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Modified MicroSecure Vitrification: A Safe, Simple and Highly Effective Cryopreservation Procedure for Human Blastocysts

Clinical embryo vitrification evolved with the development of unique vitrification devices in the 21(st) century and with the misconception that ultra-rapid cooling in an "open" system (i.e., direct LN(2) contact) was a necessity to optimize vitrification success. The dogma surrounding the...

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Autores principales: Schiewe, Mitchel C., Zozula, Shane, Nugent, Nancy, Waggoner, Kelley, Borba, Jessica, Gamboa, Lisa, Whitney, John B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5407698/
https://www.ncbi.nlm.nih.gov/pubmed/28287560
http://dx.doi.org/10.3791/54871
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author Schiewe, Mitchel C.
Zozula, Shane
Nugent, Nancy
Waggoner, Kelley
Borba, Jessica
Gamboa, Lisa
Whitney, John B.
author_facet Schiewe, Mitchel C.
Zozula, Shane
Nugent, Nancy
Waggoner, Kelley
Borba, Jessica
Gamboa, Lisa
Whitney, John B.
author_sort Schiewe, Mitchel C.
collection PubMed
description Clinical embryo vitrification evolved with the development of unique vitrification devices in the 21(st) century and with the misconception that ultra-rapid cooling in an "open" system (i.e., direct LN(2) contact) was a necessity to optimize vitrification success. The dogma surrounding the importance of cooling rates led to unsafe practices subject to technical variation and to the creation of vitrification devices that disregarded important quality-control factors (e.g., ease of use, repeatability, reliability, labeling security, and storage safety). Understanding the quality-control flaws of other devices allowed for the development of a safe, secure, repeatable, and reliable µS-VTF method aimed to minimize intra- and inter-technician variation. Equally important, it combined the availability of two existing FDA-compliant devices: 1) a 0.3-mL ionomeric resin embryo straw with internalized, dual-colored, tamper-proof labeling with repeatable weld seal potential; and 2) shortened, commonly-used, 300-µm ID sterile flexipettes to directly load the embryo(s) in order to create a highly-effective global vitrification device. Like other aseptic, closed vitrification systems (e.g., High Security Vitrification (HSV), Rapid-i, and VitriSafe) effectively used in reproductive medicine, microSecure Vitrification (µS-VTF) has proven that it can achieve high post-warming survival and pregnancy outcomes with its attention to simplicity, and reduced technical variation. Although the 0.3-mL embryo straw containing an internal hydrophobic plug was commercially replaced with a standard semen straw possessing cotton-polyvinyl pyrrolidone (PVP) plugs, it maintained its ionomeric resin composition to ensure weld sealing. However, the cotton plugs can wick out the fluid-embryo contents of the flexipettes upon contact. A modified µS-VTF method was adapted to include an additional internal weld seal before the plug on the device loading side. The added technical step to the µS-VTF procedure has not affected its successful application, as high survival rates (> 95%) and pregnancy rates continue today.
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spelling pubmed-54076982017-05-12 Modified MicroSecure Vitrification: A Safe, Simple and Highly Effective Cryopreservation Procedure for Human Blastocysts Schiewe, Mitchel C. Zozula, Shane Nugent, Nancy Waggoner, Kelley Borba, Jessica Gamboa, Lisa Whitney, John B. J Vis Exp Developmental Biology Clinical embryo vitrification evolved with the development of unique vitrification devices in the 21(st) century and with the misconception that ultra-rapid cooling in an "open" system (i.e., direct LN(2) contact) was a necessity to optimize vitrification success. The dogma surrounding the importance of cooling rates led to unsafe practices subject to technical variation and to the creation of vitrification devices that disregarded important quality-control factors (e.g., ease of use, repeatability, reliability, labeling security, and storage safety). Understanding the quality-control flaws of other devices allowed for the development of a safe, secure, repeatable, and reliable µS-VTF method aimed to minimize intra- and inter-technician variation. Equally important, it combined the availability of two existing FDA-compliant devices: 1) a 0.3-mL ionomeric resin embryo straw with internalized, dual-colored, tamper-proof labeling with repeatable weld seal potential; and 2) shortened, commonly-used, 300-µm ID sterile flexipettes to directly load the embryo(s) in order to create a highly-effective global vitrification device. Like other aseptic, closed vitrification systems (e.g., High Security Vitrification (HSV), Rapid-i, and VitriSafe) effectively used in reproductive medicine, microSecure Vitrification (µS-VTF) has proven that it can achieve high post-warming survival and pregnancy outcomes with its attention to simplicity, and reduced technical variation. Although the 0.3-mL embryo straw containing an internal hydrophobic plug was commercially replaced with a standard semen straw possessing cotton-polyvinyl pyrrolidone (PVP) plugs, it maintained its ionomeric resin composition to ensure weld sealing. However, the cotton plugs can wick out the fluid-embryo contents of the flexipettes upon contact. A modified µS-VTF method was adapted to include an additional internal weld seal before the plug on the device loading side. The added technical step to the µS-VTF procedure has not affected its successful application, as high survival rates (> 95%) and pregnancy rates continue today. MyJove Corporation 2017-03-02 /pmc/articles/PMC5407698/ /pubmed/28287560 http://dx.doi.org/10.3791/54871 Text en Copyright © 2017, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Developmental Biology
Schiewe, Mitchel C.
Zozula, Shane
Nugent, Nancy
Waggoner, Kelley
Borba, Jessica
Gamboa, Lisa
Whitney, John B.
Modified MicroSecure Vitrification: A Safe, Simple and Highly Effective Cryopreservation Procedure for Human Blastocysts
title Modified MicroSecure Vitrification: A Safe, Simple and Highly Effective Cryopreservation Procedure for Human Blastocysts
title_full Modified MicroSecure Vitrification: A Safe, Simple and Highly Effective Cryopreservation Procedure for Human Blastocysts
title_fullStr Modified MicroSecure Vitrification: A Safe, Simple and Highly Effective Cryopreservation Procedure for Human Blastocysts
title_full_unstemmed Modified MicroSecure Vitrification: A Safe, Simple and Highly Effective Cryopreservation Procedure for Human Blastocysts
title_short Modified MicroSecure Vitrification: A Safe, Simple and Highly Effective Cryopreservation Procedure for Human Blastocysts
title_sort modified microsecure vitrification: a safe, simple and highly effective cryopreservation procedure for human blastocysts
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5407698/
https://www.ncbi.nlm.nih.gov/pubmed/28287560
http://dx.doi.org/10.3791/54871
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