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首页> 外文期刊>Indian journal of pharmaceutical sciences. >Design and evaluation of Xanthan gum-based sustained release matrix tablets of diclofenac sodium
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Design and evaluation of Xanthan gum-based sustained release matrix tablets of diclofenac sodium

机译:黄原胶双氯芬酸钠缓释基质片的设计与评价

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摘要

In the present investigation, an attempt has been made to increase therapeutic efficacy, reduce frequency of administration, and improve patient compliance, by developing sustained release matrix tablets of diclofenac sodium. Sustained release matrix tablets of diclofenac sodium, were developed by using different drug: polymer ratios, such as F1 (1:0.12), F2 (1:0.16), F3 (1:0.20), F4 (1:0.24) and F5 (1:0.28). Xanthan gum was used as matrix former, and microcrystalline cellulose as diluent. All the lubricated formulations were compressed using 8 mm flat faced punches. Compressed tablets were evaluated for uniformity of weight, content of active ingredient, friability, hardness, thickness, in vitro dissolution using basket method, and swelling index. All the formulations showed compliance with pharmacopoeial standards. Among different formulations, F1 showed sustained release of drug for 12 hours with 89.67% release. The effect of other parameters like addition of release modifier (PEG 6000), gum concentration, pH of dissolution medium, rotation speed and dissolution by paddle method, were also studied. Selected formulation (F1) was subjected to stability studies for three months at 0-4°, room temperature (28 °), and 45° with RH 75±5%, and showed stability with respect to release pattern. The kinetic treatment showed that the release of drug follows zero order kinetic (R2 0.9758). Korsmeyer and Peppas equation gave value of n to one, indicating that the drug was released by zero order kinetic. Thus, Xanthan gum can be used as an effective matrix former, to extend the release of diclofenac sodium.
机译:在本研究中,已经尝试通过开发双氯芬酸钠的持续释放基质片剂来提高治疗功效,减少给药频率并改善患者依从性。通过使用不同的药物:聚合物比率,例如F1(1:0.12),F2(1:0.16),F3(1:0.20),F4(1:0.24)和F5( 1:0.28)。黄原胶用作基质形成剂,微晶纤维素用作稀释剂。所有润滑配方均使用8 mm平面冲头压缩。评价压制片剂的重量均匀性,活性成分含量,易碎性,硬度,厚度,使用篮法的体外溶出度和溶胀指数。所有制剂均符合药典标准。在不同的配方中,F1显示药物持续释放12小时,释放率为89.67%。还研究了其他参数的影响,如添加脱模改性剂(PEG 6000),胶基糖浓度,溶出介质的pH值,转速和桨式溶出度。将选择的制剂(F1)在0-4°,室温(28°)和45°,RH 75±5%的条件下进行三个月的稳定性研究,并显示出相对于释放模式的稳定性。动力学处理表明药物的释放遵循零级动力学(R2 0.9758)。 Korsmeyer和Peppas方程将n的值设为1,表明该药物以零级动力学释放。因此,黄原胶可以用作有效的基质形成剂,以延长双氯芬酸钠的释放。

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