A photoacoustic detection device and method for glucose concentration in biological fluid
A technology for glucose concentration and biological fluids, applied in the field of photoacoustic detection and analysis
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Embodiment 1
[0059] A photoacoustic detection device for glucose concentration in biological fluids, including a photoacoustic detection system and a sample reaction module. The schematic diagram of the device structure is shown in figure 1 Shown:
[0060] The photoacoustic device is composed of a laser 4, a chopper 5, a sample holder 7, a photoacoustic cell 8, a microphone 10, a preamplifier 11 and a notebook computer 12, and the laser 4 is modulated into a periodic light source through the chopper 5; The structural representation of the sample holder 7 is as image 3 As shown, the size schematic diagram of the photoacoustic cell 8 is shown as figure 2 As shown, the schematic diagram of the sample holder structure is shown in image 3 As shown, the photoacoustic pool 8 is made of polytetrafluoroethylene, and its length, width, and height are 40mm, 20mm, and 20mm respectively. The pool body is drilled. The hole A on the left side of the photoacoustic pool 8 has an aperture of 13.5mm and...
Embodiment 2
[0066] The structure of the device in this embodiment is the same as in Embodiment 1.
[0067] The method for photoacoustic detection of glucose concentration in human blood by using the above device, comprising the following steps:
[0068] Dilute the freshly obtained blood to the linear range of glucose, add 3 μL of chitosan solution with a mass concentration of 0.6% to the paper chip detection area 3, after drying at room temperature (25°C), add 2 μL of starch potassium iodide solution dropwise, and continue at room temperature Dry (25°C), then add 2 μL of glucose oxidase solution with a concentration of 2 mg / mL dropwise;
[0069] Add 20 μL of diluted human blood dropwise to the paper chip sample area 2, the diluted human blood flows to the paper chip detection area 3 through capillary action, and react at room temperature (25°C) for 30 minutes to form a purple inclusion compound; then the paper chip is detected Area 3 is transferred to the photoacoustic cell 8, the laser ...
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