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Preparation cryopreservation method and application of human placental subchorionic villi aorta tissue

A cryopreservation method and chorion technology, which is applied in the preservation, application, and animal husbandry of human or animal bodies, can solve the problems of affecting cell activity and losing the function of protecting cells in cryopreserved tissues, and achieve the effect of improving activity

Active Publication Date: 2018-12-21
JIANGXI YINFENG DINGCHENG BIO ENG
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Therefore, if the volume of cryopreserved tissue is too small, the cells will be more exposed to the toxic components of the cryoprotectant, the cell viability will be affected, and the function of cryopreserved tissue to protect cells will be lost.

Method used

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  • Preparation cryopreservation method and application of human placental subchorionic villi aorta tissue
  • Preparation cryopreservation method and application of human placental subchorionic villi aorta tissue
  • Preparation cryopreservation method and application of human placental subchorionic villi aorta tissue

Examples

Experimental program
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Effect test

Embodiment 1

[0038] The cryopreservation method of human placental subchorionic large blood vessel tissue of embodiment 1

[0039] Placenta collection: Select a healthy placenta without infectious diseases and obstetric complications, obtain the consent of the parturient and sign the informed consent; for normal collection, the collected placenta will be transported to the laboratory within 48 hours, and various necessary tests will be carried out, such as Detection of infectious diseases such as viruses, detection of bacterial contamination, etc.

[0040] The method of cryopreservation, the steps are as follows:

[0041] (1) Wash the placenta (to remove dirt and microbial contamination); cut off the decidua along the edge of the placenta, and remove the amniotic membrane.

[0042] (2) Separate the above-mentioned placental fetal surface chorion and large blood vessels from which the amniotic membrane has been removed (keep the subchorionic large blood vessels intact as much as possible),...

Embodiment 2

[0050] Recovery after embodiment 2 cryopreservation

[0051] According to the method of Example 1, after cryopreservation for 6 months, recovery was carried out, and mesenchymal stem cells were induced and isolated. The steps were as follows:

[0052] Take the cryopreserved placental subchorionic large blood vessel tissue out of the liquid nitrogen, place it in the gas phase for 10 minutes to equilibrate, and then quickly place the cryopreservation bag in a water bath at 37°C to 42°C; quickly transfer the cryopreservation bag to a safety cabinet after dissolving , open the cryopreservation bag, gently remove the placental subchorionic large blood vessel tissue with tweezers, put it into the resuscitation solution of three times the reference concentration at 4°C (pre-cooled to 4°C in advance), equilibrate for 1 minute, take it out, and then put it in 4°C ℃ double standard concentration resuscitation solution (pre-cooled to 4 ℃ in advance), equilibrate for 1 to 3 minutes, take ...

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Abstract

The invention discloses a preparation cryopreservation method of the human placental subchorionic villi aorta tissue. The method comprises the steps that (1) a placenta is washed cleanly; the abscisicdecidua is cut off along the edge of the placenta, and the amniotic membrane is removed; (2) the placenta fetal surface chorion with the amniotic membrane and the aortas are separated and washed withnormal saline or PBS buffer liquid, the blood vessels are washed so as to remove the stranded blood clots in the blood vessels; and then, the aortas connected with the chorion lamina membranacea is cut off one by one; and (3) the blood vessels are transferred into a cryopreserved pipe or a cryopreserved bag, vitrified cryopreservation liquid is guided through a three-step method, the blood vessels are transferred into a programmed freezer so as to be cooled at -80 - -90 DEG C, and then the blood vessels are transferred to liquid nitrogen cryopreservation. The cryopreservation method is beneficial for improvement of the activity of the cryopreserved tissue and the cells, the morphology, the function and the structure are consistent with the fresh tissue after being recovered, the preservedtissue can not only be applied to fields of separation of stem cells and epithelial cells, but also can be applied to fields of tissue engineering transplantation.

Description

technical field [0001] The invention relates to a method for preparing and freezing human placental subchorionic large blood vessel tissue and its application, in particular to a method for cryopreserving and resuscitating human placental subchorionic large blood vessel tissue. Background technique [0002] The placenta is an important organ for material exchange between the fetus and the mother. It is a tissue-combining organ between the mother and the child formed by the joint growth of the embryonic embryonic membrane and the maternal endometrium during human pregnancy. In recent years, with the deepening of scientific research, people can classify various types of cells from placenta, including hematopoietic stem cells, mesenchymal stem cells, epithelial cells, etc., thus changing the long-term status of placenta as medical waste. [0003] Modern scientific research suggests that placental amniotic membrane can be used not only to expand amniotic membrane-derived mesench...

Claims

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Application Information

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IPC IPC(8): A01N1/02
CPCA01N1/0221
Inventor 王肇光徐峰波王圣川宋现收生德伟李德柱
Owner JIANGXI YINFENG DINGCHENG BIO ENG
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