HPLC Set-up



        The flow sequence of LC system used in present study was from HPLC

column to PDA detector, to PHRE...
Table 1. The gradient elution of mobile phase




Time (min)   Flow    Methanol (%)     0.1% H3PO3 (%)     Acetonitrile (%...
Figure 1. Representative HPLC chromatogram of corn sample containing 11
mycotoxins. The spiking levels in this figure were...
Separation column:

Waters Symmetry C18, 3.5µm 3.9 x 150mm.




Order information:

  • PCRM includes: the Temperature Con...
HPLC Set-Up For Myco6in1
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HPLC Set-Up For Myco6in1

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HPLC Set-Up For Myco6in1

  1. 1. HPLC Set-up The flow sequence of LC system used in present study was from HPLC column to PDA detector, to PHRED, to post column reactor, and then to fluorescence detector. The reagent manager was connected to the post column reactor and controlled by Empower software. The flow rate for derivatization mixture was 0.5ml/min. The reagent manager was set to pump derivatization mixture at 18.5min and stop at 23min in the section of event of Waters’ 2795 Separation Module. The column temperature was set to 30 ± 5ºC. The mobile phase consisted of acetonitrile, methanol, and 0.1% phosphate acid in water; and the flow rate was 1.0ml/min. Gradient elution, and the events of fluorescent detector were shown in Table 1 and 2. The derivatization of aflatoxins was performed by photochemical reactor for enhanced detection. The derivatization of fumonisins was done according the procedure described previously. Briefly, borate buffer was made by dissolving 19g of sodium tetraborate decahydrate in 1 liter purified water and filtering through 0.45µm membrane, and stored in room temperature. Dissolve 150mg of OPA in 5ml methanol, add to 500ml borate buffer, and add 500ul of 2- mercaptoethanol, mix well, filter through 0.45µm membrane and place in a bottle protecting from light. The mixture of fumonisin derivatization can be used for a week.
  2. 2. Table 1. The gradient elution of mobile phase Time (min) Flow Methanol (%) 0.1% H3PO3 (%) Acetonitrile (%) Curve 1.00 0.0 85.0 15.0 4.00 1.00 0.0 85.0 15.0 6 5.00 1.00 25.0 60.0 15.0 6 16.00 1.00 25.0 60.0 15.0 6 17.00 1.00 30.0 40.0 30.0 6 30.01 1.00 0.0 85.0 15.0 11 Table 2. The event of fluorescent detector Time Parameter Wavelength Value (min) (nm) 0.1 Ex 365 Em 455 Gain 10 Auto zero 11.0 Auto zero 18.0 Ex 329 Em 465 20.0 Auto zero 23.0 Ex 276 Em 460 26.5 Auto zero 27.0 Gain 100 27.9 Ex 329 Em 460 Gain 10
  3. 3. Figure 1. Representative HPLC chromatogram of corn sample containing 11 mycotoxins. The spiking levels in this figure were: 300ppb for DON, 100ppb for HT-2 and T-2, 2.23ppb forAFG2, 6.45ppb for AFG1, 2.48ppb for AFB2, 12.93 for AFB1, 200ppb for FB1 and FB2, 150ppb for ZEA, and 50ppb for OTA. HT-2 T-2 DON FB1 FB2 ZEA OTA G2 G2 B2 B2
  4. 4. Separation column: Waters Symmetry C18, 3.5µm 3.9 x 150mm. Order information: • PCRM includes: the Temperature Control and the Heater, the Waters part # is WAT 038039, please see the attachment. • Reaction coil: it is a optional, part # is WAT 030844 • Reagent manager: 725000108, Japanese version is 725000109 see the attachment.

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