纳米材料
体内分布
粘附
药物输送
纳米技术
肽
化学
血液蛋白质类
细胞粘附
生物物理学
材料科学
生物化学
体外
生物
有机化学
作者
Yijing Li,Lingze Zhang,Pei‐Pei Yang,Kuo Zhang,Xue-Feng Gong,Da‐Yong Hou,Hui Cao,Xiaochun Wu,Ruiwu Liu,Kit S. Lam,Lei Wang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-09-22
卷期号:22 (20): 8076-8085
被引量:6
标识
DOI:10.1021/acs.nanolett.2c02243
摘要
Nanomaterials (NMs) inevitably adsorb proteins in blood and form "protein corona" upon intravenous administration as drug carriers, potentially changing the biological properties and intended functions. Inspired by anti-adhesion properties of natural proteins, herein, we employed the one-bead one-compound (OBOC) combinatorial peptide library method to screen anti-adhesion peptides (AAPs) against proteins. The library beads displaying random peptides were screened with three fluorescent-labeled plasma proteins. The nonfluorescence beads, presumed to have anti-adhesion property against the proteins, were isolated for sequence determination. These identified AAPs were coated on gold nanorods (GNRs), enabling significant extension of the blood circulating half-life of these GNRs in mice to 37.8 h, much longer than that (26.6 h) of PEG-coated GNRs. In addition, such AAP coating was found to alter the biodistribution profile of GNRs in mice. The bioinspired screening strategy and resulting peptides show great potential for enhancing the delivery efficiency and targeting ability of NMs.
科研通智能强力驱动
Strongly Powered by AbleSci AI