High-throughput microfuidic device for motile sperm selection

2013 ◽  
Vol 100 (3) ◽  
pp. S220
Author(s):  
K. Zeidan ◽  
M.C. San Gabriel ◽  
R. Nosrati ◽  
L. Eamer ◽  
D. Sinton ◽  
...  
Lab on a Chip ◽  
2021 ◽  
Vol 21 (4) ◽  
pp. 775-783
Author(s):  
Sa Xiao ◽  
Jason Riordon ◽  
Mohammad Simchi ◽  
Alexander Lagunov ◽  
Thomas Hannam ◽  
...  

The FertDish features a clinically applicable sperm processing format, and enables high recovery of motile sperm with high DNA quality.


2019 ◽  
Vol 20 (6) ◽  
pp. 1037-1045 ◽  
Author(s):  
Bohyun Hwang ◽  
Dongkyu Lee ◽  
Seung-Jun Hwang ◽  
Joong-Hwan Baek ◽  
Byungkyu Kim

Andrologia ◽  
2017 ◽  
Vol 50 (2) ◽  
pp. e12840 ◽  
Author(s):  
R. Lafuente ◽  
E. Bosch-Rue ◽  
J. Ribas-Maynou ◽  
J. Alvarez ◽  
C. Brassesco ◽  
...  

2015 ◽  
Vol 7 (14) ◽  
pp. 5981-5988 ◽  
Author(s):  
B. Zhang ◽  
T. L. Yin ◽  
J. Yang

We assessed a microfluidic method of sperm selection.


2020 ◽  
Author(s):  
Mohammad Yaghoobi ◽  
Morteza Azizi ◽  
Amir Mokhtare ◽  
Alireza Abbaspourrad

AbstractMotility is one of the most important factors in sperm migration toward egg. Therefore, sperm separation based on motility increases the chance of the best sperm selection in the process of infertility treatments. Unfortunately, it is now vastly done by conventional procedures which lack certain delicacy and precision and increase the risk of damage to sperm cells. Microfluidic systems, on the other hand, can sort sperm in a less intrusive way. However, microfluidic techniques have yet to receive widespread adoption in clinical settings, not only due to their relatively cumbersome operation, but also their extremely low outcome, leaving them inefficient in practice. Here we propose a microchamber-based microfluidic platform that can separate progressive motile sperm from nonviable sperm and debris as well as trapped nonprogressive sperm in the microchambers. Our platform is operated in a short period of time (<10 min) with an excellent degree of controllability, without any prior sample preparation. Our results show that the microchambers’ depth does not affect the residence time of motile sperm. Therefore, we are able to inspect high sample volumes (1 mL) within the same time. Furthermore, we maximize the concentration of the collected sperm by tuning the washing medium flow rate above the sperm rheotactic threshold. We foresee that our microfluidic platform may provide a facile solution for high-throughput, robust, and easy-to-modify for collection of progressive sperm needed for assisted reproductive technologies (ARTs).Significance StatementAssisted Reproductive Technologies require efficient, minimally invasive, and fast methods of sperm separation. Centrifugation methods used in clinics and biological research labs, fall short in these aspects as they are low-yield, intrusive to sperm’s DNA, and time consuming. We have developed a microchamber-based microfluidic platform for high-throughput separation of progressive motile sperm from undiluted raw semen samples. The method was further optimized to increase the concentration of collected samples. Higher concentration of collected samples combined with higher motility of the separated sperm compared to those in raw semen, make it a suitable choice in clinical applications, fertility diagnostics, and fundamental research.


Lab on a Chip ◽  
2021 ◽  
Author(s):  
Mohammad Yaghoobi ◽  
Morteza Azizi ◽  
Amir Mokhtare ◽  
Alireza Abbaspourrad

Motility is one of the most important factors in sperm migration toward an egg. Therefore, sperm separation based on motility might enhance sperm selection for infertility treatments. Conventional centrifugation-based methods...


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Iman Ramazani Sarbandi ◽  
Ali Lesani ◽  
Mahdi Moghimi Zand ◽  
Reza Nosrati

AbstractSperm selection is crucial to assisted reproduction, influencing the success rate of the treatment cycle and offspring health. However, in the current clinical sperm selection practices, bypassing almost all the natural selection barriers is a major concern. Here, we present a biomimicry microfluidic method, inspired by the anatomy of the female reproductive tract, that separates motile sperm based on their rheotaxis behavior to swim against the flow into low shear rate regions. The device includes micropocket geometries that recall the oval-shaped microstructures of the female fallopian tube to create shear protected zones for sperm separation. Clinical tests with human samples indicate that the device is capable of isolating viable and highly motile sperm based on their rheotaxis responses, resulting in a separation efficiency of 100%. The device presents an automated alternative for the current sperm selection practices in assisted reproduction.


The Analyst ◽  
2017 ◽  
Vol 142 (6) ◽  
pp. 938-944 ◽  
Author(s):  
Jen-Kuei Wu ◽  
Peng-Chun Chen ◽  
Yu-Nan Lin ◽  
Chia-Woei Wang ◽  
Li-Chern Pan ◽  
...  

In this paper, we propose a microfluidic device capable of generating a retarding flow field for the sorting and separation of human motile sperm in a high-throughput manner.


2018 ◽  
Vol 115 (33) ◽  
pp. 8272-8277 ◽  
Author(s):  
Meisam Zaferani ◽  
Soon Hon Cheong ◽  
Alireza Abbaspourrad

The separation of motile sperm from semen samples is sought after for medical infertility treatments. In this work, we demonstrate a high-throughput microfluidic device that can passively isolate motile sperm within corrals inside a fluid channel, separating them from the rest of the diluted sample. Using finite element method simulations and proposing a model for sperm motion, we investigated how flow rate can provide a rheotaxis zone in front of the corral for sperm to move upstream/downstream depending on their motility. Using three different flow rates that provided shear rates above the minimum value within the rheotaxis zone, we experimentally tested the device with human and bovine semen. By taking advantage of the rheotactic behavior of sperm, this microfluidic device is able to corral motile sperm with progressive velocities in the range of 48–93 μm⋅s−1 and 51–82 μm⋅s−1 for bovine and human samples, respectively. More importantly, we demonstrate that the separated fractions of both human and bovine samples feature 100% normal progressive motility. Furthermore, by extracting the sperm swimming distribution within the rheotaxis zone and sperm velocity distribution inside the corral, we show that the minimum velocity of the corralled sperm can be adjusted by changing the flow rate; that is, we are able to control the motility of the separated sample. This microfluidic device is simple to use, is robust, and has a high throughput compared with traditional methods of motile sperm separation, fulfilling the needs for sperm sample preparation for medical treatments, clinical applications, and fundamental studies.


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