Injectable and self-healing polysaccharide-based hydrogel for pH-responsive drug release

被引:114
|
作者
Qian, Chao [1 ]
Zhang, Tingbin [2 ]
Gravesande, Joel [1 ]
Baysah, Charles [1 ]
Song, Xiaoyan [3 ]
Xing, Jinfeng [1 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300350, Peoples R China
[2] Northwest Univ, Coll Chem & Mat Sci, Xian 710069, Shaanxi, Peoples R China
[3] Tianjin Polytech Univ, Coll Mat Sci & Engn, Tianjin 300387, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogel; Injectability; Self-healing; pH-responsive; Drug release; ACID-BASED HYDROGELS; HYALURONIC-ACID; SUPRAMOLECULAR HYDROGELS; CHITOSAN; DELIVERY; CELL; GELATIN; SYSTEM;
D O I
10.1016/j.ijbiomac.2018.11.048
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
Injectable hydrogels with self-healing and pH-responsive property are appealing for biomedical applications. Herein, we developed a facile and green method to prepare a multifunctional polysaccharide-based hydrogel as a new carrier of drug. The hydrogels were prepared by forming reversible chemical bond between carboxyethyl-modified chitosan (CEC) and aldehyde modified hyaluronic acid (A-HA). The morphology and rheological property of the hydrogels with different solid content were systematically characterized. Owing to the dynamic equilibrium of the Schiff base bonds between amine groups on CEC and aldehyde groups on A-HA, the rapid self-healing performance of hydrogels was confirmed through qualitative and quantitative methods without any external stimulus. The pH-responsive behaviour was demonstrated by equilibrium swelling and in vitro Doxorubicin (Dox) release in PBS medium with various pH. In acidic condition, Dox can be release more rapidly compared with weak alkaline medium. Furthermore, the kill effect of Dox released from hydrogels for cancer cells was investigated. In vitro degradation and cytotoxicity examinations showed that the hydrogel is biodegradable and biocompatible. Therefore, such polysaccharide-based injectable self-healing and pH-responsive hydrogel is a promising candidate as drug delivery carrier. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:140 / 148
页数:9
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