Micromanipulation dish and sperm selection method for preferred sperms
A technology of micromanipulation and sperm, which is applied in the field of assisted reproduction, can solve the problems affecting the fertilization process of sperm eggs and embryo development, the limited ability to select high-quality sperm, and increase the inheritance of offspring of patients, etc., and achieve great practical value and application prospects. Strong, low-cost effect
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Embodiment 1
[0039] In this embodiment, a micromanipulation dish for preferred sperm is made of a transparent, hard, high temperature-resistant, corrosion-resistant, non-toxic and non-pyrogenic polymer material. Such as figure 1 As shown, the micromanipulation dish includes: a dish plate and a dish cover, and the upper surface of the dish plate is concavely provided with a sample pool 1, a first channel 21, and a second channel 22, and the sample 1 passes through the middle of the first channel 21 and the second channel 22. point connection, two induction chambers 3 are respectively arranged on both sides of the midpoint of the second channel 22, and the upper surface of the dish is also divided into a sperm collection area 4, a sperm braking area 5 and a microinjection area 6, and the second channel 22 The two ends of the tube are respectively connected to the sperm collection area 4 through an upwardly inclined third channel 23, and the sperm braking area 5 and the microinjection area 6 ...
Embodiment 2
[0056] The experimental group used the preferred sperm micromanipulation dish of the present invention, and the test preparation was the same as in the first part of Example 1.
[0057] Take an appropriate amount of sperm specimens and slowly and gently add them to the sample pool 1, cover the dish, and put it in the carbon dioxide incubator for 30-60 minutes. The sperm with normal physiological functions and fertilization ability will swim to the sperm collection area 4. Sperm in sperm collection area 4 are immediately available for intracytoplasmic sperm microinjection. That is, use a micropuncture needle to draw a sperm in the sperm collection area 4, move to the sperm braking area 5 to immobilize the sperm, and then move to the microinjection area 6. Fix the egg in the microinjection area 6 with a microfixation needle, make its polar body at the 6 o'clock or 12 o'clock position, and inject the sperm into the egg to complete in vitro fertilization. In the experimental grou...
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