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Preparation of Biodegradable Gelatin Nanospheres with a Narrow Size Distribution for Carrier of Cellular Internalization of Plasmid DNA.

机译:制备具有窄尺寸分布的可降解明胶纳米球,用于载体质粒DNA的细胞内在化。

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摘要

The objective of this study is to design biodegradable nanospheres of cationized gelatin as a carrier of cellular internalization of plasmid DNA. Ethylenediamine was chemically introduced into the carboxyl groups of gelatin to obtain cationized gelatin. The gelatin solution was filtered through a glass membrane under high pressure and dropped into 2-butanol, acetone or a mixture of the two to form nanospheres of cationized gelatin. The microspheres of cationized gelatin were prepared by the conventional water-in-oil emulsion method. The resulting nano- and microspheres of cationized gelatin were dehydrothermally treated at 160°C for different time periods to allow them to cross-link chemically. The size of nanospheres, prepared by the filtration method and changed by the type of solvents, was 1.86, 0.83 or 0.24 μm. The in vitro degradation of spheres became faster as the time period of dehydrothermal treatment was shorter. The degradation time of spheres in HCl solution linearly increased with an increase in the cross-linking time, irrespective of the sphere size. However, in the collagenase solution, when compared at the similar cross-linking density, the smaller spheres were degraded more slowly than the larger ones. The plasmid DNA incorporated in the nanospheres was released from the nanospheres with their degradation. The nanospheres incorporating plasmid DNA were internalized into cells, and intracellularly degraded with time to release plasmid DNA. The time period of plasmid DNA release was prolonged by increasing the nanosphere degradation time.
机译:这项研究的目的是设计阳离子明胶的可生物降解的纳米球作为质粒DNA细胞内在化的载体。将乙二胺化学引入明胶的羧基中以获得阳离子化的明胶。将明胶溶液在高压下通过玻璃膜过滤,然后滴入2-丁醇,丙酮或两者的混合物中,形成阳离子化明胶的纳米球。阳离子化明胶微球是通过常规油包水乳液法制备的。将阳离子化明胶的纳米球和微球在160°C下进行不同时间的脱氢热处理,以使其发生化学交联。通过过滤方法制备并随溶剂类型改变的纳米球的尺寸为1.86、0.83或0.24μm。随着脱氢热处理时间的缩短,球体的体外降解变得更快。球体在HCl溶液中的降解时间随交联时间的增加而线性增加,而与球体的大小无关。但是,在胶原酶溶液中,当以相似的交联密度比较时,较小的球比较大的球降解得更慢。掺入纳米球的质粒DNA随着降解而从纳米球释放。将掺入质粒DNA的纳米球内化到细胞中,并随时间进行细胞内降解以释放质粒DNA。通过增加纳米球的降解时间可以延长质粒DNA的释放时间。

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