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Multiple and time-scheduled in situ DNA delivery mediated by β-cyclodextrin embedded in a polyelectrolyte multilayer

机译:β-环糊精在聚电解质多层膜中嵌入介导的多种时间安排的原位DNA递送

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摘要

The basic premise of gene therapy is that genes can be used to produce in situ therapeutic proteins. The controlled delivery of DNA complexes from biomaterials offers the potential to enhance gene transfer by maintaining an elevated concentration of DNA within the cellular microenvironment. Immobilization of the DNA to the substrate to which cells adhere maintains the DNA in the cell microenvironment for subsequent cellular internalization. Here, layer-by-layer (LBL) films made from poly(l-glutamic acid) (PLGA) and poly(l-lysine) (PLL) containing DNA were built in the presence of charged cyclodextrins. The biological activities of these polyelectrolyte films were tested by means of induced production of a specific protein in the nucleus or in the cytoplasm by cells in contact with the films. This type of coating offers the possibility for either simultaneous or sequential interfacial delivery of different DNA molecules aimed at cell transfection. These results open the route to numerous potential applications in patch vaccination, for example.
机译:基因治疗的基本前提是基因可用于生产原位治疗蛋白。来自生物材料的DNA复合物的受控递送通过保持细胞微环境中DNA浓度的升高,提供了增强基因转移的潜力。将DNA固定在细胞粘附的基质上,可将DNA保留在细胞微环境中,以用于随后的细胞内在化。在此,在存在带电环糊精的情况下,构建了由含有DNA的聚(1-谷氨酸)(PLGA)和聚(1-赖氨酸)(PLL)制成的逐层(LBL)膜。这些聚电解质膜的生物活性通过与膜接触的细胞在细胞核或细胞质中诱导产生特定蛋白的方式进行测试。这种类型的涂层提供了针对细胞转染的不同DNA分子同时或顺序界面递送的可能性。例如,这些结果打开了通往补丁疫苗接种的众多潜在应用的途径。

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