Method for rapidly sensitively detecting fentanyl in blood
A blood and sensitive technology, applied in the direction of measuring devices, preparation of test samples, material analysis by electromagnetic means, etc., can solve the problems of popularization, application limitations, experimental repeatability, poor selectivity, etc., and achieve simple sample pretreatment, The effect of fast detection speed and high sensitivity
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Embodiment 1
[0036] figure 2 In the positive ion mode, the air reagent ion peak appears at about 6.3ms; under the detection conditions, a 10μL blank blood sample is drawn at the sampling place of the thin slice with a micro-sampler, and the detection signal of the blood sample is at about 6.7ms, such as image 3 Shown; The ion mobility spectrogram of extractant monochlorobutane is as Figure 4 Shown; Compared with the follow-up results, it can be seen that the endogenous substances in the blank blood do not interfere with the detection of fentanyl.
Embodiment 2
[0038] Such as Figure 5 As shown, the ion mobility spectrum of 10 μL, 50 ppm fentanyl standard detected in positive ion mode, the detection signal of fentanyl is at about 8.7ms.
Embodiment 3
[0040] Dissolve 2 mL, 100 ng / mL, and 1000 ng / mL blood samples of fentanyl to be tested in 2 mL of chlorobutane organic solvent, sonicate for 1-3 min, centrifuge for 1-3 min, and take the supernatant for detection; extract 10 μL of the upper The clear liquid is dropped on the sample injection sheet, and the ion mobility spectrometer is used to carry out in the positive ion high pressure mode, and the detection time and peak signal intensity of the ion reaching the ion mobility spectrometer are measured;
[0041] Such as Figure 6-7 , to detect 0.5mg / L and 0.05mg / L fentanyl samples in 10μL blood, the detection signal of fentanyl is about 8.7ms, but the signal intensity is different at different concentrations.
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