Organ preserving liquid
A technology of preservation solution and protective agent, applied in the field of organ preservation solution, can solve the problems of discarding, long-term preservation of organ transplant donors, and low preservation quality, and achieve the effects of good preservation, preservation of activity and function, and strong tolerance
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Embodiment 1
[0065] Embodiment 1 A kind of organ preservation solution
[0066] The preparation method of the organ preservation solution in this example: under sterile conditions, take part of the deionized water, first add the substance into the deionized water, mix well and adjust the pH to 7.35-7.45 with hydrochloric acid and sodium hydroxide, and finally dilute to 7.35-7.45. 1000mL, and perform supersaturated oxygen blowing to make the liquid full of oxygen and supersaturated.
[0067] Each 1000mL preservation solution contains the components in the following table:
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Embodiment 2
[0070] Example 2 Detection of Rat Liver Transplantation Donor Preservation Effect (HE Staining)
[0071] 20 male SD rats were divided into two groups, 10 in each group. The liver was separated by aseptic operation. During the separation process, it was washed with preservation solution. The warm ischemia time was less than 30 minutes. The isolated livers of the 10 rats in the first group were treated with UW Liquid static 4 ℃ cold storage, the second group of organ preservation solution described in Example 1 low-temperature cycle mechanical perfusion preservation, perfusion pressure and perfusion volume are physiological volume, organ preservation solution in the process of perfusion preservation immediately after supersaturated oxygen The portal vein and hepatic artery immediately enter the liver.
[0072] After the rat liver was preserved by the method of the present invention for 24 hours, samples were taken immediately for HE staining section histological examination acco...
Embodiment 3
[0073] Example 3 Rat liver preservation experiment (BrdU cell proliferation detection)
[0074] 20 male SD rats were divided into two groups, 10 in each group. The liver was separated by aseptic operation. During the separation process, it was washed with preservation solution. The warm ischemia time was less than 5 minutes. The isolated livers of 10 rats in the first group were treated with UW Liquid static 4 ℃ cold storage, the second group of organ preservation solution described in Example 1 low-temperature cycle mechanical perfusion preservation, perfusion pressure and perfusion volume are physiological volume, organ preservation solution in the process of perfusion preservation immediately after supersaturated oxygen The portal vein and hepatic artery immediately enter the liver. At the beginning of in vitro preservation, BrdU (MedChem Express HY-15910) was added to the preservation solution of each experimental group. The initial concentration of BrdU in the preservat...
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