| Literature DB >> 31931050 |
Zhenbao Li1, Yongqi Wang2, Jiaojiao Zhu2, Yachao Zhang2, Wenjing Zhang2, Mei Zhou3, Cong Luo4, Zegeng Li5, Biao Cai6, Shuangying Gui7, Zhonggui He4, Jin Sun4.
Abstract
The protein corona significantly changes the nanoparticle (NP) identity both physicochemically and biologically, and in situ regulation of specific plasma protein adsorption on NP surfaces has emerged as a promising strategy for disease-targeting therapy. In the past decade, great progress in protein corona regulation has been achieved via surface chemistry-based nanomedicine development. This review first outlines the latest advances in bio-nano interactions, with special attention to factors that influence the protein corona, including NP physicochemical properties, the biological environment and the duration time. Second, NP surface chemistry strategies designed to inhibit and regulate protein corona formation are highlighted, with special emphasis on albumin, transferrin, apolipoprotein (apo) E, vascular endothelial growth factor (VEGF) and retinol binding protein 4 (RBP4). Finally, the current techniques used to characterize the protein corona are briefly discussed.Entities:
Keywords: Disease-targeting therapy; In situ regulation; Protein corona; Specific plasma protein adsorption; Surface chemistry
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Year: 2020 PMID: 31931050 DOI: 10.1016/j.jconrel.2020.01.007
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776