Department of Chemistry and Biochemistry, The University of Texas at Dallas, 800 W. Campbell Rd., Richardson, TX, 75080, USA.
Department of Radiology, The University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX, 75390, USA.
Angew Chem Int Ed Engl. 2017 Apr 3;56(15):4314-4319. doi: 10.1002/anie.201612647. Epub 2017 Mar 13.
The success of nanomedicines in the clinic depends on our comprehensive understanding of nano-bio interactions in tumor microenvironments, which are characterized by dense leaky microvasculature and acidic extracellular pH (pH ) values. Herein, we investigated the accumulation of ultrasmall renal-clearable gold NPs (AuNPs) with and without acidity targeting in xenograft mouse models of two prostate cancer types, PC-3 and LNCaP, with distinct microenvironments. Our results show that both sets of AuNPs could easily penetrate into the tumors but their uptake and retention were mainly dictated by the tumor microvasculature and the enhanced permeability and retention effect over the entire targeting process. On the other hand, increased tumor acidity indeed enhanced the uptake of AuNPs with acidity targeting, but only for a limited period of time. By making use of simple surface chemistry, these two effects can be synchronized in time for high tumor targeting, opening new possibilities to further improve the targeting efficiencies of nanomedicines.
纳米药物在临床上的成功取决于我们对肿瘤微环境中纳米-生物相互作用的全面理解,肿瘤微环境的特点是致密渗漏的微血管和酸性细胞外 pH 值(pH 值)。在此,我们研究了具有和不具有酸性靶向的超小肾脏可清除金纳米颗粒(AuNPs)在两种具有不同微环境的前列腺癌类型(PC-3 和 LNCaP)的异种移植小鼠模型中的积累情况。我们的结果表明,两组 AuNPs 都可以轻松穿透肿瘤,但它们的摄取和保留主要由肿瘤微血管和整个靶向过程中的增强通透性和保留效应决定。另一方面,肿瘤酸度的增加确实增强了具有酸性靶向的 AuNPs 的摄取,但仅在有限的时间内。通过利用简单的表面化学,这两种效应可以在时间上同步进行,以实现高肿瘤靶向,为进一步提高纳米药物的靶向效率开辟了新的可能性。