2022
DOI: 10.1039/d1lc01144h
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Lab on a chip devices for fertility: from proof-of-concept to clinical impact

Abstract: Microfluidics offers tremendous opportunities to understand the underlying biology of fertilization at the single-cell level and improve infertility management, however, its true clinical impact is yet to be realized. Lab-on-a-chip...

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Cited by 9 publications
(3 citation statements)
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References 66 publications
(81 reference statements)
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“…Fresh samples were incubated at 37°C for 30 min to liquefy. The swim-up method ( 73 ) was then used to isolate motile sperm from immotile cells and debris. Hepes-buffered salt solution (117 mM NaCl, 5.3 mM KCl, 2.3 mM CaCl 2 , 0.8 mM MgSO 4 , 1 mM NaH 2 PO 4 , 5.5 mM d -glucose, 0.03 mM phenol red, 4 mM NaHCO 3 , 21 mM Hepes, 0.33 mM Na-pyruvate, and 21.4 mM Na-lactate) supplemented with polyvinyl alcohol (1 mg ml −1 ) was used to run the swim-up assay.…”
Section: Methodsmentioning
confidence: 99%
“…Fresh samples were incubated at 37°C for 30 min to liquefy. The swim-up method ( 73 ) was then used to isolate motile sperm from immotile cells and debris. Hepes-buffered salt solution (117 mM NaCl, 5.3 mM KCl, 2.3 mM CaCl 2 , 0.8 mM MgSO 4 , 1 mM NaH 2 PO 4 , 5.5 mM d -glucose, 0.03 mM phenol red, 4 mM NaHCO 3 , 21 mM Hepes, 0.33 mM Na-pyruvate, and 21.4 mM Na-lactate) supplemented with polyvinyl alcohol (1 mg ml −1 ) was used to run the swim-up assay.…”
Section: Methodsmentioning
confidence: 99%
“…Microfluidic devices have been developed to select sperm typically through motility-based behavioral mechanisms, thereby preventing the oxidative stress and DNA fragmentation induced by centrifugation 3,4,16 . The clinical translation of these technologies has been infrequent 17 , largely due to their complexity of operation. Without an intuitive user interface, many devices have not undergone side-by-side clinical testing to evaluate their performance by clinicians.…”
Section: Introductionmentioning
confidence: 99%
“…In another study, 17 sperm with almost 100% motility and high DNA integrity were separated by guiding the cells to swim against a secondary flow from an inlet chamber to a collection chamber, but it suffered from a relatively low retrieval efficiency (a low number of isolated cells) or a long processing time (∼1 hour). Boundaryfollowing is another natural swimming characteristic of sperm to accumulate near surfaces and follow boundaries 18,19 and corners in microconfined environments. Boundary-following behaviour has been used to develop high-throughput platforms with parallelized networks of microchannels [20][21][22] or microarrays 23 to separate highly motile sperm with normal morphology and improved DNA integrity.…”
Section: Introductionmentioning
confidence: 99%