Circulating tumor cell detection method based on SERS (Surface-enhanced Raman Scattering)
A technology of tumor cells and detection methods, which is applied in the direction of measuring devices, instruments, and material analysis through optical means, and can solve problems such as uncontrollable cell identification and detection, poor reproducibility and reliability of SERS detection results, and loss of cell information.
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Embodiment example 1
[0061] Differentiate tumor cells.
[0062] Take the purchased liver cancer cell line (SMMC7721), laryngeal cancer cell line (Hep2), cervical cancer cell line (Hela), human neuroblastoma cell line (SH-SY5Y), breast tumor cell line (MCF-7), lung cancer cell line (NCI- H446) were respectively inoculated in cell culture plates, after culture, digested with trypsin in the culture medium, then put into a centrifuge tube and centrifuged at 1500 rpm for 5 minutes, poured out the upper layer of trypsin, then added PBS to wash, centrifuged again, and repeated 3 times, the cell suspension was made, and then 2 μl of the solution was added dropwise on the metal silver nanofilm substrate (purchased from Yunyang Photoelectric Co., Ltd., China), and the surface-enhanced Raman spectrum was detected by a confocal Raman spectrometer with a detection range of 600 ~1800cm -1 , the excitation wavelength is 785nm, the sampling time is 2s, and the excitation light power is 1mw. use
[0063] The Va...
Embodiment example 2
[0065] Determination of white blood cells
[0066] Take an appropriate amount of human blood sample, add an appropriate amount of EDTA anticoagulant and hemolysin into the centrifuge tube containing the blood sample, let it stand at room temperature for 15 minutes, and after the red blood cells are dissolved, use 1500 rpm to centrifuge for 5 minutes and directly pour the upper layer, add After mixing with PBS shaker, centrifuge, pour off the supernatant liquid, and then add PBS to resuspend to prepare white blood cell suspension. Then 2 μl of the solution was added dropwise on the metal silver nano film substrate (purchased from Yunyang Photoelectric Co., Ltd., China), and the surface-enhanced Raman spectrum was detected by a confocal Raman spectrometer, with a detection range of 600-1800cm-1 and an excitation wavelength of 785nm. The sampling time is 2s, and the excitation light power is 1mw.
[0067] Use VancouverRamanAlgorithm software to perform 5th-order polynomial proce...
Embodiment example 3
[0069] Determination of red blood cells
[0070] Sample red blood cell separation method: After taking an appropriate amount of human blood samples, use a 15ml centrifuge tube, add 3ml of separation liquid, carefully draw the blood sample with a straw and add it to the separation liquid, and let it stand for 30-40 minutes. After centrifugation, the centrifuge tube is divided into four layers from top to bottom at this time, the lowermost red blood cell layer is removed, and PBS is added to resuspend to prepare white blood cell suspension. Then 2 μl of the solution was added dropwise on the metal silver nano film substrate (purchased from Yunyang Photoelectric Co., Ltd., China), and the surface-enhanced Raman spectrum was detected by a confocal Raman spectrometer, with a detection range of 600-1800cm-1 and an excitation wavelength of 785nm. The sampling time is 2s, and the excitation light power is 1mw.
[0071] Use VancouverRamanAlgorithm software to perform 5th-order polynom...
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