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dc.date.accessioned 2020-09-10T21:46:48Z
dc.date.available 2020-09-10T21:46:48Z
dc.date.issued 2014-08
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/104393
dc.description.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) 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 the glass transition ranged from -126°C to -121°C, and devitrification was initiated at -109°C. Interestingly, samples entered rubbery state at -121°C 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 (-196°C), and two temperatures of liquid nitrogen vapors within the dewar (-50°C and -70°C) 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 30seconds. 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. Because of the reduced time-handling period before samples reach critical rubbery and devitrification values, caution should be exercised when handling samples in vapor phase. en
dc.format.extent 373-378 es
dc.language en es
dc.subject Devitrification es
dc.subject Embryo es
dc.subject Glass transition es
dc.subject Liquid nitrogen es
dc.subject Vitrification es
dc.title Implications of storage and handling conditions on glass transition and potential devitrification of oocytes and embryos en
dc.type Articulo es
sedici.identifier.uri http://hdl.handle.net/11336/99493 es
sedici.identifier.other https://doi.org/10.1016/j.theriogenology.2014.04.003 es
sedici.identifier.other hdl:11336/99493 es
sedici.identifier.issn 0093-691X es
sedici.creator.person Sansinena, Marina Julia es
sedici.creator.person Santos, María Victoria es
sedici.creator.person Taminelli, Guillermo Luis es
sedici.creator.person Zaritzky, Noemí Elisabet es
sedici.subject.materias Química es
sedici.description.fulltext true es
mods.originInfo.place Centro de Investigación y Desarrollo en Criotecnología de Alimentos es
sedici.subtype Preprint es
sedici.rights.license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by-nc-sa/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle Theriogenology es
sedici.relation.journalVolumeAndIssue vol. 82, no. 3 es


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Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)