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Non-biological gene carriers designed for overcoming the major extra- and intracellular hurdles in gene delivery, an updated review

机译:非生物学基因载体设计用于克服基因传递中主要的细胞外和细胞内障碍,最新综述

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Gene therapy as a modern therapeutic approach has not yet advanced to a globally-approved therapeutic approach. Lack of adequate reliable gene delivery system seems to be one of the major reasons from the pharmaceutical biotechnology point of view. Main obstacles delaying successful application of human gene therapy are presented in this review. The unique advantages of non-biological gene carriers as compared to their biological counterparts make them ideal alternatives for overcoming extra- and intracellular barriers in a more safely manner. We, therefore, highlight the significant contributions in non-biological gene delivery and favorable characteristics of different design attitudes with focus on in vivo approaches. Bypassing the rapid extracellular enzymatic degradation of genetic materials is covered in extracellular segment of this review with emphasis on PEGylated and targeted formulations. The successful approaches to pave the rest of the way from cellular uptake to intracellular transfer and gene expression of unpacked DNA are also discussed. From these approaches, we emphasize more on optimization of cationic-based polymers and dendrimers, developing newly designed membrane-effective components, and adjusting the hydrophilic-hydrophobic balance of the synthesized vectors
机译:基因治疗作为一种现代治疗方法尚未发展到全球认可的治疗方法。从药物生物技术的角度来看,缺乏足够可靠的基因递送系统似乎是主要原因之一。本文综述了延迟成功应用人类基因疗法的主要障碍。非生物基因载体与其生物学对应物相比的独特优势,使其成为以更安全的方式克服细胞外和细胞内壁垒的理想选择。因此,我们着重介绍了非生物基因传递中的重大贡献以及以体内方法为重点的不同设计态度的有利特征。绕过遗传物质的快速细胞外酶促降解涵盖在本综述的细胞外部分,重点是聚乙二醇化和靶向制剂。还讨论了成功的方法,为从细胞吸收到细胞内转移以及解包装DNA的基因表达铺平道路。从这些方法中,我们将重点放在优化阳离子型聚合物和树枝状聚合物,开发新设计的膜有效组分以及调节合成载体的亲水-疏水平衡上

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