pH triggered injectable amphiphilic hydrogel containing doxorubicin and paclitaxel

被引:138
作者
Zhao, Lingling [2 ]
Zhu, Lijun [2 ]
Liu, Fuyong [3 ]
Liu, Chenyang [3 ]
Shan-Dan [1 ]
Wang, Qian [2 ]
Zhang, Chengliang [2 ]
Li, Jiaoli [2 ]
Liu, Jiguang [2 ]
Qu, Xiaozhong [2 ]
Yang, Zhenzhong [2 ]
机构
[1] Capital Med Univ, Beijing Obstet & Gynecol Hosp, Beijing 100026, Peoples R China
[2] Chinese Acad Sci, Inst Chem, State Key Lab Polymer Phys & Chem, Beijing 100190, Peoples R China
[3] Chinese Acad Sci, Inst Chem, Key Lab Engn Plast, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
Injectable gel; pH triggered; Combination delivery; Cardiotoxicity; Antitumor activity; BIODEGRADABLE BLOCK-COPOLYMERS; METASTATIC BREAST-CANCER; INTRATUMORAL INJECTION; DELIVERY-SYSTEM; CHITOSAN HYDROGELS; CONTROLLED-RELEASE; EFFICACY; COMBINATION; POLYMER; BIODISTRIBUTION;
D O I
10.1016/j.ijpharm.2011.03.034
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Injectable hydrogel with hydrophobic microdomains for incorporating both hydrophilic and hydrophobic drugs, herein doxorubicin hydrochloride (DOX) and paclitaxel (PTX), was synthesized through dynamic bonding of glycol chitosan and benzaldehyde capped poly(ethylene glycol)-block-poly(propylene glycol)-block-poly(ethylene glycol) via Schiff's reaction triggered by environmental pH. Rheology tests show that the inclusion of hydrophilic drug decreases the gelation time and gains more robust gel, while the addition of hydrophobic drug has opposite influences. Dual-drug release from the DOX + PTX loaded gels was observed and the release rate can be accelerated by decreasing the environmental pH from physiological (7.4) to weak acidic pH (6.8). In vivo investigation proved that the gels were able to diminish the amount of DOX in blood circulation and limit the DOX-induced cardiotoxicity. By intratumoral administration, the hydrogel-drug formulations resulted in efficient growth inhibition of subcutaneous tumor (B16F10) on C57LB/6 mouse model. The advantage of the current system for DOX + PTX combination therapy was demonstrated by a prolongation of survival time in comparison with the single drug therapy. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:83 / 91
页数:9
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