Diclofenac sodium multisource prolonged release tablets - a comparative study on the dissolution profiles

被引:33
作者
Bertocchi, P
Antoniella, E
Valvo, L
Alimonti, S
Memoli, A
机构
[1] Ist Super Sanita, Dipartimento Farmaco, I-00161 Rome, Italy
[2] Univ Roma La Sapienza, Fac Farm, Dipartimento Chim & Tecnol Sostanze Biol Att, I-00185 Rome, Italy
关键词
dissolution test; friability; hardness; prolonged release; diclofenac sodium; multisource pharmaceutical products; interchangeability;
D O I
10.1016/j.jpba.2004.11.041
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学]; 081704 [应用化学];
摘要
The aim of this work was to compare the dissolution behaviour of six diclofenac sodium prolonged release tablets of different brands obtained from the national market. The formulations contain the same amount of drug substance but different types and/or amount of excipients. The influence of these differences in formulation on the release characteristics of the dosage forms was evaluated on the European Pharmacopoeia apparatus 2 (paddle) employing eight different dissolution media in the pH range 1.2-8. Friability and hardness were tested too according to the European Pharmacopoeia. Dissolution profiles obtained from the studied formulations showed that the release characteristics vary considerably among different manufacturers and that even identical formulations show rather dissimilar release profiles in all the studied media. Use of both SIF without pancreatin and SIF without pancreatin containing 1% (w/v) Tween 20 resulted in strong discrimination among products. A correlation between friability and hardness and in vitro dissolution was evidenced for two formulations having identical excipient composition. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:679 / 685
页数:7
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