Capture sieve and device for capturing cells or biomolecules in solutions
A technology of biomolecules and capture objects, which is applied in the field of devices for capturing biomolecules in solution, and can solve the problems of inability to capture living cells, difficulties in industrialization, and poor specificity
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example 1
[0065] Herein, a preparation method of the capture sieve for sorting CTCs is given. The preparation method includes:
[0066] (I) selection of sieves;
[0067] Gold sieve: Choose a gold sieve with pores (eg, 64 µm or 40 µm) to maximize contact time with tumor cells while preventing the risk of clogging. The size of the gold sieve used in the following tests is 2×2mm 2 . Larger sizes are preferred depending on the specific operation.
[0068] Stainless steel and gold sieves: 51µm pores are selected and AuPd is coated by magnetron sputtering. Such sieves are cheaper and mechanically stronger than gold, so they are more suitable for integration in devices.
[0069] (II) Pre-functionalization;
[0070] Various cleaning methods were used to prepare the sieves prior to functionalization, including autoclaving, oxygen plasma cleaning, and ultrasonic cleaning in various solutions, including piranha solutions. For example, the best results for a 64 µm gold sieve included sonicat...
example 2
[0080] Experiments were performed to demonstrate the efficiency of the screen in capturing EpCAM expressed by tumor cells. In this case, the mesh opening is 51 μm.
[0081] Cell Selection - Cells with high expression levels of EpCAM protein (such as CaCo2 and MCF7 cells) were used.
[0082] Cell Growth - Grow in DMEM buffer at 37°C.
[0083] Cell preparation and incubation of screens - CaCo2 and MCF7 cells differentiated 1:2. The test was performed on a rotating 37°C hot plate. After isolation, cells were diluted 1:10 in DMEM buffer, and 0.5 ml was used to incubate the capture screen for 1 hour.
[0084] Washing of non-specifically bound cells, the sieves were rinsed with pure water, incubated in pure aqueous solution for 2 minutes, and then rinsed again before microscopic observation.
[0085] Microscopic evaluation of trapped cells: photograph of the sieve taken by the microscope ( Figure 5a and 5b ). Figure 5a CaCo2 cells expressing the target capture molecule capt...
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