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具有 pH 敏感性侧基的刷型嵌段共聚物胶束用于控制药物释放。

Brushed block copolymer micelles with pH-sensitive pendant groups for controlled drug delivery.

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, 789 South Limestone, Lexington, Kentucky 40536-0596, USA.

出版信息

Pharm Res. 2013 Aug;30(8):2077-86. doi: 10.1007/s11095-013-1060-1. Epub 2013 May 2.

Abstract

PURPOSE

To investigate the effects of small aliphatic pendent groups conjugated through an acid-sensitive linker to the core of brushed block copolymer micelles on particle properties.

METHODS

The brushed block copolymers were synthesized by conjugating five types of 2-alkanone (2-butanone, 2-hexanone, 2-octanone, 2-decanone, and 2-dodecanone) through an acid-labile hydrazone linker to poly(ethylene glycol)-poly(aspartate hydrazide) block copolymers.

RESULTS

Only block copolymers with 2-hexanone and 2-octanone (PEG-HEX and PEG-OCT) formed micelles with a clinically relevant size (< 50 nm in diameter), low critical micelle concentration (CMC, < 20 μM), and drug entrapment yields (approximately 5 wt.%). Both micelles degraded in aqueous solutions in a pH-dependent manner, while the degradation was accelerated in an acidic condition (pH 5.0) in comparison to pH 7.4. Despite these similar properties, PEG-OCT micelles controlled the entrapment and pH-dependent release of a hydrophobic drug most efficiently, without altering particle size, shape, and stability. The molecular weight of PEG (12 kDa vs 5 kDa) induced no change in pH-controlled drug release rates of PEG-OCT micelles.

CONCLUSION

Acid-labile small aliphatic pendant groups are useful to control the entrapment and release of a hydrophobic drug physically entrapped in the core of brushed block copolymer micelles.

摘要

目的

研究通过酸敏感连接子连接到刷状嵌段共聚物胶束核心的小脂族侧基对颗粒性质的影响。

方法

通过将 5 种 2-烷酮(2-丁酮、2-己酮、2-辛酮、2-癸酮和 2-十二烷酮)通过酸不稳定腙键连接到聚(乙二醇)-聚(天冬氨酸酰肼)嵌段共聚物上来合成刷状嵌段共聚物。

结果

只有含有 2-己酮和 2-辛酮的嵌段共聚物(PEG-HEX 和 PEG-OCT)形成了具有临床相关尺寸(<50nm 直径)、低临界胶束浓度(CMC,<20μM)和药物包封产率(约 5wt.%)的胶束。两种胶束在水溶液中均以 pH 依赖性方式降解,而在酸性条件(pH5.0)下的降解速度比 pH7.4 更快。尽管具有这些相似的性质,但 PEG-OCT 胶束最有效地控制了疏水性药物的包封和 pH 依赖性释放,而不会改变颗粒的大小、形状和稳定性。PEG(12kDa 与 5kDa)的分子量未改变 PEG-OCT 胶束的 pH 控制药物释放速率。

结论

酸不稳定的小脂族侧基可用于控制物理包封在刷状嵌段共聚物胶束核心中的疏水性药物的包封和释放。

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