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高比表面积聚吡咯支架用于可调药物输送。

High surface area polypyrrole scaffolds for tunable drug delivery.

机构信息

School of Pharmacy, University of Auckland, Auckland, New Zealand.

出版信息

Int J Pharm. 2013 Feb 25;443(1-2):163-8. doi: 10.1016/j.ijpharm.2013.01.006. Epub 2013 Jan 11.

Abstract

Intrinsically conducting polymers such as polypyrrole (PPy) are viable platforms for efficient drug delivery, where release rates can be tuned by external electrical stimulus. In this study, the successful fabrication of 3-dimensionally ordered macroporous PPy inverse opal thin films is described, and the viability of such films for controlled drug release evaluated in vitro. The PPy inverse opal thin films were obtained by electropolymerization of PPy through the interstitial voids of a colloidal crystal template composed of poly(methyl methacrylate) colloids of diameter ∼430 nm. Chemical etching of the template yielded macroporous PPy inverse opal scaffolds. The model drug risperidone was loaded into the PPy inverse opal films, and then entrapped by electropolymerization of a non-porous PPy overlayer. The morphology and chemical composition of the PPy scaffolds were evaluated by SEM and FTIR spectroscopy, respectively. The high surface area PPy inverse opal scaffolds exhibited enhanced drug loading and releasing capabilities compared to conventional non-porous PPy films. Drug release profiles could be modified by applying electrical stimulus, which caused actuation of the porous polypyrrole films. The proposed delivery system may find use as an implantable device where drug release can be electrically tuned according to patient requirements.

摘要

本研究成功制备了 3D 有序大孔聚吡咯(PPy)反蛋白石薄膜,并评估了其在体外控制药物释放的可行性。通过聚甲基丙烯酸甲酯胶体(直径约为 430nm)的胶体晶体模板的间隙空隙进行 PPy 的电聚合,得到 PPy 反蛋白石薄膜。模板的化学刻蚀得到了大孔 PPy 反蛋白石支架。将模型药物利培酮载入 PPy 反蛋白石薄膜中,然后通过电聚合无孔 PPy 覆盖层将其包埋。通过 SEM 和 FTIR 光谱分别评估了 PPy 支架的形态和化学组成。与传统的非多孔 PPy 薄膜相比,高表面积的 PPy 反蛋白石支架表现出增强的药物负载和释放能力。通过施加电刺激可以改变药物释放曲线,从而引起多孔聚吡咯薄膜的致动。所提出的给药系统可作为植入式装置使用,根据患者的需求可以通过电调节药物释放。

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