Peng Chuanqi, Xu Jing, Yu Mengxiao, Ning Xuhui, Huang Yingyu, Du Bujie, Hernandez Elizabeth, Kapur Payal, Hsieh Jer-Tsong, Zheng Jie
Department of Chemistry and Biochemistry, The University of Texas at Dallas, 800 W. Campbell Rd., Richardson, TX, 75080, USA.
Department of Urology, The University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX, 75390, USA.
Angew Chem Int Ed Engl. 2019 Jun 17;58(25):8479-8483. doi: 10.1002/anie.201903256. Epub 2019 May 14.
Precise control of in vivo transport of anticancer drugs in normal and cancerous tissues with engineered nanoparticles is key to the future success of cancer nanomedicines in clinics. This requires a fundamental understanding of how engineered nanoparticles impact the targeting-clearance and permeation-retention paradoxes in the anticancer-drug delivery. Herein, we systematically investigated how renal-clearable gold nanoparticles (AuNPs) affect the permeation, distribution, and retention of the anticancer drug doxorubicin in both cancerous and normal tissues. Renal-clearable AuNPs retain the advantages of the free drug, including rapid tumor targeting and high tumor vascular permeability. The renal-clearable AuNPs also accelerated body clearance of off-target drug via renal elimination. These results clearly indicate that diverse in vivo transport behaviors of engineered nanoparticles can be used to reconcile long-standing paradoxes in the anticancer drug delivery.
利用工程化纳米颗粒精确控制抗癌药物在正常组织和癌组织中的体内运输,是癌症纳米药物未来在临床取得成功的关键。这需要从根本上了解工程化纳米颗粒如何影响抗癌药物递送中的靶向清除和渗透保留悖论。在此,我们系统地研究了可经肾脏清除的金纳米颗粒(AuNPs)如何影响抗癌药物阿霉素在癌组织和正常组织中的渗透、分布和保留。可经肾脏清除的AuNPs保留了游离药物的优势,包括快速的肿瘤靶向性和高肿瘤血管通透性。可经肾脏清除的AuNPs还通过肾脏排泄加速了脱靶药物的体内清除。这些结果清楚地表明,工程化纳米颗粒的多种体内运输行为可用于解决抗癌药物递送中长期存在的悖论。