Correlating Anticancer Drug Delivery Efficiency with Vascular Permeability of Renal Clearable Versus Non-renal Clearable Nanocarriers

被引:25
|
作者
Peng, Chuanqi [1 ]
Yu, Mengxiao [1 ]
Hsieh, Jer-Tsong [2 ]
Kapur, Payal [2 ,3 ]
Zheng, Jie [1 ,2 ]
机构
[1] Univ Texas Dallas, Dept Chem & Biochem, 800 W Campbell Rd, Richardson, TX 75080 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Dept Urol, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
[3] Univ Texas Southwestern Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
关键词
drug delivery; gold nanoparticles; intratumoral transport; therapeutic index; vascular permeability; SILICA NANOPARTICLES; POLYMERIC MICELLES; TUMOR; NANOMEDICINE; RETENTION;
D O I
10.1002/anie.201905738
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Enhancing tumor targeting of nanocarriers has been a major strategy for advancing clinical translation of cancer nanomedicines. Herein, we report a head-to-head comparison between 5 nm renal clearable and 30 nm non-renal clearable gold nanoparticle (AuNP)-based drug delivery systems (DDSs) in the delivery of doxorubicin (DOX). While the two DDSs themselves had comparable tumor targeting, we found their different vascular permeability played an even more important role than blood retention in the delivery and intratumoral transport of DOX, of which tumor accumulation, efficacy, and therapeutic index were enhanced 2, 7, and 10-fold, respectively, for the 5 nm DDS over 30 nm one. These findings indicate that ultrahigh vascular permeability of renal clearable nanocarriers can be utilized to further improve anticancer drug delivery without the need for prolonged blood retention.
引用
收藏
页码:12076 / 12080
页数:5
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