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通过纳米尺寸方法增强白藜芦醇的局部递送。

Enhancing Topical Delivery of Resveratrol through a Nanosizing Approach.

作者信息

Sinico Chiara, Pireddu Rosa, Pini Elena, Valenti Donatella, Caddeo Carla, Fadda Anna Maria, Lai Francesco

机构信息

Dept. Scienze della Vita e dell'Ambiente, Sezione di Scienze del Farmaco, University of Cagliari, Cagliari, Italy.

Dept. Scienze Farmaceutiche, Sezione di Chimica Generale e Organica "A. Marchesini", University of Milan, Milan, Italy.

出版信息

Planta Med. 2017 Mar;83(5):476-481. doi: 10.1055/s-0042-103688. Epub 2016 May 24.

Abstract

Resveratrol is a naturally occurring polyphenol with strong antioxidant and free radical scavenging properties, recently proposed as a therapeutic agent for skin diseases. In this study, we investigated the possibility of improving the dermal bioavailability of the poorly water-soluble drug resveratrol by nanocrystal technology. To this purpose, nanosuspensions were prepared by the wet media milling technique, using Poloxamer 188 or Tween 80 as stabilizers, and characterized by means of both solid state and morphological and dimensional studies. All analytical data demonstrated that neither a modification of the drug crystalline pattern nor the isomerization of the double bond were observed after the wet media milling particle size reduction process, which produced rounded and smooth nanocrystals with a mean diameter ranging between 0.2-0.3 µm. Resveratrol skin delivery from nanosuspension formulations was evaluated by the pig ear skin model via tape stripping. Results of the experiments showed that after application of nanosuspension formulations, higher amounts of resveratrol could penetrate the skin at deeper levels compared to drug coarse suspensions. The antioxidant activity of resveratrol in nanocrystals was assessed by the DPPH assay, which demonstrated that the size reduction process as well as the formulation compositions did not modify the drug antioxidant activity.

摘要

白藜芦醇是一种天然存在的多酚,具有强大的抗氧化和自由基清除特性,最近被提议作为治疗皮肤病的药物。在本研究中,我们研究了通过纳米晶体技术提高水溶性差的药物白藜芦醇的皮肤生物利用度的可能性。为此,使用泊洛沙姆188或吐温80作为稳定剂,通过湿介质研磨技术制备纳米混悬液,并通过固态、形态和尺寸研究对其进行表征。所有分析数据表明,在湿介质研磨粒径减小过程后,未观察到药物结晶模式的改变或双键的异构化,该过程产生了平均直径在0.2-0.3μm之间的圆形光滑纳米晶体。通过猪耳皮肤模型,通过胶带剥离评估了纳米混悬液制剂中白藜芦醇的皮肤递送情况。实验结果表明,与药物粗混悬液相比,应用纳米混悬液制剂后,更多量的白藜芦醇可以在更深层次穿透皮肤。通过DPPH法评估了纳米晶体中白藜芦醇的抗氧化活性,结果表明粒径减小过程以及制剂组成均未改变药物的抗氧化活性。

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