Department of Medical Biophysics , University of Toronto , Toronto , ON M5G 1L7 , Canada.
Leslie Dan Faculty of Pharmacy , University of Toronto , Toronto , ON M5S 3M2 , Canada.
ACS Nano. 2018 Aug 28;12(8):7583-7600. doi: 10.1021/acsnano.7b06301. Epub 2018 Jul 20.
Nanomedicine drug delivery systems are capable of transporting significant payloads to solid tumors. However, only a modest increase in antitumor efficacy relative to the standard of care has been observed. In this study, we demonstrate that a single dose of radiation or mild hyperthermia can substantially improve tumor uptake and distribution of nanotherapeutics, resulting in improved treatment efficacy. The delivery of nanomedicine was driven by a reduction in interstitial fluid pressure (IFP) and small perturbation of steady-state fluid flow. The transient effects on fluid dynamics in tumors with high IFP was also shown to dominate over immune cell endocytic capacity, another mechanism suspected of improving drug delivery. Furthermore, we demonstrate the specificity of this mechanism by showing that delivery of nanotherapeutics to low IFP tumors with high leukocyte infiltration does not benefit from pretreatment with radiation or heat. These results demonstrate that focusing on small perturbations to steady-state fluid dynamics, rather than large sustained effects or uncertain immune cell recruitment strategies, can impart a vulnerability to tumors with high IFP and enhance nanotherapeutic drug delivery and treatment efficacy.
纳米医学药物输送系统能够将大量有效载荷输送到实体瘤中。然而,与标准治疗相比,抗肿瘤疗效仅略有提高。在这项研究中,我们证明单次辐射或温和热疗可以显著增加纳米治疗剂在肿瘤中的摄取和分布,从而提高治疗效果。纳米医学的输送是通过降低间质流体压力 (IFP) 和对稳态流体流动的微小扰动来驱动的。还表明,对于具有高 IFP 的肿瘤,对流体动力学的瞬态影响超过了免疫细胞内吞能力,这是另一种被怀疑可改善药物输送的机制。此外,我们通过表明向具有高白细胞浸润的低 IFP 肿瘤输送纳米治疗剂不会受益于辐射或热预处理,证明了这种机制的特异性。这些结果表明,专注于稳态流体动力学的微小扰动,而不是大的持续影响或不确定的免疫细胞招募策略,可以使具有高 IFP 的肿瘤变得脆弱,并增强纳米治疗药物的输送和治疗效果。