Electroporation of Brain Endothelial Cells on Chip toward Permeabilizing the Blood-Brain Barrier

被引:24
|
作者
Bonakdar, Mohammad [1 ]
Wasson, Elisa M. [1 ]
Lee, Yong W. [2 ,3 ]
Davalos, Rafael V. [1 ,2 ,3 ]
机构
[1] Virginia Tech, Dept Mech Engn, Blacksburg, VA 24061 USA
[2] Virginia Tech, Dept Biomed Engn & Mech, Blacksburg, VA USA
[3] Virginia Tech Wake Forest Univ, Virginia Tech, Sch Biomed Engn & Sci, Blacksburg, VA USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
IN-VITRO MODELS; ON-A-CHIP; ELECTROMAGNETIC-FIELDS; FOCUSED ULTRASOUND; IRREVERSIBLE ELECTROPORATION; TARGETED DELIVERY; DRUG-DELIVERY; BBB; DISRUPTION; ELECTROPERMEABILIZATION;
D O I
10.1016/j.bpj.2015.11.3517
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The blood-brain barrier, mainly composed of brain microvascular endothelial cells, poses an obstacle to drug delivery to the brain. Controlled permeabilization of the constituent brain endothelial cells can result in overcoming this barrier and increasing transcellular transport across it. Electroporation is a biophysical phenomenon that has shown potential in permeabilizing and overcoming this barrier. In this study we developed a microengineered in vitro model to characterize the permeabilization of adhered brain endothelial cells to large molecules in response to applied pulsed electric fields. We found the distribution of affected cells by reversible and irreversible electroporation, and quantified the uptaken amount of naturally impermeable molecules into the cells as a result of applied pulse magnitude and number of pulses. We achieved 81 +/- 1.7% (N = 6) electroporated cells with 17 +/- 8% (N = 5) cell death using an electric-field magnitude of similar to 580 V/cm and 10 pulses. Our results provide the proper range for applied electric-field intensity and number of pulses for safe permeabilization without significantly compromising cell viability. Our results demonstrate that it is possible to permeabilize the endothelial cells of the BBB in a controlled manner, therefore lending to the feasibility of using pulsed electric fields to increase drug transport across the BBB through the transcellular pathway.
引用
收藏
页码:503 / 513
页数:11
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