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首页> 外文期刊>Journal of nanoscience and nanotechnology >Factorial Design and Development of Solid Lipid Nanoparticles (SLN) for Gene Delivery
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Factorial Design and Development of Solid Lipid Nanoparticles (SLN) for Gene Delivery

机译:用于基因传递的固体脂质纳米颗粒(SLN)的因子设计和开发

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Several scientific hurdles still have to be overcome before gene therapy becomes a reality. One of them is the development of safe and efficient gene delivery system. Here, we have employed factorial design to optimize the production of solid lipid nanoparticles (SLN) for gene delivery. A 2 x 3 full-factorial experimental design was used for the optimization of SLNs formulations. The variables were defined by the components of the formulation: concentration of stearic acid,. DOTAP, and Pluronic F68 at two levels (-1, 1) and 3 central points (0). Different SNL formulations were prepared by varying the amount of components and several properties were tested, including their capacity to accommodate DNA and protection against DNase degradation, colloidal stability, in vitro cytotoxicity, and transfection efficiency in prostate cancer cells. Finally, response Surface Methodology was used to select the most effective formulation for gene delivery to prostate cancer cells in vitro. In conclusion, this study revealed that stearic acid and Pluronic F68 were determinant to SLN size and stability, respectively, while small amounts of DOTAP are essential for a successful transfection.
机译:在基因治疗成为现实之前,还必须克服几个科学障碍。其中之一是开发安全有效的基因递送系统。在这里,我们采用析因设计来优化用于基因传递的固体脂质纳米颗粒(SLN)的生产。 2 x 3全因子实验设计用于优化SLNs配方。变量由制剂的成分定义:硬脂酸的浓度。 DOTAP和Pluronic F68在两个级别(-1、1)和3个中心点(0)。通过改变组分的数量来制备不同的SNL制剂,并测试了一些特性,包括它们容纳DNA的能力以及针对DNase降解的保护,胶体稳定性,体外细胞毒性和前列腺癌细胞的转染效率。最后,使用反应表面方法学来选择最有效的制剂,以将基因体外递送至前列腺癌细胞。总之,这项研究表明,硬脂酸和Pluronic F68分别决定SLN的大小和稳定性,而少量的DOTAP对于成功转染至关重要。

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