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Successful transfer of plasmid DNA into in vitro cells transfected with an inorganic plasmid-Mg/Al-LDH nanobiocomposite material as a vector for gene expression

机译:将质粒DNA成功转移到以无机质粒-Mg / Al-LDH纳米生物复合材料作为基因表达载体转染的体外细胞中

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The delivery of a full plasmid, encoding the green fluorescent protein gene into African monkey kidney (Vero3) cells, was successfully achieved using nanobiocomposites based on layered double hydroxides. This demonstrated the potential of using the system as an alternative DNA delivery vector. Intercalation of the circular plasmid DNA, pEGFP-N2, into Mg/Al-NO3- layered double hydroxides (LDH) was accomplished through anion exchange routes to form the nanobiocomposite material. The host was previously synthesized at the Mg2+ to Al3+ molar ratio R-i = 2 and subsequently intercalated with plasmid DNA. Size expansion of the interlamellae host from 8.8 angstrom in LDH to 42 angstrom was observed in the resulting nanobiocomposite, indicating stable hybridization of the plasmid DNA. The powder x-ray diffraction (PXRD) results, supplemented with Fourier-transform infrared (FTIR) spectroscopy, compositional and electrophoresis studies confirmed the encapsulation episode of the biomaterial. In order to elucidate the use of this resulting nanobiocomposite as a delivery vector, an MTT assay was performed to determine any cytotoxic effects of the host towards cells. The intercalated pEGFP-N2 anion was later successfully recovered through acidification with HNO3 after treatment with DNA-degrading enzymes, thus also showing the ability of the LDH host to protect the intercalated biomaterial from degradation. Cell transfection studies on Vero3 cells were then performed, where cells transfected with the nanobiocomposite exhibited fluorescence as early as 12 h post-treatment compared to naked delivery of the plasmid itself.
机译:使用基于层状双氢氧化物的纳米生物复合物成功地将编码绿色荧光蛋白基因的完整质粒递送至非洲猴肾(Vero3)细胞。这证明了将该系统用作替代DNA传递载体的潜力。通过阴离子交换途径将环状质粒DNA pEGFP-N2插入Mg / Al-NO3-层状双氢氧化物(LDH)中,以形成纳米生物复合材料。预先以Mg 2+与Al 3+的摩尔比R-1 = 2合成宿主,随后将其插入质粒DNA。在所得的纳米生物复合物中观察到层间宿主的大小从LDH中的8.8埃扩展到42埃,表明质粒DNA的稳定杂交。粉末X射线衍射(PXRD)结果,辅以傅里叶变换红外(FTIR)光谱,成分和电泳研究证实了该生物材料的包封过程。为了阐明这种所得纳米生物复合物作为递送载体的用途,进行了MTT测定以确定宿主对细胞的任何细胞毒性作用。插入的pEGFP-N2阴离子随后在用DNA降解酶处理后,通过用HNO3酸化而成功回收,因此也显示了LDH宿主保护插入的生物材料免于降解的能力。然后进行了对Vero3细胞的细胞转染研究,与质​​粒本身裸递送相比,用纳米生物复合物转染的细胞早在处理后12小时就显示出荧光。

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