Investigation of the sustained-release mechanism of hydroxypropyl methyl cellulose skeleton type Acipimox tablets
In this study, we investigate the production of hypolipidemic agents in the form of Acipimox sustained-release tablets, using a wet pelleting process. The purpose of this research is to reduce the total intake time for patients and to lower the initial dose in such that the adverse reactions could b...
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De Gruyter
2018-04-01
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Series: | Open Chemistry |
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Online Access: | https://doi.org/10.1515/chem-2018-0036 |
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author | Liu Wanying Huo Qing Wang Yue Yu Na Shi Rongjian |
author_facet | Liu Wanying Huo Qing Wang Yue Yu Na Shi Rongjian |
author_sort | Liu Wanying |
collection | DOAJ |
description | In this study, we investigate the production of hypolipidemic agents in the form of Acipimox sustained-release tablets, using a wet pelleting process. The purpose of this research is to reduce the total intake time for patients and to lower the initial dose in such that the adverse reactions could be reduced. This study adopts the single-factor method and orthogonal experiments by using hydroxypropyl methyl cellulose (HPMC K15M) as the main sustained-release prescription composition. The final prescription is Acipimox 20%, HPMC K15M 26.67%, sodium carboxymethyl cellulose 30%, polyethylene glycol (PEG 6000) 1%, ethyl cellulose 16.6%, lactose 4.67% and magnesium stearate 1%. The dissolution of tablets reached 85.88% in 8 h. The difference in the weight, hardness and friability of the tables met the requirements in the Chinese Pharmacopoeia; to test the stability, a temperature and illumination accelerated test method was used, the results indicate that the Acipimox sustained-release tablets should be sealed and stored in a dark, cool area. A preliminary study on the tablets’ releasing mechanism showed that their release curve fitted the Higuchi model (the formula is Mt/M∞ = 31.137 t1/2–3.605 (R2 = 0.9903)). The Acipimox tablets’ release principle is dominated by the diffusion mechanism. |
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institution | Directory Open Access Journal |
issn | 2391-5420 |
language | English |
last_indexed | 2024-12-24T03:40:34Z |
publishDate | 2018-04-01 |
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spelling | doaj.art-f2df5b3046724bc2910967ab3b2a692a2022-12-21T17:16:56ZengDe GruyterOpen Chemistry2391-54202018-04-0116133333910.1515/chem-2018-0036chem-2018-0036Investigation of the sustained-release mechanism of hydroxypropyl methyl cellulose skeleton type Acipimox tabletsLiu Wanying0Huo Qing1Wang Yue2Yu Na3Shi Rongjian4Department of Biomedicine, Biochemical Engineering College, Beijing Union University, Fatou xili 3 region 18#, Chaoyang district, Beijing100023, ChinaDepartment of Biomedicine, Biochemical Engineering College, Beijing Union University, Fatou xili 3 region 18#, Chaoyang district, Beijing100023, ChinaDepartment of Biomedicine, Biochemical Engineering College, Beijing Union University, Fatou xili 3 region 18#, Chaoyang district, Beijing100023, ChinaDepartment of Biomedicine, Biochemical Engineering College, Beijing Union University, Fatou xili 3 region 18#, Chaoyang district, Beijing100023, ChinaResearch and Development Center, Institute of High Energy Physics, Chinese Academy of Sciences, Yuquan road 19hao, yiyuan, Shijingshan district, Beijing100049, P.R. ChinaIn this study, we investigate the production of hypolipidemic agents in the form of Acipimox sustained-release tablets, using a wet pelleting process. The purpose of this research is to reduce the total intake time for patients and to lower the initial dose in such that the adverse reactions could be reduced. This study adopts the single-factor method and orthogonal experiments by using hydroxypropyl methyl cellulose (HPMC K15M) as the main sustained-release prescription composition. The final prescription is Acipimox 20%, HPMC K15M 26.67%, sodium carboxymethyl cellulose 30%, polyethylene glycol (PEG 6000) 1%, ethyl cellulose 16.6%, lactose 4.67% and magnesium stearate 1%. The dissolution of tablets reached 85.88% in 8 h. The difference in the weight, hardness and friability of the tables met the requirements in the Chinese Pharmacopoeia; to test the stability, a temperature and illumination accelerated test method was used, the results indicate that the Acipimox sustained-release tablets should be sealed and stored in a dark, cool area. A preliminary study on the tablets’ releasing mechanism showed that their release curve fitted the Higuchi model (the formula is Mt/M∞ = 31.137 t1/2–3.605 (R2 = 0.9903)). The Acipimox tablets’ release principle is dominated by the diffusion mechanism.https://doi.org/10.1515/chem-2018-0036acipimoxsustained-release tabletsodium carboxymethylcellulosehydroxypropyl methyl cellulose |
spellingShingle | Liu Wanying Huo Qing Wang Yue Yu Na Shi Rongjian Investigation of the sustained-release mechanism of hydroxypropyl methyl cellulose skeleton type Acipimox tablets Open Chemistry acipimox sustained-release tablet sodium carboxymethylcellulose hydroxypropyl methyl cellulose |
title | Investigation of the sustained-release mechanism of hydroxypropyl methyl cellulose skeleton type Acipimox tablets |
title_full | Investigation of the sustained-release mechanism of hydroxypropyl methyl cellulose skeleton type Acipimox tablets |
title_fullStr | Investigation of the sustained-release mechanism of hydroxypropyl methyl cellulose skeleton type Acipimox tablets |
title_full_unstemmed | Investigation of the sustained-release mechanism of hydroxypropyl methyl cellulose skeleton type Acipimox tablets |
title_short | Investigation of the sustained-release mechanism of hydroxypropyl methyl cellulose skeleton type Acipimox tablets |
title_sort | investigation of the sustained release mechanism of hydroxypropyl methyl cellulose skeleton type acipimox tablets |
topic | acipimox sustained-release tablet sodium carboxymethylcellulose hydroxypropyl methyl cellulose |
url | https://doi.org/10.1515/chem-2018-0036 |
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