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Tablets of paliperidone using compression-coated technology for controlled ascending release
The aim of this work was to prepare ascending release compression-coated (CC) tablets with paliperidone (PAL) using a simple manufacturing technique and short manufacturing process. The release behavior and mechanisms in vitro of the final tablets was investigated and evaluated. The PAL CC tablets w...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shenyang Pharmaceutical University
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7032237/ https://www.ncbi.nlm.nih.gov/pubmed/32104387 http://dx.doi.org/10.1016/j.ajps.2017.09.005 |
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author | Tang, Yingying Teng, Huan Shi, Yanan He, Haibing Zhang, Yu Yin, Tian Cai, Cuifang Tang, Xing |
author_facet | Tang, Yingying Teng, Huan Shi, Yanan He, Haibing Zhang, Yu Yin, Tian Cai, Cuifang Tang, Xing |
author_sort | Tang, Yingying |
collection | PubMed |
description | The aim of this work was to prepare ascending release compression-coated (CC) tablets with paliperidone (PAL) using a simple manufacturing technique and short manufacturing process. The release behavior and mechanisms in vitro of the final tablets was investigated and evaluated. The PAL CC tablets were comprised of a core layer of high viscosity hydroxypropyl cellulose (HPC-H) and a coating layer of high viscosity hydroxypropyl methylcellulose (HPMC-K100M). Several factors such as materials and core tablet compositions were studied for their influence in the formulation procedure. The drug release mechanism was studied using gravimetric analysis. The data could be fitted to the Peppas model. The ascending drug release results were expressed in terms of the slope of the release curve at different time points. Results showed that the formulation could achieve a good ascending drug release when the weight ratio of PAL was 5:1 (core:layer). The fraction of HPC and HPMC was 33 %, and the combination of Eudragit RL-PO was 10%. The ascending release mechanism was due to solvent penetration into the PAL CC tablets, and subsequent drug dissolution from the gelatinous HPC and HPMC matrix erosion. The release mechanism was therefore a combination of diffusion and erosion. This work demonstrated that the compression-coated tablets could achieve controlled ascending release over 24 h for the oral administration systems. |
format | Online Article Text |
id | pubmed-7032237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Shenyang Pharmaceutical University |
record_format | MEDLINE/PubMed |
spelling | pubmed-70322372020-02-26 Tablets of paliperidone using compression-coated technology for controlled ascending release Tang, Yingying Teng, Huan Shi, Yanan He, Haibing Zhang, Yu Yin, Tian Cai, Cuifang Tang, Xing Asian J Pharm Sci Original Research Article The aim of this work was to prepare ascending release compression-coated (CC) tablets with paliperidone (PAL) using a simple manufacturing technique and short manufacturing process. The release behavior and mechanisms in vitro of the final tablets was investigated and evaluated. The PAL CC tablets were comprised of a core layer of high viscosity hydroxypropyl cellulose (HPC-H) and a coating layer of high viscosity hydroxypropyl methylcellulose (HPMC-K100M). Several factors such as materials and core tablet compositions were studied for their influence in the formulation procedure. The drug release mechanism was studied using gravimetric analysis. The data could be fitted to the Peppas model. The ascending drug release results were expressed in terms of the slope of the release curve at different time points. Results showed that the formulation could achieve a good ascending drug release when the weight ratio of PAL was 5:1 (core:layer). The fraction of HPC and HPMC was 33 %, and the combination of Eudragit RL-PO was 10%. The ascending release mechanism was due to solvent penetration into the PAL CC tablets, and subsequent drug dissolution from the gelatinous HPC and HPMC matrix erosion. The release mechanism was therefore a combination of diffusion and erosion. This work demonstrated that the compression-coated tablets could achieve controlled ascending release over 24 h for the oral administration systems. Shenyang Pharmaceutical University 2018-03 2017-10-13 /pmc/articles/PMC7032237/ /pubmed/32104387 http://dx.doi.org/10.1016/j.ajps.2017.09.005 Text en © 2018 Shenyang Pharmaceutical University. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research Article Tang, Yingying Teng, Huan Shi, Yanan He, Haibing Zhang, Yu Yin, Tian Cai, Cuifang Tang, Xing Tablets of paliperidone using compression-coated technology for controlled ascending release |
title | Tablets of paliperidone using compression-coated technology for controlled ascending release |
title_full | Tablets of paliperidone using compression-coated technology for controlled ascending release |
title_fullStr | Tablets of paliperidone using compression-coated technology for controlled ascending release |
title_full_unstemmed | Tablets of paliperidone using compression-coated technology for controlled ascending release |
title_short | Tablets of paliperidone using compression-coated technology for controlled ascending release |
title_sort | tablets of paliperidone using compression-coated technology for controlled ascending release |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7032237/ https://www.ncbi.nlm.nih.gov/pubmed/32104387 http://dx.doi.org/10.1016/j.ajps.2017.09.005 |
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