Preparation method of human anatomy viscera specimen
A production method and anatomical technology, applied in the field of visceral specimens, can solve problems such as tissue structure fixation, tissue structure deformation, and unfavorable anatomical research operations, and achieve the effects of simple and easy method, natural color and soft texture.
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Embodiment 1
[0045] A method for preparing a human anatomical internal organ specimen, comprising the steps of:
[0046] 1) Rinse the viscera with normal saline through the artery;
[0047] 2) After the visceral artery was perfused and soaked in the pretreatment solution for 12 hours, vacuum treatment was performed at 80mm Hg, 60mm Hg, 40mmHg, and 20mm Hg, each level was 0.5h, and the viscera were pretreated twice by step 2), Before each pretreatment, fresh pretreatment liquid is replaced; wherein said pretreatment liquid includes 32wt% phenylacetaldehyde, 15wt% ethylenediaminetetraacetic acid, 2wt% 4-aminopyrrole-2-carboxylic acid, 6wt% Disodium hydrogen phosphate, 45 wt% ethanol;
[0048] 3) After the pretreatment solution was rinsed with normal saline, the internal organs were pre-cooled at 2°C for 3-5 hours, then soaked in the dehydration solution for 18 hours, and the internal organs soaked in the dehydration solution were placed In an environment at 5°C, wherein the dehydration sol...
Embodiment 2
[0053] A method for preparing a human anatomical internal organ specimen, comprising the steps of:
[0054] 1) Rinse the viscera with normal saline through the artery;
[0055] 2) After the visceral artery is perfused and soaked in the pretreatment solution for 16 hours, vacuum treatment is carried out at 80mm Hg, 60mm Hg, 40mmHg, and 20mm Hg, each level is 0.8h; the viscera are subjected to step 2) pretreatment 2 times, before each pretreatment, fresh pretreatment liquid was replaced; wherein said pretreatment liquid included 40wt% phenylacetaldehyde, 12t% ethylenediaminetetraacetic acid, 1wt% 4-aminopyrrole-2-carboxylic acid, 7wt% disodium hydrogen phosphate, 40wt% ethanol;
[0056] 3) After the pretreatment solution was rinsed with normal saline, the internal organs were pre-cooled at 2°C for 3 hours, and then soaked in the dehydration solution for 18 hours, wherein the internal organs soaked in the dehydration solution were placed at 6°C In the environment; Wherein, desc...
Embodiment 3
[0061] A method for preparing a human anatomical internal organ specimen, comprising the steps of:
[0062] 1) Rinse the viscera with normal saline through the artery;
[0063] 2) After perfusing the visceral artery and immersing it in the pretreatment solution for 24 hours, perform vacuum treatment at 80 mm Hg, 60 mm Hg, 40 mmHg, and 20 mm Hg, each level is 1 hour, and the internal organs are pretreated in step 2) 2 times, all replace fresh pretreatment liquid before each pretreatment; Wherein said pretreatment liquid comprises 45wt% phenylacetaldehyde, 12wt% ethylenediaminetetraacetic acid, 2wt% 4-aminopyrrole-2-carboxylic acid , the disodium hydrogen phosphate of 6wt%, the ethanol of 35wt%;
[0064] 3) After the pretreatment solution was rinsed with physiological saline, the internal organs were pre-cooled at 2°C for 5 hours, then soaked in the dehydration solution for 24 hours, and the internal organs soaked in the dehydration solution were placed in In an environment of...
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