Cationic cell-penetrating peptides as vehicles for siRNA delivery. (April 2015)
- Record Type:
- Journal Article
- Title:
- Cationic cell-penetrating peptides as vehicles for siRNA delivery. (April 2015)
- Main Title:
- Cationic cell-penetrating peptides as vehicles for siRNA delivery
- Authors:
- Beloor, Jagadish
Zeller, Skye
Choi, Chang Seon
Lee, Sang-Kyung
Kumar, Priti - Abstract:
- RNA interference mediated gene silencing has tremendous applicability in fields ranging from basic biological research to clinical therapy. However, delivery of siRNA across the cell membrane into the cytoplasm, where the RNA silencing machinery is located, is a significant hurdle in most primary cells. Cell-penetrating peptides (CPPs), peptides that possess an intrinsic ability to translocate across cell membranes, have been explored as a means to achieve cellular delivery of siRNA. Approaches using CPPs by themselves or through incorporation into other siRNA delivery platforms have been investigated with the intent of improving cytoplasmic delivery. Here, we review the utilization of CPPs for siRNA delivery with a focus on strategies developed to enhance cellular uptake, endosomal escape and cytoplasmic localization of CPP/siRNA complexes.
- Is Part Of:
- Therapeutic delivery. Volume 6:Number 4(2015)
- Journal:
- Therapeutic delivery
- Issue:
- Volume 6:Number 4(2015)
- Issue Display:
- Volume 6, Issue 4 (2015)
- Year:
- 2015
- Volume:
- 6
- Issue:
- 4
- Issue Sort Value:
- 2015-0006-0004-0000
- Page Start:
- 491
- Page End:
- 507
- Publication Date:
- 2015-04
- Subjects:
- Drug delivery systems -- Periodicals
Therapeutics -- Periodicals
615.6 - Journal URLs:
- http://www.future-science.com/loi/tde ↗
http://www.future-science.com/ ↗ - DOI:
- 10.4155/tde.15.2 ↗
- Languages:
- English
- ISSNs:
- 2041-5990
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 17675.xml