DESIGN AND OPTIMIZATION OF ESCITALOPRAM OXALATE ORAL DISSOLVING FILMS BY RESPONSE SURFACE METHODOLOGY

Q2 Pharmacology, Toxicology and Pharmaceutics
Chennupati Venu Babu, Venkata Ramana MURTHY KOLAPALLI
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引用次数: 0

Abstract

Objective: To develop and optimise the oral dissolving films of escitalopram oxalate by response surface methodology. Methods: Oral dissolving film compositions were optimized by central composite design. The films are prepared by solvent casting method. Initially, different polymers were screened and based on the results polyvinyl alcohol was selected as polymer, propylene glycol was selected as plasticizer. Concentration of polymer and concentration of plasticizer were fixed as independent variables; tensile strength, percent elongation, elastic modulus and amount dissolved up to 5 min (%D5 min) were taken as responses. Results: The prepared films exhibited good surface characteristics. The thickness, uniformity of weight, surface pH and drug content are within acceptable range. The mechanical properties like tensile strength, folding endurance, percent elongation and elastic modulus were determined. The statistical analysis showed that polymer concentration has a positive effect on disintegration time and the plasticizer concentration has a significant effect on folding endurance. The prepared film relesases nearly 95% at the end of 5 min. The design space was used to optimize the quantities of polymer and plasticizer. The comparison of checkpoint experiment batch responses are corelating with the predicted responses. Conclusion: Escitalopram oxalate oral dissolving films was successfully designed and optimized by response surface method. It was concluded that the prepared films exhibit good mechanical properties and maximum release within 10 min.
用响应面方法设计和优化草酸艾司西酞普兰口腔溶解膜
目的:采用响应面方法开发和优化草酸艾司西酞普兰口腔溶解膜:采用响应面方法开发和优化草酸艾司西酞普兰口腔溶解膜:方法:采用中心复合设计法优化口腔溶解膜成分。薄膜采用溶剂浇铸法制备。首先筛选了不同的聚合物,根据筛选结果,选择聚乙烯醇作为聚合物,丙二醇作为增塑剂。聚合物浓度和增塑剂浓度被定为自变量;拉伸强度、伸长率、弹性模量和 5 分钟内的溶解量(%D5 min)被定为响应变量:制备的薄膜具有良好的表面特性。厚度、重量均匀性、表面 pH 值和药物含量都在可接受的范围内。测定了拉伸强度、耐折度、伸长率和弹性模量等机械性能。统计分析显示,聚合物浓度对崩解时间有积极影响,增塑剂浓度对耐折性有显著影响。所制备的薄膜在 5 分钟后的再释放率接近 95%。设计空间用于优化聚合物和增塑剂的用量。检查点实验批次反应与预测反应的比较结果一致:结论:草酸艾司西酞普兰口腔溶解膜采用响应面法成功地进行了设计和优化。结论:采用响应面法成功设计并优化了草酸艾司西酞普兰口腔溶解膜,所制备的薄膜具有良好的机械性能,并能在 10 分钟内达到最大释放量。
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来源期刊
International Journal of Applied Pharmaceutics
International Journal of Applied Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
1.40
自引率
0.00%
发文量
219
期刊介绍: International Journal of Applied Pharmaceutics (Int J App Pharm) is a peer-reviewed, bimonthly (onward March 2017) open access journal devoted to the excellence and research in the pure pharmaceutics. This Journal publishes original research work that contributes significantly to further the scientific knowledge in conventional dosage forms, formulation development and characterization, controlled and novel drug delivery, biopharmaceutics, pharmacokinetics, molecular drug design, polymer-based drug delivery, nanotechnology, nanocarrier based drug delivery, novel routes and modes of delivery; responsive delivery systems, prodrug design, development and characterization of the targeted drug delivery systems, ligand carrier interactions etc. However, the other areas which are related to the pharmaceutics are also entertained includes physical pharmacy and API (active pharmaceutical ingredients) analysis. The Journal publishes original research work either as a Original Article or as a Short Communication. Review Articles on a current topic in the said fields are also considered for publication in the Journal.
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