| Literature DB >> 33650872 |
Bozhao Li1,2, Tianjiao Chu1,2, Jingyan Wei1, Yinlong Zhang2,3, Feilong Qi2, Zefang Lu2,3, Chao Gao1,2, Tianjiao Zhang1,2, Ershuai Jiang2,3, Junchao Xu2,3, Jiaqi Xu2,3, Suping Li2,3,4, Guangjun Nie2,3,4.
Abstract
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.Entities:
Keywords: Platelet membrane; combination therapy; nanoparticle; self-assembled tumor accumulation; tumor vessels
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Year: 2021 PMID: 33650872 DOI: 10.1021/acs.nanolett.1c00168
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189