{"title":"Fundamentals of electroporative delivery of drugs and genes","authors":"Eberhard Neumann, Sergej Kakorin, Katja Tœnsing","doi":"10.1016/S0302-4598(99)00008-2","DOIUrl":null,"url":null,"abstract":"<div><p>Electrooptical and conductometrical relaxation methods have given a new insight in the molecular mechanisms of the electroporative delivery of drug-like dyes and genes (DNA) to cells and tissues. Key findings are: (1) Membrane electroporation (ME) and hence the electroporative transmembrane transport of macromolecules are facilitated by a higher curvature of the membrane as well as by a gradient of the ionic strength across charged membranes, affecting the spontaneous curvature. (2) The degree of pore formation as the primary field response increases continuously without a threshold field strength, whereas secondary phenomena, such as a dramatic increase in the membrane permeability to drug-like dyes and DNA (also called electropermeabilization), indicate threshold field strength ranges. (3) The transfer of DNA by ME requires surface adsorption and surface insertion of the permeant molecule or part of it. The diffusion coefficient for the translocation of DNA (<em>M</em><sub>r</sub>≈3.5×10<sup>6</sup>) through the electroporated membrane is <em>D</em><sub>m</sub>=6.7×10<sup>−13</sup> cm<sup>2</sup> s<sup>−1</sup> and <em>D</em><sub>m</sub> for the drug-like dye Serva Blue G (<em>M</em><sub>r</sub>≈854) is <em>D</em><sub>m</sub>=2.0×10<sup>−12</sup> cm<sup>2</sup> s<sup>−1</sup>. The slow electroporative transport of both DNA and drugs across the electroporated membrane reflects highly interactive (electro-) diffusion, involving many small pores coalesced into large, but transiently occluded pores (DNA). The data on mouse B-cells and yeast cells provide directly the flow and permeability coefficients of Serva blue G and plasmid DNA at different electroporation protocols. The physico-chemical theory of ME and electroporative transport in terms of time-dependent flow coefficients has been developed to such a degree that analytical expressions are available to handle curvature and ionic strength effects on ME and transport. The theory presents further useful tools for the optimization of the ME techniques in biotechnology and medicine, in particular in the new field of electroporative delivery of drugs (electrochemotherapy) and of DNA transfer and gene therapy.</p></div>","PeriodicalId":79804,"journal":{"name":"Bioelectrochemistry and bioenergetics (Lausanne, Switzerland)","volume":"48 1","pages":"Pages 3-16"},"PeriodicalIF":0.0000,"publicationDate":"1999-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0302-4598(99)00008-2","citationCount":"392","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioelectrochemistry and bioenergetics (Lausanne, Switzerland)","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0302459899000082","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 392
Abstract
Electrooptical and conductometrical relaxation methods have given a new insight in the molecular mechanisms of the electroporative delivery of drug-like dyes and genes (DNA) to cells and tissues. Key findings are: (1) Membrane electroporation (ME) and hence the electroporative transmembrane transport of macromolecules are facilitated by a higher curvature of the membrane as well as by a gradient of the ionic strength across charged membranes, affecting the spontaneous curvature. (2) The degree of pore formation as the primary field response increases continuously without a threshold field strength, whereas secondary phenomena, such as a dramatic increase in the membrane permeability to drug-like dyes and DNA (also called electropermeabilization), indicate threshold field strength ranges. (3) The transfer of DNA by ME requires surface adsorption and surface insertion of the permeant molecule or part of it. The diffusion coefficient for the translocation of DNA (Mr≈3.5×106) through the electroporated membrane is Dm=6.7×10−13 cm2 s−1 and Dm for the drug-like dye Serva Blue G (Mr≈854) is Dm=2.0×10−12 cm2 s−1. The slow electroporative transport of both DNA and drugs across the electroporated membrane reflects highly interactive (electro-) diffusion, involving many small pores coalesced into large, but transiently occluded pores (DNA). The data on mouse B-cells and yeast cells provide directly the flow and permeability coefficients of Serva blue G and plasmid DNA at different electroporation protocols. The physico-chemical theory of ME and electroporative transport in terms of time-dependent flow coefficients has been developed to such a degree that analytical expressions are available to handle curvature and ionic strength effects on ME and transport. The theory presents further useful tools for the optimization of the ME techniques in biotechnology and medicine, in particular in the new field of electroporative delivery of drugs (electrochemotherapy) and of DNA transfer and gene therapy.
电光和电导弛豫方法对药物样染料和基因(DNA)在细胞和组织中的电穿孔传递的分子机制有了新的认识。主要发现有:(1)膜电穿孔(ME)和大分子的电穿孔跨膜运输通过膜的高曲率和带电膜上离子强度的梯度来促进,从而影响自发曲率。(2)随着初级场响应的不断增加,孔隙形成程度没有阈值场强,而次级现象,如膜对药物样染料和DNA的渗透性(也称为电渗透)的急剧增加,表明阈值场强范围。(3) ME转移DNA需要渗透分子或部分分子的表面吸附和表面插入。DNA (Mr≈3.5×106)通过电孔膜易位的扩散系数为Dm=6.7×10−13 cm2 s−1,药物样染料Serva Blue G (Mr≈854)的扩散系数为Dm=2.0×10−12 cm2 s−1。DNA和药物在电穿孔膜上的缓慢电传导运输反映了高度相互作用(电)扩散,包括许多小孔隙合并成大的,但短暂闭塞的孔隙(DNA)。小鼠b细胞和酵母细胞的数据直接提供了Serva blue G和质粒DNA在不同电穿孔方案下的流动和渗透系数。根据随时间变化的流动系数的ME和电穿孔输运的物理化学理论已经发展到这样的程度,可以用解析表达式来处理曲率和离子强度对ME和输运的影响。该理论为生物技术和医学中ME技术的优化提供了进一步有用的工具,特别是在药物的电穿孔递送(电化学疗法)和DNA转移和基因治疗的新领域。