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East Mediterr Health J ; 13(6): 1427-37, 2007.
Article in English | MEDLINE | ID: mdl-18341192

ABSTRACT

The pharmaceutical quality of 7 local omeprazole capsule brands in Egypt was assessed relative to the proprietary product (Losec). Drug content, content uniformity, drug release (using USP test for enteric coated articles and a modified release test) were determined. Products were subjected to a 3-month stability study. Of the 7 brands, 6 had satisfactory drug content and content uniformity. All brands passed the USP drug release test. The modified release test proved to be more discriminative. After 3 months storage, drug content of 3 brands remained > 90% and 2 of these brands maintained drug release above 75%. Changes in pellet appearance during storage were indicative of omeprazole chemical degradation.


Subject(s)
Anti-Ulcer Agents/standards , Omeprazole/standards , Analysis of Variance , Anti-Ulcer Agents/chemistry , Anti-Ulcer Agents/economics , Anti-Ulcer Agents/supply & distribution , Biological Availability , Capsules , Chemistry, Pharmaceutical , Drug Costs/statistics & numerical data , Drug Packaging/standards , Drug Stability , Drug Storage , Drug and Narcotic Control , Egypt , Humans , Humidity , Hydrogen-Ion Concentration , Omeprazole/chemistry , Omeprazole/economics , Omeprazole/supply & distribution , Product Surveillance, Postmarketing , Solubility , Tablets, Enteric-Coated/chemistry , Tablets, Enteric-Coated/standards , Tablets, Enteric-Coated/supply & distribution , Time Factors
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