首页> 外文期刊>Journal of Drug Delivery >Preparation of a Nanoscaled Poly(vinyl alcohol)/Hydroxyapatite/DNA Complex Using High Hydrostatic Pressure Technology forIn VitroandIn VivoGene Delivery
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Preparation of a Nanoscaled Poly(vinyl alcohol)/Hydroxyapatite/DNA Complex Using High Hydrostatic Pressure Technology forIn VitroandIn VivoGene Delivery

机译:使用高静水压技术制备纳米级聚乙烯醇/羟基磷灰石/ DNA复合物用于体内和体内基因传递

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Our previous research showed that poly(vinyl alcohol) (PVA) nanoparticles incorporating DNA with hydrogen bonds obtained by high hydrostatic pressurization are able to deliver DNA without any significant cytotoxicity. To enhance transfection efficiency of PVA/DNA nanoparticles, we describe a novel method to prepare PVA/DNA nanoparticles encapsulating nanoscaled hydroxyapatites (HAps) prepared by high hydrostatic pressurization (980 MPa), which is designed to facilitate endosomal escape induced by dissolving HAps in an endosome. Scanning electron microscopic observation and dynamic light scattering measurement revealed that HAps were significantly encapsulated in PVA/HAp/DNA nanoparticles. The cytotoxicity, cellular uptake, and transgene expression of PVA/HAp/DNA nanoparticles were investigated using COS-7 cells. It was found that, in contrast to PVA/DNA nanoparticles, their internalization and transgene expression increased without cytotoxicity occurring. Furthermore, a similar level of transgene expression between plasmid DNA and PVA/HAp/DNA nanoparticles was achieved usingin vivohydrodynamic injection. Our results show a novel method of preparing PVA/DNA nanoparticles encapsulating HAp nano-crystals by using high hydrostatic pressure technology and the potential use of HAps as an enhancer of the transfection efficiency of PVA/DNA nanoparticles without significant cytotoxicity.
机译:我们以前的研究表明,通过高静水压力获得的并带有氢键的DNA的聚乙烯醇(PVA)纳米颗粒能够传递DNA,而没有任何明显的细胞毒性。为了提高PVA / DNA纳米颗粒的转染效率,我们描述了一种制备通过高静水压力(980 MPa)制备的包裹纳米级羟基磷灰石(HAps)的PVA / DNA纳米颗粒的新方法,该方法旨在促进通过将HAps溶解在小鼠体内而引起的内体逸出。内体。扫描电子显微镜观察和动态光散射测量表明,HAps被显着封装在PVA / HAp / DNA纳米颗粒中。使用COS-7细胞研究了PVA / HAp / DNA纳米颗粒的细胞毒性,细胞摄取和转基因表达。已经发现,与PVA / DNA纳米颗粒相反,它们的内在化和转基因表达增加而没有细胞毒性发生。此外,使用体内流体动力注射可以实现质粒DNA和PVA / HAp / DNA纳米颗粒之间相似水平的转基因表达。我们的结果显示了一种通过使用高静水压力技术制备封装HAp纳米晶体的PVA / DNA纳米颗粒的新方法,并且潜在地将HAps用作PVA / DNA纳米颗粒转染效率的增强剂,而没有明显的细胞毒性。

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