Angiopep-2-Modified Carboxymethyl Chitosan-Based pH/Reduction Dual-Stimuli-Responsive Nanogels for Enhanced Targeting Glioblastoma

被引:47
作者
Song, Panpan [1 ]
Song, Nannan [1 ]
Li, Li [1 ]
Wu, Minghao [1 ]
Lu, Zhongxia [1 ]
Zhao, Xia [1 ,2 ,3 ]
机构
[1] Ocean Univ China, Sch Med & Pharm, Shandong Prov Key Lab Glycosci & Glycoengn, Minist Educ,Key Lab Marine Drugs, Qingdao 266003, Peoples R China
[2] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Drugs & Bioprod, Qingdao 266237, Peoples R China
[3] Marine Biomed Res Inst Qingdao, Qingdao 266071, Peoples R China
关键词
CENTRAL-NERVOUS-SYSTEM; DRUG-DELIVERY; ANTIBACTERIAL ACTIVITY; SURFACE-CHARGE; PH; NANOPARTICLES; OPTIMIZATION; CHALLENGES; TRANSPORT; MICELLES;
D O I
10.1021/acs.biomac.1c00314
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glioblastoma (GBM) is a fatal brain tumor with poor prognosis. Blood-brain barrier (BBB) prevents the effective delivery of chemotherapeutic agents to GBM. Herein, we developed a pH/reduction-sensitive carboxymethyl chitosan nanogel (CMCSN) modified by targeting peptide angiopep-2 (ANG) and loaded with doxorubicin (DOX). The multifunctional nanogel (DOX-ANG-CMCSN) exhibited good pH and reduction sensitivity, ideal stability, and biocompatibility. Its hydrodynamic diameter was 190 nm, drug loading was 12.7%, and the cumulative release rate of 24 h was 82.3% under the simulated tumor microenvironment. More importantly, the modification of ANG significantly enhanced BBB penetration and tumor targeting ability both in vivo and in vitro. DOX-ANG-CMCSN achieved 2-3-fold higher uptake and an enhanced antitumor activity compared with nontargeted DOX-CMCSN. Therefore, the targeted nanogels with the pH/reduction dual-stimuli response may provide a promising platform for GBM-targeted chemotherapy.
引用
收藏
页码:2921 / 2934
页数:14
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