Dose Dependencies and Biocompatibility of Renal Clearable Gold Nanoparticles: From Mice to Non-human Primates

被引:71
|
作者
Xu, Jing [1 ]
Yu, Mengxiao [1 ]
Peng, Chuanqi [1 ]
Carter, Phoebe [1 ]
Tian, Jia [2 ]
Ning, Xuhui [1 ]
Zhou, Qinhan [1 ]
Tu, Qiu [5 ]
Zhang, Greg [1 ]
Dao, Anthony [1 ]
Jiang, Xingya [1 ]
Kapur, Payal [3 ,4 ]
Hsieh, Jer-Tsong [4 ]
Zhao, Xudong [5 ]
Liu, Pengyu [2 ]
Zheng, Jie [1 ,4 ]
机构
[1] Univ Texas Dallas, Dept Chem & Biochem, 800 W Campbell Rd, Richardson, TX 75080 USA
[2] Gen Res Inst Nonferrous Met, 2 Xinjiekou Outer St, Beijing 100088, Peoples R China
[3] Univ Texas Southwestern Med Ctr Dallas, Dept Pathol, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
[4] Univ Texas Southwestern Med Ctr Dallas, Dept Urol, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
[5] Chinese Acad Sci, Kunming Inst Zool, 32 Jiaochang Donglu, Kunming KUNMING, Yunnan, Peoples R China
关键词
biocompatibility; dose dependencies; nanoparticles; non-human primates; renal clearance; PHARMACOKINETICS; RATS; VASCULATURE; PARTICLES; KINETICS; EFFICACY; SAFETY;
D O I
10.1002/anie.201710584
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 invivo 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 invivo transport of ultrasmall AuNPs open up a pathway to maximize their biomedical potentials and minimize their toxicity in the future clinical translation.
引用
收藏
页码:266 / 271
页数:6
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