Dodecyl Amino Glucoside Enhances Transdermal and Topical Drug Delivery via Reversible Interaction with Skin Barrier Lipids
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
28070753
DOI
10.1007/s11095-016-2093-z
PII: 10.1007/s11095-016-2093-z
Knihovny.cz E-zdroje
- Klíčová slova
- penetration enhancers, sugar, topical drug delivery, transdermal drug delivery,
- MeSH
- antivirové látky aplikace a dávkování metabolismus MeSH
- aplikace kožní MeSH
- aplikace lokální MeSH
- buněčné linie MeSH
- chemie farmaceutická MeSH
- cidofovir MeSH
- cytosin aplikace a dávkování analogy a deriváty metabolismus MeSH
- epidermis účinky léků metabolismus MeSH
- glukosidy chemická syntéza farmakologie MeSH
- hexosy farmakologie MeSH
- hydrofobní a hydrofilní interakce MeSH
- keratinocyty účinky léků metabolismus MeSH
- kožní absorpce MeSH
- kůže účinky léků metabolismus MeSH
- lidé MeSH
- lipidy fyziologie MeSH
- organofosfonáty aplikace a dávkování metabolismus MeSH
- permeabilita MeSH
- systémy cílené aplikace léků MeSH
- theofylin aplikace a dávkování metabolismus MeSH
- viabilita buněk MeSH
- vztahy mezi strukturou a aktivitou MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antivirové látky MeSH
- cidofovir MeSH
- cytosin MeSH
- glukosidy MeSH
- hexosy MeSH
- lipidy MeSH
- organofosfonáty MeSH
- sorbitan monolaurate MeSH Prohlížeč
- theofylin MeSH
PURPOSE: Skin permeation/penetration enhancers are substances that enable drug delivery through or into the skin. METHODS: To search for new enhancers with high but reversible activity and acceptable toxicity, we synthesized a series of D-glucose derivatives, both hydrophilic and amphiphilic. RESULTS: Initial evaluation of the ability of these sugar derivatives to increase permeation and penetration of theophylline through/into human skin compared with a control (no enhancer) or sorbitan monolaurate (Span 20; positive control) revealed dodecyl 6-amino-6-deoxy-α-D-glucopyranoside 5 as a promising enhancer. Furthermore, this amino sugar 5 increased epidermal concentration of a highly hydrophilic antiviral cidofovir by a factor of 7. The effect of compound 5 on skin electrical impedance suggested its direct interaction with the skin barrier. Infrared spectroscopy of isolated stratum corneum revealed no effect of enhancer 5 on the stratum corneum proteins but an overall decrease in the lipid chain order. The enhancer showed acceptable toxicity on HaCaT keratinocyte and 3T3 fibroblast cell lines. Finally, transepidermal water loss returned to baseline values after enhancer 5 had been removed from the skin. CONCLUSIONS: Compound 5, a dodecyl amino glucoside, is a promising enhancer that acts through a reversible interaction with the stratum corneum lipids.
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Curr Med Chem. 2005;12(19):2273-91 PubMed
Eur J Drug Metab Pharmacokinet. 1998 Apr-Jun;23 (2):307-12 PubMed
Int J Pharm. 2000 Jul 20;202(1-2):133-40 PubMed
Eur J Pharm Biopharm. 2007 Apr;66(1):127-34 PubMed
Biochim Biophys Acta. 2006 Jul;1758(7):923-33 PubMed
Pharm Res. 2009 Apr;26(4):811-21 PubMed
Br J Dermatol. 1995 Nov;133(5):679-85 PubMed
Bioorg Med Chem. 2011 Sep 15;19(18):5679-92 PubMed
Eur J Pharm Sci. 2001 Sep;14(2):101-14 PubMed
Arch Dermatol. 1963 Dec;88:702-5 PubMed
J Control Release. 2013 Jan 28;165(2):91-100 PubMed
Nat Rev Drug Discov. 2005 Nov;4(11):928-40 PubMed
Eur J Pharm Biopharm. 2011 Jan;77(1):43-55 PubMed
Eur J Pharm Biopharm. 2005 Sep;61(1-2):50-5 PubMed
Arch Dermatol. 1982 Jul;118(7):474-7 PubMed
Skin Pharmacol Physiol. 2009;22(1):22-30 PubMed
Carbohydr Res. 2009 May 26;344(8):966-71 PubMed
Dermatol Online J. 2000 Sep;6(1):3 PubMed
Bioconjug Chem. 2011 Feb 16;22(2):289-98 PubMed
Int J Pharm. 2000 Aug 10;203(1-2):245-53 PubMed
J Control Release. 2001 Jun 15;73(2-3):183-96 PubMed
Eur J Pharm Biopharm. 2008 Jun;69(2):597-604 PubMed
Skin Pharmacol Appl Skin Physiol. 1998 Mar-Apr;11(2):87-97 PubMed
Chem Phys Lipids. 2004 Jan;127(1):47-63 PubMed
Eur J Dermatol. 2001 Sep-Oct;11(5):416-9 PubMed
Nat Rev Drug Discov. 2004 Feb;3(2):115-24 PubMed
Pharm Res. 2006 May;23(5):912-9 PubMed
J Pharm Bioallied Sci. 2012 Jan;4(1):2-9 PubMed
Pharm Res. 2014 Apr;31(4):1071-81 PubMed
Contact Dermatitis. 1999 Feb;40(2):98-103 PubMed
Nat Biotechnol. 2004 Feb;22(2):192-7 PubMed
Biochim Biophys Acta. 2007 Sep;1770(9):1317-23 PubMed
Int J Pharm. 2012 Aug 20;433(1-2):1-9 PubMed
Int J Pharm. 2005 Jun 13;297(1-2):204-12 PubMed
Dermatology. 1998;197(2):141-5 PubMed
Biochim Biophys Acta. 2011 Mar;1811(3):129-37 PubMed
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