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新型没食子酰基橙皮苷和盐酸西替利嗪包衣漂浮片的配方与评价及其胃部给药研究。

Formulation and evaluation of novel coated floating tablets of bergenin and cetirizine dihydrochloride for gastric delivery.

机构信息

Key Laboratory of Drug Targeting and Drug Delivery System, Ministry of Education, West China School of Pharmacy, Sichuan University . No. 17, Block 3, Southern Renmin Road, Chengdu 610041, PR China.

出版信息

Drug Dev Ind Pharm. 2012 Oct;38(10):1280-8. doi: 10.3109/03639045.2011.645836. Epub 2011 Dec 30.

Abstract

A novel coated gastric floating drug-delivery system (GFDDS) of bergenin (BN) and cetirizine dihydrochloride (CET) was developed. First, the pharmacodynamic studies were performed and the results revealed that the new compounds of bergenin/cetirizine dihydrochloride had comparative efficacy as commercial products (bergenin/chlorphenamine maleate) but with fewer side effects on central nervous system (CNS). Subsequently, bergenin was formulated as an extended-release core tablet while cetirizine dihydrochloride was incorporated into the gastric coating film for immediate release. The formulation of GFDDS was optimized by CET content uniformity test, in vitro buoyancy and drug release. Herein, the effects of sodium bicarbonate (effervescent), hydroxypropyl methylcellulose (HPMC, matrix polymer) and coating weight gain were investigated respectively. The optimized GFDDS exhibited good floating properties (buoyancy lag time < 2 min; floating duration > 10 h) and satisfactory drug-release profiles (immediate release of CET in 10 min and sustained release of BN for 12 h). In vivo gamma scintigraphy proved that the optimized GFDDS could retain in the stomach with a prolonged gastric retention time (GRT) of 5 h, and the coating layer showed no side effect for gastric retention. The novel coated gastric floating drug-delivery system offers a new approach to enhance BN's absorption at its absorption site and the efficacy of both CET and BN.

摘要

开发了一种新型包衣胃漂浮型给药系统(GFDDS)的小檗碱(BN)和盐酸西替利嗪(CET)。首先进行了药效学研究,结果表明,新的小檗碱/盐酸西替利嗪化合物与商业产品(小檗碱/马来酸氯苯那敏)具有相当的疗效,但对中枢神经系统(CNS)的副作用较少。随后,将小檗碱制成缓释核心片剂,而盐酸西替利嗪则被包入胃溶膜中以实现即时释放。通过 CET 含量均匀度试验、体外漂浮和药物释放对 GFDDS 的配方进行了优化。在此,分别考察了碳酸氢钠(泡腾剂)、羟丙甲纤维素(HPMC,基质聚合物)和包衣增重的影响。优化后的 GFDDS 表现出良好的漂浮性能(漂浮滞后时间<2min;漂浮持续时间>10h)和令人满意的药物释放曲线(CET 在 10min 内快速释放,BN 持续释放 12h)。体内伽马闪烁成像证明,优化后的 GFDDS 可以在胃中保持较长的胃滞留时间(GRT)5h,且包衣层对胃滞留无副作用。新型包衣胃漂浮型给药系统为提高 BN 在吸收部位的吸收和 CET 和 BN 的疗效提供了一种新方法。

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