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Comparative single-dose pharmacokinetics of sildenafil after oral and rectal administration in healthy beagle dogs
BACKGROUND: Sildenafil citrate, a highly selective phosphodiesterase type 5 inhibitor, is used to treat pulmonary hypertension (PH) in veterinary medicine. The objective of this study was to investigate pharmacokinetic profiles by oral administration of orally disintegrating film (ODF) and film coat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154896/ https://www.ncbi.nlm.nih.gov/pubmed/30249242 http://dx.doi.org/10.1186/s12917-018-1617-7 |
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author | Yang, Hyuck-Joo Oh, Ye-In Jeong, Jong-Woo Song, Kun-Ho Koo, Tae-Sung Seo, Kyoung-Won |
author_facet | Yang, Hyuck-Joo Oh, Ye-In Jeong, Jong-Woo Song, Kun-Ho Koo, Tae-Sung Seo, Kyoung-Won |
author_sort | Yang, Hyuck-Joo |
collection | PubMed |
description | BACKGROUND: Sildenafil citrate, a highly selective phosphodiesterase type 5 inhibitor, is used to treat pulmonary hypertension (PH) in veterinary medicine. The objective of this study was to investigate pharmacokinetic profiles by oral administration of orally disintegrating film (ODF) and film coated tablet (FCT) formulations and rectal administration of ODF formulation in healthy dogs. Twelve healthy beagle dogs were administered four separate doses of sildenafil: FCT formulation 2 mg/kg orally, ODF formulation 2 mg/kg orally, ODF formulation 2 mg/kg rectally, and ODF formulation 10 mg/kg rectally. For 24 hours following administration, blood samples were collected and the plasma concentrations of sildenafil were assayed by liquid chromatography-tandem mass spectrometry. RESULTS: There were no significant differences in all the pharmacokinetic parameters between FCT and ODF formulations when administrated orally. C(max) at the time of rectal administration was lower when the same dose was given as that orally administered. No serious systemic adverse events (AEs) were observed. CONCLUSIONS: These findings suggest that sildenafil ODF formulation can be used as an alternative to FCT formulation in the treatment of canine PH patients; additionally, rectal administration of sildenafil ODF may be a beneficial treatment option for canine patients who are unable to receive medication orally. |
format | Online Article Text |
id | pubmed-6154896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61548962018-09-26 Comparative single-dose pharmacokinetics of sildenafil after oral and rectal administration in healthy beagle dogs Yang, Hyuck-Joo Oh, Ye-In Jeong, Jong-Woo Song, Kun-Ho Koo, Tae-Sung Seo, Kyoung-Won BMC Vet Res Research Article BACKGROUND: Sildenafil citrate, a highly selective phosphodiesterase type 5 inhibitor, is used to treat pulmonary hypertension (PH) in veterinary medicine. The objective of this study was to investigate pharmacokinetic profiles by oral administration of orally disintegrating film (ODF) and film coated tablet (FCT) formulations and rectal administration of ODF formulation in healthy dogs. Twelve healthy beagle dogs were administered four separate doses of sildenafil: FCT formulation 2 mg/kg orally, ODF formulation 2 mg/kg orally, ODF formulation 2 mg/kg rectally, and ODF formulation 10 mg/kg rectally. For 24 hours following administration, blood samples were collected and the plasma concentrations of sildenafil were assayed by liquid chromatography-tandem mass spectrometry. RESULTS: There were no significant differences in all the pharmacokinetic parameters between FCT and ODF formulations when administrated orally. C(max) at the time of rectal administration was lower when the same dose was given as that orally administered. No serious systemic adverse events (AEs) were observed. CONCLUSIONS: These findings suggest that sildenafil ODF formulation can be used as an alternative to FCT formulation in the treatment of canine PH patients; additionally, rectal administration of sildenafil ODF may be a beneficial treatment option for canine patients who are unable to receive medication orally. BioMed Central 2018-09-24 /pmc/articles/PMC6154896/ /pubmed/30249242 http://dx.doi.org/10.1186/s12917-018-1617-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Yang, Hyuck-Joo Oh, Ye-In Jeong, Jong-Woo Song, Kun-Ho Koo, Tae-Sung Seo, Kyoung-Won Comparative single-dose pharmacokinetics of sildenafil after oral and rectal administration in healthy beagle dogs |
title | Comparative single-dose pharmacokinetics of sildenafil after oral and rectal administration in healthy beagle dogs |
title_full | Comparative single-dose pharmacokinetics of sildenafil after oral and rectal administration in healthy beagle dogs |
title_fullStr | Comparative single-dose pharmacokinetics of sildenafil after oral and rectal administration in healthy beagle dogs |
title_full_unstemmed | Comparative single-dose pharmacokinetics of sildenafil after oral and rectal administration in healthy beagle dogs |
title_short | Comparative single-dose pharmacokinetics of sildenafil after oral and rectal administration in healthy beagle dogs |
title_sort | comparative single-dose pharmacokinetics of sildenafil after oral and rectal administration in healthy beagle dogs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154896/ https://www.ncbi.nlm.nih.gov/pubmed/30249242 http://dx.doi.org/10.1186/s12917-018-1617-7 |
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