메뉴 건너뛰기




Volumn 25, Issue 10, 2008, Pages 2309-2311

A modified approach to predict dissolution and absorption of polydisperse powders

Author keywords

Absorption; Dissolution rate prediction; Particle size; Polydisperse powders; Solubility

Indexed keywords

ABSORPTION; ARTICLE; DISSOLUTION; PARTICLE SIZE; POLYDISPERSE POWDER; POWDER; PREDICTION; PRIORITY JOURNAL; SIMULATION; SOLUBILITY; TECHNIQUE; THERMODYNAMICS;

EID: 51649086857     PISSN: 07248741     EISSN: 1573904X     Source Type: Journal    
DOI: 10.1007/s11095-008-9630-3     Document Type: Article
Times cited : (7)

References (8)
  • 1
    • 0035289779 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • 1-3
    • A. Lipinski F. Lombardo W. Dominy J. Feeney 2001 Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings Adv. Drug Deliv. Rev. 46 1-3 3 26
    • (2001) Adv. Drug Deliv. Rev. , vol.46 , pp. 3-26
    • Lipinski, A.1    Lombardo, F.2    Dominy, W.3    Feeney, J.4
  • 3
    • 0024596954 scopus 로고
    • The effect of particle size distribution on dissolution rate and oral absorption
    • 1
    • J. Hintz C. Johnson 1989 The effect of particle size distribution on dissolution rate and oral absorption Int. J. Pharm. 51 1 9 17
    • (1989) Int. J. Pharm. , vol.51 , pp. 9-17
    • Hintz, J.1    Johnson, C.2
  • 4
    • 0141680647 scopus 로고    scopus 로고
    • Dissolution and absorption modeling: Model expansion to simulate the effects of precipitation, water absorption, longitudinally changing intestinal permeability, and controlled release on drug absorption
    • 8
    • C. Johnson 2003 Dissolution and absorption modeling: model expansion to simulate the effects of precipitation, water absorption, longitudinally changing intestinal permeability, and controlled release on drug absorption Drug Dev. Ind. Pharm. 29 8 833 842
    • (2003) Drug Dev. Ind. Pharm. , vol.29 , pp. 833-842
    • Johnson, C.1
  • 5
    • 0030444550 scopus 로고    scopus 로고
    • Guidance in the setting of drug particle size specifications to minimize variability in absorption
    • 12
    • C. Johnson C. Swindell 1996 Guidance in the setting of drug particle size specifications to minimize variability in absorption Pharm. Res. 13 12 1795 1798
    • (1996) Pharm. Res. , vol.13 , pp. 1795-1798
    • Johnson, C.1    Swindell, C.2
  • 6
    • 0027275798 scopus 로고
    • Dissolution modelling: Factors affecting the dissolution rates of polydisperse powders
    • 9
    • T. Lu E. Frisella C. Johnson 1993 Dissolution modelling: factors affecting the dissolution rates of polydisperse powders Pharm. Res. 10 9 1308 1314
    • (1993) Pharm. Res. , vol.10 , pp. 1308-1314
    • Lu, T.1    Frisella, E.2    Johnson, C.3
  • 7
    • 26644466295 scopus 로고    scopus 로고
    • A new approach in the prediction of the dissolution behavior of suspended particles by means of their particle size distribution
    • 5
    • P. Tinke K. Vanhoutte R. De Maesschalck S. Verheyen H. De Winter 2005 A new approach in the prediction of the dissolution behavior of suspended particles by means of their particle size distribution J. Pharm. Biomed. Anal. 39 5 900 907
    • (2005) J. Pharm. Biomed. Anal. , vol.39 , pp. 900-907
    • Tinke, P.1    Vanhoutte, K.2    De Maesschalck, R.3    Verheyen, S.4    De Winter, H.5
  • 8
    • 3042814562 scopus 로고    scopus 로고
    • Nanosuspensions: A promising drug delivery strategy
    • 7
    • B. Patravale A. Date M. Kulkarni 2004 Nanosuspensions: a promising drug delivery strategy J. Pharm. Pharmacol. 56 7 827 840
    • (2004) J. Pharm. Pharmacol. , vol.56 , pp. 827-840
    • Patravale, B.1    Date, A.2    Kulkarni, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.