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Quality Assessment of Hydroxychloroquine Tablet: A Comparative Evaluation of Drug Produced by Different Pharmaceutical Companies in Bangladesh

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dc.contributor.author Islam, Md. Raihanur
dc.contributor.author Hossain, Md. Sakhawat
dc.contributor.author Hossain, Md. Sanower
dc.contributor.author Islam, Mohammad Touhidul
dc.contributor.author Sultana, Sharifa
dc.contributor.author Nizhum, Nisarat
dc.contributor.author Ahamed, Kutub Uddin
dc.contributor.author Choo, Chee - Yan
dc.contributor.author Tan, Ching Siang
dc.contributor.author Goh, Khang Wen
dc.date.accessioned 2024-08-19T06:04:21Z
dc.date.available 2024-08-19T06:04:21Z
dc.date.issued 2023-07-05
dc.identifier.uri http://dspace.daffodilvarsity.edu.bd:8080/handle/123456789/13087
dc.description.abstract "Hydroxychloroquine is the most commonly prescribed antimalarial extensively used to treat rheumatoid arthritis. It is extensively utilized as a repurposing drug, as well, in many countries worldwide to treat COVID-19. The pharmaceutical sector of Bangladesh is much enriched, and different pharmaceutical companies in Bangladesh produce this drug. Since the drug quality might vary significantly among different brands, assuring the quality PMMB 2023, 6, 1; a00003362of 11of medicine is absolutely necessary considering the health issues, particularly therapeutic efficacy and safety. Therefore, this study examined the quality of hydroxychloroquine produced by Bangladeshi pharmaceutical companies, concentrating on quality control parameters: the assay, dissolution, disintegration, hardness, friability, and weight fluctuation. All the brands of hydroxychloroquine tablets contained the stated amount of API between the range of 96.41±0.62 and 100.61±0.71 that met USP specification (100±5%). All brands met the pharmacopeial limit for the percentage of weight fluctuation, hardness test, friability, and disintegration time. Weight variation was between 0.31±0.01% and 0.46±0.02%, hardness was between 4.31 ± 0.88 and 7.36 ± 0.74 kgf, friability was less than 1%, and disintegration time was 5.42± 0.11 and 5.42± 0.11 min. In the dissolution test, all the samples attained more than 70% dissolution after 30 minutes. The mean percentage of hydroxychloroquine released in phosphate buffer was between 95.44±0.55 (Brand B) and 98.19±0.39 (Brand C) after 60 min. No significant difference wasamong the tested drugs from different companies, and all quality assessment parameters were within USP specifications. Therefore, hydroxychloroquine from the Bangladesh market is safe and effective" en_US
dc.language.iso en_US en_US
dc.publisher HH Publisher en_US
dc.subject Pharmaceutical technology en_US
dc.subject Bangladesh en_US
dc.subject Drug discovery en_US
dc.title Quality Assessment of Hydroxychloroquine Tablet: A Comparative Evaluation of Drug Produced by Different Pharmaceutical Companies in Bangladesh en_US
dc.type Article en_US


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