利用理化和无菌分析分析埃塞俄比亚亚的斯亚贝巴合法市场流通的注射用土霉素的质量

Yosef Nigussie, A. Melaku, Misgana Tadese, B. Belete, E. Kebede
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引用次数: 2

摘要

本研究旨在对亚的斯亚贝巴合法市场上流通的不同品牌注射用土霉素溶液的理化特性和无菌性进行质量评价。从全市兽药商店随机购买了9个品牌13个批次的土霉素。体检是根据世界卫生组织的指导方针编制的检查清单进行的。采用高效液相色谱法对活性药物成分进行定性和定量分析。无菌试验采用直接接种法。所有的样品都通过了鉴定、化验和无菌测试。不同品牌的原料药用量差异有统计学意义(P<0.05)。G品牌API含量最高(112.12%±1.86),H品牌最低(92.61%±1.5)。本研究发现,除了不同品牌的API水平存在差异外,所有品牌的理化和无菌检测均通过。需要严格的监管、监测和更广泛的监测,以确保持续控制国内不合格、未消毒和伪造的药品。
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Quality of injectable oxytetracycline circulating in legal markets of Addis Ababa, Ethiopia using physiochemical and sterility analysis
This study was conducted to evaluate the quality of different brands of injectable oxytetracycline solutions circulating in the legal markets  of Addis Ababa with respect to physicochemical characteristics and sterility. Nine brands of oxytetracycline with thirteen different batches were randomly purchased from veterinary drug stores in the city. The physical assessment was performed by using a checklist that was  prepared based on the World Health Organization guidelines. The qualitative and quantitative analysis of active pharmaceutical ingredients (API) was performed by High-Performance Liquid Chromatography. The sterility test was assessed by using the direct  inoculation method. All samples passed the identity, the assay, and the sterility tests. However, there were statistically significant  differences (P<0.05) among brands in the quantity of API. The highest percentage of the API was recorded in brand G (112.12%± 1.86) while the lowest was seen in brand H (92.61%± 1.5). This study revealed that all brands passed both physicochemical and sterility tests except for the differences in the API level among brands. Strict regulation, monitoring, and wider-scale surveillance are required to assure sustainable control of substandard, unsterile, and falsified pharmaceutical products in the country.
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