CdSe/ZnS quantum dot nano-cluster based electrochemiluminescence biological sensor, as well as manufacturing method and application thereof
A technology of luminescent biology and quantum dots, applied in chemiluminescence/bioluminescence, chemical instruments and methods, nano optics, etc., to achieve the effects of improving sensitivity, rapid analysis and detection, and excellent accuracy
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Embodiment 1
[0038] Example 1. Preparation of Electrochemiluminescent Biosensor and Its Detection of Cancer Cells
[0039] First, the magnetic gold electrodes were sequentially used α-Al of 1.0 μm, 0.3 μm and 0.05 μm 2 o 3 After polishing with polishing powder, ultrasonically wash with double distilled water and let it dry naturally, drop 8 μL of magnetic nano gold rod solution onto the surface of the electrode and let it dry naturally. Then 10 μL of aptamer DNA (C1) was dropped onto the surface of the electrode and incubated for 10 h.
[0040] Wash the electrode with the above-mentioned aptamer and immerse it into the nano-gold-DNA priming strand (solution a), incubate with shaking at 37°C for 2h, and then immerse the electrode into the CdSe / ZnS quantum dot-hair chain after cleaning. Clamp the DNA signal probe (solution b) and incubate with shaking at 37° C. for 2 hours to make a biosensor for detecting ECL of cells.
[0041] Incubate the ECL sensor with 100 μL of PBS solution containi...
Embodiment 2
[0042] Example 2. Preparation of Electrochemiluminescent Biosensor and Its Detection of Cancer Cells
[0043] "Drop 10 μL of aptamer DNA (C1) onto the surface of the electrode and incubate for 10 h" to "drop 10 μL of aptamer DNA (C1) on the surface of the electrode and incubate for 12 h". Other preparation conditions were the same as in Example 1, and a biosensor similar in appearance and properties to Example 1 was obtained. The results of cancer cell detection are the same as in Example 1.
Embodiment 3
[0044] Example 3. Preparation of Electrochemiluminescent Biosensor and Its Detection of Cancer Cells
[0045] "Incubate the ECL sensors with 100 μL of PBS solutions containing different concentrations of cells at 37°C for 60 minutes with shaking" was changed to "Incubate the ECL sensors with 100 μL of PBS solutions with different concentrations of cells at 37°C for 50 minutes with shaking". Other preparation conditions were the same as in Example 1, and a biosensor similar in appearance and properties to Example 1 was obtained. The results of cancer cell detection are the same as in Example 1.
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