Method for quantitatively determining abiraterone in blood and application thereof
A technology for quantitative determination of abiraterone, applied in measuring devices, instruments, scientific instruments, etc., can solve the problems of high cost, high toxicity, and long treatment process, and achieve the use of less sample volume, no matrix interference, and low detection cost Effect
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[0078] as attached Figure 1-9 Shown, a method for quantitative determination of abiraterone in blood, specifically comprising the following steps:
[0079] S1: Sample pretreatment
[0080] Take 20.0 μL of plasma / serum sample, add 200 μL of internal standard working solution (acetonitrile solution containing 10 ng / mL Abiraterone D4), vortex for 5 min, then centrifuge at 4°C and 4000 rpm for 10 min, take 180 μL of supernatant, and inject To the liquid mass spectrometer for measurement and analysis.
[0081] S2: Setting parameters
[0082] 1) Set the chromatographic conditions, and the elution parameters are as shown in Table 1.
[0083] Table 1
[0084] time (min) Flow rate (mL / min) Mobile phase A% Mobile phase B% 0.00 0.50 40 60 2.50 0.50 40 60
[0085] Chromatographic column: Agilent ZORBAX Eclipse Plus-C18 chromatographic column, the specification is 2.1×50mm×5μm;
[0086] Guard column: Phenomenex Security Guard Cartridges Kit C18 guar...
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