) Quality Assessment of Some Brands of Ciprofloxacin and Levofloxacin Tablets Circulating in Karu Local Government Area of Nasarawa state, Nigeria.

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Abstract

Background: Circulation of poor-quality drugs has dire consequences on the health of consumers. Introduction of branded generics to ensure availability and affordability has shown potential for spread of poor-quality drugs. In this study, quality assessment of some commonly marketed ciprofloxacin (500 mg) and levofloxacin (500 mg) tablet brands in Karu Local Government Area (LGA) of Nasarawa State, Nigeria was evaluated. Methods: Five tablet brands including an innovator, of either drug were sourced from 5 different Pharmacies in the LGA. Tablets were coded A1-A5 and B1-B5 for ciprofloxacin and levofloxacin brands respectively. Physical assessment of the tablets was done. Physico-mechanical properties, uniformity of weight, friability and disintegration time were also evaluated using pharmacopeia methods. In vitro dissolution was carried out and the profiles statistically analyzed using the similarity and difference factors in comparison with the innovator products. Results: All the tablets had uniform weights within official specification, diameter was between 16.37 and 19.44 mm. Friability values were between 0.01 and 0.06 %; within specification. Disintegration time for ciprofloxacin and levofloxacin tablets was within 1.23 - 7.20 min and 3.19 - 12.90 min respectively; all met the specification. All (100 %) the ciprofloxacin brands met pharmacopeia requirement for drug release while only 60 % of the levofloxacin brands met this requirement. Comparatively A4 with f2 value of 41.62 % may not be interchangeable with the innovator brand while brands B2 and B4 with f2 values of 53.40 and 53.03 % respectively may be interchanged with the innovator brand or with each other. Conclusion:All the tablet brands were found to have good mechanical properties but only 75 % of the ciprofloxacin and 50 % of the levofloxacin tablet brands were found to be interchangeable with the innovator drug brands. This calls for concern as it brings to question the possible interchangeability of these brands with the innovator.
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尼日利亚纳萨拉瓦州卡鲁地方政府地区流通的部分品牌环丙沙星和左氧氟沙星片剂质量评价
背景:劣质药品的流通对消费者的健康造成了可怕的后果。引进品牌仿制药以确保可获得性和可负担性已显示出劣质药物传播的潜力。本研究对尼日利亚纳萨拉瓦州卡鲁地方政府区(LGA)一些常用上市品牌环丙沙星(500 mg)和左氧氟沙星(500 mg)片剂的质量进行了评价。方法:从LGA的5个不同药房采购5个片剂品牌,其中包括1个创新品牌。环丙沙星、左氧氟沙星片剂编号分别为A1-A5、B1-B5。对药片进行了物理评估。并采用药典方法对其物理力学性能、重量均匀性、脆性和崩解时间进行了评价。对其体外溶出度进行分析,并采用异同因素对其进行统计分析。结果:所有片剂质量均匀,片剂直径在16.37 ~ 19.44 mm之间。脆性值在0.01 ~ 0.06%之间;在规范。环丙沙星片和左氧氟沙星片崩解时间分别为1.23 ~ 7.20 min和3.19 ~ 12.90 min;均符合规格要求。环丙沙星品牌全部(100%)达到药典释药要求,而左氧氟沙星品牌仅有60%达到释药要求。相比之下,f2值为41.62%的A4不能与创新品牌互换,而f2值分别为53.40和53.03%的B2和B4可以与创新品牌互换,也可以与创新品牌互换。结论:所有片剂品牌均具有良好的力学性能,但只有75%的环丙沙星和50%的左氧氟沙星片剂品牌与创新药品牌可互换。这引起了人们的关注,因为它引发了对这些品牌与创新者之间可能互换性的质疑。
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