采用质量设计方法对氯诺昔康包合物的光分散膜进行优化和研制

Q4 Pharmacology, Toxicology and Pharmaceutics Hacettepe University Journal of the Faculty of Pharmacy Pub Date : 2022-08-03 DOI:10.52794/hujpharm.1072840
Archana Nerella, Nagabhushanam Mv
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引用次数: 0

摘要

氯诺昔康是一种非甾体抗炎药,用于治疗骨关节炎和类风湿性关节炎。氯诺昔康是一种水溶性较差的药物,因此具有溶出度有限的生物利用度。本研究的目的是开发和表征氯诺昔康的非分散膜,通过质量设计(QbD)方法提高其生物利用度。采用溶剂铸造法制备氯诺昔康口腔溶膜。聚合物用量、peg400用量、聚合物种类3个配方因素均有不同程度的变化。选择崩解时间和5min后药物溶出率。在响应面法下,采用历史数据设计,利用design Expert软件进行统计分析。结果表明,该显影膜具有良好的弹性、折叠耐久性和良好的拉伸强度。崩解时间为9 ~ 17 s, 5 min后药物溶出率为49% ~ 95%。方差分析(ANOVA)结果的统计分析表明,所有配方因素对选择的反应都有显著影响(p
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QUALITY BY DESIGN APPROACH FOR OPTIMIZATION AND DEVELOPMENT OF ORODISPERSIBLE FILMS OF LORNOXICAM INCLUSION COMPLEXES
Lornoxicam is a non-steroidal anti-inflammatory drug, indicated in the treatment of osteoarthritis and rheumatoid arthritis. Lornoxicam is a poor water-soluble drug and hence possesses dissolution limited bioavailability. The aim of the current research work was to develop and characterize orodispersible films of Lornoxicam to enhance its bioavailability by employing Quality-by-Design (QbD) approach. Solvent casting method was used to formulate the Lornoxicam mouth dissolving films. Three formulation factors viz. amount of polymer, amount of PEG 400 and type of polymer were varied at different levels. The responses selected were disintegration time and percent drug dissolved after 5mins. Under the response surface methodology, historical data design was employed to perform the statistical analysis using Design Expert software. The developed films were found to have good elasticity, folding endurance and favorable tensile strength. The disintegration time was found to be 9 to 17 seconds and drug dissolved after 5 minutes was 49 to 95%. The statistical analysis of the results by ANOVA elucidated that there was a significant effect of all the formulation factors on the selected responses (p
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来源期刊
Hacettepe University Journal of the Faculty of Pharmacy
Hacettepe University Journal of the Faculty of Pharmacy Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
0.60
自引率
0.00%
发文量
18
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