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Tissue Distribution of [(14)C]-Lefamulin into the Urogenital Tract in Rats
Lefamulin, a semisynthetic pleuromutilin antibiotic approved in the United States, Canada, and Europe for intravenous and oral treatment of community-acquired bacterial pneumonia, is highly active in vitro against bacterial pathogens that cause sexually transmitted infections (STIs), including multi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380576/ https://www.ncbi.nlm.nih.gov/pubmed/35862748 http://dx.doi.org/10.1128/aac.00355-22 |
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author | Wicha, Wolfgang W. Henson, Claire Webbley, Kathryn Gelone, Steven P. |
author_facet | Wicha, Wolfgang W. Henson, Claire Webbley, Kathryn Gelone, Steven P. |
author_sort | Wicha, Wolfgang W. |
collection | PubMed |
description | Lefamulin, a semisynthetic pleuromutilin antibiotic approved in the United States, Canada, and Europe for intravenous and oral treatment of community-acquired bacterial pneumonia, is highly active in vitro against bacterial pathogens that cause sexually transmitted infections (STIs), including multidrug-resistant strains of Neisseria gonorrhoeae, Chlamydia trachomatis, and Mycoplasma genitalium. This nonclinical study used quantitative whole-body autoradiography (QWBA) and qualitative tape-transfer microautoradiography (MARG) to investigate lefamulin distribution into urogenital tract tissues down to a cellular level in male and female rats. A single intravenous dose (30 mg/kg) of [(14)C]-lefamulin was administered to 3 male and 3 female Sprague-Dawley rats. At 0.5, 6, and 24 h post dose, rats were euthanized and [(14)C]-lefamulin distribution was investigated using QWBA and MARG of sagittal planes. [(14)C]-lefamulin was well distributed throughout the carcasses of male and female rats, with the highest concentrations observed in male bulbourethral gland, urethra, prostate in female clitoral gland, uterus (particularly endometrium), and ovary. In these areas, concentrations were similar to or higher than those observed in the lungs. Concentrations peaked at 0.5 h post dose, remaining detectable in the urogenital tract up to 24 h post dose. [(14)C]-lefamulin in rats showed rapid, homogeneous distribution into urogenital tissues down to a cellular level, with high tissue:blood ratios in tissues relevant to STI treatment. These results, and the potent in vitro activity of lefamulin against multidrug-resistant bacteria known to cause STIs, will help inform further assessment of lefamulin, including potential clinical evaluation for treatment of STIs. |
format | Online Article Text |
id | pubmed-9380576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-93805762022-08-17 Tissue Distribution of [(14)C]-Lefamulin into the Urogenital Tract in Rats Wicha, Wolfgang W. Henson, Claire Webbley, Kathryn Gelone, Steven P. Antimicrob Agents Chemother Pharmacology Lefamulin, a semisynthetic pleuromutilin antibiotic approved in the United States, Canada, and Europe for intravenous and oral treatment of community-acquired bacterial pneumonia, is highly active in vitro against bacterial pathogens that cause sexually transmitted infections (STIs), including multidrug-resistant strains of Neisseria gonorrhoeae, Chlamydia trachomatis, and Mycoplasma genitalium. This nonclinical study used quantitative whole-body autoradiography (QWBA) and qualitative tape-transfer microautoradiography (MARG) to investigate lefamulin distribution into urogenital tract tissues down to a cellular level in male and female rats. A single intravenous dose (30 mg/kg) of [(14)C]-lefamulin was administered to 3 male and 3 female Sprague-Dawley rats. At 0.5, 6, and 24 h post dose, rats were euthanized and [(14)C]-lefamulin distribution was investigated using QWBA and MARG of sagittal planes. [(14)C]-lefamulin was well distributed throughout the carcasses of male and female rats, with the highest concentrations observed in male bulbourethral gland, urethra, prostate in female clitoral gland, uterus (particularly endometrium), and ovary. In these areas, concentrations were similar to or higher than those observed in the lungs. Concentrations peaked at 0.5 h post dose, remaining detectable in the urogenital tract up to 24 h post dose. [(14)C]-lefamulin in rats showed rapid, homogeneous distribution into urogenital tissues down to a cellular level, with high tissue:blood ratios in tissues relevant to STI treatment. These results, and the potent in vitro activity of lefamulin against multidrug-resistant bacteria known to cause STIs, will help inform further assessment of lefamulin, including potential clinical evaluation for treatment of STIs. American Society for Microbiology 2022-07-11 /pmc/articles/PMC9380576/ /pubmed/35862748 http://dx.doi.org/10.1128/aac.00355-22 Text en Copyright © 2022 Wicha et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Pharmacology Wicha, Wolfgang W. Henson, Claire Webbley, Kathryn Gelone, Steven P. Tissue Distribution of [(14)C]-Lefamulin into the Urogenital Tract in Rats |
title | Tissue Distribution of [(14)C]-Lefamulin into the Urogenital Tract in Rats |
title_full | Tissue Distribution of [(14)C]-Lefamulin into the Urogenital Tract in Rats |
title_fullStr | Tissue Distribution of [(14)C]-Lefamulin into the Urogenital Tract in Rats |
title_full_unstemmed | Tissue Distribution of [(14)C]-Lefamulin into the Urogenital Tract in Rats |
title_short | Tissue Distribution of [(14)C]-Lefamulin into the Urogenital Tract in Rats |
title_sort | tissue distribution of [(14)c]-lefamulin into the urogenital tract in rats |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380576/ https://www.ncbi.nlm.nih.gov/pubmed/35862748 http://dx.doi.org/10.1128/aac.00355-22 |
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