Comparison of blastocyst and sage media for in vitro maturation of human immature oocytes

© The Author(s) 2014. In vitro maturation (IVM) of human oocytes is an attractive alternative to conventional assisted reproductive technology (ART) treatment, as it involves no or minimal ovarian stimulation. Currently, commercialized media specifically designed for IVM are often used. These media...

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Main Authors: Pallop Pongsuthirak, Sorramon Songveeratham, Teraporn Vutyavanich
Format: Journal
Published: 2018
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Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84924757438&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/54775
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spelling th-cmuir.6653943832-547752018-09-04T10:23:10Z Comparison of blastocyst and sage media for in vitro maturation of human immature oocytes Pallop Pongsuthirak Sorramon Songveeratham Teraporn Vutyavanich Medicine © The Author(s) 2014. In vitro maturation (IVM) of human oocytes is an attractive alternative to conventional assisted reproductive technology (ART) treatment, as it involves no or minimal ovarian stimulation. Currently, commercialized media specifically designed for IVM are often used. These media are expensive, have limited shelf life, and must be ordered in advance. If standard culture media can be used in place of the specialized IVM media, it would simplify management and make IVM more feasible and more widely employed in ART centers around the world, especially in developing countries where resources are scarce. This study was, therefore, conducted to test the hypothesis that blastocyst medium was as good as commercial IVM medium to support maturation and developmental competence of human immature oocytes as previously shown in the mouse system. Immature oocytes were obtained by needle aspiration from 89 pregnant women during cesarean deliveries between April 2012 and February 2013. Sibling oocytes were allocated to Sage IVM media (512 oocytes) or blastocyst medium (520 oocytes) and assessed for maturation 36 hours later. Mature oocytes were inseminated by intracytoplasmic sperm injection and cultured up to 144 hours. There was no difference in maturation rate (65.0% vs 68.7%; P =.218) or fertilization rate (66.9% vs 66.4%; P =.872) of oocytes matured in vitro in both media. There was also no difference in the formation of good-quality blastocysts (46.6% vs 45.9%; P =.889) in the 2 groups. Further study should be done to ascertain implantation and pregnancy potential of these embryos. 2018-09-04T10:23:10Z 2018-09-04T10:23:10Z 2015-01-01 Journal 19337205 19337191 2-s2.0-84924757438 10.1177/1933719114542027 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84924757438&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/54775
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Medicine
spellingShingle Medicine
Pallop Pongsuthirak
Sorramon Songveeratham
Teraporn Vutyavanich
Comparison of blastocyst and sage media for in vitro maturation of human immature oocytes
description © The Author(s) 2014. In vitro maturation (IVM) of human oocytes is an attractive alternative to conventional assisted reproductive technology (ART) treatment, as it involves no or minimal ovarian stimulation. Currently, commercialized media specifically designed for IVM are often used. These media are expensive, have limited shelf life, and must be ordered in advance. If standard culture media can be used in place of the specialized IVM media, it would simplify management and make IVM more feasible and more widely employed in ART centers around the world, especially in developing countries where resources are scarce. This study was, therefore, conducted to test the hypothesis that blastocyst medium was as good as commercial IVM medium to support maturation and developmental competence of human immature oocytes as previously shown in the mouse system. Immature oocytes were obtained by needle aspiration from 89 pregnant women during cesarean deliveries between April 2012 and February 2013. Sibling oocytes were allocated to Sage IVM media (512 oocytes) or blastocyst medium (520 oocytes) and assessed for maturation 36 hours later. Mature oocytes were inseminated by intracytoplasmic sperm injection and cultured up to 144 hours. There was no difference in maturation rate (65.0% vs 68.7%; P =.218) or fertilization rate (66.9% vs 66.4%; P =.872) of oocytes matured in vitro in both media. There was also no difference in the formation of good-quality blastocysts (46.6% vs 45.9%; P =.889) in the 2 groups. Further study should be done to ascertain implantation and pregnancy potential of these embryos.
format Journal
author Pallop Pongsuthirak
Sorramon Songveeratham
Teraporn Vutyavanich
author_facet Pallop Pongsuthirak
Sorramon Songveeratham
Teraporn Vutyavanich
author_sort Pallop Pongsuthirak
title Comparison of blastocyst and sage media for in vitro maturation of human immature oocytes
title_short Comparison of blastocyst and sage media for in vitro maturation of human immature oocytes
title_full Comparison of blastocyst and sage media for in vitro maturation of human immature oocytes
title_fullStr Comparison of blastocyst and sage media for in vitro maturation of human immature oocytes
title_full_unstemmed Comparison of blastocyst and sage media for in vitro maturation of human immature oocytes
title_sort comparison of blastocyst and sage media for in vitro maturation of human immature oocytes
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84924757438&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/54775
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