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Swine as the Animal Model for Testing New Formulations of Anti-Inflammatory Drugs: Carprofen Pharmacokinetics and Bioavailability of the Intramuscular Route
Carprofen (CP) is a non-steroidal anti-inflammatory drug (NSAID) frequently used to treat respiratory diseases in numerous small animals, but also in large species. CP is a formidable candidate for further therapeutic research of human inflammatory diseases using the pig as an animal model. However,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9143053/ https://www.ncbi.nlm.nih.gov/pubmed/35631631 http://dx.doi.org/10.3390/pharmaceutics14051045 |
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author | Gómez-Segura, Lidia Boix-Montañes, Antoni Mallandrich, Mireia Parra-Coca, Alexander Soriano-Ruiz, José L. Calpena, Ana Cristina Gimeno, Álvaro Bellido, David Colom, Helena |
author_facet | Gómez-Segura, Lidia Boix-Montañes, Antoni Mallandrich, Mireia Parra-Coca, Alexander Soriano-Ruiz, José L. Calpena, Ana Cristina Gimeno, Álvaro Bellido, David Colom, Helena |
author_sort | Gómez-Segura, Lidia |
collection | PubMed |
description | Carprofen (CP) is a non-steroidal anti-inflammatory drug (NSAID) frequently used to treat respiratory diseases in numerous small animals, but also in large species. CP is a formidable candidate for further therapeutic research of human inflammatory diseases using the pig as an animal model. However, CP administration in swine is very uncommon and respective pharmacokinetics/bioavailability studies are scarce. A simultaneous population pharmacokinetic analysis after CP intravenous and intramuscular administrations in pigs has shown high extent and rate of absorption and a similar distribution profile with respect to man and other mammals. However, clearance and half-life values found in swine suggest a slower elimination process than that observed in man and some other animal species. Although not reported in other species, liver and kidney concentrations achieved at 48 h post-intramuscular administration in pigs were ten times lower than those found in plasma. Simulations pointed to 4 mg/kg every 24 h as the best dosage regimen to achieve similar therapeutic levels to those observed in other animal species. All these findings support the use of pig as an animal model to study the anti-inflammatory effects of CP in humans. |
format | Online Article Text |
id | pubmed-9143053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91430532022-05-29 Swine as the Animal Model for Testing New Formulations of Anti-Inflammatory Drugs: Carprofen Pharmacokinetics and Bioavailability of the Intramuscular Route Gómez-Segura, Lidia Boix-Montañes, Antoni Mallandrich, Mireia Parra-Coca, Alexander Soriano-Ruiz, José L. Calpena, Ana Cristina Gimeno, Álvaro Bellido, David Colom, Helena Pharmaceutics Article Carprofen (CP) is a non-steroidal anti-inflammatory drug (NSAID) frequently used to treat respiratory diseases in numerous small animals, but also in large species. CP is a formidable candidate for further therapeutic research of human inflammatory diseases using the pig as an animal model. However, CP administration in swine is very uncommon and respective pharmacokinetics/bioavailability studies are scarce. A simultaneous population pharmacokinetic analysis after CP intravenous and intramuscular administrations in pigs has shown high extent and rate of absorption and a similar distribution profile with respect to man and other mammals. However, clearance and half-life values found in swine suggest a slower elimination process than that observed in man and some other animal species. Although not reported in other species, liver and kidney concentrations achieved at 48 h post-intramuscular administration in pigs were ten times lower than those found in plasma. Simulations pointed to 4 mg/kg every 24 h as the best dosage regimen to achieve similar therapeutic levels to those observed in other animal species. All these findings support the use of pig as an animal model to study the anti-inflammatory effects of CP in humans. MDPI 2022-05-12 /pmc/articles/PMC9143053/ /pubmed/35631631 http://dx.doi.org/10.3390/pharmaceutics14051045 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gómez-Segura, Lidia Boix-Montañes, Antoni Mallandrich, Mireia Parra-Coca, Alexander Soriano-Ruiz, José L. Calpena, Ana Cristina Gimeno, Álvaro Bellido, David Colom, Helena Swine as the Animal Model for Testing New Formulations of Anti-Inflammatory Drugs: Carprofen Pharmacokinetics and Bioavailability of the Intramuscular Route |
title | Swine as the Animal Model for Testing New Formulations of Anti-Inflammatory Drugs: Carprofen Pharmacokinetics and Bioavailability of the Intramuscular Route |
title_full | Swine as the Animal Model for Testing New Formulations of Anti-Inflammatory Drugs: Carprofen Pharmacokinetics and Bioavailability of the Intramuscular Route |
title_fullStr | Swine as the Animal Model for Testing New Formulations of Anti-Inflammatory Drugs: Carprofen Pharmacokinetics and Bioavailability of the Intramuscular Route |
title_full_unstemmed | Swine as the Animal Model for Testing New Formulations of Anti-Inflammatory Drugs: Carprofen Pharmacokinetics and Bioavailability of the Intramuscular Route |
title_short | Swine as the Animal Model for Testing New Formulations of Anti-Inflammatory Drugs: Carprofen Pharmacokinetics and Bioavailability of the Intramuscular Route |
title_sort | swine as the animal model for testing new formulations of anti-inflammatory drugs: carprofen pharmacokinetics and bioavailability of the intramuscular route |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9143053/ https://www.ncbi.nlm.nih.gov/pubmed/35631631 http://dx.doi.org/10.3390/pharmaceutics14051045 |
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