The biomimetic cell membrane camouflaged
approach provides numerous
opportunities in designing therapeutic platforms for various biomedical
applications. It is necessary to understand the engineering of physicochemical
properties on materials’ surfaces for target biological functions
to develop the next-generation anticancer nanomedicines. Herein, we
envelope mesoporous silica nanoparticles (MSNs) with red blood cell
(RBC) membrane ghosts to obtain MSN@RBC, which possesses significantly
stronger physiological stability and longer circulation time than
bare MSNs. The surface functionalization of the core material is a
critical design parameter for RBC membrane coating efficiency. Therefore,
various surface functionalization (−COOH, −SH, −NH2) modifications were performed on MSNs. Compared with other
groups, MSN-COOH possessed a better RBC membrane coating efficiency.
Then, MSN-COOH of different particle sizes were coated by RBC-derived
vesicle membranes. The results indicated that smaller types were able
to last longer in blood circulation and accumulate more in target
sites than the larger ones. Overall, MSN-ICG@RBC with surface functionalization
of −COOH and optimized particle size of 60 nm led to efficient
imaging-guided photothermal cancer treatment and could be potentially
appealing to actual clinical applications in the future.