I. Piergentili, P. Bouwmans, Luuk Reinalda, Reece W. Lewis, Benjamin Klemm, Huanhuan Liu, R. D. de Kruijff, A. Denkova, R. Eelkema
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引用次数: 0
摘要
在某些肿瘤和病变组织中,活性氧(ROS)(如H2O2)的产生浓度高于健康细胞。到目前为止,只有少数药物递送和释放系统对这些小但显著升高的ROS浓度做出选择性反应。此外,在氧化敏感材料领域,确保聚合物基载体在“健康”生物条件下的稳定性仍然是一个挑战。在这里,我们提出了ROS响应性嵌段共聚物胶束,其能够在2 mM H2O2存在下数天内和在更高浓度H2O2(60–600 mM)下数小时内实现胶束破坏。同时,这些胶束在无氧化剂的生理条件(pH=7.4,37°C)下稳定两周以上,在弱酸性(pH=5.0和pH=6.0,37°C)条件下稳定至少六天。使用基于4-(甲硫基)苯基酯的逻辑门将观察到的选择性编程到材料中。在这里,硫醚部分的氧化导致酯水解不稳定性的大幅增加,有效地将酯水解从关闭切换到打开。这一概念代表着实现能够在生物环境中选择性作用的信号响应性药物递送材料向前迈出了一步。
Poly(thioether phenyl acrylate) Based Micelles Show Exclusively ROS-triggered Breakdown
In certain tumor and diseased tissues, reactive oxygen species (ROS), such as H2O2, are produced in higher concentrations than in healthy cells. To date, only few examples of drug delivery and release systems responds selectively to these small but significantly elevated ROS concentrations. In addition, assuring the stability of the polymer-based carrier in “healthy” biological conditions is still a challenge in the field of oxidation-sensitive materials. Here, we present ROS-responsive block copolymer micelles capable of achieving micellar disruption over days in the presence of 2 mM H2O2 and within hours under higher concentrations of H2O2 (60 – 600 mM). At the same time, these micelles are stable for over two weeks in oxidant-free physiological (pH = 7.4, 37°C) and for at least six days in mildly acidic (pH = 5.0 and pH = 6.0, 37°C) conditions. The observed selectivity is programmed into the material using a 4-(methylthio)phenyl ester based logic gate. Here, oxidation of the thioether moiety results in a large increase in ester hydrolytic lability, effectively switching the ester hydrolysis from off to on. The concept represents a step forward to realize signal responsive drug delivery materials capable of selective action in biological environments.