研究目的
Investigating the effect of biocompatible polymers of gold nanoparticles on cellular responses, specifically cytotoxicity and cell cycle progression.
研究成果
GNPs causing cell cycle arrest was highly dependent on the surface biocompatibility of GNPs. Residual toxic CTAB on the naked GNPs typically caused cell cycle arrest in G0/G1 phase, whereas the coating of GNPs with BSA resulted in the inhibition of lysosome rupture ability, microtubule stabilization, and a switch to G2/M arrest. This will greatly help us to regulate the cell cycle progression through modulating surface coating and biocompatibility of nanoparticles and direct us to set the guidelines for the formulation of nanoparticles in different biomedical applications.
研究不足
The study focuses on the effects of BSA and CTAB coatings on GNPs, and the findings may not be directly applicable to other biocompatible coatings or nanoparticle types. The mechanisms behind the observed effects require further investigation.