| Literature DB >> 30408347 |
Minmin Chen1, Suwei Jiang1, Feng Zhang1, Linlin Li1, Hailiang Hu2, Hualin Wang1.
Abstract
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 π-π 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 π-π stacking between PDA and GO.Entities:
Keywords: HT-29 cells; activated reactive oxygen species; cytotoxicity; graphene oxide; nanofibrous scaffold
Mesh:
Substances:
Year: 2018 PMID: 30408347 DOI: 10.1002/mabi.201800321
Source DB: PubMed Journal: Macromol Biosci ISSN: 1616-5187 Impact factor: 4.979