Denzi Agnese, Della Valle Elena, Apollonio Francesca, Breton Marie, Mir Lluis M, Liberti Micaela
Center for Life Nano Science at Sapienza, Istituto Italiano di Tecnologia, 00161, Rome, Italy.
Italian Inter-University Centre of Electromagnetic Fields and Bio-Systems (ICEmB)@Department of Information Engineering, Electronics and Telecommunication (DIET), University of Rome "La Sapienza", 00184, Rome, Italy.
J Membr Biol. 2017 Feb;250(1):31-40. doi: 10.1007/s00232-016-9922-1. Epub 2016 Aug 25.
Smart drug delivery systems represent an interesting tool to significantly improve the efficiency and the precision in the treatment of a broad category of diseases. In this context, a drug delivery mediated by nanosecond pulsed electric fields seems a promising technique, allowing for a controlled release and uptake of drugs by the synergy between the electropulsation and nanocarriers with encapsulated drugs. The main concern about the use of electroporation for drug delivery applications is the difference in dimension between the liposome (nanometer range) and the cell (micrometer range). The choice of liposome dimension is not trivial. Liposomes larger than 500 nm of diameter could be recognized as pathogen agents by the immune system, while liposomes of smaller size would require external electric field of high amplitudes for the membrane electroporation that could compromise the cell viability. The aim of this work is to theoretically study the possibility of a simultaneous cell and liposomes electroporation. The numerical simulations reported the possibility to electroporate the cell and a significant percentage of liposomes with comparable values of external electric field, when a 12 nsPEF is used.
智能药物递送系统是一种有趣的工具,可显著提高广泛疾病治疗的效率和精准度。在此背景下,纳秒级脉冲电场介导的药物递送似乎是一种很有前景的技术,通过电脉冲与载有药物的纳米载体之间的协同作用,实现药物的控释和摄取。对于将电穿孔用于药物递送应用,主要关注点在于脂质体(纳米范围)与细胞(微米范围)之间的尺寸差异。脂质体尺寸的选择并非易事。直径大于500 nm的脂质体可能会被免疫系统识别为病原体,而较小尺寸的脂质体则需要高幅值的外部电场来进行膜电穿孔,这可能会损害细胞活力。这项工作的目的是从理论上研究细胞和脂质体同时进行电穿孔的可能性。数值模拟表明,当使用12 nsPEF时,在具有相当外部电场值的情况下,有可能使细胞和相当比例的脂质体发生电穿孔。