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Allometric analysis of tylosin tartrate pharmacokinetics in growing male turkeys
BACKGROUND: Despite common use of tylosin in turkeys, the pharmacokinetic (PK) data for this drug in turkeys is limited. Within a few months of growth, PK of drugs in turkeys undergoes changes that may decrease their efficacy due to variable internal exposure. OBJECTIVES: The objective of this study...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Veterinary Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263918/ https://www.ncbi.nlm.nih.gov/pubmed/32476311 http://dx.doi.org/10.4142/jvs.2020.21.e35 |
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author | Poźniak, Błażej Tikhomirov, Marta Motykiewicz-Pers, Karolina Bobrek, Kamila Świtała, Marcin |
author_facet | Poźniak, Błażej Tikhomirov, Marta Motykiewicz-Pers, Karolina Bobrek, Kamila Świtała, Marcin |
author_sort | Poźniak, Błażej |
collection | PubMed |
description | BACKGROUND: Despite common use of tylosin in turkeys, the pharmacokinetic (PK) data for this drug in turkeys is limited. Within a few months of growth, PK of drugs in turkeys undergoes changes that may decrease their efficacy due to variable internal exposure. OBJECTIVES: The objective of this study was to investigate the influence of age on the PK of a single intravenous (i.v.) and oral administration of tylosin to turkeys at a dose of 10 and 50 mg/kg, respectively. METHODS: Plasma drug concentrations were measured using high-performance liquid chromatography with UV detection. The PK parameters were assessed by means of non-compartmental approach and were subjected to allometric analysis. RESULTS: During a 2.5-month-long period of growth from 1.4 to 14.7 kg, the median value for area under the concentration-time curve after i.v. administration increased from 2.61 to 7.15 mg × h/L and the body clearance decreased from a median of 3.81 to 1.42 L/h/kg. Over the same time, the median elimination half-life increased from 1.03 to 2.96 h. For the oral administration a similar trend was noted but the differences were less pronounced. Bioavailability was variable (5.76%–21.59%) and age-independent. For both routes, the plasma concentration of the major tylosin metabolite, tylosin D, was minimal. Protein binding was age-independent and did not exceed 50%. Allometric analysis indicated a relatively poor predictivity of clearance, volume of distribution and elimination half-life for tylosin in turkeys. CONCLUSIONS: Age has a significant impact on tylosin PK in turkeys and dosage adjustment may be needed, particularly in young individuals. |
format | Online Article Text |
id | pubmed-7263918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Korean Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-72639182020-06-10 Allometric analysis of tylosin tartrate pharmacokinetics in growing male turkeys Poźniak, Błażej Tikhomirov, Marta Motykiewicz-Pers, Karolina Bobrek, Kamila Świtała, Marcin J Vet Sci Original Article BACKGROUND: Despite common use of tylosin in turkeys, the pharmacokinetic (PK) data for this drug in turkeys is limited. Within a few months of growth, PK of drugs in turkeys undergoes changes that may decrease their efficacy due to variable internal exposure. OBJECTIVES: The objective of this study was to investigate the influence of age on the PK of a single intravenous (i.v.) and oral administration of tylosin to turkeys at a dose of 10 and 50 mg/kg, respectively. METHODS: Plasma drug concentrations were measured using high-performance liquid chromatography with UV detection. The PK parameters were assessed by means of non-compartmental approach and were subjected to allometric analysis. RESULTS: During a 2.5-month-long period of growth from 1.4 to 14.7 kg, the median value for area under the concentration-time curve after i.v. administration increased from 2.61 to 7.15 mg × h/L and the body clearance decreased from a median of 3.81 to 1.42 L/h/kg. Over the same time, the median elimination half-life increased from 1.03 to 2.96 h. For the oral administration a similar trend was noted but the differences were less pronounced. Bioavailability was variable (5.76%–21.59%) and age-independent. For both routes, the plasma concentration of the major tylosin metabolite, tylosin D, was minimal. Protein binding was age-independent and did not exceed 50%. Allometric analysis indicated a relatively poor predictivity of clearance, volume of distribution and elimination half-life for tylosin in turkeys. CONCLUSIONS: Age has a significant impact on tylosin PK in turkeys and dosage adjustment may be needed, particularly in young individuals. The Korean Society of Veterinary Science 2020-05 2020-03-11 /pmc/articles/PMC7263918/ /pubmed/32476311 http://dx.doi.org/10.4142/jvs.2020.21.e35 Text en © 2020 The Korean Society of Veterinary Science https://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Poźniak, Błażej Tikhomirov, Marta Motykiewicz-Pers, Karolina Bobrek, Kamila Świtała, Marcin Allometric analysis of tylosin tartrate pharmacokinetics in growing male turkeys |
title | Allometric analysis of tylosin tartrate pharmacokinetics in growing male turkeys |
title_full | Allometric analysis of tylosin tartrate pharmacokinetics in growing male turkeys |
title_fullStr | Allometric analysis of tylosin tartrate pharmacokinetics in growing male turkeys |
title_full_unstemmed | Allometric analysis of tylosin tartrate pharmacokinetics in growing male turkeys |
title_short | Allometric analysis of tylosin tartrate pharmacokinetics in growing male turkeys |
title_sort | allometric analysis of tylosin tartrate pharmacokinetics in growing male turkeys |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263918/ https://www.ncbi.nlm.nih.gov/pubmed/32476311 http://dx.doi.org/10.4142/jvs.2020.21.e35 |
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