Method for improving capture accuracy of circulating tumor cells and microfluidic material
A tumor cell and precision technology, applied in the field of medical materials, can solve problems such as false positives, achieve the effect of improving accuracy and capture accuracy
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[0023] S1. Preparation of polydimethylsiloxane chip
[0024] Please combine figure 1 , making a polydimethylsiloxane (PDMS) chip with a micropillar array structure on a silicon wafer template, and doping a conductive material in the polydimethylsiloxane chip to obtain a conductive PDMS microchip. The microarray structure formed by PDMS is used to form a microfluidic chip to capture circulating tumor cell CTCs. The addition of conductive materials enables the materials to deposit electrospun fibers by electrospinning.
[0025] It should be noted that under the conventional parameter conditions, the size of the micro-pillars is relatively large, mainly due to the obstruction of the micro-pillars to the fluid, which causes the shunt to flow laterally, and produces an uneven velocity field distribution on the surface of the micro-pillars, making The particles therein have more movement trajectories and more collisions with the micro-pillars in the three-dimensional space on the m...
Embodiment 1
[0048] This embodiment provides a method for improving the accuracy of capturing circulating tumor cells, which includes the following steps:
[0049] (1) Take a clean silicon wafer template, blow it off with nitrogen, place it in a petri dish with a flat bottom, and then perform silanization treatment (drop 3 drops of hexamethyldisilazane on the silicon substrate, wait until the volatilization is complete, and drop it again , repeated 3 times). Next, weigh a certain amount of PDMS prepolymer and tetraethyl orthosilicate at a mass ratio of 10:1, mix for about 2 minutes, and pour it into a petri dish with a silicon template to control the thickness of PDMS to about 3.5mm. Place the petri dish with PDMS and silicon template in a vacuum drying oven, vacuum for 2 minutes to remove air bubbles, then let it stand at room temperature for 15 minutes, and then transfer it to a constant temperature drying oven at 80°C for about 60 minutes to cure crosslinking. Peel off the cured PDMS ...
Embodiment 2
[0054] This embodiment provides a method for improving the accuracy of capturing circulating tumor cells, which includes the following steps:
[0055] (1) Take a clean silicon wafer template, blow it off with nitrogen, place it in a petri dish with a flat bottom, and then perform silanization treatment (drop 4 drops of hexamethyldisilazane on the silicon substrate, wait until the volatilization is complete, and drop it again , repeat 2 times). Next, weigh a certain amount of PDMS prepolymer and phenyltrimethoxysilane according to the mass ratio of 8:1, mix for about 2 minutes, pour it into a petri dish with a silicon template, and control the thickness of PDMS to about 4.5mm. Place the petri dish with PDMS and silicon template in a vacuum drying oven, vacuum for 2 minutes to remove air bubbles, then let it stand at room temperature for 20 minutes, and then transfer it to a constant temperature drying oven at 80°C for about 60 minutes to cure crosslinking. Peel off the cured ...
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