Quality Assessment of Hydroxychloroquine Tablet: A Comparative Evaluation of Drug Produced by Different Pharmaceutical Companies in Bangladesh
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 pharmaceut...
Published in: | Progress in Microbes and Molecular Biology |
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2023
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2-s2.0-85165186638 Islam R.; Hossain S.; Hossain S.; Islam M.T.; Sultana S.; Nizhum N.; Ahamed K.U.; Choo C.-Y.; Tan C.S.; Goh K.W. Quality Assessment of Hydroxychloroquine Tablet: A Comparative Evaluation of Drug Produced by Different Pharmaceutical Companies in Bangladesh 2023 Progress in Microbes and Molecular Biology 6 1 10.36877/pmmb.a0000336 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85165186638&doi=10.36877%2fpmmb.a0000336&partnerID=40&md5=9dfa2983ca4865c7d7dba7a5794c4c72 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 of 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 was among 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. © 2023, HH Publisher. All rights reserved. HH Publisher 26371049 English Article All Open Access; Gold Open Access |
author |
Islam R.; Hossain S.; Hossain S.; Islam M.T.; Sultana S.; Nizhum N.; Ahamed K.U.; Choo C.-Y.; Tan C.S.; Goh K.W. |
spellingShingle |
Islam R.; Hossain S.; Hossain S.; Islam M.T.; Sultana S.; Nizhum N.; Ahamed K.U.; Choo C.-Y.; Tan C.S.; Goh K.W. Quality Assessment of Hydroxychloroquine Tablet: A Comparative Evaluation of Drug Produced by Different Pharmaceutical Companies in Bangladesh |
author_facet |
Islam R.; Hossain S.; Hossain S.; Islam M.T.; Sultana S.; Nizhum N.; Ahamed K.U.; Choo C.-Y.; Tan C.S.; Goh K.W. |
author_sort |
Islam R.; Hossain S.; Hossain S.; Islam M.T.; Sultana S.; Nizhum N.; Ahamed K.U.; Choo C.-Y.; Tan C.S.; Goh K.W. |
title |
Quality Assessment of Hydroxychloroquine Tablet: A Comparative Evaluation of Drug Produced by Different Pharmaceutical Companies in Bangladesh |
title_short |
Quality Assessment of Hydroxychloroquine Tablet: A Comparative Evaluation of Drug Produced by Different Pharmaceutical Companies in Bangladesh |
title_full |
Quality Assessment of Hydroxychloroquine Tablet: A Comparative Evaluation of Drug Produced by Different Pharmaceutical Companies in Bangladesh |
title_fullStr |
Quality Assessment of Hydroxychloroquine Tablet: A Comparative Evaluation of Drug Produced by Different Pharmaceutical Companies in Bangladesh |
title_full_unstemmed |
Quality Assessment of Hydroxychloroquine Tablet: A Comparative Evaluation of Drug Produced by Different Pharmaceutical Companies in Bangladesh |
title_sort |
Quality Assessment of Hydroxychloroquine Tablet: A Comparative Evaluation of Drug Produced by Different Pharmaceutical Companies in Bangladesh |
publishDate |
2023 |
container_title |
Progress in Microbes and Molecular Biology |
container_volume |
6 |
container_issue |
1 |
doi_str_mv |
10.36877/pmmb.a0000336 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85165186638&doi=10.36877%2fpmmb.a0000336&partnerID=40&md5=9dfa2983ca4865c7d7dba7a5794c4c72 |
description |
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 of 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 was among 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. © 2023, HH Publisher. All rights reserved. |
publisher |
HH Publisher |
issn |
26371049 |
language |
English |
format |
Article |
accesstype |
All Open Access; Gold Open Access |
record_format |
scopus |
collection |
Scopus |
_version_ |
1809678477638500352 |