Formulation and Evaluation of Indomethacin Sustained Release Tablet by using Natural Polymers

Sudhir Kathane, Shruti Rathore, Shashikant Chandrakar
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Abstract

Arthritis is most prevalent disorder and Indomethacin is choice of drug for arthritis. Oral route is most preferred route of drug administration and tablets are the more convenient dosage form. In present research natural polymers guar gum and xanthan gum were used to make sustained release tablet of Indomethacin. Indomethacin release from the tablets was studied in phosphate buffer pH 7.2. The drug release pattern of six different formulations in which xanthan gum and guar gum were used as a retarding material in different proportions was shown in table no. 6. The formulation F1 releases (75.20%) upto 12 hrs whereas the formulation F2 releases the drug (98.81%) in same time. The formulations F3, F4, F5 and F6 release 98.32%, 99.29%, 98.79% and 82.40% respectively. The dissolution pattern of both gums was similar i.e. with drug to polymer ratio (1:1). In present work F1 shows best sustained release upto 12 hrs in which Drug to Polymer ratio was 1:1:0 (Drug : Xanthan gum : Guar gum). In formulation F2 drug release was not sustained and complete release occurs in 12 hrs where the Drug to Polymer ratio was 1:1.67:0 (Drug: Xanthan gum : Guar gum). It was found that on the concentration of xanthan gum decreases the release rate of the drug also decreases. For sustain release there is not much role of Guar Gum reported. Indomethacin drug has been selected which has half-life 4.5 hrs. Hence the present work, an attempt has been made to provide sustained release drug delivery using polymers with Indomethacin as the model drug. Xanthan gum was best able to retard Indomethacin release mechanism even in the presence of a polymer. Polymer can be used to formulate successful sustained release Indomethacin matrix tablets that have desirable characteristics.
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使用天然聚合物配制和评估吲哚美辛缓释片剂
关节炎是最常见的疾病,而吲哚美辛是治疗关节炎的首选药物。口服是最常用的给药途径,而片剂是更方便的剂型。本研究使用天然聚合物瓜尔豆胶和黄原胶来制作吲哚美辛缓释片。在 pH 值为 7.2 的磷酸盐缓冲液中研究了片剂中吲哚美辛的释放情况。表 6 列出了黄原胶和瓜尔胶作为缓释材料的六种不同配方的药物释放模式。6.配方 F1 在 12 小时内的药物释放率为 75.20%,而配方 F2 在同一时间内的药物释放率为 98.81%。配方 F3、F4、F5 和 F6 的药物释放率分别为 98.32%、99.29%、98.79% 和 82.40%。两种胶的溶解模式相似,即药物与聚合物的比例为 1:1。在目前的研究中,药物与聚合物的比例为 1:1:0(药物:黄原胶:瓜尔豆胶)时,F1 的药物释放持续时间最长可达 12 小时。在配方 F2 中,药物与聚合物的比例为 1:1.67:0(药物:黄原胶:瓜尔豆胶),药物释放不持久,12 小时后完全释放。研究发现,随着黄原胶浓度的降低,药物的释放速率也会降低。据报道,瓜尔胶对药物的持续释放作用不大。吲哚美辛的半衰期为 4.5 小时。因此,本研究以吲哚美辛为模型药物,尝试使用聚合物进行持续释放给药。即使在聚合物存在的情况下,黄原胶也能最好地延缓吲哚美辛的释放机制。聚合物可用于成功配制具有理想特性的吲哚美辛缓释基质片剂。
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