A colon targeted drug delivery system based on alginate modificated graphene oxide for colorectal liver metastasis

被引:64
作者
Zhang, Bin [1 ]
Yan, Yayuan [1 ]
Shen, Qiujuan [1 ]
Ma, Dong [3 ]
Huang, Langhuan [1 ]
Cai, Xiang [2 ]
Tan, Shaozao [1 ]
机构
[1] Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China
[2] Guangdong Polytech, Dept Light Chem Engn, Foshan 528041, Peoples R China
[3] Jinan Univ, Dept Biomed Engn, Guangdong Higher Educ Inst, Key Lab Biomat, Guangzhou 510632, Guangdong, Peoples R China
来源
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2017年 / 79卷
基金
中国国家自然科学基金;
关键词
Graphene oxide; Drug delivery; Anti-cancer; 5-fluorouracil; Liver metastasis; IN-VITRO; HEPATOCELLULAR-CARCINOMA; CONTROLLED-RELEASE; CHEMOTHERAPY; CANCER; NANOPARTICLES; MICROSPHERES; HEPATECTOMY; NANOCARRIER; HYDROGELS;
D O I
10.1016/j.msec.2017.05.054
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
A major problem associated with colon cancer is liver metastasis. A colon-targeted drug delivery system is one way to address this problem after the resection of colorectal cancer. However, traditional drug delivery systems face many challenges, such as an inability to control the release rate, inaccurate targeting, susceptibility to the microenvironment and poor stability. Here, we report the development of a graphene oxide (GO)-based, sodium alginate (ALG) functionalized colon-targeting drug delivery system, that is loaded with 5-fluorouracil (5-FU) as the anti-cancer drug (denoted as GO-ALG/5-FU). Our results demonstrate that the as-prepared drug delivery system possesses a much lower toxicity and better colon-targeting controlled-release behaviours. We show that GOALG/5-FU significantly inhibited tumour growth and liver metastasis and prolonged the survival time of mice. We anticipate that our assay will help improve basic research of colon-targeted drug delivery systems and provide a new way to treat colon cancer liver metastasis. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:185 / 190
页数:6
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