Human sperm vitrification: the state of the art

Abstract Sperm cryopreservation has been widely used in assisted reproductive technology (ART) and has resulted in millions of live births. Two principal approaches have been adopted: conventional (slow) freezing and vitrification. As a traditional technique, slow freezing has been successfully empl...

Full description

Bibliographic Details
Main Authors: Yong Tao, Erika Sanger, Arpornrad Saewu, Marie-Claude Leveille
Format: Article
Language:English
Published: BMC 2020-03-01
Series:Reproductive Biology and Endocrinology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12958-020-00580-5
id doaj-8d733509a53f438ab2b06ff140570182
record_format Article
spelling doaj-8d733509a53f438ab2b06ff1405701822020-11-25T02:10:15ZengBMCReproductive Biology and Endocrinology1477-78272020-03-0118111010.1186/s12958-020-00580-5Human sperm vitrification: the state of the artYong Tao0Erika Sanger1Arpornrad Saewu2Marie-Claude Leveille3Ottawa Fertility CenterOttawa Fertility CenterOttawa Fertility CenterOttawa Fertility CenterAbstract Sperm cryopreservation has been widely used in assisted reproductive technology (ART) and has resulted in millions of live births. Two principal approaches have been adopted: conventional (slow) freezing and vitrification. As a traditional technique, slow freezing has been successfully employed and widely used at ART clinics whereas the latter, a process to solidify liquid into an amorphous or glassy state, may become a faster alternative method of sperm cryopreservation with significant benefits in regard to simple equipment and applicability to fertility centers. Sperm vitrification has its own limitations. Firstly, small volume of load is usually plunged to liquid nitrogen to achieve high cooling rate, which makes large volume sample cryopreservation less feasible. Secondly, direct contact with liquid nitrogen increases the potential risk of contamination. Recently, new carriers have been developed to facilitate improved control over the volume and speed, and new strategies have been implemented to minimize the contamination risk. In summary, although sperm vitrification has not yet been applied in routine sperm cryopreservation, its potential as a standard procedure is growing.http://link.springer.com/article/10.1186/s12958-020-00580-5CryopreservationVitrificationContaminationLiquid nitrogenSpermatozoaSemen
collection DOAJ
language English
format Article
sources DOAJ
author Yong Tao
Erika Sanger
Arpornrad Saewu
Marie-Claude Leveille
spellingShingle Yong Tao
Erika Sanger
Arpornrad Saewu
Marie-Claude Leveille
Human sperm vitrification: the state of the art
Reproductive Biology and Endocrinology
Cryopreservation
Vitrification
Contamination
Liquid nitrogen
Spermatozoa
Semen
author_facet Yong Tao
Erika Sanger
Arpornrad Saewu
Marie-Claude Leveille
author_sort Yong Tao
title Human sperm vitrification: the state of the art
title_short Human sperm vitrification: the state of the art
title_full Human sperm vitrification: the state of the art
title_fullStr Human sperm vitrification: the state of the art
title_full_unstemmed Human sperm vitrification: the state of the art
title_sort human sperm vitrification: the state of the art
publisher BMC
series Reproductive Biology and Endocrinology
issn 1477-7827
publishDate 2020-03-01
description Abstract Sperm cryopreservation has been widely used in assisted reproductive technology (ART) and has resulted in millions of live births. Two principal approaches have been adopted: conventional (slow) freezing and vitrification. As a traditional technique, slow freezing has been successfully employed and widely used at ART clinics whereas the latter, a process to solidify liquid into an amorphous or glassy state, may become a faster alternative method of sperm cryopreservation with significant benefits in regard to simple equipment and applicability to fertility centers. Sperm vitrification has its own limitations. Firstly, small volume of load is usually plunged to liquid nitrogen to achieve high cooling rate, which makes large volume sample cryopreservation less feasible. Secondly, direct contact with liquid nitrogen increases the potential risk of contamination. Recently, new carriers have been developed to facilitate improved control over the volume and speed, and new strategies have been implemented to minimize the contamination risk. In summary, although sperm vitrification has not yet been applied in routine sperm cryopreservation, its potential as a standard procedure is growing.
topic Cryopreservation
Vitrification
Contamination
Liquid nitrogen
Spermatozoa
Semen
url http://link.springer.com/article/10.1186/s12958-020-00580-5
work_keys_str_mv AT yongtao humanspermvitrificationthestateoftheart
AT erikasanger humanspermvitrificationthestateoftheart
AT arpornradsaewu humanspermvitrificationthestateoftheart
AT marieclaudeleveille humanspermvitrificationthestateoftheart
_version_ 1724919887604744192