This is an Application Brief and does not contain a detailed Experimental section.
This application brief demonstrates analysis of niflumic acid/camphor sulfonic acid extracted from rat plasma.
The compounds used in this study are - Niflumic Acid and (1S)-Camphor-10-sulfonic acid.
 
            
        | 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 | 
| 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 | 
 
            
         
            
         
            
        WA41895, May 2005