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

M. Ahmed, R. Chaudhari, Ankit Acharya
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引用次数: 8

Abstract

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 29 o -39 o 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.
阿托伐他汀原位凝胶治疗牙周炎的配方及疗效评价
目的:制备并评价甲基纤维素基阿托伐他汀原位牙周凝胶。方法:采用不同浓度的甲基纤维素制备原位凝胶,并对凝胶的pH、粘度和流变性、注射性、药物含量、体外释药和释药动力学进行评价。结果:用FTIR进行配伍研究,与其他辅料无相互作用。所有配方的粘度在320-570厘泊范围内,所有配方都表现出假塑性行为。凝胶时间为6 ~ 17 min,凝胶温度为29 ~ 39 min。除配方G6和G7外,其余配方均因聚合物浓度较低而具有较好的注射性。体外释药研究结果表明,G5为最佳处方,24 h释药率为96.87%。体外释药研究表明,原位凝胶的释药率呈浓度依赖性;随着甲基纤维素浓度的增加,药物释放速度减慢。结论:以添加0.9%w/v的甲基纤维素为最佳配方。
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