Transdermal protein delivery by a coadministered peptide identified via phage display
- PMID: 16565728
- DOI: 10.1038/nbt1193
Transdermal protein delivery by a coadministered peptide identified via phage display
Abstract
Efficient transdermal drug delivery of large hydrophilic drugs is challenging. Here we report that the short synthetic peptide, ACSSSPSKHCG, identified by in vivo phage display, facilitated efficient transdermal protein drug delivery through intact skin. Coadministration of the peptide and insulin to the abdominal skin of diabetic rats resulted in elevated systemic levels of insulin and suppressed serum glucose levels for at least 11 h. Significant systemic bioavailability of human growth hormone was also achieved when topically coadministered with the peptide. The transdermal-enhancing activity of the peptide was sequence specific and dose dependent, did not involve direct interaction with insulin and enabled penetration of insulin into hair follicles beyond a depth of 600 microm. Time-lapse studies suggested that the peptide creates a transient opening in the skin barrier to enable macromolecular drugs to reach systemic circulation.
Comment in
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A peptide chaperone for transdermal drug delivery.Nat Biotechnol. 2006 Apr;24(4):416-7. doi: 10.1038/nbt0406-416. Nat Biotechnol. 2006. PMID: 16601723 No abstract available.
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