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Volumn 98, Issue 9, 2009, Pages 2875-2885

Current status of amorphous formulation and other special dosage forms as formulations for early clinical phases

Author keywords

Amorphous; Crystallization; Developmental strategy; Early clinical phases; Molecular mobility; Special dosage form; Stability

Indexed keywords

CARBAMAZEPINE; CREMOPHOR; CYCLODEXTRIN DERIVATIVE; ER 34122; EXCIPIENT; GELATIN; HYDROXYPROPYLMETHYLCELLULOSE; HYDROXYPROPYLMETHYLCELLULOSE ACETATE SUCCINATE; HYDROXYPROPYLMETHYLCELLULOSE PHTHALATE; IBUPROFEN; INSULIN; ITRACONAZOLE; JNJ 25894934; MACROGOL; MACROGOL 6000; MACROGOL DERIVATIVE; METHYLCELLULOSE; NIFEDIPINE; NITRENDIPINE; OIL; POLOXAMER; POLYSORBATE 80; POVIDONE; PRANLUKAST; RECOMBINANT HUMAN INSULIN; RICINOMACROGOL; TACROLIMUS; TOCOPHEROL DERIVATIVE; TOCOPHERYLPOLYETHYLENEGLYCOL SUCCINATE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 68949105637     PISSN: 00223549     EISSN: 15206017     Source Type: Journal    
DOI: 10.1002/jps.21816     Document Type: Article
Times cited : (68)

References (64)
  • 1
    • 0031024171 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • DOI 10.1016/S0169-409X(96)00423-1, PII S0169409X96004231
    • Lipinski CA, Lombardo F, Dominy BW, Feeney PJ. 1997. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv Drug Deliv Rev 23:3-25. (Pubitemid 27046991)
    • (1997) Advanced Drug Delivery Reviews , vol.23 , Issue.1-3 , pp. 3-25
    • Lipinski, C.A.1    Lombardo, F.2    Dominy, B.W.3    Feeney, P.J.4
  • 2
    • 2942564021 scopus 로고    scopus 로고
    • Pursuing the leadlikeness concept in pharmaceutical research
    • Hann MM, Oprea TI. 2004. Pursuing the leadlikeness concept in pharmaceutical research. Curr Opin Chem Biol 8:255-263.
    • (2004) Curr Opin Chem Biol , vol.8 , pp. 255-263
    • Hann, M.M.1    Oprea, T.I.2
  • 3
    • 37549071045 scopus 로고    scopus 로고
    • Drug discovery beyond the 'rule-of-five.'
    • Zhang M-Q, Wilkinson B. 2007. Drug discovery beyond the 'rule-of-five.' Curr Opin Biotechnol 18:478-488.
    • (2007) Curr Opin Biotechnol , vol.18 , pp. 478-488
    • Zhang, M.-Q.1    Wilkinson, B.2
  • 4
    • 41549115075 scopus 로고    scopus 로고
    • Assessing drug-likeness - What are we missing?
    • Vistoli G, Pedretti A, Testaet B. 2008. Assessing drug-likeness - What are we missing? Drug Discov Today 13:285-294.
    • (2008) Drug Discov Today , vol.13 , pp. 285-294
    • Vistoli, G.1    Pedretti, A.2    Testaet, B.3
  • 5
    • 36549010477 scopus 로고    scopus 로고
    • Unfinished business: Target-based drug discovery
    • DOI 10.1016/j.drudis.2007.10.017, PII S1359644607004576
    • Brown D. 2007. Unfinished business: Target-based drug discovery. Drug Discov Today 12:1007-1012. (Pubitemid 350180564)
    • (2007) Drug Discovery Today , vol.12 , Issue.23-24 , pp. 1007-1012
    • Brown, D.1
  • 6
    • 33847295225 scopus 로고    scopus 로고
    • Designing a molecular delivery system within a preclinical timeframe
    • DOI 10.1016/j.drudis.2007.01.006, PII S1359644607000463
    • Henck J-O, Byrn S. 2007. Designing a molecular delivery system within a preclinical timeframe. Drug Discov Today 12:189-199. (Pubitemid 46316891)
    • (2007) Drug Discovery Today , vol.12 , Issue.5-6 , pp. 189-199
    • Henck, J.-O.1    Byrn, S.R.2
  • 7
    • 34447646495 scopus 로고    scopus 로고
    • Developing early formulations: Practice and perspective
    • DOI 10.1016/j.ijpharm.2007.05.049, PII S0378517307004553
    • Li P, Zhao L. 2007. Developing early formulations: Practice and perspective. Int J Pharm 341:1-19. (Pubitemid 47088122)
    • (2007) International Journal of Pharmaceutics , vol.341 , Issue.1-2 , pp. 1-19
    • Li, P.1    Zhao, L.2
  • 9
    • 0034614208 scopus 로고    scopus 로고
    • Microemulsion-based media as novel drug delivery systems
    • DOI 10.1016/S0169-409X(00)00103-4, PII S0169409X00001034
    • Lawrence MJ, Rees GD. 2000. Microemulsion-based media as novel drug delivery systems. Adv Drug Deliv Rev 45:89-121. (Pubitemid 30943127)
    • (2000) Advanced Drug Delivery Reviews , vol.45 , Issue.1 , pp. 89-121
    • Lawrence, M.J.1    Rees, G.D.2
  • 10
    • 85031359422 scopus 로고    scopus 로고
    • Oil-in-water microemulsions containing tricyclic compounds or preconcentrates thereof
    • WO01/076582. Shionogi & Co., Ltd.
    • Kawakami K, Yoshikawa T. Oil-in-water microemulsions containing tricyclic compounds or preconcentrates thereof, WO01/076582. Shionogi & Co., Ltd.
    • Kawakami, K.1    Yoshikawa, T.2
  • 11
    • 0037123703 scopus 로고    scopus 로고
    • Microemulsion formulation for enhanced absorption of poorly soluble drugs: I. Prescription design
    • DOI 10.1016/S0168-3659(02)00049-4, PII S0168365902000494
    • Kawakami K, Yoshikawa T, Moroto Y, Kanaoka E, Takahashi K, Nishihara Y, Masuda K. 2002. Microemulsion formulation for enhanced absorption of poorly soluble drugs. I. Prescription design. J Control Release 81:65-74. (Pubitemid 34454850)
    • (2002) Journal of Controlled Release , vol.81 , Issue.1-2 , pp. 65-74
    • Kawakami, K.1    Yoshikawa, T.2    Moroto, Y.3    Kanaoka, E.4    Takahashi, K.5    Nishihara, Y.6    Masuda, K.7
  • 12
    • 0037123701 scopus 로고    scopus 로고
    • Microemulsion formulation for enhanced absorption of poorly soluble drugs: II. In vivo study
    • DOI 10.1016/S0168-3659(02)00050-0, PII S0168365902000500
    • Kawakami K, Yoshikawa T, Hayashi T, Nishihara Y, Masuda K. 2002. Microemulsion formulation for enhanced absorption of poorly soluble drugs. II. In vivo study. J Control Release 81:75-82. (Pubitemid 34454851)
    • (2002) Journal of Controlled Release , vol.81 , Issue.1-2 , pp. 75-82
    • Kawakami, K.1    Yoshikawa, T.2    Hayashi, T.3    Nishihara, Y.4    Masuda, K.5
  • 13
    • 39149113817 scopus 로고    scopus 로고
    • Formulation of lipid-based delivery systems for oral administration: Materials, methods and strategies
    • Pouton CW, Porter CJH. 2008. Formulation of lipid-based delivery systems for oral administration: Materials, methods and strategies. Adv Drug Deliv Rev 60:625-637.
    • (2008) Adv Drug Deliv Rev , vol.60 , pp. 625-637
    • Pouton, C.W.1    Porter, C.J.H.2
  • 14
    • 0030638567 scopus 로고    scopus 로고
    • Characteristics and Significance of the Amorphous State in Pharmaceutical Systems
    • Hancock BC, Zografi G. 1997. Characteristics and significance of the amorphous state in pharmaceutical systems. J Pharm Sci 86:1-12. (Pubitemid 127489650)
    • (1997) Journal of Pharmaceutical Sciences , vol.86 , Issue.1
    • Hancock, B.C.1    Zografi, G.2
  • 15
    • 0032885450 scopus 로고    scopus 로고
    • Solid dispersion of poorly-soluble drugs: Early promises, subsequent problems, and recent breakthroughs
    • Serajuddin ATM. 1999. Solid dispersion of poorly-soluble drugs: Early promises, subsequent problems, and recent breakthroughs. J Pharm Sci 88:1058-1066.
    • (1999) J Pharm Sci , vol.88 , pp. 1058-1066
    • Serajuddin, A.T.M.1
  • 16
    • 0035897584 scopus 로고    scopus 로고
    • Amorphous pharmaceutical solids: Preparation, characterization and stabilization
    • DOI 10.1016/S0169-409X(01)00098-9, PII S0169409X01000989
    • Yu L. 2001. Amorphous pharmaceutical solids: Preparation, characterization and stabilization. Adv Drug Deliv Rev 48:27-42. (Pubitemid 32454482)
    • (2001) Advanced Drug Delivery Reviews , vol.48 , Issue.1 , pp. 27-42
    • Yu, L.1
  • 17
    • 1842865536 scopus 로고    scopus 로고
    • Melt extrusion: From process to drug delivery technology
    • DOI 10.1016/S0939-6411(02)00061-9, PII S0939641102000619
    • Breitenbach J. 2002. Melt extrusion: From process to drug delivery technology. Eur J Pharm Biopharm 54:107-117. (Pubitemid 34919382)
    • (2002) European Journal of Pharmaceutics and Biopharmaceutics , vol.54 , Issue.2 , pp. 107-117
    • Breitenbach, J.1
  • 18
    • 0036181889 scopus 로고    scopus 로고
    • Practical aspects of lyophilization using non-aqueous co-solvent systems
    • Teagarden DL, Baker DS. 2002. Practical aspects of lyophilization using non-aqueous co-solvent systems. Eur J Pharm Sci 15:115-133.
    • (2002) Eur J Pharm Sci , vol.15 , pp. 115-133
    • Teagarden, D.L.1    Baker, D.S.2
  • 19
    • 1442334238 scopus 로고    scopus 로고
    • Incorporation of lipophilic drugs in sugar glasses by lyophilization using a mixture of water and tertiary butyl alcohol as solvent
    • Van Drooge DJ, Hinrichs WLJ, Frijlink HW. 2004. Incorporation of lipophilic drugs in sugar glasses by lyophilization using a mixture of water and tertiary butyl alcohol as solvent. J Pharm Sci 93:713-725.
    • (2004) J Pharm Sci , vol.93 , pp. 713-725
    • Van Drooge, D.J.1    Hinrichs, W.L.J.2    Frijlink, H.W.3
  • 20
    • 20344400666 scopus 로고    scopus 로고
    • Pharmaceutical development of a lyophilised dosage form for the investigational anticancer agent imexon using dimethyl sulfoxide as solubilising and stabilising agent
    • DOI 10.1002/jps.20331
    • den Brok MWJ, Nuijen B, Lutz C, Opitz HG, Beijnen JH. 2005. Pharmaceutical development of a lyophilised dosage form for the investigational anticancer agent Imexon using dimethyl sulfoxide as solubilising and stabilising agent. J Pharm Sci 94:1101-1114. (Pubitemid 40780776)
    • (2005) Journal of Pharmaceutical Sciences , vol.94 , Issue.5 , pp. 1101-1114
    • Den Brok, M.W.J.1    Nuijen, B.2    Lutz, C.3    Opitz, H.-G.4    Beijnen, J.H.5
  • 21
    • 38349180826 scopus 로고    scopus 로고
    • Prediction of onset of crystallization from experimental relaxation times. II. Comparison between predicted and experimental onset times
    • Bhugra C, Shmeis R, Krill SL, Pikal MJ. 2008. Prediction of onset of crystallization from experimental relaxation times. II. Comparison between predicted and experimental onset times. J Pharm Sci 97:455-472.
    • (2008) J Pharm Sci , vol.97 , pp. 455-472
    • Bhugra, C.1    Shmeis, R.2    Krill, S.L.3    Pikal, M.J.4
  • 22
    • 43249092894 scopus 로고    scopus 로고
    • Role of thermodynamic, molecular, and kinetic factors in crystallization from the amorphous state
    • Bhugra C, Pikal MJ. 2008. Role of thermodynamic, molecular, and kinetic factors in crystallization from the amorphous state. J Pharm Sci 97:1329-1349.
    • (2008) J Pharm Sci , vol.97 , pp. 1329-1349
    • Bhugra, C.1    Pikal, M.J.2
  • 23
    • 0034061182 scopus 로고    scopus 로고
    • 1H NMR relaxation times
    • DOI 10.1002/(SICI)1520-6017(200003)89:3<408::AID-JPS11>3.0.CO;2-#
    • Aso Y, Yoshioka S, Kojima S. 2000. Relationship between the crystallization rates of amorphous nifedipine, phenobarbital, and flopropione, and their molecular mobility as measured by their enthalpy relaxation and 1H NMR relaxation times. J Pharm Sci 89:408-416. (Pubitemid 30152440)
    • (2000) Journal of Pharmaceutical Sciences , vol.89 , Issue.3 , pp. 408-416
    • Aso, Y.1    Yoshioka, S.2    Kojima, S.3
  • 24
    • 0035991640 scopus 로고    scopus 로고
    • Physical stability of amorphous pharmaceuticals: Importance of configurational thermodynamic quantities and molecular mobility
    • DOI 10.1002/jps.10169
    • Zhou D, Zhang GGZ, Law D, Grant DJW, Schmitt EA. 2002. Physical stability of amorphous pharmaceuticals: Importance of configurational thermodynamic quantities and molecular mobility. J Pharm Sci 91:1863-1872. (Pubitemid 34810531)
    • (2002) Journal of Pharmaceutical Sciences , vol.91 , Issue.8 , pp. 1863-1872
    • Zhou, D.1    Zhang, G.G.Z.2    Law, D.3    Grant, D.J.W.4    Schmitt, E.A.5
  • 25
    • 0036171845 scopus 로고    scopus 로고
    • Cryogenic grinding of indomethacin polymorphs and solvates: Assessment of amorphous phase formation and amorphous phase physical stability
    • DOI 10.1002/jps.10028
    • Crowley KJ, Zografi G. 2002. Cryogenic grinding of indomethacin polymorphs and solvates: Assessment of amorphous phase formation and amorphous phase physical stability. J Pharm Sci 91:492-507. (Pubitemid 34139812)
    • (2002) Journal of Pharmaceutical Sciences , vol.91 , Issue.2 , pp. 492-507
    • Crowley, K.J.1    Zografi, G.2
  • 26
    • 3242714321 scopus 로고    scopus 로고
    • Effect of preparation method on physical properties of amorphous trehalose
    • DOI 10.1023/B:PHAM.0000033003.17251.c3
    • Surana R, Pyne A, Suryanarayanan R. 2004. Effect of preparation method on physical properties of amorphous trehalose. Pharm Res 21:1167-1176. (Pubitemid 38960768)
    • (2004) Pharmaceutical Research , vol.21 , Issue.7 , pp. 1167-1176
    • Surana, R.1    Pyne, A.2    Suryanarayanan, R.3
  • 27
    • 6344247455 scopus 로고    scopus 로고
    • Stability and solubility of celecoxib-PVP amorphous dispersions: A molecular perspective
    • DOI 10.1023/B:PHAM.0000045226.42859.b8
    • Gupta P, Kakumanu VK, Bansal AK. 2004. Stability and solubility of celecoxib-PVP amorphous dispersions: A molecular perspective. Pharm Res 21:1762-1769. (Pubitemid 39390086)
    • (2004) Pharmaceutical Research , vol.21 , Issue.10 , pp. 1762-1769
    • Gupta, P.1    Kakumanu, V.K.2    Bansal, A.K.3
  • 28
    • 20344362926 scopus 로고    scopus 로고
    • Calorimetric investigation of the structural relaxation of amorphous materials: Evaluating validity of the methodologies
    • DOI 10.1002/jps.20298
    • Kawakami K, Pikal MJ. 2005. Calorimetric investigation of the structural relaxation of amorphous materials: Evaluating validity of the methodologies. J Pharm Sci 94:948-965. (Pubitemid 40789961)
    • (2005) Journal of Pharmaceutical Sciences , vol.94 , Issue.5 , pp. 948-965
    • Kawakami, K.1    Pikal, M.J.2
  • 29
    • 33749435820 scopus 로고    scopus 로고
    • A calorimetric method to estimate molecular mobility of amorphous solids at relatively low temperatures
    • DOI 10.1007/s11095-006-9071-9
    • Mao C, Chamarthy SP, Byrn SR, Pinal R. 2006. A calorimetric method to estimate molecular mobility of amorphous solids at relatively low temperatures. Pharm Res 23:2269-2276. (Pubitemid 44511508)
    • (2006) Pharmaceutical Research , vol.23 , Issue.10 , pp. 2269-2276
    • Mao, C.1    Prasanth Chamarthy, S.2    Byrn, S.R.3    Pinal, R.4
  • 32
    • 36549025974 scopus 로고    scopus 로고
    • Enhancement of the dissolution rate and gastrointestinal absorption of pranlukast as a model poorly water-soluble drug by grinding with gelatin
    • DOI 10.1016/j.ijpharm.2007.06.037, PII S0378517307005546
    • Chono S, Takeda E, Seki T, Morimoto K. 2008. Enhancement of the dissolution rate and gastrointestinal absorption of pranlukast as a model poorly water-soluble drug by grinding with gelatin. Int J Pharm 347:71-78. (Pubitemid 350180324)
    • (2008) International Journal of Pharmaceutics , vol.347 , Issue.1-2 , pp. 71-78
    • Chono, S.1    Takeda, E.2    Seki, T.3    Morimoto, K.4
  • 33
    • 38749130125 scopus 로고    scopus 로고
    • Method for screening of solid dispersion formulations of low-solubility compounds-Miniaturization and automation of solvent casting and dissolution testing
    • DOI 10.1016/j.ijpharm.2007.09.042, PII S0378517307008228
    • Shanbhag A, Rabel S, Nauka E, Casadevall G, Shivanand P, Eichenbaum G, Mansky P. 2008. Method for screening of solid dispersion formulations of low-solubility compounds - Miniaturization and automation of solvent casting and dissolution testing. Int J Pharm 351:209-218. (Pubitemid 351186860)
    • (2008) International Journal of Pharmaceutics , vol.351 , Issue.1-2 , pp. 209-218
    • Shanbhag, A.1    Rabel, S.2    Nauka, E.3    Casadevall, G.4    Shivanand, P.5    Eichenbaum, G.6    Mansky, P.7
  • 34
    • 0035964465 scopus 로고    scopus 로고
    • In vitro and in vivo evaluation of carbamazepine-PEG 6000 solid dispersions
    • Zerrouk N, Chemtob C, Arnaud P, Toscani S, Dugue J. 2001. In vitro and in vivo evaluation of carbamazepine-PEG 6000 solid dispersions. Int J Pharm 225:49-62.
    • (2001) Int J Pharm , vol.225 , pp. 49-62
    • Zerrouk, N.1    Chemtob, C.2    Arnaud, P.3    Toscani, S.4    Dugue, J.5
  • 35
    • 0019201676 scopus 로고
    • Dissolution and absorption of nifedipine from nifedipine- polyvinylpyrrolidone coprecipitate
    • Sugimoto I, Kuchiki A, Nakagawa H, Tohgo K, Kondo S, Iwane I, Takahashi K. 1980. Dissolution and absorption of nifedipine from nifedipine- polyvinylpyrrolidone coprecipitate. Drug Dev Ind Pharm 6:137-160. (Pubitemid 11236605)
    • (1980) Drug Development and Industrial Pharmacy , vol.6 , Issue.2 , pp. 137-160
    • Sugimoto, I.1    Kuchiki, A.2    Nakagawa, H.3
  • 36
    • 0036141742 scopus 로고    scopus 로고
    • Improvement of dissolution and oral absorption of ER-34122, a poorly water-soluble dual 5-lipoxygenase/cyclooxygenase inhibitor with anti-inflammatory activity by preparing solid dispersion
    • DOI 10.1002/jps.10020
    • Kushida I, Ichikawa M, Asakawa N. 2002. Improvement of dissolution and oral absorption of ER-34122, a poorly water-soluble dual 5-lipoxygenase/ cyclooxygenase inhibitor with anti-inflammatory activity by preparing solid dispersion. J Pharm Sci 91:258-266. (Pubitemid 34074484)
    • (2002) Journal of Pharmaceutical Sciences , vol.91 , Issue.1 , pp. 258-266
    • Kushida, I.1    Ichikawa, M.2    Asakawa, N.3
  • 39
    • 4544383493 scopus 로고    scopus 로고
    • Nanosuspensions in drug delivery
    • Rabinow BE. 2004. Nanosuspensions in drug delivery. Nat Rev Drug Discov 3:785-796.
    • (2004) Nat Rev Drug Discov , vol.3 , pp. 785-796
    • Rabinow, B.E.1
  • 40
    • 34548049483 scopus 로고    scopus 로고
    • Nanosizing - Oral formulation development and biopharmaceutical evaluation
    • DOI 10.1016/j.addr.2007.05.003, PII S0169409X0700083X
    • Kesisoglou F, Panmai S, Wu Y. 2007. Nanosizing - Oral formulation development and biopharmaceutical evaluation. Adv Drug Deliv Rev 59:631-644. (Pubitemid 47285408)
    • (2007) Advanced Drug Delivery Reviews , vol.59 , Issue.7 , pp. 631-644
    • Kesisoglou, F.1    Panmai, S.2    Wu, Y.3
  • 41
    • 1242308254 scopus 로고    scopus 로고
    • Current status and future potential of transdermal drug delivery
    • Prausnitz MR, Mitragotri S, Langer R. 2004. Current status and future potential of transdermal drug delivery. Nat Rev Drug Discov 3:115-124. (Pubitemid 38239773)
    • (2004) Nature Reviews Drug Discovery , vol.3 , Issue.2 , pp. 115-124
    • Prausnitz, M.R.1    Mitragotri, S.2    Langer, R.3
  • 42
    • 33845906339 scopus 로고    scopus 로고
    • Inhaling medicines: Delivering drugs to the body through the lungs
    • Patton JS, Byron PR. 2007. Inhaling medicines: Delivering drugs to the body through the lungs. Nat Rev Drug Discov 6:67-74.
    • (2007) Nat Rev Drug Discov , vol.6 , pp. 67-74
    • Patton, J.S.1    Byron, P.R.2
  • 44
    • 36849085410 scopus 로고    scopus 로고
    • Pfizer dumps Exubera
    • Mack GS. 2007. Pfizer dumps Exubera. Nat Biotechnol 25:1331-1332.
    • (2007) Nat Biotechnol , vol.25 , pp. 1331-1332
    • Mack, G.S.1
  • 45
    • 43449134352 scopus 로고    scopus 로고
    • Inhaled insulin's last gasp?
    • Kling J. 2008. Inhaled insulin's last gasp? Nat Biotechnol 26:479-480.
    • (2008) Nat Biotechnol , vol.26 , pp. 479-480
    • Kling, J.1
  • 47
    • 49449090136 scopus 로고    scopus 로고
    • Inhaled Technosphere insulin in comparison to subcutaneous regular human insulin: Time action profile and variability in subjects with type 2 diabetes
    • Rave K, Heise T, Heinemann L, Boss AH. 2008. Inhaled Technosphere insulin in comparison to subcutaneous regular human insulin: Time action profile and variability in subjects with type 2 diabetes. J Diabetes Sci Technol 2:205-212.
    • (2008) J Diabetes Sci Technol , vol.2 , pp. 205-212
    • Rave, K.1    Heise, T.2    Heinemann, L.3    Boss, A.H.4
  • 48
    • 20344391910 scopus 로고    scopus 로고
    • Trends in solubility of polymorphs
    • Pudipeddi M, Serajuddin ATM. 2005. Trends in solubility of polymorphs. J Pharm Sci 94:929-939.
    • (2005) J Pharm Sci , vol.94 , pp. 929-939
    • Pudipeddi, M.1    Serajuddin, A.T.M.2
  • 49
    • 52449088248 scopus 로고    scopus 로고
    • Biodegradable films developed by electrospray deposition for sustained drug delivery
    • Xie J, Tan JC, Wang C-H. 2008. Biodegradable films developed by electrospray deposition for sustained drug delivery. J Pharm Sci 97:3109-3122.
    • (2008) J Pharm Sci , vol.97 , pp. 3109-3122
    • Xie, J.1    Tan, J.C.2    Wang, C.-H.3
  • 50
    • 0346639267 scopus 로고    scopus 로고
    • Physics of amorphous solids
    • Hilden LR, Morris KR. 2004. Physics of amorphous solids. J Pharm Sci 93:3-12.
    • (2004) J Pharm Sci , vol.93 , pp. 3-12
    • Hilden, L.R.1    Morris, K.R.2
  • 51
    • 0141678823 scopus 로고    scopus 로고
    • The effect of low concentrations of molecularly dispersed poly(vinylpyrrolidone) on indomethacin crystallization from the amorphous state
    • DOI 10.1023/A:1025706110520
    • Crowley KJ, Zografi G. 2003. The effect of low concentrations of molecularly dispersed poly(vinylpyrrolidone) on indomethacin crystallization from the amorphous state. Pharm Res 20:1417-1422. (Pubitemid 37164050)
    • (2003) Pharmaceutical Research , vol.20 , Issue.9 , pp. 1417-1422
    • Crowley, K.J.1    Zografi, G.2
  • 52
    • 33745018390 scopus 로고    scopus 로고
    • Crystallization of sucrose glass under ambient conditions: Evaluation of crystallization rate and unusual melting behavior of resultant crystals
    • DOI 10.1002/jps.20458
    • Kawakami K, Miyoshi K, Tamura N, Yamaguchi T, Ida Y. 2006. Crystallization of sucrose glass under ambient conditions: Evaluation of crystallization rate and unusual melting behavior of resultant crystals. J Pharm Sci 95:1354-1363. (Pubitemid 43874449)
    • (2006) Journal of Pharmaceutical Sciences , vol.95 , Issue.6 , pp. 1354-1363
    • Kawakami, K.1    Miyoshi, K.2    Tamura, N.3    Yamaguchi, T.4    Ida, Y.5
  • 53
    • 33947154406 scopus 로고    scopus 로고
    • Isothermal crystallization of Imwitor 742 from supercooled liquid state
    • DOI 10.1007/s11095-006-9193-0
    • Kawakami K. 2007. Isothermal crystallization of Imwitor 742 from supercooled liquid state. Pharm Res 24:738-747. (Pubitemid 46411962)
    • (2007) Pharmaceutical Research , vol.24 , Issue.4 , pp. 738-747
    • Kawakami, K.1
  • 54
    • 38949119344 scopus 로고    scopus 로고
    • Diffusionless crystal growth from glass has precursor in equilibrium liquid
    • DOI 10.1021/jp709616c
    • Sun Y, Xi H, Ediger MD, Yu L. 2008. Difussionless crystal growth from glass has precursor in equilibrium liquid. J Phys Chem B 112:661-664. (Pubitemid 351212499)
    • (2008) Journal of Physical Chemistry B , vol.112 , Issue.3 , pp. 661-664
    • Sun, Y.1    Xi, H.2    Ediger, M.D.3    Yu, L.4
  • 55
    • 43949132112 scopus 로고    scopus 로고
    • Crystallization near glass transition: Transition from diffusion-controlled to diffusionless crystal growth studied with seven polymorphs
    • DOI 10.1021/jp7120577
    • Sun Y, Xi H, Chen S, Ediger MD, Yu L. 2008. Crystallization near glass transition: Transition from difussion-controlled to diffusionless crystal growth studied with seven polymorphs. J Phys Chem B 112:5594-5601. (Pubitemid 351704577)
    • (2008) Journal of Physical Chemistry B , vol.112 , Issue.18 , pp. 5594-5601
    • Sun, Y.1    Xi, H.2    Chen, S.3    Ediger, M.D.4    Yu, L.5
  • 57
    • 0038058782 scopus 로고    scopus 로고
    • In situ monitoring of crystallization processes using synchrotron x-ray diffraction: The search for structural precursors
    • Davey RJ, Liu W, Quayle MJ, Tiddy GJT. 2002. In situ monitoring of crystallization processes using synchrotron x-ray diffraction: The search for structural precursors. Cryst Growth Des 2:269-272.
    • (2002) Cryst Growth Des , vol.2 , pp. 269-272
    • Davey, R.J.1    Liu, W.2    Quayle, M.J.3    Tiddy, G.J.T.4
  • 58
    • 34249018624 scopus 로고    scopus 로고
    • Correlations between molecular mobility and chemical stability during storage of amorphous pharmaceuticals
    • DOI 10.1002/jps.20926
    • Yoshioka S, Aso Y. 2007. Correlations between molecular mobility and chemical stability during storage of amorphous pharmaceuticals. J Pharm Sci 96:960-981. (Pubitemid 46797468)
    • (2007) Journal of Pharmaceutical Sciences , vol.96 , Issue.5 , pp. 960-981
    • Yoshioka, S.1    Aso, Y.2
  • 59
    • 17644414570 scopus 로고    scopus 로고
    • Phase behavior of amorphous molecular dispersions. I: Determination of the degree and mechanism of solid solubility
    • Vasanthavada M, Tong WQ, Joshi Y, Kislalioglu MS. 2004. Phase behavior of amorphous molecular dispersions. I: Determination of the degree and mechanism of solid solubility. Pharm Res 21:1598-1606.
    • (2004) Pharm Res , vol.21 , pp. 1598-1606
    • Vasanthavada, M.1    Tong, W.Q.2    Joshi, Y.3    Kislalioglu, M.S.4
  • 60
    • 17644395269 scopus 로고    scopus 로고
    • Phase behavior of amorphous molecular dispersions. II: Role of hydrogen bonding in solid solubility and phase separation kinetics
    • Vasanthavada M, Tong WQ, Joshi Y, Kislalioglu MS. 2005. Phase behavior of amorphous molecular dispersions. II: Role of hydrogen bonding in solid solubility and phase separation kinetics. Pharm Res 22:440-448.
    • (2005) Pharm Res , vol.22 , pp. 440-448
    • Vasanthavada, M.1    Tong, W.Q.2    Joshi, Y.3    Kislalioglu, M.S.4
  • 61
    • 24044470016 scopus 로고    scopus 로고
    • Impact of the amount of excess solids on apparent solubility
    • DOI 10.1007/s11095-005-6247-7
    • Kawakami K, Miyoshi K, Ida Y. 2005. Impact of the amount of excess solids on apparent solubility. Pharm Res 22:1537-1543. (Pubitemid 41215895)
    • (2005) Pharmaceutical Research , vol.22 , Issue.9 , pp. 1537-1543
    • Kawakami, K.1    Miyoshi, K.2    Ida, Y.3
  • 62
    • 33749442356 scopus 로고    scopus 로고
    • Theoretical and practical approaches for prediction of drug-polymer miscibility and solubility
    • Marsac PJ, Shamblin SL, Taylor LS. 2006. Theoretical and practical approaches for prediction of drug-polymer miscibility and solubility. Pharm Res 23:2417-2426.
    • (2006) Pharm Res , vol.23 , pp. 2417-2426
    • Marsac, P.J.1    Shamblin, S.L.2    Taylor, L.S.3
  • 63
    • 57749206650 scopus 로고    scopus 로고
    • Estimation of drug-polymer miscibility and solubility in amorphous solid dispersions using experimentally determined interaction parameters
    • Marsac PJ, Li T, Taylor LS. 2009. Estimation of drug-polymer miscibility and solubility in amorphous solid dispersions using experimentally determined interaction parameters. Pharm Res 26:139-151.
    • (2009) Pharm Res , vol.26 , pp. 139-151
    • Marsac, P.J.1    Li, T.2    Taylor, L.S.3
  • 64
    • 61449135800 scopus 로고    scopus 로고
    • Solubility of small-molecule crystals in polymers: D-mannitol in PVP, indomethacin in PVP/VA, and nifedipine in PVP/VA
    • Tao J, Sun Y, Zhang GGZ, Yu L. 2009. Solubility of small-molecule crystals in polymers: D-mannitol in PVP, indomethacin in PVP/VA, and nifedipine in PVP/VA. Pharm Res 26:855-864.
    • (2009) Pharm Res , vol.26 , pp. 855-864
    • Tao, J.1    Sun, Y.2    Zhang, G.G.Z.3    Yu, L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.