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采用压制包衣技术实现控释递增释放的帕利哌酮片剂。

Tablets of paliperidone using compression-coated technology for controlled ascending release.

作者信息

Tang Yingying, Teng Huan, Shi Yanan, He Haibing, Zhang Yu, Yin Tian, Cai Cuifang, Tang Xing

机构信息

School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.

出版信息

Asian J Pharm Sci. 2018 Mar;13(2):143-154. doi: 10.1016/j.ajps.2017.09.005. Epub 2017 Oct 13.

Abstract

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 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.

摘要

本研究旨在采用简单的制备技术和较短的制备工艺制备帕利哌酮(PAL)的梯度释放包衣(CC)片。对最终片剂的释放行为和机制进行了研究和评估。PAL CC片由高粘度羟丙基纤维素(HPC-H)的核心层和高粘度羟丙基甲基纤维素(HPMC-K100M)的包衣层组成。研究了材料和片芯组成等几个因素在制剂过程中的影响。采用重量分析法研究药物释放机制。数据可拟合到Peppas模型。梯度释药结果用不同时间点释放曲线的斜率表示。结果表明,当PAL的重量比为5:1(片芯:包衣层)时,该制剂可实现良好的梯度释药。HPC和HPMC的比例为33%,丙烯酸树脂RL-PO的用量为10%。梯度释放机制是由于溶剂渗透到PAL CC片中,随后药物从凝胶状的HPC和HPMC基质侵蚀中溶解出来。因此,释放机制是扩散和侵蚀的结合。本研究表明,对于口服给药系统,包衣片可在24小时内实现可控的梯度释放。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d35/7032237/d415792fc695/ajps470-ga-5001.jpg

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