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蛋白冠对纳米粒体内循环的影响和应用研究进展
引用本文:周冬艳,姜晟,关志宇,朱卫丰,钟凌云,刘婧,刘荣华.蛋白冠对纳米粒体内循环的影响和应用研究进展[J].药学学报,2021(2):487-495.
作者姓名:周冬艳  姜晟  关志宇  朱卫丰  钟凌云  刘婧  刘荣华
作者单位:江西中医药大学药学院
基金项目:国家重点研发计划中医药现代化研究重点专项(2017YFC1702904);国家重大新药创制科技重大专项(2018ZX09721002-008);江西省教育厅科技计划项目(GJJ170718);江西省博士后研究人员科研项目(2020KY51).
摘    要:纳米粒在检测、治疗癌症以及各种疑难杂症方面具有较佳的适用性,但单核吞噬系统可严重缩短纳米粒的体内循环时间,降低药物疗效。纳米粒进入机体后在其表面形成的蛋白冠可改变其表面性质,干扰吞噬细胞的识别,从而影响其在体内的循环时间。本文概述了蛋白冠的一般组成和形成过程,总结了纳米粒物理化学性质如粒径、表面电荷、亲水性和表面材料对蛋白冠形成的影响。蛋白冠影响纳米粒体内循环,主要在于吸附的调理蛋白促进细胞吞噬。因此,本文还介绍了应用蛋白冠促进纳米粒体内长循环的方法,通过设计合适的理化性质、表面修饰和定向设计蛋白冠,减少蛋白质在纳米粒表面的吸附。以减少纳米粒在单核吞噬系统(主要是肝脏和脾脏的吞噬细胞)的清除,实现纳米粒在体内长循环的目标。

关 键 词:蛋白冠  纳米粒  吞噬作用  长循环  理化性质  表面修饰

Research advances in the effect and utilization of protein corona on the circulation of nanoparticles in vivo
ZHOU Dong-yan,JIANG Cheng,GUAN Zhi-yu,ZHU Wei-feng,ZHONG Ling-yun,LIU Jing,LIU Rong-hua.Research advances in the effect and utilization of protein corona on the circulation of nanoparticles in vivo[J].Acta Pharmaceutica Sinica,2021(2):487-495.
Authors:ZHOU Dong-yan  JIANG Cheng  GUAN Zhi-yu  ZHU Wei-feng  ZHONG Ling-yun  LIU Jing  LIU Rong-hua
Institution:(School of Pharmacy,Jiangxi University of Traditional Chinese Medicine,Nanchang 330004,China)
Abstract:Nanoparticles have better applicability in the detection,treatment of cancer and various difficult diseases,but mononuclear phagocytosis system can seriously shorten the time of nanoparticles in vivo circulation,reduce the drug efficacy.The protein crown formed on the surface of the nanoparticle after entering the body can change its surface properties,interfere with the recognition of phagocytes,and thus affect its circulation time in vivo.This article outlines the general composition and formation process of protein crowns.It also summarizes the influence of the physical and chemical properties of nanoparticles,such as particle size,surface charge,hydrophilicity and surface materials on the formation of protein crowns.The protein crown affects the circulation of nanoparticles in vivo,mainly because the adsorbed opsonic protein promotes cell phagocytosis.Therefore,we also introduce the method of using protein crowns to promote the long circulation of nanoparticles in vivo.By designing appropriate physical and chemical properties,surface modification,and directed design of protein crowns,the adsorption of proteins on the surface of nanoparticles can be reduced.Therefore,it can reduce the clearance of nanoparticles in the mononuclear phagocytic system(mainly the phagocytes of the liver and spleen),and achieve the goal of long circulation of nanoparticles in the body.
Keywords:protein corona  nanoparticle  phagocytosis  long circulation  physical and chemical property  surface modification
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