Method and device for detecting tumor cell in blood by using stimulated Raman spectrum
A tumor cell and stimulated Raman technology, applied in the field of bioinformatics, can solve the problems of cumbersome blood sample processing, low sensitivity, complicated reagent labeling and operation, and achieve short signal acquisition time, improved sensitivity, and high Raman Effect of Signal Intensity or Brightness
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Embodiment 1
[0024] like figure 1 As shown, the present invention provides a device for detecting tumor cells in blood by using stimulated Raman spectroscopy, comprising a capillary glass tube 5, the two ends of the capillary glass tube 5 are respectively provided with a first optical window 4 and a second optical window 6;
[0025] It also includes a pump laser source 9, and a second collimating lens 10, a beam splitter 11, a pair of axicon mirrors 12 and a reflector 13 are sequentially arranged on the optical path of the pump laser source 9. An objective lens 14 is provided between the reflecting mirror 13 and the second optical window 6; the beam splitter 11 and the laser light path emitted by the pump laser source 9 are at an angle of 45 degrees. , an angle of 90 degrees is formed between the reflecting mirror 13 and the beam splitter 11, and the reflecting mirror 13 reflects the light beam of the pump laser source 9 into the capillary glass tube 5;
[0026] Also includes a Stokes la...
Embodiment 2
[0031]Using the device shown in Example 1 of the present invention, the present invention performs stimulated Raman spectroscopic analysis on lipid droplets in blood. Lipid droplets are composed of a monolayer of phospholipids and a hydrophobic core composed of neutral lipids, and there are many proteins distributed on the surface. Is an "inert" cell inclusion. We take the capillary glass tube length 2mm, internal diameter: 100um. We take 5 ml of blood sample and pump it into the capillary glass tube to circulate, and adjust the Raman scattered light transmission to 2,850 cm -1 the CH 2 Symmetrical vibration for stimulated Raman imaging of lipid droplets. The Stokes laser source 7 and the pump laser source 9 generate two synchronized laser beams with a repetition rate of 80 MHz. Among them, the Stokes laser 7 has a fixed wavelength of 1,040 nm. The pump laser 9 has a tunable wavelength of 680 to 1,300 nm. The beams are then spatially combined by a beam splitter 11 . Tw...
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