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埃塞俄比亚西南部吉马市可获得的八个品牌盐酸二甲双胍片的溶出度曲线评价

Dissolution Profile Evaluation of Eight Brands of Metformin Hydrochloride Tablets Available in Jimma, Southwest Ethiopia.

作者信息

Umeta Belachew, Bekele Anbessa, Mohammed Tesfaye, Duguma Markos, Teshome Henok, Mekonnen Yimer

机构信息

Department of Pharmaceutical Sciences, School of Pharmacy, Institute of Health, Jimma University, Jimma, Oromia, Ethiopia.

Jimma University Laboratory of Drug Quality (JULaDQ), Jimma University, Jimma, Oromia, Ethiopia.

出版信息

Diabetes Metab Syndr Obes. 2021 Aug 5;14:3499-3506. doi: 10.2147/DMSO.S316187. eCollection 2021.

Abstract

BACKGROUND

Dissolution is the critical quality control parameter and used to predict an in vivo oral bioavailability, and it is used to support bio-waiver.

AIM

To evaluate and compare the dissolution profile of eight brands of metformin HCL 500 mg tablets available in Jimma town, Southwest Ethiopia.

METHODS

The study was conducted in Jimma town, Ethiopia. Eight (seven brands and one comparator) metformin HCL 500 mg tablets were included. The dissolution study was conducted as per United States Pharmacopeia, and the dissolution profile was compared by one-way ANOVA, model-dependent and model-independent approaches.

RESULTS

All of the included tablet brands complied with single-point dissolution study specification. Statistical comparisons of the dissolution profile by one-way ANOVA revealed that all brands had similar dissolution profiles (=0.89). All of the brands had a similarity factor (f) >50% and the difference factor (f) <15. The entire brands followed the Weibull curve approach (the highest coefficient of determination and lowest Akaike Information Criteria) for the release of an active pharmaceutical ingredient.

CONCLUSION

All of the brands complied with single point dissolution study and all of them could be used interchangeably with the innovator drug. All brands followed the Weibull method for the release of the drug substance.

摘要

背景

溶出度是关键的质量控制参数,用于预测体内口服生物利用度,并用于支持生物豁免。

目的

评估和比较埃塞俄比亚西南部吉马镇市售的8个品牌的500毫克盐酸二甲双胍片的溶出曲线。

方法

该研究在埃塞俄比亚吉马镇进行。纳入了8种(7个品牌和1个对照品)500毫克盐酸二甲双胍片。溶出度研究按照美国药典进行,溶出曲线通过单向方差分析、模型依赖和模型独立方法进行比较。

结果

所有纳入的片剂品牌均符合单点溶出度研究规范。通过单向方差分析对溶出曲线进行统计比较显示,所有品牌的溶出曲线相似(=0.89)。所有品牌的相似性因子(f)>50%,差异因子(f)<15。所有品牌在活性药物成分释放方面均遵循威布尔曲线方法(决定系数最高,赤池信息准则最低)。

结论

所有品牌均符合单点溶出度研究,且均可与创新药物互换使用。所有品牌在药物释放方面均遵循威布尔方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/662b/8352574/6e397a6ac640/DMSO-14-3499-g0001.jpg

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