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

被引:17
|
作者
Tang, Yingying [1 ]
Teng, Huan [1 ]
Shi, Yanan [1 ]
He, Haibing [1 ]
Zhang, Yu [1 ]
Yin, Tian [1 ]
Cai, Cuifang [1 ]
Tang, Xing [1 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
Paliperidone; Compression-coated tablet; Ascending release; Controlled release; HYDROPHILIC MATRIX TABLETS; EXTENDED-RELEASE; DELIVERY-SYSTEM; DRUG-DELIVERY; ORAL PALIPERIDONE; IN-VITRO; LAYER; HYDROXYPROPYLCELLULOSE; THEOPHYLLINE; DISSOLUTION;
D O I
10.1016/j.ajps.2017.09.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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. (C) 2018 Shenyang Pharmaceutical University. Production and hosting by Elsevier B.V.
引用
收藏
页码:143 / 154
页数:12
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