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Simple separation of good quality bovine oocytes using a microfluidic device
We fabricated a simple microfluidic device for separation of bovine oocytes based on the oocyte quality to improve the conception rate of in vitro fertilization (IVF) by using good quality oocytes. The microfluidic device separates oocytes based on sedimentation rate differences in a sucrose buffer,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155318/ https://www.ncbi.nlm.nih.gov/pubmed/30250059 http://dx.doi.org/10.1038/s41598-018-32687-6 |
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author | Iwasaki, Wataru Yamanaka, Kenichi Sugiyama, Daisuke Teshima, Yuki Briones-Nagata, Maria Portia Maeki, Masatoshi Yamashita, Kenichi Takahashi, Masashi Miyazaki, Masaya |
author_facet | Iwasaki, Wataru Yamanaka, Kenichi Sugiyama, Daisuke Teshima, Yuki Briones-Nagata, Maria Portia Maeki, Masatoshi Yamashita, Kenichi Takahashi, Masashi Miyazaki, Masaya |
author_sort | Iwasaki, Wataru |
collection | PubMed |
description | We fabricated a simple microfluidic device for separation of bovine oocytes based on the oocyte quality to improve the conception rate of in vitro fertilization (IVF) by using good quality oocytes. The microfluidic device separates oocytes based on sedimentation rate differences in a sucrose buffer, which is dependent on oocyte quality. The microfluidic device has a 700 µm width, 1 mm height, and 10 mm long separation channel. Oocytes were injected from the upper half of the separation channel, and they flowed while sinking. The outlets of the separation channel were divided into upper and lower chambers. Good quality oocytes settled faster than poor quality oocytes in sucrose buffer; therefore, good quality oocytes were collected from the lower outlet. We performed IVF after the microfluidic separation of oocytes. The developmental rate to blastocysts of oocytes collected from the lower outlet was significantly higher than those collected from the upper outlet (36.0% vs. 14.1%). This result was comparable to that in the BCB staining method performed as a comparison method (BCB+ : 35.7%, BCB−: 15.4%). These findings indicate that our microfluidic device could be applied to oocyte separation and contribute to improvement of in vitro embryo production system. |
format | Online Article Text |
id | pubmed-6155318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61553182018-09-28 Simple separation of good quality bovine oocytes using a microfluidic device Iwasaki, Wataru Yamanaka, Kenichi Sugiyama, Daisuke Teshima, Yuki Briones-Nagata, Maria Portia Maeki, Masatoshi Yamashita, Kenichi Takahashi, Masashi Miyazaki, Masaya Sci Rep Article We fabricated a simple microfluidic device for separation of bovine oocytes based on the oocyte quality to improve the conception rate of in vitro fertilization (IVF) by using good quality oocytes. The microfluidic device separates oocytes based on sedimentation rate differences in a sucrose buffer, which is dependent on oocyte quality. The microfluidic device has a 700 µm width, 1 mm height, and 10 mm long separation channel. Oocytes were injected from the upper half of the separation channel, and they flowed while sinking. The outlets of the separation channel were divided into upper and lower chambers. Good quality oocytes settled faster than poor quality oocytes in sucrose buffer; therefore, good quality oocytes were collected from the lower outlet. We performed IVF after the microfluidic separation of oocytes. The developmental rate to blastocysts of oocytes collected from the lower outlet was significantly higher than those collected from the upper outlet (36.0% vs. 14.1%). This result was comparable to that in the BCB staining method performed as a comparison method (BCB+ : 35.7%, BCB−: 15.4%). These findings indicate that our microfluidic device could be applied to oocyte separation and contribute to improvement of in vitro embryo production system. Nature Publishing Group UK 2018-09-24 /pmc/articles/PMC6155318/ /pubmed/30250059 http://dx.doi.org/10.1038/s41598-018-32687-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Iwasaki, Wataru Yamanaka, Kenichi Sugiyama, Daisuke Teshima, Yuki Briones-Nagata, Maria Portia Maeki, Masatoshi Yamashita, Kenichi Takahashi, Masashi Miyazaki, Masaya Simple separation of good quality bovine oocytes using a microfluidic device |
title | Simple separation of good quality bovine oocytes using a microfluidic device |
title_full | Simple separation of good quality bovine oocytes using a microfluidic device |
title_fullStr | Simple separation of good quality bovine oocytes using a microfluidic device |
title_full_unstemmed | Simple separation of good quality bovine oocytes using a microfluidic device |
title_short | Simple separation of good quality bovine oocytes using a microfluidic device |
title_sort | simple separation of good quality bovine oocytes using a microfluidic device |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155318/ https://www.ncbi.nlm.nih.gov/pubmed/30250059 http://dx.doi.org/10.1038/s41598-018-32687-6 |
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