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基于沉淀聚合的分子印迹聚合物:一种用于姜黄素经皮递送的新方法。

Precipitation Polymerization-Based Molecularly Imprinted Polymers: A Novel Approach for Transdermal Curcumin Delivery.

作者信息

Djunaidi Muhammad Cholid, Putri Viona Resda, Maharani Nesti Dwi, Lusiana Retno Ariadi, Siahaan Parsaoran, Sunarno Sunarno

机构信息

Department of Chemistry, Faculty of Science and Mathematics, Diponegoro University, Jl. Prof. Soedharto SH, Tembalang, Semarang 50275, Indonesia.

Department of Biology, Faculty of Science and Mathematics, Diponegoro University, Jl. Prof. Soedharto SH, Tembalang, Semarang 50275, Indonesia.

出版信息

Polymers (Basel). 2024 Dec 10;16(24):3456. doi: 10.3390/polym16243456.

Abstract

This research describes the synthesis and characterization of a molecularly imprinted polymer (MIP) as a candidate for the transdermal delivery of curcumin. The MIP was synthesized through precipitation polymerization using methacrylic acid as the functional monomer and ethylene glycol dimethacrylate as the cross-linking agent. MIP characterization studies were conducted using SEM-EDX and FTIR spectroscopy to determine the morphology and interaction between curcumin and polymers. The MIP obtained through precipitation polymerization was in the form of a fine powder with a surface morphology resembling a collection of small granules with a uniform shape. The adsorption capacity of the MIP follows the Langmuir adsorption isotherm model, with a maximum capacity of 4.239 mg/g, which is greater than that of the NIP (3.219 mg/g), resulting in an imprinting efficiency of 1.317. The percentage of curcumin released from the MIP after 8 h was 41.26%, which is lower than that from the NIP, at 51.50%. The drug release kinetics study follows the Higuchi model, indicating drug diffusion from the polymer matrix. Imprinting on the MIP can modify drug diffusion from the polymer matrix, resulting in a reduced release rate in the MIP. Therefore, the MIP can be considered a candidate for the controlled transdermal delivery of curcumin.

摘要

本研究描述了一种分子印迹聚合物(MIP)的合成与表征,该聚合物作为姜黄素经皮给药的候选材料。以甲基丙烯酸为功能单体、乙二醇二甲基丙烯酸酯为交联剂,通过沉淀聚合法合成了MIP。利用扫描电子显微镜-能谱仪(SEM-EDX)和傅里叶变换红外光谱(FTIR)对MIP进行表征研究,以确定姜黄素与聚合物之间的形态和相互作用。通过沉淀聚合法得到的MIP为细粉形式,其表面形态类似于形状均匀的小颗粒集合。MIP的吸附容量符合朗缪尔吸附等温线模型,最大容量为4.239 mg/g,大于非印迹聚合物(NIP,3.219 mg/g),印迹效率为1.317。8小时后,MIP中姜黄素的释放百分比为41.26%,低于NIP的51.50%。药物释放动力学研究符合 Higuchi 模型,表明药物从聚合物基质中扩散。MIP上的印迹可以改变药物从聚合物基质中的扩散,导致MIP中药物释放速率降低。因此,MIP可被视为姜黄素控释经皮给药的候选材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28cc/11678942/599dc631b8a3/polymers-16-03456-g001.jpg

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