Microfluidic chip, tumor metastasis model based on chip, model construction method and application
A microfluidic chip and tumor metastasis technology, which is applied in the fields of cell biology and tissue engineering, can solve the problems of seldom simulated anti-tumor drug screening, etc.
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Embodiment 2
[0059] Example 2 Microfluidic chip-based tumor metastasis model and its construction method
[0060] Such as Figure 5 As shown, a tumor metastasis model based on a microfluidic chip, the porous membrane in the microfluidic chip is coated with collagen to form a three-dimensional microenvironment; the microfluidic channels of the second chip layer are perfused with vascular endothelial cells to form dense blood vessels in vitro Lumen; Tumor cells are injected into the microfluidic channels of the first chip layer by continuous perfusion.
[0061] The construction method of above-mentioned tumor metastasis model, described construction method comprises the following steps:
[0062] Step 1: Perfusion of collagen within the chip
[0063] Configure collagen with a final concentration of 0.1-10 mg / ml, use a syringe pump to pour collagen from the channel inlet of each layer of the chip into the three-dimensional channel channel by continuous perfusion flow, place the chip in a 37°...
Embodiment 3
[0068] Embodiment 3 Real-time monitoring of the whole process of tumor metastasis
[0069] Using the tumor metastasis model established by the microfluidic chip described in Example 1-2, the cultured vascular endothelial cells (EAhy926) were digested into a single cell suspension, and the cell suspension (0.2*10 6 cells / ml) were injected into the microfluidic channel of the second chip layer by continuous perfusion. After filling the cell suspension, the chip was placed in a 37°C incubator for 2 hours, and the lower surface of the cell culture chamber of the second chip layer Form a dense cell layer; then turn the chip upside down, perfuse the cell suspension twice to form a dense cell layer on the upper surface, and then use a syringe pump to drive the liquid to continue culturing vascular endothelial cells for 3 days to form a dense vascular cavity in vitro. The cultured tumor cells were digested into a single cell suspension, and the cell suspension (0.1*10 6 cells / ml) was...
Embodiment 4
[0070] Example 4 Migration characteristics of different tumor cells
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