An in vitro culture system kit for improving human sperm motility and its application
An in vitro culture system and in vitro culture technology, applied in the field of in vitro culture system kits, can solve the problems of ineffective improvement of sperm motility, achieve the effects of improving forward motility, increasing fertilization rate, and improving pregnancy outcomes
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Embodiment 1
[0023] Sample source: three normal motility sperm samples (the standard is according to the fifth edition of WHO)
[0024] Sperm processing:
[0025] 1. Preheat 10 mL of mHTF containing 10% SSS by volume fraction (as a control group before cultivation), 2 mL of Isolate sperm separation liquid and 10 mL of in vitro culture liquid of the present invention.
[0026] 2. Place the semen collection cup in a 37°C water bath, and take it out after liquefaction.
[0027] 3. Mix the preheated mHTF with a volume fraction of 10% SSS and the liquefied semen, slowly add it to the Isolate sperm separation solution, and centrifuge at 300g for 10 minutes.
[0028] 4. Discard the supernatant after centrifugation, remove the lower layer and separate the sperm for microscopic examination, record the sperm motility, and serve as the control group before culture.
[0029] 5. Mix the remaining sperm in step 4 with the sperm in vitro culture solution of the present invention at a concentration of 1...
Embodiment 2
[0033] Sample source: three sperm samples from patients with asthenozoospermia (the standard is according to the fifth edition of WHO)
[0034] Sperm processing:
[0035] 1. Preheat 10 mL of mHTF containing 10% SSS by volume fraction (as a control group before cultivation), 2 mL of Isolate sperm separation liquid and 10 mL of in vitro culture liquid of the present invention.
[0036] 2. Place the semen collection cup in a 37°C water bath, and take it out after liquefaction.
[0037] 3. Mix the preheated mHTF with a volume fraction of 10% SSS and the liquefied semen, slowly add it to the Isolate separation solution, and centrifuge at 300g for 10 minutes.
[0038] 4. Discard the supernatant after centrifugation, remove the lower layer and separate the sperm for microscopic examination, record the sperm motility, and serve as the control group before culture.
[0039] 5. Mix the remaining sperm in step 4 with the sperm culture system of the present invention at a concentration ...
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