In-vitro Evaluations of Quality Control Parameters of Paracetamol Tablets Marketed in Gondar City, Northwest Ethiopia.

IF 2.2 Q2 HEALTH CARE SCIENCES & SERVICES Drug, Healthcare and Patient Safety Pub Date : 2020-12-21 eCollection Date: 2020-01-01 DOI:10.2147/DHPS.S282420
Konjit Abebe, Tamirat Bekele Beressa, Bilal Tessema Yimer
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引用次数: 6

Abstract

Background: The aim of this research was to evaluate quality control parameters of available brands of paracetamol tablets in Gondar city since standard quality parameters are essential for a better quality of the product. The different brands of paracetamol tablets were obtained from local pharmacies in Gondar town and the University of Gondar (UOG) hospital pharmacies.

Methods: Five brands of paracetamol, from each, 102 tablets were collected from private pharmacies, government health centers, and UOG pharmacies. The popular brands in the city, Panadol, Para-denk, Paramol, Paracetamol (EPHARM), and Cadimol, conventional tablets of 500 mg strength were chosen and the tablets were assessed for different quality parameters: weight variation, hardness, friability, disintegration, dissolution, and drug content (assay) using compendial methods. The tablets were evaluated to check if they comply with the specifications of USP (United States Pharmacopeia).

Results: From the results, it was observed that all the brands of paracetamol have passed the tests and met the specifications of USP. Results of weight variation, hardness, friability, and disintegration time ranged from 0.46 to 1.11%, 117.0 to 174.70 N, 0.07 to 0.63%, and 01 to 08 minutes for all the tablets, respectively. The dissolution profiles of all the brands are within the acceptable label claim. The assay results showed that the drug content of the paracetamol brands ranged from 95.04% to 106.81%. The dissolution rate was significantly different (p < 0.05) as compared to code 1 with all brands tested at 30 minutes. The disintegration time of different brands was also significantly different from the comparator (code 1) except code 2.

Conclusion: Based on the finding from this study, there were no significant deviations from pharmacopeia standards and specifications. The brands studied were safe enough and could be used to achieve the desired therapeutic effect.

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埃塞俄比亚西北部贡达尔市市售扑热息痛片质量控制参数的体外评价
背景:本研究的目的是评价贡达市现有品牌扑热息痛片的质量控制参数,因为标准的质量参数对提高产品质量至关重要。不同品牌的扑热息痛片分别从贡达尔镇当地药房和贡达尔大学(UOG)医院药房获得。方法:在民营药店、政府卫生院和UOG药店收集5个品牌的扑热息痛,每个品牌102片。采用药典法对市售常用品牌Panadol、Para-denk、Paramol、Paracetamol (EPHARM)、caddimol等500 mg常规片剂的质量参数:重量变化、硬度、脆度、崩解度、溶出度、含量(测定)进行评价。对所制片剂进行评价,检查其是否符合《美国药典》的规定。结果:各品牌对乙酰氨基酚均通过检验,符合美国药典的要求。重量变化、硬度、脆度、崩解时间分别为0.46 ~ 1.11%、117.0 ~ 174.70 N、0.07 ~ 0.63%、01 ~ 08 min。所有品牌的溶解情况都在可接受的标签声明范围内。结果表明,各品牌对乙酰氨基酚的含量范围为95.04% ~ 106.81%。与代码1相比,所有品牌在30分钟内的溶出率有显著差异(p < 0.05)。除代码2外,不同品牌的崩解时间与比较品(代码1)也存在显著差异。结论:本研究结果与药典标准、规范无明显偏差。所研究的品牌是足够安全的,可以达到预期的治疗效果。
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来源期刊
Drug, Healthcare and Patient Safety
Drug, Healthcare and Patient Safety HEALTH CARE SCIENCES & SERVICES-
CiteScore
4.10
自引率
0.00%
发文量
24
审稿时长
16 weeks
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