Cell block collection device and cell block collection method
A collection device and collection method technology, applied in the direction of measuring devices, sampling, instruments, etc., can solve the problems of wrong or missed detection, unfavorable microscopic inspection, and affecting the accuracy of exfoliated cells, etc.
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preparation example
[0043] Preparation example Gelatin preparation: To prepare an aqueous solution of gelatin, add agar, tissue fixative and water at a mass ratio of 1:1:8, and then stir evenly. Wherein, the tissue fixative is medical formaldehyde or medical alcohol; the medical formaldehyde is a formaldehyde aqueous solution with a formaldehyde mass fraction of 35-40%, and the medical alcohol is an ethanol aqueous solution with a volume fraction of 75%. The tissue fixative selected in this preparation example is an aqueous formaldehyde solution with a mass fraction of formaldehyde of 38%.
Embodiment 1
[0047] A cell block collection device, such as figure 1 and figure 2 As shown, it includes a support plate 1 and several auxiliary parts. The support plate 1 is made of plastic and has certain deformation capabilities. The support plate 1 is provided with grooves of different shapes. The opening shape of each groove and the corresponding The shape of the auxiliary parts is adapted so that each auxiliary part can be securely snapped into the corresponding groove. The auxiliary parts include auxiliary material tubes, a fixed support plate 4, a special centrifuge tube 3 for containing exfoliated cell liquid during centrifugation, a limiter 5 and a tissue embedding box 6. The auxiliary material tube includes a sealed cell fixing glue tube 21 with built-in cell fixing glue.
[0048] Such as figure 2 As shown, the grooves include auxiliary material tube grooves 11 , centrifuge tube grooves 12 , pallet grooves 13 , stopper grooves 14 and embedding cassette grooves 15 . Specific...
Embodiment 2
[0067] The difference between this embodiment and embodiment 1 is that the operating process parameters are different, specifically:
[0068] In step S1, after the obtained body fluid is pretreated to obtain exfoliated cell fluid with less impurity content, the specific steps of the pretreatment are as follows: 1. Take a clean common centrifuge tube with a volume of 50 mL, and take the obtained body fluid Pour 20mL into an ordinary centrifuge tube, then centrifuge at 3000rpm for 5min. Other operations of step S1 are the same as those in Embodiment 1.
[0069] In step S2, the special centrifuge tube 3 containing the treated exfoliated cell liquid is placed in the centrifuge, centrifuged at a speed of 3000rpm for 5 minutes, and then the supernatant is poured off, and the exfoliated cells are collected in the straight tube 32; step S3-S6 is the same as embodiment 1.
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