...
首页> 外文期刊>International Journal of Pharmaceutics >Novel non-viral gene delivery systems composed of carbosilane dendron functionalized nanoparticles prepared from nano-emulsions as non-viral carriers for antisense oligonucleotides
【24h】

Novel non-viral gene delivery systems composed of carbosilane dendron functionalized nanoparticles prepared from nano-emulsions as non-viral carriers for antisense oligonucleotides

机译:由碳硅烷树枝状分子官能化的纳米颗粒组成的新型非病毒基因递送系统,该纳米颗粒由纳米乳液制备为反义寡核苷酸的非病毒载体

获取原文
获取原文并翻译 | 示例
           

摘要

The development of novel and efficient delivery systems is often the limiting step in fields such as antisense therapies. In this context, poly(D,L-lactide-co-glycolide) acid (PLGA) nanoparticles have been obtained by a versatile and simple technology based on nano-emulsion templating and low-energy emulsification methods, performed in mild conditions, providing good size control. O/W polymeric nano-emulsions were prepared by the phase inversion composition method at 25 degrees C using the aqueous solution/polysorbate80/[4 wt% PLGA in ethyl acetate] system. Nano-emulsions formed at oil-to-surfactant (O/S) ratios between 10/90-90/10 and aqueous contents above 70 wt%. Nano-emulsion with 90 wt% of aqueous solution and O/S ratio of 70/30 was chosen for further studies, since they showed the appropriate characteristics to be used as nanoparticle template: hydrodynamic radii lower than 50 nm and enough kinetic stability. Nanoparticles, prepared from nano-emulsions by solvent evaporation, showed spherical shape, sizes about 40 nm, negative surface charges and high stability. The as-prepared nanoparticles were functionalized with carbosilane cationic dendrons through a carbodiimide-mediated reaction achieving positively charged surfaces. Antisense oligonucleotides were electrostatically attached to nanoparticles surface to perform gene-silencing studies. These complexes were non-haemolytic and non-cytotoxic at the concentrations required. The ability of the complexes to impart cellular uptake was also promising. Therefore, these novel nanoparticulate complexes might be considered as potential non-viral carriers in antisense therapy. (C) 2014 Elsevier B.V. All rights reserved.
机译:在诸如反义疗法等领域中,新颖且有效的递送系统的开发通常是限制步骤。在这种情况下,聚(D,L-丙交酯-共-乙交酯)酸(PLGA)纳米粒子是通过基于纳米乳液模板和低能乳化方法的通用且简单的技术获得的,该技术在温和的条件下进行,提供了良好的大小控制。在25℃下,使用水溶液/聚山梨酯80 / [乙酸乙酯中的4wt%PLGA]体系通过相转化组成法制备O / W聚合物纳米乳液。以油/表面活性剂(O / S)比率介于10 / 90-90 / 10和含水量超过70 wt%形成的纳米乳液。选择具有90 wt%水溶液和O / S比为70/30的纳米乳液进行进一步研究,因为它们显示出用作纳米粒子模板的适当特性:低于50 nm的流体力学半径和足够的动力学稳定性。由纳米乳液通过溶剂蒸发制备的纳米颗粒呈球形,尺寸约为40 nm,具有负表面电荷和高稳定性。通过碳二亚胺介导的反应,用碳硅烷阳离子树突将所制备的纳米颗粒官能化,从而获得带正电的表面。将反义寡核苷酸静电附着至纳米颗粒表面以进行基因沉默研究。这些复合物在所需浓度下是非溶血性和非细胞毒性的。复合物赋予细胞摄取的能力也是有希望的。因此,在反义疗法中,这些新颖的纳米颗粒复合物可被认为是潜在的非病毒载体。 (C)2014 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号