使用3D打印技术制造的精子冷冻装置的开发和验证。

IF 1.9 Q3 OBSTETRICS & GYNECOLOGY
Vera Lucia Lângaro Amaral, Gabriela Reif, Rafael Alonso Salvador, Cleiton Alves de Oliveira, Alfred Paul Senn, Tiago Góss Dos Santos
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引用次数: 0

摘要

目的:开发和评估在安全和可复制的条件下,在冷冻过程中保存精液吸管的3d打印原型的有效性。方法:3D打印一个能够在液氮蒸汽(LN2)中容纳十根吸管的原型。第二种常用的支撑物是由膨胀聚乙烯(EPS)片组装而成的,考虑到吸管和LN2表面之间的相同距离。温度是用放在吸管里的热电偶记录的。在两个独立的系列测量中,使用原型(n=20)和EPS支架(n=20)在冷冻保护剂存在下冷冻精液样本。对新鲜和冻融样品的精子参数(活力、活力和DNA片段)进行测量。结果:在样品上测得的温度冷却曲线重现性好。原型材料经受了超过300次的冰冻循环而没有损坏。新鲜样品(64.2%,72.0%)和冻融样品(25.7%,38.8%)的平均运动性和活力差异显著(p)结论:该装置可实现均匀、可量化、可重复的液氮蒸汽冷却。两种测试支撑的回收率与文献报道的回收率相当。设计的3d打印原型有利于吸管的安全处理,一种明确描述冷冻条件的方式,以及更好的操作员内部和实验室间冷冻保存过程的可重复性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development and validation of a sperm-freezing device created using 3D printer technology.

Development and validation of a sperm-freezing device created using 3D printer technology.

Development and validation of a sperm-freezing device created using 3D printer technology.

Development and validation of a sperm-freezing device created using 3D printer technology.

Objective: To develop and evaluate the effectiveness of a 3D-printed prototype to hold semen straws during the freezing process under safe and reproducible conditions.

Methods: A prototype capable of holding ten straws in liquid nitrogen vapor (LN2) was 3D printed. A second support that is commonly used was assembled from pieces of expanded polyethylene (EPS), respecting the identical distance between the straws and the LN2 surface. Temperatures were registered with a thermocouple placed inside a straw. Semen samples were frozen in the presence of cryoprotectant using the prototype (n=20) and the EPS support (n=20) in two independent series of measurements. Sperm parameters (motility, vitality, and DNA fragmentation) were measured for fresh and frozen-thawed samples.

Results: The temperature cooling curves measured on the prototype were remarkably reproducible. The prototype material withstood over 300 freezing cycles without damage. The mean motility and vitality of fresh (64.2%, 72.0%) and frozen-thawed (25.7%, 38.8%) samples were significantly different (p<0.001) using either support. Recovery rates of motility, vitality, and sperm DNA fragmentation in frozen-thawed sperm samples were equal regardless of straw position on the prototype or support type used.

Conclusions: The developed device allows a homogeneous, quantifiable, reproducible cooling of the straws in liquid nitrogen vapor. The recovery rates are comparable to those reported in the literature for both tested supports. The designed 3-D printed prototype favors the safe handling of the straws, an explicit way of describing freezing conditions, and a better intra-operator and inter-laboratory reproducibility of the cryopreservation process.

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来源期刊
CiteScore
3.30
自引率
6.70%
发文量
56
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