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A 3D Printed Vitrification Device for Storage in Cryopreservation Vials
Sperm cryopreservation by vitrification is a promising approach for small-bodied animals such as zebrafish (Danio rerio). However, most vitrification tools adopted in aquatic research were initially designed for applications other than sperm (such as human embryo freezing) and, thus, pose challenges...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910574/ https://www.ncbi.nlm.nih.gov/pubmed/36777919 http://dx.doi.org/10.3390/app11177977 |
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author | Liu, Yue Lin, Andy Tiersch, Terrence R. Monroe, William Todd |
author_facet | Liu, Yue Lin, Andy Tiersch, Terrence R. Monroe, William Todd |
author_sort | Liu, Yue |
collection | PubMed |
description | Sperm cryopreservation by vitrification is a promising approach for small-bodied animals such as zebrafish (Danio rerio). However, most vitrification tools adopted in aquatic research were initially designed for applications other than sperm (such as human embryo freezing) and, thus, pose challenges for adoption to sperm vitrification. Three-dimensional (3D) printing combined with open hardware sharing is an emerging strategy to address challenges in the development of cryopreservation tools. The goal of this study was to develop a 3D printed Vitrification Device for Cryo-Vials (VDCV) that can be integrated with the existing vial storage systems. The VDCV combined the vitrification and handling components to achieve functions of sample handling, vitrification, storage, and identification. The vitrification component featured a base, a stem, and a loop. A total of 36 configurations with various loop lengths (8, 10, and 12 mm); loop widths (2.0, 2.5, 3.0, and 3.5 mm); and support structures (open, transverse, and axial) of the VDCD prototypes were designed, fabricated, and tested. Device handling orientations (horizontal and vertical holding angles prior to and during freezing) were also investigated. Computer simulations estimated that the cooling rate of the samples ranged from 0.6–1.5 × 10(5) °C/min in all the configurations. Prior to freezing, loops with axial supports produced a minimum of 92% film retention. The overall trends of full vitrification occurrence were observed: horizontal plunging > vertical plunging, and axial support > transverse support and open loop. A loop length of 8 mm had the highest overall vitrification occurrence (86–100%). No significant differences (p = 0.6584) were shown in a volume capacity (5.7–6.0 μL) among the three supporting configurations. A single unit of VDCV can provide loading efficiencies of about 6 × 10(7) sperm/vial, pooling of samples from 3–6 males/vial, and fertilization for 1800 eggs/vial. The VDCV are low-cost (<$0.5 material cost per unit) and can be customized, standardized, securely labeled, and efficiently stored. The prototypes can be accessed by user communities through open-fabrication file sharing and fabricated with consumer-level 3D printers, thus facilitating community-level standardization. |
format | Online Article Text |
id | pubmed-9910574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-99105742023-02-09 A 3D Printed Vitrification Device for Storage in Cryopreservation Vials Liu, Yue Lin, Andy Tiersch, Terrence R. Monroe, William Todd Appl Sci (Basel) Article Sperm cryopreservation by vitrification is a promising approach for small-bodied animals such as zebrafish (Danio rerio). However, most vitrification tools adopted in aquatic research were initially designed for applications other than sperm (such as human embryo freezing) and, thus, pose challenges for adoption to sperm vitrification. Three-dimensional (3D) printing combined with open hardware sharing is an emerging strategy to address challenges in the development of cryopreservation tools. The goal of this study was to develop a 3D printed Vitrification Device for Cryo-Vials (VDCV) that can be integrated with the existing vial storage systems. The VDCV combined the vitrification and handling components to achieve functions of sample handling, vitrification, storage, and identification. The vitrification component featured a base, a stem, and a loop. A total of 36 configurations with various loop lengths (8, 10, and 12 mm); loop widths (2.0, 2.5, 3.0, and 3.5 mm); and support structures (open, transverse, and axial) of the VDCD prototypes were designed, fabricated, and tested. Device handling orientations (horizontal and vertical holding angles prior to and during freezing) were also investigated. Computer simulations estimated that the cooling rate of the samples ranged from 0.6–1.5 × 10(5) °C/min in all the configurations. Prior to freezing, loops with axial supports produced a minimum of 92% film retention. The overall trends of full vitrification occurrence were observed: horizontal plunging > vertical plunging, and axial support > transverse support and open loop. A loop length of 8 mm had the highest overall vitrification occurrence (86–100%). No significant differences (p = 0.6584) were shown in a volume capacity (5.7–6.0 μL) among the three supporting configurations. A single unit of VDCV can provide loading efficiencies of about 6 × 10(7) sperm/vial, pooling of samples from 3–6 males/vial, and fertilization for 1800 eggs/vial. The VDCV are low-cost (<$0.5 material cost per unit) and can be customized, standardized, securely labeled, and efficiently stored. The prototypes can be accessed by user communities through open-fabrication file sharing and fabricated with consumer-level 3D printers, thus facilitating community-level standardization. 2021-09-01 2021-08-28 /pmc/articles/PMC9910574/ /pubmed/36777919 http://dx.doi.org/10.3390/app11177977 Text en https://creativecommons.org/licenses/by/4.0/This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Liu, Yue Lin, Andy Tiersch, Terrence R. Monroe, William Todd A 3D Printed Vitrification Device for Storage in Cryopreservation Vials |
title | A 3D Printed Vitrification Device for Storage in Cryopreservation Vials |
title_full | A 3D Printed Vitrification Device for Storage in Cryopreservation Vials |
title_fullStr | A 3D Printed Vitrification Device for Storage in Cryopreservation Vials |
title_full_unstemmed | A 3D Printed Vitrification Device for Storage in Cryopreservation Vials |
title_short | A 3D Printed Vitrification Device for Storage in Cryopreservation Vials |
title_sort | 3d printed vitrification device for storage in cryopreservation vials |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910574/ https://www.ncbi.nlm.nih.gov/pubmed/36777919 http://dx.doi.org/10.3390/app11177977 |
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