Decellularized blood vessel matrix gel, preparation method therefor and applications thereof
A technology of decellularization and blood vessels, which is applied in the field of decellularized vascular matrix gel and its preparation, can solve the problems that the preparation method of decellularized vascular matrix gel has not been reported, and achieve thorough removal effect, appropriate diameter and uniformity Effect
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Embodiment 1
[0045] Example 1 Preparation and detection of acellular vascular matrix gel (1)
[0046] 1. Preparation of acellular vascular matrix gel
[0047] 1. Preparation of acellular vascular matrix powder
[0048] Purchase the aorta of an adult pig (about 120kg) from a slaughterhouse, remove the outer membrane and fascia, cut it into small pieces of irregular blood vessels, place it in 1% Triton X-100 solution, shake at 37°C, and shake at 200rpm to decellularize After 6.5 days of treatment, wash with water every other day and replace with 1% Triton X-100 solution until the blood vessel pieces turn white. The decellularized blood vessel slices were frozen overnight in a -80°C refrigerator, and then placed in a vacuum freeze-dryer (Labconco Triad 2.5L, the United States) for freeze-drying at a temperature of -50°C for about 48 hours until the blood vessel slices became dry. Dry and hard. Then use a small pulverizer to crush it into powder, and filter through a 60-mesh sieve.
[00...
Embodiment 2
[0073] Example 2 Preparation and detection of acellular vascular matrix gel (2)
[0074] 1. Preparation of acellular vascular matrix gel
[0075] 1. Preparation of acellular vascular matrix powder
[0076] Purchase the aorta of an adult pig (about 120kg) from a slaughterhouse, remove the outer membrane and fascia, cut it into small pieces of irregular blood vessels, place it in 0.9% Triton X-100 solution, shake at 37°C, shake at 200rpm, and decellularize After 7 days of treatment, wash with water every other day and replace with 0.9% Triton X-100 solution until the blood vessels turn white. The blood vessel slices after decellularization were placed in a -80°C refrigerator overnight, and then placed in a vacuum freeze-dryer (Labconco Triad 2.5L, the United States) for freeze-drying at a temperature of -50°C for about 46 hours until the blood vessel slices became Dry and hard. Then use a small pulverizer to crush it into powder, and filter through a 60-mesh sieve.
[0077...
Embodiment 3
[0094] Example 3 Preparation and detection of acellular vascular matrix gel (3)
[0095] 1. Preparation of acellular vascular matrix gel
[0096] 1. Preparation of acellular vascular matrix powder
[0097] Purchase the aorta of adult pigs (about 120kg) from the slaughterhouse, remove the adventitia and fascia, cut into small pieces of irregular blood vessels, place them in 1.1% Triton X-100 solution, shake at 37°C, and shake at 200rpm to decellularize After 6 days of treatment, wash with water every other day and replace with 1.1% Triton X-100 solution until the blood vessel pieces turn white. The decellularized blood vessel slices were frozen overnight in a -80°C refrigerator, and then placed in a vacuum freeze-dryer (Labconco Triad 2.5L, the United States) for freeze-drying at a temperature of -50°C for about 50 hours until the blood vessel slices became Dry and hard. Then use a small pulverizer to crush it into powder, and filter through a 60-mesh sieve.
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