Structure, chip and use method for capturing circulating tumor cells of peripheral blood
A technology for peripheral blood circulation and tumor cells, which is applied in the structural field of capturing peripheral blood circulation tumor cells, can solve the problems of fast local flow velocity, uneven distribution of fluid pressure, and CTCs that cannot be captured, and achieve the effect of avoiding blockage
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Embodiment 1
[0025] if figure 2 As shown, the length L of the chip is 47 mm, the width D is 15.5 mm, and the length L' of the intermediate cell capture region is 36 mm.
[0026] Such as image 3 As shown, the first capture block (1) and the second capture block (1') constituting the capture unit are both in the shape of a microcolumn (column) with a triangular cross-section. The two sides a of the triangle are 12.5 microns long and the bottom is b is 15 microns long, the interval c between the two opposite triangular micropillars in the capture unit is 8 microns, the longitudinal interval e and the transverse interval e' of the capture unit are both 20 microns, and the inclination angle β of the capture unit array is 1 degree, that is to say, The cells are arranged in a staggered arrangement so that if the first row does not capture the blood as it flows through, the second row in the staggered arrangement may capture it, and because there are many permutations, the tumor cells are captu...
Embodiment 2
[0031] if figure 2 As shown, the chip has a length of 47 mm, a width of 15.5 mm, and a length of 36 mm in the middle cell capture region. Such as Figure 5 As shown, the two sides of the triangular micropillars in the capture unit are 12.5 microns long, and the length of one side is 15 microns. The distance between the two opposite triangular microcolumns in the capture unit is 8 microns. All are 20 microns, the capture unit array has a tilt angle of 1 degree, the height of all microcolumns in the chip is 30 microns, and the total number of capture units in the chip is about 35*10 5 indivual.
[0032]A549 cells were stained with fluorescent dyes in advance, and about 1000 A549 cells labeled with fluorescent dyes were added to 2 ml of healthy human blood, and then 2 ml of blood was diluted to 10 ml with PBS (phosphate buffer saline) solution, and 10 One milliliter of blood is passed into the chip inlet through the syringe pump, and the flow rate of the solution is respectiv...
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