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首页> 外文期刊>Bulletin of experimental biology and medicine >Study of the Efficiency of the Hydroporation for Delivery of Plasmid DNA to the Cells on the Model of Toxic Neuropathy
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Study of the Efficiency of the Hydroporation for Delivery of Plasmid DNA to the Cells on the Model of Toxic Neuropathy

机译:研究水质流体效率,将质粒DNA递送给毒性神经病变模型中的细胞

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We compared the efficiency of delivery of plasmid DNA (active ingredient concentration 1 mg/kg) that provides production of nerve growth factor (NGF) after intravenous administration to rats and after administration by hydroporation. The method of hydroporation ensured plasmid penetration into the liver tissue and lengthened the time of its detection in the organ. DNA concentration in 1 h after its introduction by hydroporation or intravenous route was 0.7 and 0.05 ng/mg tissue, respectively. The use of this transfection method ensured preservation of NGF DNA in the liver tissue at a level of 0.24 ng/mg of tissue 1 day after administration of the plasmid construct, while after intravenous administration, expression of the analyzed DNA was not detected in blood and liver samples. After hydroporation, the maximum of relative normalized expression of cDNA (270 rel. units) was observed after 4 h, and after 1 day, this parameter decreased to 35 rel. units. Introduction of plasmid DNA of NGF by hydroporation prevented the development of disorders of neuromuscular conduction in a rats model of toxic neuropathy induced by subacute administration of malathion in a dose of 0.5 LD50.
机译:我们比较了质粒DNA的递送效率(活性成分浓度1mg / kg),其在静脉内施用到大鼠和通过水层施用后提供神经生长因子(NGF)的产生。水煤的方法确保质粒渗透到肝脏组织中并加长在器官中的检测时间。通过水能流体或静脉内途径引入后1小时的DNA浓度分别为0.7和0.05ng / mg组织。使用该转染方法的使用确保在施用质粒构建体后1天在肝组织中保存肝组织中的NGF DNA,同时在静脉内给药后,在血液中未检测到分析的DNA的表达肝脏样本。水下过孔后,4小时后观察到cDNA(270 kem,单位)的相对归一化表达的最大值,并且在1天后,该参数降低至35 rel。单位。 NGF通过水流引入NGF的质粒DNA阻止了在0.5 LD50剂量的亚急性泌尿外毒病诱导的毒性神经病变大鼠中的神经肌肉传导紊乱的发育。

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