Bio-fluid uptake and release of Indomethacin of direct-compressed HPMC tablets

被引:10
作者
Bin, Chen [1 ]
Joshi, Sunil C. [1 ]
Lam, Y. C. [1 ]
机构
[1] Nanyang Technol Univ, Sch Mech & Aerosp Engn, Singapore 639798, Singapore
关键词
HPMC; Tablets; Swelling; Indomethacin; Release; CONTROLLED DRUG-DELIVERY; THERMOREVERSIBLE GELATION; METHYLCELLULOSE; MATRICES; KINETICS; MODEL; HYDROXYPROPYLMETHYLCELLULOSE; MECHANISMS; DIFFUSION; HYDROGELS;
D O I
10.1016/j.carbpol.2008.07.025
中图分类号
O69 [应用化学];
学科分类号
070301 [无机化学];
摘要
Tablets of three different grades of hydroxypropyl methyl cellulose (HPMC), having different viscosity, were prepared using the direct-compression technique with no additive or binder. The fluid uptake behavior of these HPMC tablets was studied in three types of bio-media - water, simulated gastric fluid (SGF), and simulated intestinal fluid (SIF). The amount of fluid uptake by the tablets followed a power law relationship with time for all three media. Variants such as pH value, type of salts and salt concentration in the media were found to have little influence on the swelling process for the tablet. On the contrary, viscosity and molecular weight of HPMC were the controlling parameters for the swelling process. Subsequently, Indomethacin was added in certain percentage to the tablets as a model drug. It was to examine and elucidate drug releasing properties of the HPMC tablets. The possible mechanisms involved in the process of drug dispersion are proposed and discussed. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:282 / 286
页数:5
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