School of Chemistry and Chemical Engineering, Hefei University of Technology, Hefei, 230009, P. R. China.
First Affiliated Hospital of Anhui Medical University, Hefei, 230022, P. R. China.
Macromol Biosci. 2018 Dec;18(12):e1800321. doi: 10.1002/mabi.201800321. Epub 2018 Nov 8.
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.
氧化石墨烯(GO)/聚(乳酸-共-乙醇酸)(PLGA)支架在生物医学领域有很好的应用前景。但是,人们更加关注的是掺入系统及其在正常细胞中的应用。在这项工作中,通过聚多巴胺(PDA)辅助,开发了一种新型的 GO 固定化的 PLGA 纳米纤维支架(PLGA-PDA-GO),用于抑制 HT-29 结肠癌细胞的生长。GO 和 PDA 之间的相互作用归因于π-π共轭相互作用和静电吸引。除了增强热稳定性和机械强度外,GO 的固定化还显著提高了支架的表面粗糙度、亲水性和电活性。支架对 HT-29 具有良好的抑制作用,固定化的 GO 被观察到与 HT-29 细胞接触但未被内化。支架对 HT-29 的细胞毒性机制归因于细胞内活性氧的产生,这是由于 GO 边缘的物理相互作用和 PDA 与 GO 之间的π-π堆积的电信号。