Synthesis of oxidized carboxymethyl cellulose/chitosan hydrogels doped with graphene oxide for pH- and NIR-responsive drug delivery

被引:11
|
作者
Zhao, Zherui [1 ]
Gao, Jun [2 ]
Cai, Wenrong [1 ]
Li, Junyao [1 ]
Kong, Yong [1 ]
Zhou, Min [3 ]
机构
[1] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Peoples R China
[2] Changzhou Municipal Hosp Tradit Chinese Med, Dept Orthoped, Changzhou 213003, Peoples R China
[3] Changzhou 3 Peoples Hosp, Dept Hematol & Oncol, Changzhou 213001, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxidized carboxymethyl cellulose; Chitosan; Hydrogels; Graphene oxide; Controlled delivery; INJECTABLE HYDROGELS; CHITOSAN; ACID;
D O I
10.1016/j.eurpolymj.2023.112437
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Biological macromolecules hydrogels are synthesized via the Schiff base reaction between oxidized carboxymethyl cellulose (oxCMC) and chitosan (CS), and graphene oxide (GO) and 5-fluorouracil (5-FU) are co-doped in the oxCMC/CS hydrogels during the cross-linking process. The acylhydrazone bonds (-HC = N-) between oxCMC and CS can be easily hydrolyzed in acidic solutions, leading to the swelling of the hydrogels and facilitated delivery of 5-FU. On the other hand, the doped GO is a promising photothermal agent, and the delivery of 5-FU can also be facilitated by the generated hyperthermia upon near infrared (NIR) irradiation. Therefore, pHand NIR-responsive delivery of 5-FU from the hydrogels can be achieved. The kinetics of drug delivery indicate that the delivery of 5-FU from the hydrogels is controlled by first-order model. The drug-free carrier (oxCMC/CS/ GO) has excellent biocompatibility while the developed drug delivery system (oxCMC/CS/GO/5-FU) exhibits high cytotoxicity against human hepatoma SMMC-7721 cells.
引用
收藏
页数:8
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