Microfluidic chip capable of realizing cell three-dimensional culture and drug screening and application
A microfluidic chip, three-dimensional culture technology, used in drug screening, tissue cell/virus culture devices, compound screening, etc., can solve the problems of inability to meet concentration gradients, low mixing efficiency, instability, etc. and detection effect
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Embodiment 1
[0041] As shown in Figures 1 and 2, a microfluidic chip that can realize three-dimensional cell culture and drug screening includes an upper chip 8 and a lower chip 7, the upper chip 8 is provided with channels of different geometric structures, and the channels Including cell culture chamber 3, serpentine channel 4, and triangular baffle 5; fluid inlet 1 is set on concentric circles, the concentric circles are not closed, and the center of the circle is set as fluid outlet 2, and the channel depth is 100 microns, except for oval cell culture chamber 3 , the width of the overall channel is 100 microns, and the angle α between the branch channel connecting the two concentric circles and the tangent line of the outer circle is 40°. Described lower layer chip 7 is provided with spherical groove 6 (as Figure 1bAs shown, each small circle is called a spherical groove), its cross-sectional diameter is 120 microns, and the depth of the spheres is 100 microns, which are evenly distrib...
Embodiment 2
[0043] As shown in Figure 3, the difference from Example 1 is that on the basis of three concentric circles, one concentric circle is added to form four different fluid concentration gradients, and the number of concentric circles can be increased or decreased according to the needs of the experiment. Concentration gradients of various fluids can be formed, and the layout is not limited to this embodiment.
experiment example 1
[0045] In order to calculate the substance concentration gradient in the cell culture chamber, three parallel experiments were carried out on the microfluidic chip of Example 1 of the present invention. Specifically, in these three experiments, the fluorescent reagent Rh123 was introduced into the outer ring, middle ring and inner ring respectively, and ultrapure water was loaded into the other two inlets of each experiment, and after perfusion at a flow rate of 1 μL / min for 10 min, Take fluorescence pictures with an inverted fluorescence microscope. Obtained by calculating the fluorescence intensity in the cell culture chamber as Figure 4 The line graph shown. It can be seen that the fluids of the three inlets are distributed in different proportions under the final concentration gradient, which verifies that the design of the middle and upper chip of the present invention can accurately control the fluids and quickly and stably generate the concentration gradients of the t...
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