School of Chemistry and Chemical Engineering, Tianjin University of Technology, Tianjin 300384, China.
Eur J Pharm Sci. 2012 Oct 9;47(3):556-63. doi: 10.1016/j.ejps.2012.07.009. Epub 2012 Aug 2.
A series of polymers were synthesized by cross-linking carboxyl poly(glycerol methacrylate) (PGOHMA) using hexamethylene diisocyanate (HDI). The structures and molecular weight were characterized by ¹H NMR and gel permeation chromatography (GPC). Nanoparticles were then fabricated for encapsulation of doxorubicin hydrochloride (DOX). The encapsulation and release were affected by the chemical structure and degree of cross-linking of the polymers. The polymers were quite effective in the encapsulation of DOX, and exhibited pH-dependent drug release. Specifically, the stability of nanoparticles in neutral pH was significant enhanced and the release rate was enhanced at acidic pH after cross-linking, which could be potential useful as a controlled drug release carrier, especially for anti-cancer drug.
通过使用六亚甲基二异氰酸酯 (HDI) 交联羧酸聚 (甘油甲基丙烯酸酯) (PGOHMA),合成了一系列聚合物。通过 ¹H NMR 和凝胶渗透色谱 (GPC) 对其结构和分子量进行了表征。然后制备了纳米粒子以包封盐酸阿霉素 (DOX)。包封和释放受聚合物的化学结构和交联度的影响。聚合物在包封 DOX 方面非常有效,并表现出 pH 依赖性药物释放。具体而言,交联后在中性 pH 下纳米粒子的稳定性显著提高,在酸性 pH 下的释放速率提高,这可能是作为控制药物释放载体的潜在有用,特别是对于抗癌药物。