Composite alginate microparticles for controlled drug release

A. Hubatová-Vacková, D. Lizoňová, A. Pittermannová, V. Tokárová, O. Kašpar, F. Štěpánek
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Abstract

: Microparticles introduced in this work are made of hydrophilic polymers with the ability to incorporate various functional components such as magnetic nanoparticles, liposomes, or enzymes [1, 2]. Microfluidics allows us to fabricate such microparticles in sizes comparable to blood cells, which makes them suitable for drug delivery [3]. The advantage is that these microparticles can be used as tiny chemical or biochemical reactors to locally produce and release pharmaceutically active substances, which are highly reactive or unstable, and therefore cannot be delivered using conventional drug formulations. Another advantage of such system is the possibility of active targeting using surface modification by specific ligands. The goal of this project was to prepare, test and analyse alginate particles, starting by encapsulating a model fluorescent dye and aiming to prepare microparticles able to deliver an antimicrobial compound. Therefore, the methods of preparation of hydrogel microparticles, more specifically microfluidics and microencapsulation, as well as the encapsulation of active compounds within liposomes will be presented in this work. Methods of controlled release are studied, in particular the delivery of doxycycline and the on-demand production of resorufin by the reaction of resazurin with ascorbic acid.
控制药物释放的复合海藻酸盐微颗粒
本研究中引入的微颗粒是由亲水性聚合物制成的,具有结合各种功能成分的能力,如磁性纳米颗粒、脂质体或酶[1,2]。微流体技术使我们能够制造出与血细胞大小相当的微颗粒,这使得它们适合于药物输送[3]。其优点是,这些微粒可以用作微小的化学或生化反应器,在局部生产和释放具有高度活性或不稳定的药物活性物质,因此不能使用传统的药物配方来输送。这种系统的另一个优点是可以通过特定配体进行表面修饰来实现主动靶向。该项目的目标是制备、测试和分析海藻酸盐颗粒,从封装一种模型荧光染料开始,旨在制备能够传递抗菌化合物的微粒。因此,本工作将介绍水凝胶微颗粒的制备方法,特别是微流体和微胶囊化方法,以及活性化合物在脂质体内的胶囊化方法。本文研究了多西环素的控释方法,特别是多西环素的释药方法和去甲绿素与抗坏血酸反应按需生产去甲绿素的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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