Bertocchi Paola, Antoniella Eleonora, Valvo Luisa, Alimonti Stefano, Memoli Adriana
Dipartimento del Farmaco, Istituto Superiore di Sanità, Viale Regina Elena, 299-00161 Rome, Italy.
J Pharm Biomed Anal. 2005 Apr 1;37(4):679-85. doi: 10.1016/j.jpba.2004.11.041. Epub 2004 Dec 22.
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.
本研究的目的是比较从国内市场获得的六个不同品牌双氯芬酸钠缓释片的溶出行为。这些制剂含有相同量的原料药,但辅料的类型和/或用量不同。在欧洲药典装置2(桨法)上,采用pH值范围为1.2 - 8的八种不同溶出介质,评估这些制剂差异对剂型释放特性的影响。还根据欧洲药典测试了脆碎度和硬度。从所研究制剂获得的溶出曲线表明,不同厂家的释放特性差异很大,而且即使是相同的制剂在所有研究介质中的释放曲线也相当不同。使用不含胰酶的模拟肠液和含1%(w/v)吐温20的不含胰酶的模拟肠液,导致产品之间有很强的区分度。对于两种辅料组成相同的制剂,脆碎度和硬度与体外溶出之间存在相关性。