UHPLC Analysis of Aflatoxins on Titan C18 with TFA Derivatization and Fluoresence Detection

CONDITIONS
sample preparation
200 μL of standard solution of aflatoxins was mixed with 300 μL of derivatization solution (7:1:2 water:acetic acid:trifluoroacetic acid). (The mixture was kept at 65 °C for 25 minutes, then cooled down to room temperature. 550 μL of water was added.)
column
Titan C18, 10 cm x 2.1 mm I.D., 1.9 μm particles (577124-U)
mobile phase
[A] 5% acetonitrile in water; [B] acetonitrile.
gradient
10 to 30% B in 3 min; to 100% B in 2 min; held at 100% B for 2 min; to 10% B in 0.5 min; held at 10% B for 2.5 min
flow rate
0.4 mL/min
column temp.
35 °C
detector
Fluorescence, 360/440 Ex/Em
injection
20 μL
sample
standard solution of aflatoxins contained 1.2 ng/mL each of afltoxin B1 and aflatoxin G1, and 0.3 ng/mL each of aflatoxin B2 and afltoxin G2 in acetonitrile:water (84:16)
说明
分析说明
An optimized method for sensitive detection of low levels of aflatoxins using a TFA-derivatization procedure is shown here.
法律信息
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