Butler D, Bonadeo D, Maroni A, Foppoli A, Zema L, Giordano F
Helsinn Birex Pharmaceuticals LTD, Damastown, Mulhuddart, Dublin 15, Ireland.
Boll Chim Farm. 2000 Nov-Dec;139(6):237-41.
Nimesulide is a quite popular non-steroidal anti-inflammatory drug (NSAID), which has been demonstrated to preferentially inhibit cycloxygenase-2 (COX-2), thus exerting milder gastrointestinal and renal side effects. Apart from the original products (Aulin and Mesulid), several copy and generic nimesulide-containing preparations are presently available on the Italian market. Generics are defined by the World Health Organization (WHO) as interchangeable multi-source pharmaceutical products and, according to international regulatory issues, their bioequivalence to an already marketed reference product has to be proven. Due to its physico-chemical properties, and in particular to the low solubility, nimesulide appears to be a critical molecule from a biopharmaceutical point of view. On the basis of these premises, the aim of the present work was to perform a comparative evaluation of tablets in vitro behaviour for the best-selling copy (Sulidamor) and generic (Nimesulide Dorom) in reference to the original products. The results provided by the dissolution test pointed out statistically significant differences in the in vitro behaviour displayed by the original products on one hand and by the copy as well as generic preparations in exam on the other.
尼美舒利是一种非常受欢迎的非甾体抗炎药(NSAID),已证明其能优先抑制环氧化酶-2(COX-2),因此胃肠道和肾脏副作用较轻。除了原研产品(奥鲁林和美舒利)外,目前意大利市场上还有几种含尼美舒利的仿制药和通用制剂。世界卫生组织(WHO)将通用制剂定义为可互换的多源药品,根据国际监管问题,必须证明其与已上市的参比产品具有生物等效性。由于其物理化学性质,特别是低溶解度,从生物制药的角度来看,尼美舒利似乎是一个关键分子。基于这些前提,本研究的目的是针对最畅销的仿制药(舒利莫)和通用制剂(多罗美尼美舒利),参照原研产品,对片剂的体外行为进行比较评估。溶出度试验结果表明,一方面原研产品与另一方面受试的仿制药和通用制剂所表现出的体外行为存在统计学上的显著差异。