体内
药物输送
胶体金
阿霉素
抗癌药
药品
纳米颗粒
纳米技术
化学
纳米医学
渗透
间隙
药理学
材料科学
医学
膜
内科学
生物化学
生物技术
化疗
泌尿科
生物
作者
Chuanqi Peng,Jing Xu,Mengxiao Yu,Xuhui Ning,Yingyu Huang,Bujie Du,Elizabeth Hernández,Payal Kapur,Jer‐Tsong Hsieh,Jie Zheng
标识
DOI:10.1002/anie.201903256
摘要
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.
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