首页> 外文OA文献 >Decationized polyplexes as stable and safe carrier systems for improved biodistribution in systemic gene therapy
【2h】

Decationized polyplexes as stable and safe carrier systems for improved biodistribution in systemic gene therapy

机译:修饰多聚体作为稳定和安全的载体系统,可改善系统基因治疗中的生物分布

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Many polycation-based gene delivery vectors show high transfection in vitro, but their cationic nature generally leads to significant toxicity and poor in vivo performance which significantly hampers their clinical applicability. Unlike conventional polycation-based systems, decationized polyplexes are based on hydrophilic and neutral polymers. They are obtained by a 3-step process: charge-driven condensation followed by disulfide crosslinking stabilization and finally polyplex decationization. They consist of a disulfide-crosslinked poly(hydroxypropyl methacrylamide) (pHPMA) core stably entrapping plasmid DNA (pDNA), surrounded by a shell of poly(ethylene glycol) (PEG). In the present paper the applicability of decationized polyplexes for systemic administration was evaluated. Cy5-labeled decationized polyplexes were evaluated for stability in plasma by fluorescence single particle tracking (fSPT), which technique showed stable size distribution for 48 h unlike its cationic counterpart. Upon the incubation of the polymers used for the formation of polyplexes with HUVEC cells, MTT assay showed excellent cytocompatibility of the neutral polymers. The safety was further demonstrated by a remarkable low teratogenicity and mortality activity of the polymers in a zebrafish assay, in great contrast with their cationic counterpart. Near infrared (NIR) dye-labeled polyplexes were evaluated for biodistribution and tumor accumulation by noninvasive optical imaging when administered systemically in tumor bearing mice. Decationized polyplexes exhibited an increased circulation time and higher tumor accumulation, when compared to their cationic precursors. Histology of tumors sections showed that decationized polyplexes induced reporter transgene expression in vivo. In conclusion, decationized polyplexes are a platform for safer polymeric vectors with improved biodistribution properties when systemically administered
机译:许多基于聚阳离子的基因递送载体在体外显示出高转染率,但它们的阳离子性质通常会导致明显的毒性和体内不良的性能,从而大大阻碍其临床应用。与传统的基于聚阳离子的体系不同,去离子化的多链体是基于亲水性和中性的聚合物。它们是通过三步过程获得的:电荷驱动的缩合,然后进行二硫键的交联稳定化,最后进行多聚体的阳离子化。它们由稳定包裹质粒DNA(pDNA)的二硫键交联的聚(羟丙基甲基丙烯酰胺)(pHPMA)核心组成,被聚(乙二醇)(PEG)的壳包围。在本文中,评估了去离子多链体在全身给药中的适用性。 Cy5标记的阳离子化多聚体通过荧光单粒子跟踪(fSPT)在血浆中的稳定性进行了评估,该技术显示了48小时稳定的粒径分布,这与阳离子对应物不同。与HUVEC细胞一起孵育用于形成多链体的聚合物后,MTT分析显示中性聚合物具有出色的细胞相容性。在斑马鱼试验中,该聚合物的致畸性和致死性极低,这与它们的阳离子对应物形成鲜明对比,进一步证明了安全性。当在荷瘤小鼠中全身给药时,通过无创光学成像评估近红外(NIR)染料标记的多聚体的生物分布和肿瘤蓄积。与阳离子前体相比,去离子化的多链体表现出更长的循环时间和更高的肿瘤积累。肿瘤切片的组织学显示,去离子多聚体在体内诱导报告基因转基因表达。总之,去离子多聚体是用于更安全的聚合物载体的平台,当全身给药时,该载体具有改善的生物分布特性

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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