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Cationic nioplexes-in-polysaccharide-based hydrogels as versatile biodegradable hybrid materials to deliver nucleic acids

机译:基于多糖的阳离子Nioplexes水凝胶作为通用的可生物降解杂化材料来传递核酸

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摘要

Two polysaccharide-based hydrogels made of only κ-carrageenan (4%; w/v) or of a mixture of methylcellulose:κ-carrageenan (2%; w/v) were used to encapsulate cationic nioplexes. These vesicular particles were made of a synthetic aminolipid and polysorbate-80 (Tween-80), as a non-ionic surfactant agent. According to oscillatory rheological measurements, the presence of nioplexes did not compromise the mechanical integrity of the gels. In vitro niosomal release experiments demonstrated the liberation of nioplexes up to 24 h, and the curves were fitted according to Higuchi, Korsmeyer–Peppas and Weibull equation models, which indicated Fickian-diffusion controlled mechanisms. Besides nioplexes, cervical cancer cells were also entrapped within the biohydrogels. Cell release confirmed that these materials did not affect the cell viability, allowing cells to spread and proliferate after 24 h. The applicability of these biocompatible hydrogels was also extended to gene delivery. In this regard, the best silencing activities were found when cationic niosomes were complexed with antisense oligonucleotides in KC hydrogels. Nioplexes were able to release through the hydrogel and promoted silencing of luciferase expression in the presence of serum without using commercially available cationic lipids. Overall, the formation of such hybrid materials by integrating cationic nioplexes within biodegradable hydrogels provides a new perspective for the delivery of macromolecular therapeutics.
机译:两种仅由κ-角叉菜胶(4%; w / v)或甲基纤维素∶κ-角叉菜胶(2%; w / v)的混合物制成的基于多糖的水凝胶被用于封装阳离子尼克络合物。这些囊状颗粒由合成的氨基脂质和聚山梨酯80(Tween-80)制成,作为非离子表面活性剂。根据振荡流变学测量,复合物的存在不损害凝胶的机械完整性。体外的释放释放实验表明,在24小时内释放了神经复合物,并根据Higuchi,Korsmeyer-Peppas和Weibull方程模型拟合了曲线,表明了Fickian扩散控制的机理。除了生物复合物外,宫颈癌细胞也被包裹在生物水凝胶中。细胞释放证实这些物质不影响细胞活力,允许细胞在24小时后扩散和增殖。这些生物相容性水凝胶的适用性也扩展到基因传递。在这方面,当阳离子腈与反义寡核苷酸在KC水凝胶中复合时,发现了最佳的沉默活性。 Nioplex能够通过水凝胶释放并在血清存在下促进萤光素酶表达的沉默,而无需使用市售的阳离子脂质。总体而言,通过在可生物降解的水凝胶中整合阳离子Nioplex来形成此类杂化材料,为高分子药物的递送提供了新的视角。

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