Independent Consultant, London, UK.
Concept Foundation, Geneva, Switzerland.
Int J Gynaecol Obstet. 2024 May;165(2):405-415. doi: 10.1002/ijgo.15148. Epub 2023 Sep 29.
Previous studies have demonstrated quality concerns with misoprostol. Mifepristone, however, has not been extensively assessed for quality. Between 2020 and 2021, Concept Foundation and the International Planned Parenthood Federation conducted a study to determine the quality of these medical abortion drugs in low- and middle-income countries (LMIC).
The collection of batch samples of misoprostol and mifepristone was carried out by trained sampling agents in selected LMIC. Single drug packs and combipacks were sampled. A World Health Organization prequalified laboratory conducted testing method verifications and subsequent sample analysis. Tests included identification, assay, related substances, and content uniformity for misoprostol, and identification, assay, related substances, and dissolution for mifepristone.
Samples were collected from Burkina Faso, Cambodia, Democratic Republic of Congo, India, Kyrgyzstan, Moldova, Nepal, Nigeria, Pakistan, Uganda and Vietnam. Sixty-four pooled batch samples were tested, consisting of 31 combipacks, 26 misoprostol-only and seven mifepristone-only products. Overall, 54.7% of samples were non-compliant with one or more of the specifications, representing 51.6% of combipack products, 57.1% of misoprostol tablets analyzed and 23.7% of mifepristone tablets. One falsified misoprostol-only product was found.
The present study confirms that a significant problem still exists in relation to the quality of medical abortion drugs in LMIC. For misoprostol, our findings suggest that historical concerns around primary packaging may have been largely resolved but that manufacturing processes for both finished product and active pharmaceutical ingredient need to be improved. The present study also provides evidence of mifepristone quality issues.
先前的研究表明米索前列醇存在质量问题。然而,米非司酮的质量尚未得到广泛评估。2020 年至 2021 年期间,概念基金会和国际计划生育联合会开展了一项研究,以确定中低收入国家(LMIC)这些药物流产药物的质量。
在选定的 LMIC 中,经过培训的抽样代理收集米索前列醇和米非司酮的批次样本。对单一药物包装和组合包装进行抽样。世界卫生组织预认证实验室进行了测试方法验证和随后的样品分析。测试包括米索前列醇的鉴别、含量测定、有关物质和含量均匀度,以及米非司酮的鉴别、含量测定、有关物质和溶出度。
从布基纳法索、柬埔寨、刚果民主共和国、印度、吉尔吉斯斯坦、摩尔多瓦、尼泊尔、尼日利亚、巴基斯坦、乌干达和越南收集了样本。共测试了 64 个混合批次样本,包括 31 个组合包装、26 个米索前列醇单药和 7 个米非司酮单药产品。总体而言,有 54.7%的样本不符合一项或多项规格,这代表了 51.6%的组合包装产品、57.1%的米索前列醇片剂和 23.7%的米非司酮片剂。发现一个伪造的米索前列醇单药产品。
本研究证实,中低收入国家药物流产药物的质量仍存在重大问题。对于米索前列醇,我们的研究结果表明,过去对初级包装的担忧可能在很大程度上得到了解决,但成品和原料药的生产工艺仍需改进。本研究还提供了米非司酮质量问题的证据。