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细胞穿透肽在 siRNA 细胞内递送中的多功能性。

Versatility of cell-penetrating peptides for intracellular delivery of siRNA.

机构信息

a Department of Chemical Engineering , Soonchunhyang University , Asan , Republic of Korea.

出版信息

Drug Deliv. 2018 Nov;25(1):1996-2006. doi: 10.1080/10717544.2018.1543366.

Abstract

The plasma membrane is a large barrier to systemic drug delivery into cells, and it limits the efficacy of drug cargo. This issue has been overcome using cell-penetrating peptides (CPPs). CPPs are short peptides (6-30 amino acid residues) that are potentially capable of intracellular penetration to deliver drug molecules. CPPs broadened biomedical applications and provide a means to deliver a range of biologically active molecules, such as small molecules, proteins, imaging agents, and pharmaceutical nanocarriers, across the plasma membrane with high efficacy and low toxicity. This review is focused on the versatility of CPPs and advanced approaches for siRNA delivery.

摘要

细胞膜是药物进入细胞的系统性输送的一大障碍,限制了药物有效载荷的功效。这个问题已经通过使用细胞穿透肽(CPPs)得到解决。CPPs 是短肽(6-30 个氨基酸残基),具有潜在的细胞内穿透能力,可输送药物分子。CPPs 拓宽了生物医学的应用,并提供了一种有效的方法来输送一系列具有生物活性的分子,如小分子、蛋白质、成像剂和药物纳米载体,穿过细胞膜,具有高效和低毒性。本文重点介绍 CPPs 的多功能性和用于 siRNA 递送的先进方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81da/6319457/00b9765ea769/IDRD_A_1543366_F0001_C.jpg

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