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一种基于质量源于设计的方法用于开发和评估含聚合物膜的依托度酸-磷脂复合物以提高抗炎效果

A QbD-Navigated Approach to the Development and Evaluation of Etodolac-Phospholipid Complex Containing Polymeric Films for Improved Anti-Inflammatory Effect.

作者信息

Singh Jangjeet Karan, Kaur Simran, Chandrasekaran Balakumar, Kaur Gurpreet, Saini Balraj, Kaur Rajwinder, Silakari Pragati, Kaur Narinderpal, Bassi Pallavi

机构信息

Chitkara College of Pharmacy, Chitkara University, Rajpura 140401, Punjab, India.

Faculty of Pharmacy, Philadelphia University, P.O. Box 1, Amman 19392, Jordan.

出版信息

Polymers (Basel). 2024 Sep 4;16(17):2517. doi: 10.3390/polym16172517.

Abstract

The current study focuses on development of phospholipid complex-loaded films of etodolac for enhanced transdermal permeation and anti-inflammatory effect. An etodolac-phospholipid complex was developed using the solvent evaporation method and was characterized by DSC, XRD, FTIR, and H-NMR studies. The formation of the complex led to conversion of a crystalline drug to an amorphous form. A stoichiometric ratio of 1:1 (drug-phospholipid) was selected as the optimized ratio. Further, the developed complex was incorporated into films and systematic optimization using a central composite design was carried out using a response surface methodological approach. The desirable design space based on minimum contact angle and maximum tensile strength was selected, while the water vapour transmission rate and swelling index were set within limits. The results for swelling index, contact angle, tensile strength, and water vapour transmission rate were 60.14 ± 1.01%, 31.6 ± 0.03, 2.44 ± 0.39 kg/cm, and 15.38 g/hm, respectively. These values exhibited a good correlation with the model-predicted values. The optimized formulation exhibited improved diffusion and permeation across skin. In vivo studies revealed enhanced anti-inflammatory potential of the developed films in comparison to the un-complexed drug. Hence, the study demonstrated that etodolac-phospholipid complex-loaded films improve the transdermal permeation and provided enhanced anti-inflammatory effect.

摘要

本研究聚焦于依托度酸磷脂复合物载药膜的研发,以增强其透皮渗透及抗炎效果。采用溶剂蒸发法制备了依托度酸 - 磷脂复合物,并通过差示扫描量热法(DSC)、X射线衍射法(XRD)、傅里叶变换红外光谱法(FTIR)和氢核磁共振(H-NMR)研究对其进行了表征。复合物的形成导致结晶药物转变为无定形形式。选择1:1(药物 - 磷脂)的化学计量比作为优化比例。此外,将所制备的复合物掺入薄膜中,并采用响应面法通过中心复合设计进行系统优化。基于最小接触角和最大拉伸强度选择了理想的设计空间,同时将水蒸气透过率和溶胀指数控制在一定范围内。溶胀指数、接触角、拉伸强度和水蒸气透过率的结果分别为60.14±1.01%、31.6±0.03、2.44±0.39 kg/cm和15.38 g/hm。这些值与模型预测值具有良好的相关性。优化后的制剂在皮肤表面表现出更好的扩散和渗透性能。体内研究表明,与未复合的药物相比,所制备的薄膜具有更强的抗炎潜力。因此,该研究表明依托度酸磷脂复合物载药膜可改善透皮渗透并提供增强的抗炎效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d590/11398249/c81cb0e451c8/polymers-16-02517-g001.jpg

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