埃塞俄比亚西南部Jimma镇不同品牌甲硝唑的质量:一项横断面药品质量研究

Teshome Sosengo, Tesfaye Mohammed, Ramanjireddy Tatiparthi
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引用次数: 0

摘要

背景:劣质药品包括不合格和伪造(即假药)药品。世卫组织2017年的报告估计,低收入和中等收入国家的不合格和伪造医疗产品率约为10.5%,估计支出为305亿美元。目的:对埃塞俄比亚西南部奥罗米亚地区Jimma镇不同品牌甲硝唑的质量进行评价。方法:在埃塞俄比亚奥罗米亚州Jimma镇进行横断面研究。该研究于2018年5月3日至7月30日进行。采用方便取样技术采集样本。样品采用2013年英国药典和2015年美国药典规定的方法进行分析。将7个品牌甲硝唑的检测结果和3个品牌甲硝唑胶囊的溶出度检测结果输入window社会科学软件24.0版统计软件包中。然后采用Tukey检验进行单因素方差分析,确定各剂型品牌内及品牌间含量测定和溶出度试验结果是否存在显著差异(p<0.05)。结果与讨论:按照《英国药典2013》和《美国药典2015》规定的方法,对3种甲硝唑胶囊和4种甲硝唑注射剂品牌进行了质量评价。所分析的7个品牌的甲硝唑均通过了BP 2013的一致性检测规范。三个品牌的甲硝唑胶囊均通过了USP 2015的重量均匀度和溶出度试验规范。7个品牌的甲硝唑均通过了USP 2015的测定(即药物含量)检验规范。甲硝唑(仿制药)胶囊和尼美特(注射剂)的药物含量最高,分别为107.81%和105.56%。但在95%置信区间对各剂型各品牌含量进行统计比较,各剂型各品牌内部含量和各品牌之间含量差异显著(p<0.05)。4个品牌的甲硝唑注射液均通过了USP 2015内毒素限量,内毒素限量< 0.35 Eu/ml。在纳入研究的4个品牌的甲硝唑注射液中,Aldezol和Metris两个品牌的甲硝唑注射液无菌检测不合格,质量较差。甲硝唑注射液pH值在BP 2013标准范围内。结论:本研究结果表明,吉马镇存在劣质甲硝唑的发生率。因此,应定期进行上市后质量评估,以确定药品在市场上的质量状况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quality of Different Brands of Metronidazole Available in Jimma Town, South West Ethiopia: A Cross-Sectional PharmaceuticalQuality Study
Background: Poor quality medicines include substandard and falsified (i.e., counterfeited) medicines. WHO report of 2017 estimates that the rates of substandard and falsified medical products in low- and middle-income countries is approximately 10.5% with an estimated spend of US$ 30.5 billion. Objective: The purpose of the study is to assess the quality of different brands of metronidazole available in Jimma town, Oromia region, South West Ethiopia. Methods: Cross-sectional study was conducted in Jimma town, Oromia regional state, Ethiopia. The study was conducted from May 03 – July 30, 2018. Samples were collected using convenience sampling technique. The samples were analyzed using a methods specified in British Pharmacopoeia 2013 and United States Pharmacopoeia 2015. The assay result of all the seven brands of metronidazole and dissolution test result of the three brands of metronidazole capsules was entered to statistical package for social sciences software version 24.0 for windows. Then, one way analysis of variance was performed using Tukey test to determine whether there exists significant difference in assay and dissolution test results within and among the brands of the respective dosage forms (p<0.05). Results and Discussion: The quality of brands (three Metronidazole capsules and four Metronidazole injections brands) of Metronidazole was assessed based up on a method specified in BP 2013 and USP 2015. All the seven brands of Metronidazole analyzed for quality passed identity test specification of BP 2013. The three brands of Metronidazole capsules passed weight uniformity and dissolution test specification of USP 2015. The seven brands of Metronidazole passed assay (i.e., drug content) test specification of USP 2015. The highest percentage of drug content, 107.81% and 105.56%, obtained for Metronidazole (generic) (capsule), Nirmet (injection) respectively. However, statistical comparison of assay of respective brands of the respective dosage forms at 95% confidence interval indicates that there exists significant difference in assay within and among the brands of the respective dosage forms (p<0.05). All the four brands of Metronidazole injections passed USP 2015 limit for Endotoxin, Endotoxin limit < 0.35 Eu/ml. Two brands of Metronidazole injection, Aldezol and Metris, failed sterility test from the four brands of Metronidazole injections included in the study and hence of poor quality. The pH of Metronidazole injections were within BP 2013 specification range. Conclusion: The result of the current study revealed that there was incidence of poor quality Metronidazole in Jimma town. Therefore, post marketing quality assessment should be performed routinely to determine quality status of the drug on market.
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