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用于筛选药物递送系统的合成肿瘤网络

Synthetic tumor networks for screening drug delivery systems.

作者信息

Prabhakarpandian Balabhaskar, Shen Ming-Che, Nichols Joseph B, Garson Charles J, Mills Ivy R, Matar Majed M, Fewell Jason G, Pant Kapil

机构信息

Biomedical Technology, CFD Research Corporation, Huntsville, AL 35806, USA.

Biomedical Technology, CFD Research Corporation, Huntsville, AL 35806, USA.

出版信息

J Control Release. 2015 Mar 10;201:49-55. doi: 10.1016/j.jconrel.2015.01.018. Epub 2015 Jan 17.

Abstract

Tumor drug delivery is a complex phenomenon affected by several elements in addition to drug or delivery vehicle's physico-chemical properties. A key factor is tumor microvasculature with complex effects including convective transport, high interstitial pressure and enhanced vascular permeability due to the presence of "leaky vessels". Current in vitro models of the tumor microenvironment for evaluating drug delivery are oversimplified and, as a result, show poor correlation with in vivo performance. In this study, we report on the development of a novel microfluidic platform that models the tumor microenvironment more accurately, with physiologically and morphologically realistic microvasculature including endothelial cell lined leaky capillary vessels along with 3D solid tumors. Endothelial cells and 3D spheroids of cervical tumor cells were co-cultured in the networks. Drug vehicle screening was demonstrated using GFP gene delivery by different formulations of nanopolymers. The synthetic tumor network was successful in predicting in vivo delivery efficiencies of the drug vehicles. The developed assay will have critical applications both in basic research, where it can be used to develop next generation delivery vehicles, and in drug discovery where it can be used to study drug transport and delivery efficacy in realistic tumor microenvironment, thereby enabling drug compound and/or delivery vehicle screening.

摘要

肿瘤药物递送是一种复杂的现象,除了药物或递送载体的物理化学性质外,还受到多种因素的影响。一个关键因素是肿瘤微血管系统,它具有复杂的作用,包括对流运输、高间质压力以及由于“渗漏血管”的存在而增强的血管通透性。目前用于评估药物递送的肿瘤微环境体外模型过于简化,因此与体内性能的相关性较差。在本研究中,我们报告了一种新型微流控平台的开发,该平台能更准确地模拟肿瘤微环境,具有生理和形态逼真的微血管系统,包括内衬内皮细胞的渗漏毛细血管以及三维实体肿瘤。内皮细胞和宫颈肿瘤细胞的三维球体在网络中共同培养。通过不同配方的纳米聚合物进行绿色荧光蛋白基因递送,展示了药物载体筛选。合成肿瘤网络成功预测了药物载体的体内递送效率。所开发的检测方法在基础研究中具有关键应用,可用于开发下一代递送载体;在药物发现中也可用于研究在真实肿瘤微环境中的药物运输和递送效率,从而实现药物化合物和/或递送载体的筛选。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d971/4418523/ed74893c311a/nihms658418f1.jpg

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