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Niflumic Acid/Camphorsulfonic Acid Extracted from Rat Plasma

Niflumic Acid/Camphorsulfonic Acid Extracted from Rat Plasma

  • Waters Corporation
White laboratory rat on vials

This is an Application Brief and does not contain a detailed Experimental section.

Abstract

This application brief demonstrates analysis of niflumic acid/camphor sulfonic acid extracted from rat plasma.

Introduction

The compounds used in this study are - Niflumic Acid and (1S)-Camphor-10-sulfonic acid.

Experimental

Oasis WAX SPE Protocol

Plate:

Oasis WAX μElution Plate

Condition:

200 μL MeOH

Equilibrate:

200 μL H2O

Load:

100 μL 1:1 diluted rat plasma, 10 pg/μL, w/2% H3PO4

Wash 1:

200 μL 25 mM NH4CH2COOH buffer in H2O, pH 5

Wash 2:

200 μL MeOH

Elute:

50 μL (25 μL x 2) MeOH w/2% NH4OH

Dilute:

50 μL H2O with 2% HCOOH

Inject:

10 μL

Conditions

Column:

SunFire C18 2.1 x 20 mm IS, 3.5 μm

Part number:

186002531

Mobile phase A:

H2O with 10 mM NH4CH3COOH, pH 5.5

Mobile phase B:

MeOH with 10 mM NH4CH3COOH, pH 5.5

Flow rate:

0.4 mL/min

Injection volume:

10 μL

Sample concentration:

10 pg/μL each analyte

Temperature:

Ambient

Instrument:

Waters Alliance 2695

Waters Micromass Quattro micro API

ESI source temp.:

150 °C

Desolvation temp.:

350 °C

Cone gas flow:

50 L/Hr

Desolvation gas flow:

600 L/Hr

Collision Cell:

1.23e-3 bar (Ar gas)

Compounds

MRM Transition

Cone (V)

CID(eV)

Niflumic Acid

m/z 281.1 → 237.1

30

17

Camphorsulfonic Acid

m/z 231.1 → 79.9

45

30

Gradient

Gradient.

Results and Discussion

Featured Products

WA41895, May 2005

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