Preparation and evaluation of dual-mode floating gastroretentive tablets containing itraconazole

被引:11
|
作者
Kim, Ju-Young [1 ]
Rhee, Yun-Seok [2 ,3 ]
Park, Chun-Woong [4 ]
Ha, Jung-Myung [1 ]
Park, Eun-Seok [1 ]
机构
[1] Sungkyunkwan Univ, Sch Pharm, Suwon 440746, Gyeonggi Do, South Korea
[2] Gyeongsang Natl Univ, Coll Pharm, Jinju, South Korea
[3] Gyeongsang Natl Univ, Pharmaceut Sci Res Inst, Jinju, South Korea
[4] Chungbuk Natl Univ, Coll Pharm, Cheongju, South Korea
关键词
Controlled release; gastro-floating system; miniature pigs; oral administration; porous matrix; site-specific drug delivery; PHARMACOKINETIC INTERACTION; ANTIFUNGAL AGENTS; SOLID DISPERSION; MATRIX TABLETS; DRUG-DELIVERY; FORMULATION; DISSOLUTION; BIOAVAILABILITY; ENHANCEMENT; DISPOSITION;
D O I
10.3109/10717544.2013.853212
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aims of the present study were to prepare new dual-mode floating gastroretentive tablets (DF-GRT) containing itraconazole (ITR) and to evaluate influence of the dosage forms on pharmacokinetic parameters of ITR. The solubility of ITR was enhanced around 200 times (from 1.54 to 248.38 mu g/mL) by preparing solid dispersion (SD) with hydroxypropylmethyl cellulose. Buoyancy of DF-GRT containing ITR-SD was established by both camphor sublimation and gas generation. Camphor sublimation decreased density of DF-GRT by making pores in tablet matrix, which led to elimination of lag time for floating. Carbon dioxide generated by sodium bicarbonate and citric acid helped to maintain buoyancy of DF-GRT. Therefore DF-GRT floated on the medium without lag time until disintegrated entirely during in vitro release study. They released 89.11% of the drug at 2 h. Residual camphor was <0.5 wt% after sublimation. The pharmacokinetics of DF-GRT was evaluated in six miniature pigs and compared to immediate release tablets (IRT). Mean AUC ratio of GRT/IRT was 1.36 but there was no statistical difference between AUC values. However delayed t(max), increased MRT and equivalent C-max of DF-GRT supposed it could be a promising tool for gastroretentive drug delivery system containing ITR.
引用
收藏
页码:519 / 529
页数:11
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