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Effect of solution composition of plasmid DNA on gene transfection following liver surface administration in mice

机译:小鼠肝脏表面给药后质粒DNA溶液组成对基因转染的影响

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We investigated the effect of plasmid DNA (pDNA) solution composition on gene transfection following liver surface administration in mice. Gene transfection experiments in situ and in vivo were performed using the following pDNA solutions: dextrose solution, NaCl solution, phosphate buffer, phosphate-buffered saline, Tris/HCl buffer with EDTA, Tris/HCl buffer with EDTA and Triton X-100, and water. In in situ experiments, we used a glass cylindrical diffusion cell that limited the contact area between the liver surface and the naked pDNA solution. The gene transfection at the site of diffusion cell attachment increased in hypotonic solution, and decreased in hypertonic solution, compared with isotonic solution. In in vivo experiments, instillation of naked pDNA solution onto the liver surface using a micropipette caused no significant differences in gene transfection in the applied lobe. These results suggest that it is important to select the optimal pDNA solution composition to control the gene transfection.
机译:我们调查了小鼠肝脏表面给药后质粒DNA(pDNA)溶液成分对基因转染的影响。使用以下pDNA溶液进行原位和体内基因转染实验:葡萄糖溶液,NaCl溶液,磷酸盐缓冲液,磷酸盐缓冲盐水,带EDTA的Tris / HCl缓冲液,带EDTA和Triton X-100的Tris / HCl缓冲液,以及水。在原位实验中,我们使用玻璃圆柱状扩散池限制了肝脏表面与裸露的pDNA溶液之间的接触面积。与等渗溶液相比,低渗溶液中扩散细胞附着部位的基因转染增加,而高渗溶液中基因转染减少。在体内实验中,使用微量移液管将裸露的pDNA溶液滴注到肝脏表面不会导致所应用的叶在基因转染方面产生显着差异。这些结果表明选择最佳的pDNA溶液组成来控制基因转染非常重要。

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