Formulation and in vitro evaluation of sustained release matrix tablets using cross-linked natural gum

被引:0
|
作者
Jamil, Qurrat Ul Ain [1 ,4 ]
Masood, Muhammad Irfan [1 ]
Jamil, Muhammad Nauman [2 ]
Masood, Imran [3 ]
Iqbal, Shahid Muhammad [4 ]
机构
[1] Univ Vet & Anim Sci, Inst Pharmaceut Sci, Lahore, Pakistan
[2] Univ Sargodha, Fac Pharm, Sargodha, Pakistan
[3] Islamia Univ Bahawalpur, Fac Pharm & Alternat Med, Bahawalpur, Pakistan
[4] Drugs Regulatory Author Pakistan, Islamabad, Pakistan
关键词
Sustained release tablet; isoniazid; dissolution release profile; release models; swelling index; OPTIMIZATION;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Polysaccharide gums because of their biocompatibility, biodegiadability and non-immunogenic properties are considered as the best choice for preparing sustained release tablets as compared to their synthetic counterpart. The cross linking of natural gums in matrix tablets increase the sustained release property of matrix tablets. Isoniazid is a first line therapy of tuberculosis, belongs to BCS I with half-life of 3-4 hours. These characteristics make isoniazid a good candidate for sustained release dosage form. Karaya gum crossed linked with trisodium tri metaphosphate was used as release rate retardant for preparing isoniazid cross-linked matrix tablet. Total 8 sustained release formulations were prepared. Both granules and tablets were evaluated under in vitro condition against different parameters. Dissolution studies were performed with all eight formulations for 12 hours using USP apparatus I. Four formulations designated as F1, F2, F3, F4 have drug and karaya gum while other four formulations F5, F6, F7, F8 have drug and crossed linked polymer in ratios of 1:1, 1:2, 1:3 and 1:4 respectively. Dissolution data was analyzed by using different kinetic models. Best fit model for most efficient formulation was zero order while release mechanism was super case I. Formulation 8 showed sufficiently slow release kinetics and about 83% of drug was released in 10 hours, indicating that cross-linked karaya gum proved efficient in preparing sustained release tablets.
引用
收藏
页码:355 / 362
页数:8
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