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一种用于向内耳局部递送蛋白质的新型载体:负载PLGA纳米颗粒的可注射且可生物降解的热敏水凝胶。

A novel vehicle for local protein delivery to the inner ear: injectable and biodegradable thermosensitive hydrogel loaded with PLGA nanoparticles.

作者信息

Dai Juan, Long Wei, Liang Zhongping, Wen Lu, Yang Fan, Chen Gang

机构信息

a School of Pharmacy , Guangdong Pharmaceutical University , Guangzhou , China.

b Guangdong Provincial Key Laboratory of Advanced Drug Delivery , Guangdong Pharmaceutical University , Guangzhou , China.

出版信息

Drug Dev Ind Pharm. 2018 Jan;44(1):89-98. doi: 10.1080/03639045.2017.1373803. Epub 2017 Sep 13.

DOI:10.1080/03639045.2017.1373803
PMID:28851247
Abstract

Delivery of biomacromolecular drugs into the inner ear is challenging, mainly because of their inherent instability as well as physiological and anatomical barriers. Therefore, protein-friendly, hydrogel-based delivery systems following local administration are being developed for inner ear therapy. Herein, biodegradable poly(lactic-co-glycolic acid) (PLGA) nanoparticles (NPs) containing interferon α-2 b (IFN α-2 b) were loaded in chitosan/glycerophosphate (CS/GP)-based thermosensitive hydrogel for IFN delivery by intratympanic injection. The injectable hydrogel possessed a physiological pH and formed semi-solid gel at 37 °C, with good swelling and deswelling properties. The CS/GP hydrogel could slowly degrade as visualized by scanning electron microscopy (SEM). The presence of NPs in CS/GP gel largely influenced in vitro drug release. In the guinea pig cochlea, a 1.5- to 3-fold increase in the drug exposure time of NPs-CS/GP was found than those of the solution, NPs and IFN-loaded hydrogel. Most importantly, a prolonged residence time was attained without obvious histological changes in the inner ear. This biodegradable, injectable, and thermosensitive NPs-CS/GP system may allow longer delivery of protein drugs to the inner ear, thus may be a potential novel vehicle for inner ear therapy.

摘要

将生物大分子药物递送至内耳具有挑战性,主要是因为它们固有的不稳定性以及生理和解剖学屏障。因此,正在开发基于水凝胶的蛋白质友好型局部给药递送系统用于内耳治疗。在此,将含有干扰素α-2b(IFNα-2b)的可生物降解聚乳酸-羟基乙酸共聚物(PLGA)纳米颗粒(NPs)负载于基于壳聚糖/甘油磷酸酯(CS/GP)的热敏水凝胶中,通过鼓膜内注射进行IFN递送。该可注射水凝胶具有生理pH值,在37°C时形成半固体凝胶,具有良好的溶胀和消溶胀性能。通过扫描电子显微镜(SEM)观察发现,CS/GP水凝胶可缓慢降解。CS/GP凝胶中NPs的存在极大地影响了体外药物释放。在豚鼠耳蜗中,发现NPs-CS/GP的药物暴露时间比溶液、NPs和负载IFN的水凝胶增加了1.5至3倍。最重要的是,实现了延长的停留时间,且内耳无明显组织学变化。这种可生物降解、可注射且热敏的NPs-CS/GP系统可能使蛋白质药物向内耳的递送时间更长,因此可能是一种潜在的内耳治疗新型载体。

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