药代动力学
胶体金
体内
药理学
化学
生物相容性
间隙
纳米颗粒
肾脏生理学
体内分布
不利影响
排泄
生物物理学
肾功能
纳米技术
体外
医学
材料科学
泌尿科
生物化学
生物
生物技术
有机化学
作者
Jing Xu,Mengxiao Yu,Chuanqi Peng,Phoebe Carter,Jia Tian,Xuhui Ning,Qinhan Zhou,Qiu Tu,Greg Zhang,Anthony Dao,Xingya Jiang,Payal Kapur,Jer‐Tsong Hsieh,Xudong Zhao,Pengyu Liu,Jie Zheng
标识
DOI:10.1002/ange.201710584
摘要
Abstract While dose dependencies in pharmacokinetics and clearance are often observed in clinically used small molecules, very few studies have been dedicated to the understandings of potential dose‐dependent in vivo transport of nanomedicines. Here we report that the pharmacokinetics and clearance of renal clearable gold nanoparticles (GS‐AuNPs) are strongly dose‐dependent once injection doses are above 15 mg kg −1 : high dose expedited the renal excretion and shortened the blood retention. As a result, the no‐observed‐adverse‐effect‐level (NOAEL) of GS‐AuNPs was >1000 mg kg −1 in CD‐1 mice. The efficient renal clearance and high compatibility can be translated to the non‐human primates: no adverse effects were observed within 90 days after intravenous injection of 250 mg kg −1 GS‐AuNPs. These fundamental understandings of dose effect on the in vivo transport of ultrasmall AuNPs open up a pathway to maximize their biomedical potentials and minimize their toxicity in the future clinical translation.
科研通智能强力驱动
Strongly Powered by AbleSci AI