Graphene Oxide Immobilized PLGA-polydopamine Nanofibrous Scaffolds for Growth Inhibition of Colon Cancer Cells

被引:19
作者
Chen, Minmin [1 ]
Jiang, Suwei [1 ]
Zhang, Feng [1 ]
Li, Linlin [1 ]
Hu, Hailiang [2 ]
Wang, Hualin [1 ]
机构
[1] Hefei Univ Technol, Sch Chem & Chem Engn, Hefei 230009, Anhui, Peoples R China
[2] Anhui Med Univ, Affiliated Hosp 1, Hefei 230022, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
activated reactive oxygen species; cytotoxicity; graphene oxide; HT-29; cells; nanofibrous scaffold; STEM-CELLS; POLY(DOPAMINE)-ASSISTED IMMOBILIZATION; DIFFERENTIATION; NANOPARTICLES; OSTEOGENESIS; CYTOTOXICITY; DEGRADATION; COMPOSITE; ADHESION; COLLAGEN;
D O I
10.1002/mabi.201800321
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
Graphene oxide (GO)/poly (lactide-co-glycolic acid) (PLGA) scaffolds have promising applications in the biomedical field. However, greater attention is focused on the incorporated system and its applications in normal cells. In this work, a novel GO immobilized PLGA nanofibrous scaffold assisted by polydopamine (PLGA-PDA-GO) is developed for growth inhibition of HT-29 colon cancer cells. The interactions between GO and PDA are attributed to a pi-pi conjugate interaction and electrostatic attraction. In addition to the enhancement of thermal stability and mechanical strength, the surface roughness, hydrophilicity, and electro-activity of the scaffolds are significantly improved by immobilization of GO. The scaffolds show good inhibition of HT-29, and immobilized GO is observed to be in contact with but not internalized in HT-29 cells. The cytotoxicity mechanism of scaffolds toward HT-29 is attributed to intracellular activated reactive oxygen species that result from the physical interaction of the sharp GO edges and electrical signals of pi-pi stacking between PDA and GO.
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页数:9
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