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Azoospermia in rabbits following an intravas injection of Vasalgel ™
BACKGROUND: Vasectomy is currently the only long-acting contraceptive option available for men, despite increasing demand and potentially significant positive impacts on human health of additional male contraceptive options. Vasalgel ™ is a high molecular weight hydrogel polymer being developed as a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4812607/ https://www.ncbi.nlm.nih.gov/pubmed/27030808 http://dx.doi.org/10.1186/s12610-016-0033-8 |
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author | Waller, Donald Bolick, David Lissner, Elaine Premanandan, Christopher Gamerman, Gary |
author_facet | Waller, Donald Bolick, David Lissner, Elaine Premanandan, Christopher Gamerman, Gary |
author_sort | Waller, Donald |
collection | PubMed |
description | BACKGROUND: Vasectomy is currently the only long-acting contraceptive option available for men, despite increasing demand and potentially significant positive impacts on human health of additional male contraceptive options. Vasalgel ™ is a high molecular weight hydrogel polymer being developed as a non-hormonal long-acting reversible male contraceptive. Vasalgel consists of styrene-alt-maleic acid dissolved in dimethyl sulfoxide, which is distinct from styrene-alt-maleic anhydride materials previously studied. METHODS: The goal of the study was to determine the contraceptive efficacy of two test articles with different levels of styrene maleic acid (100 %, and 80 % acid/20 % anhydride). The test articles were injected bilaterally in the vasa deferentia of mature male rabbits. Post-implantation analyses of semen parameters were completed over a 12 month period and compared to baseline measures of sperm concentration, motility and forward progression. RESULTS: Both test articles were effective in blocking the passage of spermatozoa through the vasa deferentia in the 12 subjects completing the study. A significant decrease in sperm concentration occurred following implantation of the test material, with no measurable sperm concentration except for a few samples in one animal that were markedly oligospermic. Vasalgel produced a rapid onset of azoospermia, with no sperm in semen samples collected as early as 29–36 days post-implantation, and was durable over a 12 month period. CONCLUSION: This study indicated that Vasalgel is an effective non-hormonal long-acting male contraceptive in a rabbit model. |
format | Online Article Text |
id | pubmed-4812607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48126072016-03-31 Azoospermia in rabbits following an intravas injection of Vasalgel ™ Waller, Donald Bolick, David Lissner, Elaine Premanandan, Christopher Gamerman, Gary Basic Clin Androl Research Article BACKGROUND: Vasectomy is currently the only long-acting contraceptive option available for men, despite increasing demand and potentially significant positive impacts on human health of additional male contraceptive options. Vasalgel ™ is a high molecular weight hydrogel polymer being developed as a non-hormonal long-acting reversible male contraceptive. Vasalgel consists of styrene-alt-maleic acid dissolved in dimethyl sulfoxide, which is distinct from styrene-alt-maleic anhydride materials previously studied. METHODS: The goal of the study was to determine the contraceptive efficacy of two test articles with different levels of styrene maleic acid (100 %, and 80 % acid/20 % anhydride). The test articles were injected bilaterally in the vasa deferentia of mature male rabbits. Post-implantation analyses of semen parameters were completed over a 12 month period and compared to baseline measures of sperm concentration, motility and forward progression. RESULTS: Both test articles were effective in blocking the passage of spermatozoa through the vasa deferentia in the 12 subjects completing the study. A significant decrease in sperm concentration occurred following implantation of the test material, with no measurable sperm concentration except for a few samples in one animal that were markedly oligospermic. Vasalgel produced a rapid onset of azoospermia, with no sperm in semen samples collected as early as 29–36 days post-implantation, and was durable over a 12 month period. CONCLUSION: This study indicated that Vasalgel is an effective non-hormonal long-acting male contraceptive in a rabbit model. BioMed Central 2016-03-30 /pmc/articles/PMC4812607/ /pubmed/27030808 http://dx.doi.org/10.1186/s12610-016-0033-8 Text en © Waller et al. 2016 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 Waller, Donald Bolick, David Lissner, Elaine Premanandan, Christopher Gamerman, Gary Azoospermia in rabbits following an intravas injection of Vasalgel ™ |
title | Azoospermia in rabbits following an intravas injection of Vasalgel ™ |
title_full | Azoospermia in rabbits following an intravas injection of Vasalgel ™ |
title_fullStr | Azoospermia in rabbits following an intravas injection of Vasalgel ™ |
title_full_unstemmed | Azoospermia in rabbits following an intravas injection of Vasalgel ™ |
title_short | Azoospermia in rabbits following an intravas injection of Vasalgel ™ |
title_sort | azoospermia in rabbits following an intravas injection of vasalgel ™ |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4812607/ https://www.ncbi.nlm.nih.gov/pubmed/27030808 http://dx.doi.org/10.1186/s12610-016-0033-8 |
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