Literature DB >> 13954443

Dissolution rates of finely divided drug powders. I. Effect of a distribution of particle sizes in a diffusion-controlled process.

W I HIGUCHI, E N HIESTAND.   

Abstract

Keywords:  CHEMISTRY, PHARMACEUTICAL; POWDERS

Mesh：

Substances：

Year:  1963        PMID： 13954443     DOI： 10.1002/jps.2600520114

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN： 0022-3549            Impact factor:   3.534


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  6 in total

1.  Powder dissolution method for estimating rotating disk intrinsic dissolution rates of low solubility drugs.

Authors:  Konstantin Tsinman; Alex Avdeef; Oksana Tsinman; Dmytro Voloboy
Journal:  Pharm Res       Date:  2009-06-19       Impact factor: 4.200

2.  Effect of change in shape factor of a single crystal on its dissolution behavior.

Authors:  M V Dali; J T Carstensen
Journal:  Pharm Res       Date:  1996-01       Impact factor: 4.200

3.  Dissolution studies of poorly soluble drug nanosuspensions in non-sink conditions.

Authors:  Peng Liu; Odile De Wulf; Johanna Laru; Teemu Heikkilä; Bert van Veen; Juha Kiesvaara; Jouni Hirvonen; Leena Peltonen; Timo Laaksonen
Journal:  AAPS PharmSciTech       Date:  2013-04-25       Impact factor: 3.246

4.  Estimating the fraction dose absorbed from suspensions of poorly soluble compounds in humans: a mathematical model.

Authors:  D M Oh; R L Curl; G L Amidon
Journal:  Pharm Res       Date:  1993-02       Impact factor: 4.200

5.  Dissolution modeling: factors affecting the dissolution rates of polydisperse powders.

Authors:  A T Lu; M E Frisella; K C Johnson
Journal:  Pharm Res       Date:  1993-09       Impact factor: 4.200

6.  Simulating dissolution of intravitreal triamcinolone acetonide suspensions in an anatomically accurate rabbit eye model.

Authors:  Paul J Missel; Marc Horner; R Muralikrishnan
Journal:  Pharm Res       Date:  2010-05-14       Impact factor: 4.200
  6 in total

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