Influence of processing parameters and formulation factors on the drug release from tablets powder-coated with Eudragit® L 100-55-Reference-Cited by-同舟云学术

Influence of processing parameters and formulation factors on the drug release from tablets powder-coated with Eudragit® L 100-55

Published:2007-09 Issue:2 Volume:67 Page:464-475
ISSN:0939-6411
Container-title:European Journal of Pharmaceutics and Biopharmaceutics
language:en
Short-container-title:European Journal of Pharmaceutics and Biopharmaceutics

Author:

Sauer Dorothea,Zheng Weijia,Coots Lonique B.,McGinity James W.

Publisher

Elsevier BV

Subject

Pharmaceutical Science,General Medicine,Biotechnology

Reference33 articles.

1. Degradation of omeprazole induced by enteric polymer solutions and aqueous dispersions: HPLC investigations;Riedel;Drug Dev. Ind. Pharm.,2005

2. The influence of polymeric subcoats and pellet formulation on the release of chlorpheniramine maleate from enteric coated pellets;Bruce;Drug Dev. Ind. Pharm.,2003

3. Influence of hydroxyethylcellulose on the drug release properties of theophylline pellets coated with Eudragit RS 30 D;Zheng;Eur. J. Pharm. Biopharm.,2005

4. Influence of plasticizer concentration and storage conditions on the drug release rate from Eudragit RS 30 D film-coated sustained-release theophylline pellets;Amighi;Eur. J. Pharm. Biopharm.,1996

5. Influence of film additives on stabilizing drug release rates from pellets coated with acrylic polymers;Maejima;Pharm. Dev. Technol.,2001

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