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Piperine Nanoparticles for Topical Application: Preparation, Characterization, In vitro and In silico Evaluation

机译:用于局部应用的胡椒碱纳米颗粒:制备,表征,体外和计算机评估

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摘要

In this study, piperine was investigated as a drug molecule due to its analgesic and anti-inflammatory properties. Piperine was encapsulated with poly(lactic-co-glycolic acid) (PLGA) in order to increase drug bioavailability for topical applications. Charac- terization of piperine PLGA nanoparticles (NPs) were performed with spectroscopic and imaging methods. It was found that the piperine PLGA NPs were successfully prepared according to the analyses. The encapsulation efficiency and loading capacity of the piperine were calculated as 99% and 3%, respectively. In vitro release study was also performed. Besides, it was shown that piperine had no mutagenic effect. Finally, molecular docking simulation was performed by using the AutoDock Vina program to identify the interaction between piperine and COX- 1 and COX-2 enzymes. The aim of this study is to contribute to the design of plant derived nano-formulations for local anti- inflammation and pain treatment with better skin penetration.
机译:在这项研究中,由于其镇痛药和抗炎特性,对Piperine作为药物分子进行了研究。 用聚(乳酸 - 乙醇酸)(PLGA)封装了哌啶,以增加局部应用的药物生物利用度。 使用光谱和成像方法进行尖白PLGA纳米颗粒(NP)的特征。 发现根据分析成功制备了哌啶PLGA NP。 管碱的封装效率和负载能力分别计算为99%和3%。 还进行了体外释放研究。 此外,还表明佛中没有诱变作用。 最后,通过使用Autodock Vina程序来识别Piperine和Cox-1和Cox-2酶之间的相互作用,进行了分子对接模拟。 这项研究的目的是为植物衍生的纳米形成的设计做出贡献,用于局部抗炎和疼痛治疗,并以更好的皮肤渗透。

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