Deconinck E, Andriessens S, Bothy J L, Courselle P, De Beer J O
Division of Food, Medicines and Consumer Safety, Section Medicinal Products, Scientific Institute of Public Health (WIV-ISP), J. Wytmansstraat 14, B-1050 Brussels, Belgium.
J Pharm Anal. 2014 Aug;4(4):250-257. doi: 10.1016/j.jpha.2014.03.002. Epub 2014 Mar 13.
Counterfeit medicines are a growing problem in both developing and industrialised countries. In general the evaluation of these medicines is limited to the identification and the dosage of the active ingredients. In this study in vitro dissolution tests were conducted on two sets of counterfeit medicines containing PDE-5 inhibitors (sildenafil citrate and tadalafil). The dissolution profiles were statistically compared to the ones of the genuine products using the -method and a comparison at each time point using the Cochran test. The results showed low equivalences between counterfeit and genuine products as well as higher variations around the mean dissolution value at the different time points for the counterfeit products.
假药在发展中国家和工业化国家都是一个日益严重的问题。一般来说,对这些药品的评估仅限于活性成分的鉴别和剂量测定。在本研究中,对两组含有5型磷酸二酯酶(PDE-5)抑制剂(枸橼酸西地那非和他达拉非)的假药进行了体外溶出试验。使用-方法将溶出曲线与正品的溶出曲线进行统计学比较,并使用 Cochr an检验在每个时间点进行比较。结果表明,假药与正品之间的等效性较低,并且假药在不同时间点的平均溶出值周围的变异性较高。