issue.7 , pp. 631-644
    • Kesisoglou, F.1    Panmai, S.2    Wu, Y.3
  • 10
    • 77955053514 scopus 로고    scopus 로고
    • Enhanced dissolution of megestrol acetate microcrystals prepared by antisolvent precipitation process using hydrophilic additives
    • Cho E, Cho W, Cha KH, et al. Enhanced dissolution of megestrol acetate microcrystals prepared by antisolvent precipitation process using hydrophilic additives. Int J Pharm 2010;396:91-8
    • (2010) Int J Pharm , vol.396 , pp. 91-8
    • Cho, E.1    Cho, W.2    Cha, K.H.3
  • 11
    • 1142303337 scopus 로고    scopus 로고
    • What is the true solubility advantage for amorphous pharmaceuticals?
    • DOI 10.1023/A:1007516718048
    • Hancock BC, Parks M. What is the true solubility advantage for amorphous pharmaceuticals? Pharm Res 2000;17:397-404 (Pubitemid 30395293)
    • (2000) Pharmaceutical Research , vol.17 , Issue.4 , pp. 397-404
    • Hancock, B.C.1    Parks, M.2
  • 12
    • 75749094421 scopus 로고    scopus 로고
    • Review: Physical chemistry of solid dispersions
    • Janssens S, Van den Mooter G. Review: physical chemistry of solid dispersions. J Pharm Pharmacol 2009;61:1571-86
    • (2009) J Pharm Pharmacol , vol.61 , pp. 1571-86
    • Janssens, S.1    Van Den Mooter, G.2
  • 13
    • 0034601240 scopus 로고    scopus 로고
    • Improving drug solubility for oral delivery using solid dispersions
    • DOI 10.1016/S0939-6411(00)00076-X, PII S093964110000076X
    • Leuner C, Dressman J. Improving drug solubility for oral delivery using solid dispersions. Eur J Pharm Biopharm 2000;50:47-60 (Pubitemid 30326688)
    • (2000) European Journal of Pharmaceutics and Biopharmaceutics , vol.50 , Issue.1 , pp. 47-60
    • Leuner, C.1    Dressman, J.2
  • 14
    • 0037074108 scopus 로고    scopus 로고
    • The mechanisms of drug release from solid dispersions in water-soluble polymers
    • DOI 10.1016/S0378-5173(01)00891-2, PII S0378517301008912
    • Craig DQM. The mechanisms of drug release from solid dispersions in water soluble polymers. Int J Pharm 2002;231:131-44 (Pubitemid 34033673)
    • (2002) International Journal of Pharmaceutics , vol.231 , Issue.2 , pp. 131-144
    • Craig, D.Q.M.1
  • 15
    • 0032885450 scopus 로고    scopus 로고
    • Solid dispersion of poorly water-soluble drugs: Early promises, subsequent problems, and recent breakthroughs
    • Serajuddin ATM. Solid dispersion of poorly water-soluble drugs: early promises, subsequent problems, and recent breakthroughs. J Pharm Sci 1999;88:1058-66
    • (1999) J Pharm Sci , vol.88 , pp. 1058-66
    • Serajuddin, A.T.M.1
  • 17
    • 34548134519 scopus 로고    scopus 로고
    • Cyclodextrins as pharmaceutical solubilizers
    • DOI 10.1016/j.addr.2007.05.012, PII S0169409X07000841
    • Brewster ME, Loftsson T. Cyclodextrins as pharmaceutical solubilizers. Adv Drug Deliv Rev 2007;59:645-66 (Pubitemid 47299263)
    • (2007) Advanced Drug Delivery Reviews , vol.59 , Issue.7 , pp. 645-666
    • Brewster, M.E.1    Loftsson, T.2
  • 18
    • 77950673725 scopus 로고    scopus 로고
    • Formulation and evaluation of a protein-loaded solid dispersions by non-destructive methods
    • Rahman Z, Zidan AS, Khan MA. Formulation and evaluation of a protein-loaded solid dispersions by non-destructive methods. AAPS J 2010;12:158-70
    • (2010) AAPS J , vol.12 , pp. 158-70
    • Rahman, Z.1    Zidan, A.S.2    Khan, M.A.3
  • 19
    • 78650366422 scopus 로고    scopus 로고
    • Mechanism of dissolution enhancement and bioavailability of poorly water soluble celecoxib by preparing stable amorphous nanoparticles
    • Liu Y, Sun C, Hao Y, et al. Mechanism of dissolution enhancement and bioavailability of poorly water soluble celecoxib by preparing stable amorphous nanoparticles. J Pharm Pharm Sci 2010;13:589-606
    • (2010) J Pharm Pharm Sci , vol.13 , pp. 589-606
    • Liu, Y.1    Sun, C.2    Hao, Y.3
  • 20
    • 77952698655 scopus 로고    scopus 로고
    • Electrospraying, spray drying and related techniques for production and formulation of drug nanoparticles
    • Peltonen L, Valo H, Kolakovic R, et al. Electrospraying, spray drying and related techniques for production and formulation of drug nanoparticles. Expert Opin Drug Deliv 2010;7:705-19
    • (2010) Expert Opin Drug Deliv , vol.7 , pp. 705-19
    • Peltonen, L.1    Valo, H.2    Kolakovic, R.3
  • 23
    • 34249092945 scopus 로고    scopus 로고
    • Investigation of the release mechanism of a sparingly water-soluble drug from solid dispersions in hydrophilic carriers based on physical state of drug, particle size distribution and drug-polymer interactions
    • DOI 10.1016/j.ejpb.2006.11.020, PII S0939641106003390
    • Karavas E, Georgarakis E, Sigalas MP, et al. Investigation of the release mechanism of a sparingly water-soluble drug from solid dispersions in hydrophilic carriers based on physical state of drug, particle size distribution and drug-polymer interactions. Eur J Pharm Biopharm 2007;66:334-47 (Pubitemid 46778978)
    • (2007) European Journal of Pharmaceutics and Biopharmaceutics , vol.66 , Issue.3 , pp. 334-347
    • Karavas, E.1    Georgarakis, E.2    Sigalas, M.P.3    Avgoustakis, K.4    Bikiaris, D.5
  • 26
    • 74149089070 scopus 로고    scopus 로고
    • To enhance dissolution rate of poorly water-soluble drugs: Glucosamine hydrochloride as a potential carrier in solid dispersion formulations
    • Al-Hamidi H, Edwards AA, Mohammad MA, et al. To enhance dissolution rate of poorly water-soluble drugs: glucosamine hydrochloride as a potential carrier in solid dispersion formulations. Colloids Surf B Biointerfaces 2010;76:170-8
    • (2010) Colloids Surf B Biointerfaces , vol.76 , pp. 170-8
    • Al-Hamidi, H.1    Edwards, A.A.2    Mohammad, M.A.3
  • 27
    • 51449104992 scopus 로고    scopus 로고
    • Enhancement of dissolution rate of gliclazide using solid dispersions with polyethylene glycol 6000
    • Biswal S, Sahoo J, Murthy PN, et al. Enhancement of dissolution rate of gliclazide using solid dispersions with polyethylene glycol 6000. AAPS PharmSciTech 2008;9:563-70
    • (2008) AAPS PharmSciTech , vol.9 , pp. 563-70
    • Biswal, S.1    Sahoo, J.2    Murthy, P.N.3
  • 28
    • 77249138794 scopus 로고    scopus 로고
    • Dissolution rate and stability study of flavanone aglycones, naringenin and hesperetin, by drug delivery systems based on polyvinylpyrrolidone (PVP) nanodispersions
    • Kanaze FI, Kokkalou E, Niopas I, et al. Dissolution rate and stability study of flavanone aglycones, naringenin and hesperetin, by drug delivery systems based on polyvinylpyrrolidone (PVP) nanodispersions. Drug Dev Ind Pharm 2010;36:292-301
    • (2010) Drug Dev Ind Pharm , vol.36 , pp. 292-301
    • Kanaze, F.I.1    Kokkalou, E.2    Niopas, I.3
  • 29
    • 33645299283 scopus 로고    scopus 로고
    • Felodipine nanodispersions as active core for predictable pulsatile chronotherapeutics using PVP/HPMC blends as coating layer
    • Karavas E, Georgarakis E, Bikiaris D. Felodipine nanodispersions as active core for predictable pulsatile chronotherapeutics using PVP/HPMC blends as coating layer. Int J Pharm 2006;313:189-97
    • (2006) Int J Pharm , vol.313 , pp. 189-97
    • Karavas, E.1    Georgarakis, E.2    Bikiaris, D.3
  • 30
    • 34447263070 scopus 로고    scopus 로고
    • Combining SEM, TEM, and micro-Raman techniques to differentiate between the amorphous molecular level dispersions and nanodispersions of a poorly water-soluble drug within a polymer matrix
    • DOI 10.1016/j.ijpharm.2007.03.037, PII S0378517307002669
    • Karavas E, Georgarakis M, Docoslis A, et al. Combining SEM, TEM, and micro-Raman techniques to differentiate between the amorphous molecular level dispersions and nanodispersions of a poorly water-soluble drug within a polymer matrix. Int J Pharm 2007;340:76-83 (Pubitemid 47044963)
    • (2007) International Journal of Pharmaceutics , vol.340 , Issue.1-2 , pp. 76-83
    • Karavas, E.1    Georgarakis, M.2    Docoslis, A.3    Bikiaris, D.4
  • 31
    • 73749088616 scopus 로고    scopus 로고
    • The effect of physical state on the drug dissolution rate. Miscibility studies of nimodipine with PVP
    • Papageorgiou GZ, Docoslis A, Georgarakis M, et al. The effect of physical state on the drug dissolution rate. Miscibility studies of nimodipine with PVP. J Therm Anal Cal 2009;95:903-15
    • (2009) J Therm Anal Cal , vol.95 , pp. 903-15
    • Papageorgiou, G.Z.1    Docoslis, A.2    Georgarakis, M.3
  • 32
    • 70649101162 scopus 로고    scopus 로고
    • Influence of temperature on the solubilization of thiabendazole by combined action of solid dispersions and co-solvents
    • Muela S, Escalera B, Pena MA, Bustamante P. Influence of temperature on the solubilization of thiabendazole by combined action of solid dispersions and co-solvents. Int J Pharm 2010;384:93-9
    • (2010) Int J Pharm , vol.384 , pp. 93-9
    • Muela, S.1    Escalera, B.2    Pena, M.A.3    Bustamante, P.4
  • 33
    • 63649134819 scopus 로고    scopus 로고
    • Co-solvent evaporation method for enhancement of solubility and dissolution rate of poorly aqueous soluble drug simvastatin: In vitro-in vivo evaluation
    • Pandya P, Gattani S, Jain P, et al. Co-solvent evaporation method for enhancement of solubility and dissolution rate of poorly aqueous soluble drug simvastatin: in vitro-in vivo evaluation. AAPS PharmSciTech 2008;9:1247-52
    • (2008) AAPS PharmSciTech , vol.9 , pp. 1247-52
    • Pandya, P.1    Gattani, S.2    Jain, P.3
  • 34
    • 77954312179 scopus 로고    scopus 로고
    • Effect of the solid-dispersion method on the solubility and crystalline property of Tacrolimus
    • Joe JH, Lee WM, Park YJ, et al. Effect of the solid-dispersion method on the solubility and crystalline property of Tacrolimus. Int J Pharm 2010;395:161-6
    • (2010) Int J Pharm , vol.395 , pp. 161-6
    • Joe, J.H.1    Lee, W.M.2    Park, Y.J.3
  • 35
    • 79951577432 scopus 로고    scopus 로고
    • Carvedilol dissolution improvement by preparation of solid dispersions with porous silica
    • Planinsek O, Kovacic B, Vrecer F. Carvedilol dissolution improvement by preparation of solid dispersions with porous silica. Int J Pharm 2011;406:41-8
    • (2011) Int J Pharm , vol.406 , pp. 41-8
    • Planinsek, O.1    Kovacic, B.2    Vrecer, F.3
  • 36
    • 76249133449 scopus 로고    scopus 로고
    • Oxidized mesoporous silicon microparticles for improved oral delivery of poorly soluble drugs
    • Wang F, Hui H, Barnes TJ, et al. Oxidized mesoporous silicon microparticles for improved oral delivery of poorly soluble drugs. Mol Pharm 2010;7:227-36
    • (2010) Mol Pharm , vol.7 , pp. 227-36
    • Wang, F.1    Hui, H.2    Barnes, T.J.3
  • 37
    • 77955652842 scopus 로고    scopus 로고
    • Inclusion of telmisartan in MCF nanoparticles: Drug loading and release property
    • Zhang Y, Jiang T, Zhang Q, et al. Inclusion of telmisartan in MCF nanoparticles: drug loading and release property. Eur J Pharm Biopharm 2010;76:17-23
    • (2010) Eur J Pharm Biopharm , vol.76 , pp. 17-23
    • Zhang, Y.1    Jiang, T.2    Zhang, Q.3
  • 38
    • 77954805866 scopus 로고    scopus 로고
    • Solid dispersion as an approach for bioavailability enhancement of poorly water-soluble drug ritonavir
    • Sinha S, Ali M, Baboota S, et al. Solid dispersion as an approach for bioavailability enhancement of poorly water-soluble drug ritonavir. AAPS PharmSciTech 2010;11:518-27
    • (2010) AAPS PharmSciTech , vol.11 , pp. 518-27
    • Sinha, S.1    Ali, M.2    Baboota, S.3
  • 39
    • 76049117937 scopus 로고    scopus 로고
    • Enhanced solubility and bioavailability of sibutramine base by solid dispersion system with aqueous medium
    • Li DX, Jang KY, Kang WK, et al. Enhanced solubility and bioavailability of sibutramine base by solid dispersion system with aqueous medium. Biol Pharm Bull 2010;33:279-84
    • (2010) Biol Pharm Bull , vol.33 , pp. 279-84
    • Li, D.X.1    Jang, K.Y.2    Kang, W.K.3
  • 40
    • 75549090079 scopus 로고    scopus 로고
    • Kneading technique for preparation of binary solid dispersion of meloxicam with poloxamer 188
    • Ghareeb MM, Abdulrasool AA, Hussein AA, et al. Kneading technique for preparation of binary solid dispersion of meloxicam with poloxamer 188. AAPS PharmSciTech 2009;10:1206-15
    • (2009) AAPS PharmSciTech , vol.10 , pp. 1206-15
    • Ghareeb, M.M.1    Abdulrasool, A.A.2    Hussein, A.A.3
  • 41
    • 69249106944 scopus 로고    scopus 로고
    • Formulation and evaluation of solid dispersions of furosemide in sodium starch glycolate
    • Chaulang G, Patel P, Hardikar S, et al. Formulation and evaluation of solid dispersions of furosemide in sodium starch glycolate. Trop J Pharm Res 2009;8:43-51
    • (2009) Trop J Pharm Res , vol.8 , pp. 43-51
    • Chaulang, G.1    Patel, P.2    Hardikar, S.3
  • 42
    • 78751584648 scopus 로고    scopus 로고
    • Improvement of dissolution rate of aceclofenac by solid dispersion technique
    • Maulvi FA, Dalwadi SJ, Thakkar VT, et al. Improvement of dissolution rate of aceclofenac by solid dispersion technique. Powder Technol 2011;207:47-54
    • (2011) Powder Technol , vol.207 , pp. 47-54
    • Maulvi, F.A.1    Dalwadi, S.J.2    Thakkar, V.T.3
  • 43
    • 34548801947 scopus 로고    scopus 로고
    • Preparation and characterization of etoricoxib-β-cyclodextrin complexes prepared by the kneading method
    • DOI 10.2478/v10007-007-0028-2, PII 64RT7726736773H1
    • Patel HM, Suhagia BN, Shah SA, et al. Preparation and characterization of etoricoxib-beta-cyclodextrin complexes prepared by the kneading method. Acta Pharm 2007;57:351-9 (Pubitemid 47429179)
    • (2007) Acta Pharmaceutica , vol.57 , Issue.3 , pp. 351-359
    • Patel, H.M.1    Suhagia, B.N.2    Shah, S.A.3    Rathod, I.S.4    Parmar, V.K.5
  • 44
    • 70350460588 scopus 로고    scopus 로고
    • Evaluation of some methods for preparing gliclazide-beta-Cyclodextrin inclusion complexes
    • Sapkal NP, Kilor VA, Bhusari KP, et al. Evaluation of some methods for preparing gliclazide-beta-Cyclodextrin inclusion complexes. Trop J Pharm Res 2007;6:833-40
    • (2007) Trop J Pharm Res , vol.6 , pp. 833-40
    • Sapkal, N.P.1    Kilor, V.A.2    Bhusari, K.P.3
  • 45
    • 0036172264 scopus 로고    scopus 로고
    • Physicochemical characterization and in vitro dissolution behavior of nicardipine-cyclodextrins inclusion compounds
    • DOI 10.1016/S0928-0987(01)00208-1, PII S0928098701002081
    • Fernandes CM, Vieira MT, Veiga FJB. Physicochemical characterization and in vitro dissolution behavior of nicardipine-cyclodextrins inclusion compounds. Eur J Pharm Sci 2002;15:79-88 (Pubitemid 34136971)
    • (2002) European Journal of Pharmaceutical Sciences , vol.15 , Issue.1 , pp. 79-88
    • Fernandes, C.M.1    Teresa Vieira, M.2    B. Veiga, F.J.3
  • 47
    • 33846096823 scopus 로고    scopus 로고
    • Investigation of enhancement of solubility of norfloxacin β-cyclodextrin in presence of acidic solubilizing additives
    • DOI 10.2174/156720107779314776
    • Dua K, Ramana MV, Sara UVS, et al. Investigation of enhancement of solubility of norfloxacin beta-cyclodextrin in presence of acidic solubilizing additives. Curr Drug Deliv 2007;4:21-5 (Pubitemid 46066411)
    • (2007) Current Drug Delivery , vol.4 , Issue.1 , pp. 21-25
    • Dua, K.1    Ramana, M.V.2    Singh Sara, U.V.3    Himaja, M.4    Agrawal, A.5    Garg, V.6    Pabreja, K.7
  • 48
    • 78650527889 scopus 로고    scopus 로고
    • Silymarin-solid dispersions: Characterization and influence of preparation methods on dissolution
    • Sonali D, Tejal S, Vaishali T, et al. Silymarin-solid dispersions: Characterization and influence of preparation methods on dissolution. Acta Pharm 2010;60:427-43
    • (2010) Acta Pharm , vol.60 , pp. 427-43
    • Sonali, D.1    Tejal, S.2    Vaishali, T.3
  • 49
    • 1342281182 scopus 로고    scopus 로고
    • Micron-Size Drug Particles: Common and Novel Micronization Techniques
    • DOI 10.1081/PDT-120027417
    • Rasenack N, Muller BW. Micron-size drug particles: common and novel micronization techniques. Pharm Dev Technol 2004;9:1-13 (Pubitemid 38258252)
    • (2004) Pharmaceutical Development and Technology , vol.9 , Issue.1 , pp. 1-13
    • Rasenack, N.1    Muller, B.W.2
  • 50
    • 1842559836 scopus 로고    scopus 로고
    • Nanoparticle Engineering Processes for Enhancing the Dissolution Rates of Poorly Water Soluble Drugs
    • DOI 10.1081/DDC-120030422
    • Hu J, Johnston KP, Williams RO III. Nanoparticle engineering processes for enhancing the dissolution rates. Drug Dev Ind Pharm 2004;30:233-45 (Pubitemid 38451748)
    • (2004) Drug Development and Industrial Pharmacy , vol.30 , Issue.3 , pp. 233-245
    • Hu, J.1    Johnston, K.P.2    Williams III, R.O.3
  • 51
    • 38349087174 scopus 로고    scopus 로고
    • Novel technology to prepare oral formulations for preclinical safety studies
    • Niwa T, Hashimoto N. Novel technology to prepare oral formulations for preclinical safety studies. Int J Pharm 2008;350:70-8
    • (2008) Int J Pharm , vol.350 , pp. 70-8
    • Niwa, T.1    Hashimoto, N.2
  • 52
    • 21644468027 scopus 로고    scopus 로고
    • Insulin nanoparticles: A novel formulation approach for poorly water soluble Zn-insulin
    • Merisko-Liversidge E, McGurk SL, Liversidge GG. Insulin nanoparticles: a novel formulation approach for poorly water soluble Zn-insulin. Pharm Res 2004;21:1545-51
    • (2004) Pharm Res , vol.21 , pp. 1545-51
    • Merisko-Liversidge, E.1    McGurk, S.L.2    Liversidge, G.G.3
  • 53
    • 70349694077 scopus 로고    scopus 로고
    • Nanoparticulation of poorly water soluble drugs using a wet-mill process and physicochemical properties of the nanopowders
    • Tanaka Y, Inkyo M, Yumoto R, et al. Nanoparticulation of poorly water soluble drugs using a wet-mill process and physicochemical properties of the nanopowders. Chem Pharm Bull (Tokyo) 2009;57:1050-7
    • (2009) Chem Pharm Bull (Tokyo) , vol.57 , pp. 1050-7
    • Tanaka, Y.1    Inkyo, M.2    Yumoto, R.3
  • 54
    • 77951652999 scopus 로고    scopus 로고
    • Comparison of bioavailability of amorphous versus crystalline itraconazole nanoparticles via pulmonary administration in rats
    • Yang W, Johnston KP, Williams RO III. Comparison of bioavailability of amorphous versus crystalline itraconazole nanoparticles via pulmonary administration in rats. Eur J Pharm Biopharm 2010;75:33-41
    • (2010) Eur J Pharm Biopharm , vol.75 , pp. 33-41
    • Yang, W.1    Johnston, K.P.2    Williams III, R.O.3
  • 55
    • 78650574590 scopus 로고    scopus 로고
    • Development of inhalable nanocrystalline solid dispersion of tranilast for airway inflammatory diseases
    • Onoue S, Aoki Y, Matsui T, et al. Development of inhalable nanocrystalline solid dispersion of tranilast for airway inflammatory diseases. J Pharm Sci 2011;100:622-33
    • (2011) J Pharm Sci , vol.100 , pp. 622-33
    • Onoue, S.1    Aoki, Y.2    Matsui, T.3
  • 56
    • 77956880320 scopus 로고    scopus 로고
    • Improved dissolution and pharmacokinetic behavior of cyclosporine A using high-energy amorphous solid dispersion approach
    • Onoue S, Sato H, Ogawa K, et al. Improved dissolution and pharmacokinetic behavior of cyclosporine A using high-energy amorphous solid dispersion approach. Int J Pharm 2010;399:94-101
    • (2010) Int J Pharm , vol.399 , pp. 94-101
    • Onoue, S.1    Sato, H.2    Ogawa, K.3
  • 57
    • 33746253253 scopus 로고    scopus 로고
    • Increased dissolution and physical stability of micronized nifedipine particles encapsulated with a biocompatible polymer and surfactants in a wet ball milling process
    • Li N, DeGennaro MD, Liebenberg W, et al. Increased dissolution and physical stability of micronized nifedipine particles encapsulated with a biocompatible polymer and surfactants in a wet ball milling process. Pharmazie 2006;61:595-603 (Pubitemid 44098026)
    • (2006) Pharmazie , vol.61 , Issue.7 , pp. 595-603
    • Li, N.1    DeGennaro, M.D.2    Liebenberg, W.3    Tiedt, L.R.4    Zahn, A.S.5    Pishko, M.V.6    De Villiers, M.M.7
  • 58
    • 48749094715 scopus 로고    scopus 로고
    • In vitro-in vivo correlation for wet-milled tablet of poorly water-soluble cilostazol
    • Jinno J, Kamada N, Miyake M, et al. In vitro-in vivo correlation for wet-milled tablet of poorly water-soluble cilostazol. J Control Release 2008;130:29-37
    • (2008) J Control Release , vol.130 , pp. 29-37
    • Jinno, J.1    Kamada, N.2    Miyake, M.3
  • 59
    • 70350654531 scopus 로고    scopus 로고
    • Development and characterization of solid oral dosage form incorporating candesartan nanoparticles
    • Nekkanti V, Pillai R, Venkateshwarlu V, et al. Development and characterization of solid oral dosage form incorporating candesartan nanoparticles. Pharm Dev Technol 2009;14:290-8
    • (2009) Pharm Dev Technol , vol.14 , pp. 290-8
    • Nekkanti, V.1    Pillai, R.2    Venkateshwarlu, V.3
  • 60
    • 34547861305 scopus 로고    scopus 로고
    • Nanosizing of a drug/carrageenan complex to increase solubility and dissolution rate
    • DOI 10.1016/j.ijpharm.2007.04.032, PII S0378517307003626
    • Dai WG, Dong LC, Song YQ. Nanosizing of a drug/carrageenan complex to increase solubility and dissolution rate. Int J Pharm 2007;342:201-7 (Pubitemid 47259320)
    • (2007) International Journal of Pharmaceutics , vol.342 , Issue.1-2 , pp. 201-207
    • Dai, W.-G.1    Dong, L.C.2    Song, Y.-Q.3
  • 61
    • 77950992215 scopus 로고    scopus 로고
    • The preparation of ternary solid dispersions of an herbal drug via spray drying of liquid feed
    • Araujo RR, Teixeira CCC, Freitas LAP. The preparation of ternary solid dispersions of an herbal drug via spray drying of liquid feed. Drying Technol 2010;28:412-21
    • (2010) Drying Technol , vol.28 , pp. 412-21
    • Araujo, R.R.1    Ccc, T.2    Freitas, L.A.P.3
  • 62
    • 67349158352 scopus 로고    scopus 로고
    • Spray drying from complex solvent systems broadens the applicability of Kollicoat IR as a carrier in the formulation of solid dispersions
    • Janssens S, Anne M, Rombaut P, et al. Spray drying from complex solvent systems broadens the applicability of Kollicoat IR as a carrier in the formulation of solid dispersions. Eur J Pharm Sci 2009;37:241-8
    • (2009) Eur J Pharm Sci , vol.37 , pp. 241-8
    • Janssens, S.1    Anne, M.2    Rombaut, P.3
  • 63
    • 78649490164 scopus 로고    scopus 로고
    • Flavonoid microparticles by spraydrying: Influence of enhancers of the dissolution rate on properties and stability
    • Sansone F, Picerno P, Mencherini T, et al. Flavonoid microparticles by spraydrying: influence of enhancers of the dissolution rate on properties and stability. J Food Eng 2011;103:188-96
    • (2011) J Food Eng , vol.103 , pp. 188-96
    • Sansone, F.1    Picerno, P.2    Mencherini, T.3
  • 64
    • 67650806122 scopus 로고    scopus 로고
    • Particle characterization of poorly water-soluble drugs using a spray freeze drying technique
    • Kondo M, Niwa T, Okamoto H, et al. Particle characterization of poorly water-soluble drugs using a spray freeze drying technique. Chem Pharm Bull (Tokyo) 2009;57:657-62
    • (2009) Chem Pharm Bull (Tokyo) , vol.57 , pp. 657-62
    • Kondo, M.1    Niwa, T.2    Okamoto, H.3
  • 65
    • 71649105279 scopus 로고    scopus 로고
    • Anomalous properties of spray dried solid dispersions
    • Al-Obaidi H, Brocchini S, Buckton G. Anomalous properties of spray dried solid dispersions. J Pharm Sci 2009;98:4724-37
    • (2009) J Pharm Sci , vol.98 , pp. 4724-37
    • Al-Obaidi, H.1    Brocchini, S.2    Buckton, G.3
  • 66
    • 77954268900 scopus 로고    scopus 로고
    • Physicochemical and pharmacokinetic characterization of a spray-dried cefpodoxime proxetil nanosuspension
    • Gao Y, Qian S, Zhang J. Physicochemical and pharmacokinetic characterization of a spray-dried cefpodoxime proxetil nanosuspension. Chem Pharm Bull (Tokyo) 2010;58:912-17
    • (2010) Chem Pharm Bull (Tokyo) , vol.58 , pp. 912-17
    • Gao, Y.1    Qian, S.2    Zhang, J.3
  • 67
    • 77952746314 scopus 로고    scopus 로고
    • Improvement of dissolution and absorption properties of poorly water-soluble drug by preparing spray-dried powders with alpha-glucosyl hesperidin
    • Uchiyama H, Tozuka Y, Imono M, et al. Improvement of dissolution and absorption properties of poorly water-soluble drug by preparing spray-dried powders with alpha-glucosyl hesperidin. Int J Pharm 2010;392:101-6
    • (2010) Int J Pharm , vol.392 , pp. 101-6
    • Uchiyama, H.1    Tozuka, Y.2    Imono, M.3
  • 68
    • 67650178803 scopus 로고    scopus 로고
    • Formation and characterization of solid dispersions of piroxicam and polyvinylpyrrolidone using spray drying and precipitation with compressed antisolvent
    • Wu K, Li J, Wang W, Winstead DA. Formation and characterization of solid dispersions of piroxicam and polyvinylpyrrolidone using spray drying and precipitation with compressed antisolvent. J Pharm Sci 2009;98:2422-31
    • (2009) J Pharm Sci , vol.98 , pp. 2422-31
    • Wu, K.1    Li, J.2    Wang, W.3    Winstead, D.A.4
  • 69
    • 78650678715 scopus 로고    scopus 로고
    • Spray freeze drying with polyvinylpyrrolidone and sodium caprate for improved dissolution and oral bioavailability of oleanolic acid, a BCS Class IV compound
    • Tong HHY, Du Z, Wang GN, et al. Spray freeze drying with polyvinylpyrrolidone and sodium caprate for improved dissolution and oral bioavailability of oleanolic acid, a BCS Class IV compound. Int J Pharm 2011;404:148-58
    • (2011) Int J Pharm , vol.404 , pp. 148-58
    • Hhy, T.1    Du, Z.2    Wang, G.N.3
  • 70
    • 34548306554 scopus 로고    scopus 로고
    • Improvement of the dissolution rate of nitrendipine using a new pulse combustion drying method
    • DOI 10.1248/cpb.55.1119
    • Wang L, Cui FD, Sunada H. Improvement of the dissolution rate of nitrendipine using a new pulse combustion drying method. Chem Pharm Bull (Tokyo) 2007;55:1119-25 (Pubitemid 47344960)
    • (2007) Chemical and Pharmaceutical Bulletin , vol.55 , Issue.8 , pp. 1119-1125
    • Wang, L.1    Cui, F.-D.2    Sunada, H.3
  • 71
    • 78650702648 scopus 로고    scopus 로고
    • Dissolution enhancement of a poorly water-soluble antimalarial drug by means of a modified multi-fluid nozzle pilot spray drier
    • Sahoo NG, Kakran M, Li L, et al. Dissolution enhancement of a poorly water-soluble antimalarial drug by means of a modified multi-fluid nozzle pilot spray drier. Matter Sci Eng C 2011;31:391-9
    • (2011) Matter Sci Eng C , vol.31 , pp. 391-9
    • Sahoo, N.G.1    Kakran, M.2    Li, L.3
  • 73
    • 67549093409 scopus 로고    scopus 로고
    • Enhancement of oral bioavailability of cilostazol by forming its inclusion complexes
    • Patel SG, Rajput SJ. Enhancement of oral bioavailability of cilostazol by forming its inclusion complexes. AAPS PharmSciTech 2009;10:660-9
    • (2009) AAPS PharmSciTech , vol.10 , pp. 660-9
    • Patel, S.G.1    Rajput, S.J.2
  • 74
    • 35248822616 scopus 로고    scopus 로고
    • The utility of cyclodextrins for enhancing oral bioavailability
    • DOI 10.1016/j.jconrel.2007.07.018, PII S0168365907004129
    • Carrier RL, Miller LA, Ahmed I. The utility of cyclodextrins for enhancing oral bioavailability. J Control Release 2007;123:78-99 (Pubitemid 47566400)
    • (2007) Journal of Controlled Release , vol.123 , Issue.2 , pp. 78-99
    • Carrier, R.L.1    Miller, L.A.2    Ahmed, I.3
  • 75
    • 10444279209 scopus 로고    scopus 로고
    • Cyclodextrin-based pharmaceutics: Past, present and future
    • DOI 10.1038/nrd1576
    • Davis ME, Brewster ME. Cyclodextrin-based pharmaceutics: Past, present and future. Nat Rev Drug Discov 2004;3:1023-35 (Pubitemid 39642365)
    • (2004) Nature Reviews Drug Discovery , vol.3 , Issue.12 , pp. 1023-1035
    • Davis, M.E.1    Brewster, M.E.2
  • 76
    • 11044221846 scopus 로고    scopus 로고
    • Role of cyclodextrins in improving oral drug delivery
    • DOI 10.2165/00137696-200402040-00006
    • Loftsson T, Brewster ME, Masson M. Role of cyclodextrins in improving oral drug delivery. Am J Drug Deliv 2004;2:261-75 (Pubitemid 40045491)
    • (2004) American Journal of Drug Delivery , vol.2 , Issue.4 , pp. 261-275
    • Loftsson, T.1    Brewster, M.E.2    Masson, M.3
  • 77
    • 74849087408 scopus 로고    scopus 로고
    • Modeling the influence of cyclodextrins on oral absorption of low-solubility drugs: I
    • Gamsiz ED, Miller L, Thombre AG, et al. Modeling the influence of cyclodextrins on oral absorption of low-solubility drugs: I. Model development. Biotechnol Bioeng 2010;105:409-20
    • (2010) Model Development. Biotechnol Bioeng , vol.105 , pp. 409-20
    • Gamsiz, E.D.1    Miller, L.2    Thombre, A.G.3
  • 78
    • 58249102205 scopus 로고    scopus 로고
    • Preparation and evaluation of itraconazole dihydrochloride for the solubility and dissolution rate enhancement
    • Tao T, Zhao Y, Wu J, et al. Preparation and evaluation of itraconazole dihydrochloride for the solubility and dissolution rate enhancement. Int J Pharm 2009;367:109-14
    • (2009) Int J Pharm , vol.367 , pp. 109-14
    • Tao, T.1    Zhao, Y.2    Wu, J.3
  • 79
    • 42749095034 scopus 로고    scopus 로고
    • Cyclodextrins as stabilizers for the preparation of drug nanocrystals by the emulsion solvent diffusion method
    • Makhlof A, Miyazaki Y, Tozuka Y, et al. Cyclodextrins as stabilizers for the preparation of drug nanocrystals by the emulsion solvent diffusion method. Int J Pharm 2008;357:280-5
    • (2008) Int J Pharm , vol.357 , pp. 280-5
    • Makhlof, A.1    Miyazaki, Y.2    Tozuka, Y.3
  • 80
    • 34848845290 scopus 로고    scopus 로고
    • Enhancement of dissolution amount and in vivo bioavailability of itraconazole by complexation with β-cyclodextrin using supercritical carbon dioxide
    • DOI 10.1016/j.jpba.2007.06.011, PII S0731708507003329
    • Hassan HA, Al-Marzouqi AH, Jobe B, et al. Enhancement of dissolution amount and in vivo bioavailability of itraconazole by complexation with beta-cyclodextrin using supercritical carbon dioxide. J Pharm Biomed Anal 2007;45:243-50 (Pubitemid 47513421)
    • (2007) Journal of Pharmaceutical and Biomedical Analysis , vol.45 , Issue.2 , pp. 243-250
    • Hassan, H.A.1    Al-Marzouqi, A.H.2    Jobe, B.3    Hamza, A.A.4    Ramadan, G.A.5
  • 81
    • 27744575591 scopus 로고    scopus 로고
    • Cyclodextrins in drug delivery: An updated review
    • Challa R, Ahuja A, Ali J, et al. Cyclodextrins in drug delivery: an updated review. AAPS PharmSciTech 2005;6:E329-57
    • (2005) AAPS PharmSciTech , vol.6
    • Challa, R.1    Ahuja, A.2    Ali, J.3
  • 82
    • 77955982703 scopus 로고    scopus 로고
    • Enhancement of the aqueous solubility and masking the bitter taste of famotidine using drug/SBE-beta-CD/povidone K30 complexation approach
    • Mady FM, Abou-Taleb AE, Khaled KA, et al. Enhancement of the aqueous solubility and masking the bitter taste of famotidine using drug/SBE-beta-CD/ povidone K30 complexation approach. J Pharm Sci 2010;99:4285-94
    • (2010) J Pharm Sci , vol.99 , pp. 4285-94
    • Mady, F.M.1    Abou-Taleb, A.E.2    Khaled, K.A.3
  • 83
    • 70449520196 scopus 로고    scopus 로고
    • Effect of cyclodextrin complexation of curcumin on its solubility and antiangiogenic and anti-inflammatory activity in rat colitis model
    • Yadav VR, Suresh S, Devi K, et al. Effect of cyclodextrin complexation of curcumin on its solubility and antiangiogenic and anti-inflammatory activity in rat colitis model. AAPS PharmSciTech 2009;10:752-62
    • (2009) AAPS PharmSciTech , vol.10 , pp. 752-62
    • Yadav, V.R.1    Suresh, S.2    Devi, K.3
  • 85
    • 0031024463 scopus 로고    scopus 로고
    • Crystallization and polymorphic transition behavior of chloramphenicol palmitate in 2-hydroxypropyl-β-cyclodextrin matrix
    • DOI 10.1016/S0928-0987(96)00250-3, PII S0928098796002503
    • Hirayama F, Usami M, Kimura K, et al. Crystallization and polymorphic transition behavior of chloramphenicol palmitate in 2-hydroxypropyl- betacyclodextrin matrix. Eur J Pharm Sci 1997;5:23-30 (Pubitemid 27046432)
    • (1997) European Journal of Pharmaceutical Sciences , vol.5 , Issue.1 , pp. 23-30
    • Hirayama, F.1    Usami, M.2    Kimura, K.3    Uekama, K.4
  • 86
    • 77954816979 scopus 로고    scopus 로고
    • Improvement of dissolution behavior for poorly water-soluble drug by application of cyclodextrin in extrusion process: Comparison between melt extrusion and wet extrusion
    • Yano H, Kleinebudde P. Improvement of dissolution behavior for poorly water-soluble drug by application of cyclodextrin in extrusion process: Comparison between melt extrusion and wet extrusion. AAPS PharmSciTech 2010;11:885-93
    • (2010) AAPS PharmSciTech , vol.11 , pp. 885-93
    • Yano, H.1    Kleinebudde, P.2
  • 87
    • 77954312803 scopus 로고    scopus 로고
    • New "drug-in cyclodextrin-in deformable liposomes" formulations to improve the therapeutic efficacy of local anaesthetics
    • Maestrelli F, Gonzalez-Rodriguez ML, Rabasco AM, et al. New 'drug-in cyclodextrin-in deformable liposomes' formulations to improve the therapeutic efficacy of local anaesthetics. Int J Pharm 2010;395:222-3
    • (2010) Int J Pharm , vol.395 , pp. 222-3
    • Maestrelli, F.1    Gonzalez-Rodriguez, M.L.2    Rabasco, A.M.3
  • 88
    • 80054829203 scopus 로고    scopus 로고
    • Solid dispersions Part II: New strategies in manufacturing methods for dissolution rate enhancement of poorly water soluble drugs
    • Sep Epub ahead of print
    • Bikiaris D. Solid dispersions, Part II: new strategies in manufacturing methods for dissolution rate enhancement of poorly water soluble drugs. Expert Opin Drug Deliv Sep 2011. [Epub ahead of print]
    • (2011) Expert Opin Drug Deliv
    • Bikiaris, D.1
  • 89
    • 77953236977 scopus 로고    scopus 로고
    • Predicting the formation and Stability of amorphous small molecule binary mixtures from computationally determined Flory-Huggins interaction parameter and phase diagram
    • Pajula K, Taskinen M, Lehto VP, et al. Predicting the formation and Stability of amorphous small molecule binary mixtures from computationally determined Flory-Huggins interaction parameter and phase diagram. Mol Pharm 2010;7:795-04
    • (2010) Mol Pharm , vol.7 , pp. 795-04
    • Pajula, K.1    Taskinen, M.2    Lehto, V.P.3
  • 90
    • 77955243354 scopus 로고    scopus 로고
    • Theoretical and experimental investigation on the solid solubility and miscibility of naproxen in poly(vinylpyrrolidone
    • Paudel A, Van Humbeeck J, Van den Mooter G. Theoretical and experimental investigation on the solid solubility and miscibility of naproxen in poly(vinylpyrrolidone). Mol Pharm 2010;7:1133-48
    • (2010) Mol Pharm , vol.7 , pp. 1133-48
    • Paudel, A.1    Van Humbeeck, J.2    Van Den Mooter, G.3
  • 91
    • 77956361367 scopus 로고    scopus 로고
    • Prediction of onset of crystallization in amorphous pharmaceutical systems: Phenobarbital, nifedipine/PVP, and phenobarbital/PVP
    • Caron V, Bhugra C, Pikal MJ. Prediction of onset of crystallization in amorphous pharmaceutical systems: Phenobarbital, nifedipine/PVP, and phenobarbital/PVP. J Pharm Sci 2010;99:3887-00
    • (2010) J Pharm Sci , vol.99 , pp. 3887-00
    • Caron, V.1    Bhugra, C.2    Pikal, M.J.3


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