Uhl Christopher George, Muzykantov Vladimir R, Liu Yaling
Department of Bioengineering, Lehigh University, Bethlehem, Pennsylvania 18015, USA.
Department of Pharmacology, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
Biomicrofluidics. 2018 Jan 2;12(1):014101. doi: 10.1063/1.5000377. eCollection 2018 Jan.
Therapeutic delivery from microvasculature to cancerous sites is influenced by many factors including endothelial permeability, vascular flow rates/pressures, cancer secretion of cytokines and permeabilizing agents, and characteristics of the chosen therapeutics. This work uses bi-layer microfluidics capable of studying dye and therapeutic transport from a simulated vessel to a cancerous region while allowing for direct visualization and quantification of endothelial permeability. 2.5 to 13 times greater dye transport was observed when utilizing small dye sizes (FITC) when compared to larger molecules (FITC-Dextran 4 kDa and FITC-Dextran 70 kDa), respectively. The use of lower flow rates/pressures is shown to improve dye transport by factors ranging from 2.5 to 5 times, which result from increased dye diffusion times within the system. Furthermore, subjecting confluent endothelial monolayers to cancerous cells resulted in increased levels of vascular permeability. Situations of cancer induced increases in vascular permeability are shown to facilitate enhanced dye transport when compared to non-diseased endothelial monolayers. Subsequent introduction of paclitaxel or doxorubicin into the system was shown to kill cancerous cells resulting in the recovery of endothelial confluency overtime. The response of endothelial cells to paclitaxel and doxorubicin is quantified to understand the direct influence of anti-cancer therapeutics on endothelial growth and permeability. Introduction of therapeutics into the system showed the recovery of endothelial confluency and dye transport back to conditions experienced prior to cancer cell introduction after 120 h of continuous treatment. Overall, the system has been utilized to show that therapeutic transport to cancerous sites depends on the size of the chosen therapeutic, the flow rate/pressure established within the vasculature, and the degree of cancer induced endothelial permeability. In addition, treatment of the cancerous region has been demonstrated with anti-cancer therapeutics, which are shown to influence vascular permeability in direct (therapeutics themselves) and indirect (death of cancer cells) manners. Lastly, the system presented in this work is believed to function as a versatile testing platform for future anti-cancer therapeutic testing and development.
从微脉管系统到癌灶的治疗性给药受到许多因素的影响,包括内皮通透性、血管流速/压力、癌细胞分泌的细胞因子和通透剂,以及所选治疗药物的特性。这项工作使用了双层微流控技术,能够研究染料和治疗药物从模拟血管到癌区的转运,同时允许直接可视化和定量内皮通透性。与较大分子(4 kDa的异硫氰酸荧光素 - 葡聚糖和70 kDa的异硫氰酸荧光素 - 葡聚糖)相比,使用小尺寸染料(异硫氰酸荧光素)时观察到的染料转运分别大2.5至13倍。较低的流速/压力的使用显示可将染料转运提高2.5至5倍,这是由于系统内染料扩散时间增加所致。此外,使汇合的内皮单层细胞接触癌细胞会导致血管通透性水平升高。与未患病的内皮单层细胞相比,癌症诱导血管通透性增加的情况显示有助于增强染料转运。随后将紫杉醇或阿霉素引入系统显示可杀死癌细胞,导致内皮细胞汇合度随时间恢复。对内皮细胞对紫杉醇和阿霉素的反应进行定量,以了解抗癌治疗药物对内皮生长和通透性的直接影响。在连续治疗120小时后,将治疗药物引入系统显示内皮细胞汇合度恢复,染料转运回到引入癌细胞之前的状态。总体而言,该系统已被用于表明向癌灶的治疗性转运取决于所选治疗药物的大小、脉管系统内建立的流速/压力以及癌症诱导的内皮通透性程度。此外,已证明用抗癌治疗药物治疗癌区,这些药物显示以直接(治疗药物本身)和间接(癌细胞死亡)方式影响血管通透性。最后,这项工作中提出的系统被认为可作为未来抗癌治疗测试和开发的通用测试平台。