Compared
with traditional chemotherapeutics, vascular disruption
agents (VDAs) have the advantages of rapidly blocking the supply of
nutrients and starving tumors to death. Although the VDAs are effective
under certain scenarios, this treatment triggers angiogenesis in the
later stage of therapy that frequently leads to tumor recurrence and
treatment failure. Additionally, the nonspecific tumor targeting and
considerable side effects also impede the clinical applications of
VDAs. Here we develop a customized strategy that combines a VDA with
an anti-angiogenic drug (AAD) using mesoporous silica nanoparticles
(MSNs) coated with platelet membrane for the self-assembled tumor
targeting accumulation. The tailor-made nanoparticles accumulate in
tumor tissues through the targeted adhesion of platelet membrane surface
to damaged vessel sites, resulting in significant vascular disruption
and efficient anti-angiogenesis in animal models. This study demonstrates
the promising potential of combining VDA and AAD in a single nanoplatform
for tumor eradication.