Liu Yue, Lin Andy, Tiersch Terrence R, Monroe William Todd
Department of Biological and Agricultural Engineering, Louisiana State University Agricultural Center, Louisiana State University, Baton Rouge, LA 70803, USA.
Aquatic Germplasm and Genetic Resources Center, School of Renewable Natural Resources, Louisiana State University Agricultural Center, Baton Rouge, LA 70820, USA.
Appl Sci (Basel). 2021 Sep 1;11(17). doi: 10.3390/app11177977. Epub 2021 Aug 28.
Sperm cryopreservation by vitrification is a promising approach for small-bodied animals such as zebrafish (). 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 °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 ( = 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 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.
玻璃化冷冻保存精子是一种很有前景的方法,适用于斑马鱼等小型动物。然而,水生研究中采用的大多数玻璃化工具最初是为精子以外的应用设计的(如人类胚胎冷冻),因此,在应用于精子玻璃化时面临挑战。三维(3D)打印与开放硬件共享相结合是应对冷冻保存工具开发挑战的一种新兴策略。本研究的目标是开发一种可与现有冻存管存储系统集成的3D打印冻存管玻璃化装置(VDCV)。VDCV将玻璃化和操作组件结合起来,实现样品处理、玻璃化、存储和识别功能。玻璃化组件包括一个基座、一个柄和一个环。共设计、制造并测试了36种VDCD原型,这些原型具有不同的环长度(8、10和12毫米)、环宽度(2.0、2.5、3.0和3.5毫米)以及支撑结构(开放、横向和轴向)。还研究了装置的操作方向(冷冻前和冷冻过程中的水平和垂直握持角度)。计算机模拟估计,所有配置下样品的冷却速率在0.6-1.5×10℃/分钟范围内。在冷冻前,带有轴向支撑的环产生的薄膜保留率至少为92%。观察到完全玻璃化发生的总体趋势:水平投入>垂直投入,轴向支撑>横向支撑和开放环。8毫米的环长度具有最高的总体玻璃化发生率(86-100%)。三种支撑配置在体积容量(5.7-6.0微升)方面没有显著差异(P = 0.6584)。单个VDCV单元可提供约6×10个精子/冻存管的装载效率,每个冻存管可汇集3-6只雄性的样品,并可为1800枚卵子授精。VDCV成本低(每单位材料成本<0.5美元),可定制、标准化、安全标记并高效存储。用户社区可通过开放制造文件共享获取这些原型,并使用消费级3D打印机进行制造,从而促进社区层面的标准化。