Implications of storage and handling conditions on glass transition and potential devitrification of oocytes and embryos
- Autores
- Sansiñena, Marina Julia; Santos, María Victoria; Taminelli, Guillermo; Zaritzky, Noemí
- Año de publicación
- 2014
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión aceptada
- Descripción
- Fil: Sansiñena, Marina Julia. Pontificia Universidad Católica Argentina. Facultad de Ingeniería y Ciencias Agrarias; Argentina
Fil: Sansiñena, Marina Julia. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Santos, María Victoria. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Santos, María Victoria. Universidad Nacional de La Plata. Facultad de Ingeniería. Departamento de Ingeniería Química; Argentina
Fil: Santos, María Victoria. Universidad Nacional de La Plata. Centro de Investigación y Desarrollo en Criotecnología de Alimentos; Argentina
Fil: Taminelli, Guillermo. Pontificia Universidad Católica Argentina. Facultad de Ingeniería y Ciencias Agrarias; Argentina
Fil: Zaritzky, Noemí. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Zaritzky, Noemí. Universidad Nacional de La Plata. Facultad de Ingeniería. Departamento de Ingeniería Química; Argentina
Fil: Zaritzky, Noemí. Universidad Nacional de La Plata. Centro de Investigación y Desarrollo en Criotecnología de Alimentos; Argentina
Abstract: Devitrification, the process of crystallization of a formerly crystal-free, amorphous glass state, can lead to damage during the warming of cells. The objective of this study was to determine the glass transition temperature of a cryopreservation solution typically used in the vitrification, storage and warming of mammalian oocytes and embryos using Differential Scanning Calorimetry. A numerical model of the heat transfer process to analyze warming and devitrification thresholds for a common vitrification carrier (open pulled straw, OPS) was conducted. The implications on specimen handling and storage inside the dewar in contact with nitrogen vapor phase at different temperatures were determined. The time required for initiation of devitrification of a vitrified sample was determined by mathematical modeling and compared with measured temperatures in the vapor phase of liquid nitrogen cryogenic dewars. Results indicated that the glass transition ranged from -126 to -121ºC and devitrification was initiated at -109ºC. Interestingly, samples entered rubbery state at -121ºC and therefore could potentially initiate devitrification above this value, with the consequent damaging effects to cell survival. Devitrification times were calculated considering an initial temperature of material immersed in liquid nitrogen (-196ºC) and two temperatures of liquid nitrogen vapors within the dewar (-50 and -70ºC) to which the sample could be exposed for a period of time, either during storage or upon its removal. The mathematical model indicated samples could reach glass transition temperatures and undergo devitrification in 30 seconds. Results of the present study indicate storage of vitrified oocytes and embryos in the liquid nitrogen vapor phase (as opposed to completely immersed in liquid nitrogen) poses the potential risk of devitrification. Due to the reduced time-handling period before samples reach critical rubbery and devitrification values, caution should be exercised when handling samples in vapor phase - Fuente
- Theriogenology. 2014;82(3):373–378
- Materia
-
VITRIFICACION
EMBRIONES
NITROGENO LIQUIDO - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/4.0/
- Repositorio
- Institución
- Pontificia Universidad Católica Argentina
- OAI Identificador
- oai:ucacris:123456789/5495
Ver los metadatos del registro completo
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Implications of storage and handling conditions on glass transition and potential devitrification of oocytes and embryosSansiñena, Marina JuliaSantos, María VictoriaTaminelli, GuillermoZaritzky, NoemíVITRIFICACIONEMBRIONESNITROGENO LIQUIDOFil: Sansiñena, Marina Julia. Pontificia Universidad Católica Argentina. Facultad de Ingeniería y Ciencias Agrarias; ArgentinaFil: Sansiñena, Marina Julia. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Santos, María Victoria. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Santos, María Victoria. Universidad Nacional de La Plata. Facultad de Ingeniería. Departamento de Ingeniería Química; ArgentinaFil: Santos, María Victoria. Universidad Nacional de La Plata. Centro de Investigación y Desarrollo en Criotecnología de Alimentos; ArgentinaFil: Taminelli, Guillermo. Pontificia Universidad Católica Argentina. Facultad de Ingeniería y Ciencias Agrarias; ArgentinaFil: Zaritzky, Noemí. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Zaritzky, Noemí. Universidad Nacional de La Plata. Facultad de Ingeniería. Departamento de Ingeniería Química; ArgentinaFil: Zaritzky, Noemí. Universidad Nacional de La Plata. Centro de Investigación y Desarrollo en Criotecnología de Alimentos; ArgentinaAbstract: Devitrification, the process of crystallization of a formerly crystal-free, amorphous glass state, can lead to damage during the warming of cells. The objective of this study was to determine the glass transition temperature of a cryopreservation solution typically used in the vitrification, storage and warming of mammalian oocytes and embryos using Differential Scanning Calorimetry. A numerical model of the heat transfer process to analyze warming and devitrification thresholds for a common vitrification carrier (open pulled straw, OPS) was conducted. The implications on specimen handling and storage inside the dewar in contact with nitrogen vapor phase at different temperatures were determined. The time required for initiation of devitrification of a vitrified sample was determined by mathematical modeling and compared with measured temperatures in the vapor phase of liquid nitrogen cryogenic dewars. Results indicated that the glass transition ranged from -126 to -121ºC and devitrification was initiated at -109ºC. Interestingly, samples entered rubbery state at -121ºC and therefore could potentially initiate devitrification above this value, with the consequent damaging effects to cell survival. Devitrification times were calculated considering an initial temperature of material immersed in liquid nitrogen (-196ºC) and two temperatures of liquid nitrogen vapors within the dewar (-50 and -70ºC) to which the sample could be exposed for a period of time, either during storage or upon its removal. The mathematical model indicated samples could reach glass transition temperatures and undergo devitrification in 30 seconds. Results of the present study indicate storage of vitrified oocytes and embryos in the liquid nitrogen vapor phase (as opposed to completely immersed in liquid nitrogen) poses the potential risk of devitrification. Due to the reduced time-handling period before samples reach critical rubbery and devitrification values, caution should be exercised when handling samples in vapor phaseElsevier2014info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttps://repositorio.uca.edu.ar/handle/123456789/54950093-691X10.1016/j.theriogenology.2014.04.003Sansinena M, Santos MV, Taminelli G, Zaritky N. Implications of storage and handling conditions on glass transition and potential devitrification of oocytes and embryos [en línea]. Theriogenology. 2014;82(3):373–378. doi:10.1016/j.theriogenology.2014.04.003 Disponible en: https://repositorio.uca.edu.ar/handle/123456789/5495Theriogenology. 2014;82(3):373–378reponame:Repositorio Institucional (UCA)instname:Pontificia Universidad Católica Argentinaenginfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/4.0/2025-07-03T10:56:07Zoai:ucacris:123456789/5495instacron:UCAInstitucionalhttps://repositorio.uca.edu.ar/Universidad privadaNo correspondehttps://repositorio.uca.edu.ar/oaiclaudia_fernandez@uca.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:25852025-07-03 10:56:07.975Repositorio Institucional (UCA) - Pontificia Universidad Católica Argentinafalse |
dc.title.none.fl_str_mv |
Implications of storage and handling conditions on glass transition and potential devitrification of oocytes and embryos |
title |
Implications of storage and handling conditions on glass transition and potential devitrification of oocytes and embryos |
spellingShingle |
Implications of storage and handling conditions on glass transition and potential devitrification of oocytes and embryos Sansiñena, Marina Julia VITRIFICACION EMBRIONES NITROGENO LIQUIDO |
title_short |
Implications of storage and handling conditions on glass transition and potential devitrification of oocytes and embryos |
title_full |
Implications of storage and handling conditions on glass transition and potential devitrification of oocytes and embryos |
title_fullStr |
Implications of storage and handling conditions on glass transition and potential devitrification of oocytes and embryos |
title_full_unstemmed |
Implications of storage and handling conditions on glass transition and potential devitrification of oocytes and embryos |
title_sort |
Implications of storage and handling conditions on glass transition and potential devitrification of oocytes and embryos |
dc.creator.none.fl_str_mv |
Sansiñena, Marina Julia Santos, María Victoria Taminelli, Guillermo Zaritzky, Noemí |
author |
Sansiñena, Marina Julia |
author_facet |
Sansiñena, Marina Julia Santos, María Victoria Taminelli, Guillermo Zaritzky, Noemí |
author_role |
author |
author2 |
Santos, María Victoria Taminelli, Guillermo Zaritzky, Noemí |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
VITRIFICACION EMBRIONES NITROGENO LIQUIDO |
topic |
VITRIFICACION EMBRIONES NITROGENO LIQUIDO |
dc.description.none.fl_txt_mv |
Fil: Sansiñena, Marina Julia. Pontificia Universidad Católica Argentina. Facultad de Ingeniería y Ciencias Agrarias; Argentina Fil: Sansiñena, Marina Julia. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Santos, María Victoria. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Santos, María Victoria. Universidad Nacional de La Plata. Facultad de Ingeniería. Departamento de Ingeniería Química; Argentina Fil: Santos, María Victoria. Universidad Nacional de La Plata. Centro de Investigación y Desarrollo en Criotecnología de Alimentos; Argentina Fil: Taminelli, Guillermo. Pontificia Universidad Católica Argentina. Facultad de Ingeniería y Ciencias Agrarias; Argentina Fil: Zaritzky, Noemí. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Zaritzky, Noemí. Universidad Nacional de La Plata. Facultad de Ingeniería. Departamento de Ingeniería Química; Argentina Fil: Zaritzky, Noemí. Universidad Nacional de La Plata. Centro de Investigación y Desarrollo en Criotecnología de Alimentos; Argentina Abstract: Devitrification, the process of crystallization of a formerly crystal-free, amorphous glass state, can lead to damage during the warming of cells. The objective of this study was to determine the glass transition temperature of a cryopreservation solution typically used in the vitrification, storage and warming of mammalian oocytes and embryos using Differential Scanning Calorimetry. A numerical model of the heat transfer process to analyze warming and devitrification thresholds for a common vitrification carrier (open pulled straw, OPS) was conducted. The implications on specimen handling and storage inside the dewar in contact with nitrogen vapor phase at different temperatures were determined. The time required for initiation of devitrification of a vitrified sample was determined by mathematical modeling and compared with measured temperatures in the vapor phase of liquid nitrogen cryogenic dewars. Results indicated that the glass transition ranged from -126 to -121ºC and devitrification was initiated at -109ºC. Interestingly, samples entered rubbery state at -121ºC and therefore could potentially initiate devitrification above this value, with the consequent damaging effects to cell survival. Devitrification times were calculated considering an initial temperature of material immersed in liquid nitrogen (-196ºC) and two temperatures of liquid nitrogen vapors within the dewar (-50 and -70ºC) to which the sample could be exposed for a period of time, either during storage or upon its removal. The mathematical model indicated samples could reach glass transition temperatures and undergo devitrification in 30 seconds. Results of the present study indicate storage of vitrified oocytes and embryos in the liquid nitrogen vapor phase (as opposed to completely immersed in liquid nitrogen) poses the potential risk of devitrification. Due to the reduced time-handling period before samples reach critical rubbery and devitrification values, caution should be exercised when handling samples in vapor phase |
description |
Fil: Sansiñena, Marina Julia. Pontificia Universidad Católica Argentina. Facultad de Ingeniería y Ciencias Agrarias; Argentina |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
acceptedVersion |
dc.identifier.none.fl_str_mv |
https://repositorio.uca.edu.ar/handle/123456789/5495 0093-691X 10.1016/j.theriogenology.2014.04.003 Sansinena M, Santos MV, Taminelli G, Zaritky N. Implications of storage and handling conditions on glass transition and potential devitrification of oocytes and embryos [en línea]. Theriogenology. 2014;82(3):373–378. doi:10.1016/j.theriogenology.2014.04.003 Disponible en: https://repositorio.uca.edu.ar/handle/123456789/5495 |
url |
https://repositorio.uca.edu.ar/handle/123456789/5495 |
identifier_str_mv |
0093-691X 10.1016/j.theriogenology.2014.04.003 Sansinena M, Santos MV, Taminelli G, Zaritky N. Implications of storage and handling conditions on glass transition and potential devitrification of oocytes and embryos [en línea]. Theriogenology. 2014;82(3):373–378. doi:10.1016/j.theriogenology.2014.04.003 Disponible en: https://repositorio.uca.edu.ar/handle/123456789/5495 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/4.0/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/4.0/ |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier |
publisher.none.fl_str_mv |
Elsevier |
dc.source.none.fl_str_mv |
Theriogenology. 2014;82(3):373–378 reponame:Repositorio Institucional (UCA) instname:Pontificia Universidad Católica Argentina |
reponame_str |
Repositorio Institucional (UCA) |
collection |
Repositorio Institucional (UCA) |
instname_str |
Pontificia Universidad Católica Argentina |
repository.name.fl_str_mv |
Repositorio Institucional (UCA) - Pontificia Universidad Católica Argentina |
repository.mail.fl_str_mv |
claudia_fernandez@uca.edu.ar |
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1836638339667591168 |
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13.221938 |