| Literature DB >> 29476273 |
Chenxi Qu1, Jizhao Li1, Yejuan Zhou1, Shudi Yang1, Weiliang Chen1, Fang Li1, Bengang You1, Yang Liu1, Xuenong Zhang2.
Abstract
Low accumulation in tumor sites and slow intracellular drug release remain as the obstacles for nanoparticles to achieve effective delivery of chemotherapeutic drugs. In this study, multifunctional micelles were designed to deliver doxorubicin (Dox) to tumor sites to provide more efficient therapy against hepatic carcinoma. The micelles were based on pH-responsive carboxymethyl chitosan (CMCh) modified with a reactive oxygen species (ROS)-responsive segment phenylboronic acid pinacol ester (BAPE) and an active targeted ligand CD147 monoclonal antibody. The Dox-loaded micelles provided rapid and complete drug release in pH 5.3 incubation conditions with 1 mM H2O2. In addition, an in vitro cell uptake study revealed that CD147 modification significantly enhanced cellular internalization due to the high affinity to CD147 receptors, which are overexpressed on tumor cells. An in vivo study revealed that CD147-modified micellar formulations exhibited high accumulation in tumor sites and markedly enhanced antiproliferation effects with fewer side effects than other formulations. In conclusion, this CD147 receptor targeted delivery system with ROS/pH dual sensitivity provides a promising strategy for the treatment of hepatic carcinoma.Entities:
Keywords: CD147; ROS/pH dual sensitivity; doxorubicin; micelles
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Year: 2018 PMID: 29476273 DOI: 10.1208/s12248-018-0195-8
Source DB: PubMed Journal: AAPS J ISSN: 1550-7416 Impact factor: 4.009