Test method for trazodone
A detection method, the technology of trazodone, which is applied in the detection field of trazodone, can solve the problems of time-consuming and long sample detection time, etc.
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Embodiment 1
[0103] Example 1: Preparation of standard solutions of series concentrations
[0104] (a) Preparation of standard stock solution:
[0105] Accurately weigh 5 mg of standard trazodone into a 5 mL volumetric flask, dissolve in methanol, and dilute to 5 mL to obtain a standard stock solution, which is stored at -80°C.
[0106] (b) Preparation of standard working solution
[0107] Take an appropriate amount of the standard stock solution in step (a), dilute and mix with 70% methanol aqueous solution as a diluent to obtain a series of standard mixed intermediate solutions containing 500-30000ng / mL trazodone, and store at -80 °C ;
[0108] Among them, the standard working solutions of different concentrations are a series of solutions containing trazodone: 500ng / mL, 2000ng / mL, 5000ng / mL, 10000ng / mL, 15000ng / mL, 20000ng / mL, and 30000ng / mL.
[0109] (c) Preparation of internal standard stock solution
[0110] Take 5 mg of 2-naphthol standard substance and put it in a 5 mL volumetr...
Embodiment 2
[0115] Example 2: Fitting the Standard Curve Equation
[0116] The seven standard solutions in Example 1 were respectively detected by a liquid chromatograph, and the chromatograms of the standard solutions of seven different concentrations of trazodone were obtained.
[0117] From the chromatograms of the standard solutions of trazodone above, the corresponding peak areas of trazodone and the internal standard in the seven standard solutions were obtained, respectively, and the peaks of trazodone obtained from the chromatograms of the standard solutions of each concentration above were obtained. The ratio of the area to the chromatographic peak area of the internal standard is taken as the ordinate y1 of the standard curve equation, and the concentration in the above-mentioned trazodone standard working solution and the concentration of the internal standard are taken as the abscissa x1 of the standard curve equation. The data of different concentrations are subjected to li...
Embodiment 3
[0126] Example 3: Treatment of samples to be tested
[0127] 3.1 Take at least 5 mL of blood to be processed, centrifuge at 3500 rpm for 10 min, take the supernatant serum or plasma as the first supernatant, and store the above-mentioned serum or plasma at -20°C for use before analysis.
[0128] 3.2 Use a pipette to pipette 10 μL of the internal standard working solution in Example 1 into a 1.5 mL centrifuge tube, then add 100 μL of serum or plasma from step 3.1, vortex and mix for 1 min at 2000 rpm, and add protein precipitation Add 1000 μL of acetonitrile solution, vortex mixing at 2000 rpm for 5 min, and then centrifuge at 14000 rpm for 10 min, the obtained second supernatant is the sample to be tested.
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