4.8 Article

A pH-responsive drug nanovehicle constructed by reversible attachment of cholesterol to PEGylated poly(L-lysine) via catechol-boronic acid ester formation

期刊

ACTA BIOMATERIALIA
卷 10, 期 8, 页码 3686-3695

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2014.05.018

关键词

PH-responsiveness; Boronate ester; Self-assembly; Cellular uptake; Controlled drug release

资金

  1. National Key Basic Research Program of China [2011CB606202]
  2. National Natural Science Foundation of China [21374085, 21174110]
  3. Fundamental Research Funds for the Central Universities [2042014kf0193, 2012203020210]

向作者/读者索取更多资源

The present work reports the construction of a drug delivery nanovehicle via a pH-sensitive assembly strategy for improved cellular internalization and intracellular drug liberation. Through spontaneous formation of boronate linkage in physiological conditions, phenylboronic acid-modified cholesterol was able to attach onto catechol-pending methoxypoly(ethylene glycol)-block-poly(L-lysine). This comb-type polymer can self-organize into a micellar nanoconstruction that is able to effectively encapsulate poorly water-soluble agents. The blank micelles exhibited negligible in vitro cytotoxicity, yet doxorubicin (DOX)-loaded micelles could effectively induce cell death at a level comparable to free DOX. Owing to the acid-labile feature of the boronate linkage, a reduction in environmental pH from pH 7.4 to 5.0 could trigger the dissociation of the nanoconstruction, which in turn could accelerate the liberation of entrapped drugs. Importantly, the blockage of endosomal acidification in HeLa cells by NH4Cl treatment significantly decreased the nuclear uptake efficiency and cell-killing effect mediated by the DOX-loaded nanoassembly, suggesting that acid-triggered destruction of the nanoconstruction is of significant importance in enhanced drug efficacy. Moreover, confocal fluorescence microscopy and flow cytometry assay revealed the effective internalization of the nanoassemblies, and their cellular uptake exhibited a cholesterol dose-dependent profile, indicating the contribution of introduced cholesterol functionality to the transmembrane process of the nanoassembly. (C) 2014 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

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