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Versatility of cell-penetrating peptides for intracellular delivery of siRNAopen access

Authors
Singh, TejinderMurthy, Akula S. N.Yang, Hye-JinIm, Jungkyun
Issue Date
31-Dec-2018
Publisher
Taylor & Francis
Keywords
Cell-penetrating peptides; conjugation; gene therapy; cellular internalization; siRNA delivery
Citation
Drug Delivery, v.25, no.1, pp 1996 - 2006
Pages
11
Journal Title
Drug Delivery
Volume
25
Number
1
Start Page
1996
End Page
2006
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/5352
DOI
10.1080/10717544.2018.1543366
ISSN
1071-7544
1521-0464
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.
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