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Microneedle-mediated transdermal bacteriophage delivery

Interest in bacteriophages as therapeutic agents has recently been reawakened. Parenteral delivery is the most routinely-employed method of administration. However, injection of phages has numerous disadvantages, such as the requirement of a health professional for administration and the possibility...

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Autores principales: Ryan, Elizabeth, Garland, Martin J., Singh, Thakur Raghu Raj, Bambury, Eoin, O’Dea, John, Migalska, Katarzyna, Gorman, Sean P., McCarthy, Helen O., Gilmore, Brendan F., Donnelly, Ryan F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science B.V 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778942/
https://www.ncbi.nlm.nih.gov/pubmed/22750416
http://dx.doi.org/10.1016/j.ejps.2012.06.012
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author Ryan, Elizabeth
Garland, Martin J.
Singh, Thakur Raghu Raj
Bambury, Eoin
O’Dea, John
Migalska, Katarzyna
Gorman, Sean P.
McCarthy, Helen O.
Gilmore, Brendan F.
Donnelly, Ryan F.
author_facet Ryan, Elizabeth
Garland, Martin J.
Singh, Thakur Raghu Raj
Bambury, Eoin
O’Dea, John
Migalska, Katarzyna
Gorman, Sean P.
McCarthy, Helen O.
Gilmore, Brendan F.
Donnelly, Ryan F.
author_sort Ryan, Elizabeth
collection PubMed
description Interest in bacteriophages as therapeutic agents has recently been reawakened. Parenteral delivery is the most routinely-employed method of administration. However, injection of phages has numerous disadvantages, such as the requirement of a health professional for administration and the possibility of cross-contamination. Transdermal delivery offers one potential means of overcoming many of these problems. The present study utilized a novel poly (carbonate) (PC) hollow microneedle (MN) device for the transdermal delivery of Escherichia coli-specific T4 bacteriophages both in vitro and in vivo. MN successfully achieved bacteriophage delivery in vitro across dermatomed and full thickness skin. A concentration of 2.67 × 10(6) PFU/ml (plaque forming units per ml) was detected in the receiver compartment when delivered across dermatomed skin and 4.0 × 10(3) PFU/ml was detected in the receiver compartment when delivered across full thickness skin. An in vivo study resulted in 4.13 × 10(3) PFU/ml being detected in blood 30 min following initial MN-mediated phage administration. Clearance occurred rapidly, with phages being completely cleared from the systemic circulation within 24 h, which was expected in the absence of infection. We have shown here that MN-mediated delivery allows successful systemic phage absorption. Accordingly, bacteriophage-based therapeutics may now have an alternative route for systemic delivery. Once fully-investigated, this could lead to more widespread investigation of these interesting therapeutic viruses.
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spelling pubmed-37789422013-09-23 Microneedle-mediated transdermal bacteriophage delivery Ryan, Elizabeth Garland, Martin J. Singh, Thakur Raghu Raj Bambury, Eoin O’Dea, John Migalska, Katarzyna Gorman, Sean P. McCarthy, Helen O. Gilmore, Brendan F. Donnelly, Ryan F. Eur J Pharm Sci Article Interest in bacteriophages as therapeutic agents has recently been reawakened. Parenteral delivery is the most routinely-employed method of administration. However, injection of phages has numerous disadvantages, such as the requirement of a health professional for administration and the possibility of cross-contamination. Transdermal delivery offers one potential means of overcoming many of these problems. The present study utilized a novel poly (carbonate) (PC) hollow microneedle (MN) device for the transdermal delivery of Escherichia coli-specific T4 bacteriophages both in vitro and in vivo. MN successfully achieved bacteriophage delivery in vitro across dermatomed and full thickness skin. A concentration of 2.67 × 10(6) PFU/ml (plaque forming units per ml) was detected in the receiver compartment when delivered across dermatomed skin and 4.0 × 10(3) PFU/ml was detected in the receiver compartment when delivered across full thickness skin. An in vivo study resulted in 4.13 × 10(3) PFU/ml being detected in blood 30 min following initial MN-mediated phage administration. Clearance occurred rapidly, with phages being completely cleared from the systemic circulation within 24 h, which was expected in the absence of infection. We have shown here that MN-mediated delivery allows successful systemic phage absorption. Accordingly, bacteriophage-based therapeutics may now have an alternative route for systemic delivery. Once fully-investigated, this could lead to more widespread investigation of these interesting therapeutic viruses. Elsevier Science B.V 2012-09-29 /pmc/articles/PMC3778942/ /pubmed/22750416 http://dx.doi.org/10.1016/j.ejps.2012.06.012 Text en © 2012 Elsevier B.V. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Ryan, Elizabeth
Garland, Martin J.
Singh, Thakur Raghu Raj
Bambury, Eoin
O’Dea, John
Migalska, Katarzyna
Gorman, Sean P.
McCarthy, Helen O.
Gilmore, Brendan F.
Donnelly, Ryan F.
Microneedle-mediated transdermal bacteriophage delivery
title Microneedle-mediated transdermal bacteriophage delivery
title_full Microneedle-mediated transdermal bacteriophage delivery
title_fullStr Microneedle-mediated transdermal bacteriophage delivery
title_full_unstemmed Microneedle-mediated transdermal bacteriophage delivery
title_short Microneedle-mediated transdermal bacteriophage delivery
title_sort microneedle-mediated transdermal bacteriophage delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778942/
https://www.ncbi.nlm.nih.gov/pubmed/22750416
http://dx.doi.org/10.1016/j.ejps.2012.06.012
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