Literature DB >> 2235898

Particle size and content uniformity.

S H Yalkowsky1, S Bolton.   

Abstract

The requirements of the USP Content Uniformity test are translated into physical and mathematical parameters. Assuming spherical particle sizes with a log normal distribution, the mean particle size and particle size distribution required to insure a high probability of passing the content uniformity test are calculated. On the basis of these calculations it is shown that satisfactory tablets of low doses cannot be manufactured from a drug that does not meet certain particle size distribution specifications. It is recommended that particle size specifications for low dose drugs include a requirement for a limit to size distribution.

Mesh:

Substances:

Year:  1990        PMID: 2235898     DOI: 10.1023/a:1015958209643

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  7 in total

1.  Particle size and content uniformity.

Authors:  H C Caldwell
Journal:  Pharm Res       Date:  1991-03       Impact factor: 4.200

2.  The manufacture of low-dose oral solid dosage form to support early clinical studies using an automated micro-filing system.

Authors:  Mingda Bi; Changquan Calvin Sun; Francisco Alvarez; Fernando Alvarez-Nunez
Journal:  AAPS PharmSciTech       Date:  2010-12-23       Impact factor: 3.246

3.  Comments on "Particle size and content uniformity," by Yalkowsky and Bolton.

Authors:  H Egermann
Journal:  Pharm Res       Date:  1991-08       Impact factor: 4.200

4.  Towards integrated drug substance and drug product design for an active pharmaceutical ingredient using particle engineering.

Authors:  Eleftherios Kougoulos; Ian Smales; Hugh M Verrier
Journal:  AAPS PharmSciTech       Date:  2011-01-19       Impact factor: 3.246

5.  Guidance in the setting of drug particle size specifications to minimize variability in absorption.

Authors:  K C Johnson; A C Swindell
Journal:  Pharm Res       Date:  1996-12       Impact factor: 4.200

Review 6.  Process optimization and particle engineering of micronized drug powders via milling.

Authors:  A Brunaugh; H D C Smyth
Journal:  Drug Deliv Transl Res       Date:  2018-12       Impact factor: 4.617

Review 7.  Direct Compaction Drug Product Process Modeling.

Authors:  Alexander Russell; John Strong; Sean Garner; William Ketterhagen; Michelle Long; Maxx Capece
Journal:  AAPS PharmSciTech       Date:  2022-01-31       Impact factor: 3.246

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.