Gitua John, Beck Aaron, Rovers John
College of Pharmacy and Health Sciences, Drake University, 2507 University Avenue, Des Moines, IA 50311, USA.
Malar J. 2014 Dec 4;13:474. doi: 10.1186/1475-2875-13-474.
The quality and stability of anti-malarial drugs in the Global South has long been of significant concern. Drug quality can be affected by poor or fraudulent manufacturing processes, while drug stability is affected by temperature and humidity. Knowledge of drug quality and stability is often the unique contribution of pharmacists volunteering on short-term medical mission trips.
To determine the quality and stability of artemether-lumefantrine 20/120 mg under ambient storage conditions in rural Mali.
One unopened blister pack of artemether-lumefantrine 20/120 mg (IPCA Laboratories, Mumbai) was stored under ambient conditions in a warehouse in a Malian village for one year. A second pack from the same lot number was stored under temperature and humidity controlled conditions in a university laboratory. The active ingredients of tablets from both packages were analysed using thin layer chromatography, nuclear magnetic resonance and infrared spectroscopy. The IPCA samples were referenced for drug identity and content to an identical American made product (Coartem(®), Novartis Pharmaceuticals).
Thin layer chromatographs, nuclear magnetic resonance and infrared spectroscopy results were identical for both IPCA samples and the reference product.
The IPCA products contained the same drugs in the same amount as on their package label and were identical to the reference product. It is concluded that they were of good quality. Spectroscopy results demonstrate the sample stored in Mali was stable for one year. Pharmacists volunteering on medical mission trips may dispense this product with confidence. At the end of a mission trip, pharmacists may store left over artemether-lumefantrine under ambient conditions for up to one year without concern for significant degradation of the active ingredients.
长期以来,全球南方抗疟药物的质量和稳定性一直备受关注。药品质量可能会受到不良或欺诈性生产工艺的影响,而药品稳定性则受温度和湿度影响。药品质量和稳定性方面的知识往往是参与短期医疗任务旅行的药剂师的独特贡献。
确定在马里农村环境储存条件下,蒿甲醚-本芴醇20/120毫克的质量和稳定性。
将一包未开封的蒿甲醚-本芴醇20/120毫克(IPCA实验室,孟买)在马里一个村庄的仓库环境条件下储存一年。同一批号的另一包在大学实验室的温度和湿度控制条件下储存。使用薄层色谱法、核磁共振和红外光谱法分析两包片剂的活性成分。将IPCA样品的药物标识和含量与相同的美国产产品(可泰舒(®),诺华制药)进行参照。
IPCA样品和参照产品的薄层色谱图、核磁共振和红外光谱结果相同。
IPCA产品所含药物与包装标签上的相同,且与参照产品相同。得出结论,其质量良好。光谱分析结果表明,在马里储存的样品一年来是稳定的。参与医疗任务旅行的药剂师可以放心分发该产品。在任务旅行结束时,药剂师可以在环境条件下将剩余的蒿甲醚-本芴醇储存长达一年,而无需担心活性成分会大幅降解。