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Formulation and Evaluation of in situ Gel of Atorvastatin for the Treatment of Periodontitis

机译:阿托伐他汀原位凝胶治疗牙周炎的配方与评价

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Purpose: The main objective of present study is to formulate and evaluate methyl cellulose based in situ periodontal gel of Atorvastatin. Approach: The in situ gel was prepared by using different concentration of methyl cellulose and gel was evaluated for pH, viscosity and rheology, Syringeability, drug content, in vitro drug release, and drug release kinetics. Findings: Compatibility study was performed using FTIR and results showed there was no interaction between drug and other excipients. Viscosity of all formulations was found in the range of 320-570 centipoise and all formulations exhibited pseudoplastic behaviour. Gelation time and temperature was found in the range of 6-17 min and 29o-39o respectively. All the formulation except formulation G6 and G7 showed satisfactory Syringeability due to lower concentration of polymer. Based on the results of release study, formulation G5 was found to be optimum formulation as it released 96.87% drug at the end of 24 h. In vitro release study revealed that release rate of drug from the in situ gel was concentration dependent; as concentration of methyl cellulose increased the drug release rate was retarded. Conclusion: It can be concluded that formulation containing 0.9%w/v of methyl cellulose gave optimized formulation.
机译:目的:本研究的主要目的是配制和评估基于阿托伐他汀的甲基纤维素基牙周凝胶。方法:通过使用不同浓度的甲基纤维素制备原位凝胶,并评估凝胶的pH值,粘度和流变性,可注射性,药物含量,体外药物释放和药物释放动力学。结果:使用FTIR进行了兼容性研究,结果表明药物与其他赋形剂之间没有相互作用。发现所有制剂的粘度在320-570厘泊的范围内,并且所有制剂均表现出假塑性行为。胶凝时间和温度分别在6-17分钟和29o-39o范围内。由于较低的聚合物浓度,除制剂G6和G7以外的所有制剂均显示令人满意的可注射性。根据释放研究的结果,发现制剂G5是最佳制剂,因为它在24小时结束时释放了96.87%的药物。体外释放研究表明,药物从原位凝胶中的释放速率与浓度有关。随着甲基纤维素浓度的增加,药物的释放速率受到阻碍。结论:可以得出结论,含有0.9%w / v的甲基纤维素的配方可提供最佳的配方。

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