Feasibility of refreezing human spermatozoa through the technique of liquid nitrogen vapor

OBJECTIVE: To assess the feasibility of refreezing human semen using the technique of liquid nitrogen vapor with static phases. MATERIALS AND METHODS: Twenty samples from 16 subjects who required disposal of their cryopreserved semen were thawed, corresponding to 6 cancer patients and 10 participant...

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Main Authors: Sidney Verza Jr, Sandro C. Esteves
Format: Article
Language:English
Published: Sociedade Brasileira de Urologia 2004-12-01
Series:International Brazilian Journal of Urology
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382004000600006
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spelling doaj-163e392cbd7446d3b147c7ab956bf8cb2020-11-25T02:25:19ZengSociedade Brasileira de UrologiaInternational Brazilian Journal of Urology1677-55381677-61192004-12-0130648749310.1590/S1677-55382004000600006Feasibility of refreezing human spermatozoa through the technique of liquid nitrogen vaporSidney Verza JrSandro C. EstevesOBJECTIVE: To assess the feasibility of refreezing human semen using the technique of liquid nitrogen vapor with static phases. MATERIALS AND METHODS: Twenty samples from 16 subjects who required disposal of their cryopreserved semen were thawed, corresponding to 6 cancer patients and 10 participants in the assisted reproduction (AR) program. Samples were refrozen using the technique of liquid nitrogen vapor with static phases, identical to the one used for the initial freezing, and thawed again after 72 hours. We assessed the concentration of motile spermatozoa, total and progressive percent motility and spermatic vitality, according to criteria of the World Health Organization (WHO), as well as spermatic morphology according to the strict Kruger criterion, after the first and after the second thawing. RESULTS: We observed a significant decrease in all the parameters evaluated between the first and the second thawing. Median values for the concentration of motile spermatozoa decreased from 2.0x10(6)/mL to 0.1x10(6)/mL (p < 0.01); total percent motility from 42% to 22.5% (p < 0.01); progressive percent motility from 34% to 9.5% (p < 0.01); vitality from 45% to 20% (p < 0.01); and morphology from 5% to 5% (p = 0.03). There was no significant difference in the spermatic parameters between the cancer and assisted reproduction groups, both after the first and after the second thawing. We observed that in 100% of cases there was retrieval of motile spermatozoa after the second thawing. CONCLUSIONS: Refreezing of human semen by the technique of liquid nitrogen vapor allows the retrieval of viable spermatozoa after thawing.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382004000600006fertilityin vitro fertilizationspermfreezingnitrogen
collection DOAJ
language English
format Article
sources DOAJ
author Sidney Verza Jr
Sandro C. Esteves
spellingShingle Sidney Verza Jr
Sandro C. Esteves
Feasibility of refreezing human spermatozoa through the technique of liquid nitrogen vapor
International Brazilian Journal of Urology
fertility
in vitro fertilization
sperm
freezing
nitrogen
author_facet Sidney Verza Jr
Sandro C. Esteves
author_sort Sidney Verza Jr
title Feasibility of refreezing human spermatozoa through the technique of liquid nitrogen vapor
title_short Feasibility of refreezing human spermatozoa through the technique of liquid nitrogen vapor
title_full Feasibility of refreezing human spermatozoa through the technique of liquid nitrogen vapor
title_fullStr Feasibility of refreezing human spermatozoa through the technique of liquid nitrogen vapor
title_full_unstemmed Feasibility of refreezing human spermatozoa through the technique of liquid nitrogen vapor
title_sort feasibility of refreezing human spermatozoa through the technique of liquid nitrogen vapor
publisher Sociedade Brasileira de Urologia
series International Brazilian Journal of Urology
issn 1677-5538
1677-6119
publishDate 2004-12-01
description OBJECTIVE: To assess the feasibility of refreezing human semen using the technique of liquid nitrogen vapor with static phases. MATERIALS AND METHODS: Twenty samples from 16 subjects who required disposal of their cryopreserved semen were thawed, corresponding to 6 cancer patients and 10 participants in the assisted reproduction (AR) program. Samples were refrozen using the technique of liquid nitrogen vapor with static phases, identical to the one used for the initial freezing, and thawed again after 72 hours. We assessed the concentration of motile spermatozoa, total and progressive percent motility and spermatic vitality, according to criteria of the World Health Organization (WHO), as well as spermatic morphology according to the strict Kruger criterion, after the first and after the second thawing. RESULTS: We observed a significant decrease in all the parameters evaluated between the first and the second thawing. Median values for the concentration of motile spermatozoa decreased from 2.0x10(6)/mL to 0.1x10(6)/mL (p < 0.01); total percent motility from 42% to 22.5% (p < 0.01); progressive percent motility from 34% to 9.5% (p < 0.01); vitality from 45% to 20% (p < 0.01); and morphology from 5% to 5% (p = 0.03). There was no significant difference in the spermatic parameters between the cancer and assisted reproduction groups, both after the first and after the second thawing. We observed that in 100% of cases there was retrieval of motile spermatozoa after the second thawing. CONCLUSIONS: Refreezing of human semen by the technique of liquid nitrogen vapor allows the retrieval of viable spermatozoa after thawing.
topic fertility
in vitro fertilization
sperm
freezing
nitrogen
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382004000600006
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