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Chitosan-DNA nanoparticles: effect on DNA integrity, bacterial transformation and transfection efficiency.

机译:壳聚糖-DNA纳米颗粒:对DNA完整性,细菌转化和转染效率的影响。

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While somatic gene therapy has the potential to treat many genetic disorders, recent clinical trials suggest that an efficient and safe delivery vehicle for successful gene therapy is lacking. The current study examines the influence of two different preparation (the solvent evaporation method and the complex coacervation method) methods on the encapsulation of a model plasmid with chitosan. The ability of different molecular weights of chitosan to form nanoparticles with a plasmid, and particulated polymers to stabilize a plasmid in a supercoiled form, were examined by agarose gel electrophoresis. Protection of encapsulated pDNA offered by these nanoparticles from nuclease attack was confirmed by assessing degradation in the presence of DNase I, and the transformation of the plasmids with incubated nanoparticles were examined by beta-galactosidase assay. Model pDNA existed as a mixture of both supercoiled (84.2%) and open circular (15.8%) forms. Our results demonstrated that supercoiled forms decreased while open circular forms and fragmented linear forms increased during the preparation of formulations. F1 formulation prepared by the complex coacervation method protected the supercoiled form of pDNA effectively. There weren't any significant changes in nanoparticle size and zeta potential values at pH 5.5 for a period of 3 months, but differences in particle sizes were observed after lyophilization with a cryoprotective agent. The efficiency of nanoparticles mediated transformation to Escherichia coli cells was significantly higher than naked DNA or poly-L-lysine (PLL)-DNA polycation complexes. The transfection studies were performed in COS-7 cells. A 3-fold increase in gene expression was produced by nanoparticles as compared to the same amount of naked plasmid DNA (pDNA). These observations suggest that formulations with high molecular weight (HMW) chitosan can be an effective non-viral method of gene vector in animal studies.
机译:尽管体细胞基因疗法具有治疗许多遗传疾病的潜力,但最近的临床试验表明,缺乏成功进行基因疗法的有效且安全的载体。当前的研究检验了两种不同的制备方法(溶剂蒸发法和复杂凝聚法)对壳聚糖包封模型质粒的影响。通过琼脂糖凝胶电泳检查了不同分子量的壳聚糖与质粒形成纳米颗粒的能力,以及微粒聚合物以超螺旋形式稳定质粒的能力。通过评估在DNase I存在下的降解,证实了这些纳米颗粒提供的封装pDNA免受核酸酶攻击的保护,并通过β-半乳糖苷酶分析检测了孵育的纳米颗粒对质粒的转化。 pDNA模型以超螺旋形式(84.2%)和开放圆形形式(15.8%)的混合物形式存在。我们的结果表明,在制剂制备过程中,超螺旋形式减少,而开放的圆形形式和线性碎片形式增加。通过复合凝聚法制备的F1制剂可有效保护pDNA的超螺旋形式。在pH值为5.5的情况下,在3个月的时间内纳米颗粒大小和zeta电位值没有任何显着变化,但是在用冷冻保护剂冻干后,观察到了颗粒大小的差异。纳米粒子介导的向大肠杆菌细胞转化的效率显着高于裸露的DNA或聚L-赖氨酸(PLL)-DNA聚阳离子复合物。转染研究是在COS-7细胞中进行的。与相同数量的裸质粒DNA(pDNA)相比,纳米粒子使基因表达增加了3倍。这些观察结果表明,在动物研究中,具有高分子量(HMW)壳聚糖的制剂可能是一种有效的非病毒基因载体方法。

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