Determination of the enantiomers of salbutamol and its 4-O-sulphate metabolites in biological matrices by chiral liquid chromatography tandem mass spectrometry

✍ Scribed by Karina B. Joyce; Anne E. Jones; Rebecca J. Scott; Robert A. Biddlecombe; Stephen Pleasance

• Publisher: John Wiley and Sons
• Year: 1998
• Tongue: English
• Weight: 246 KB
• Volume: 12
• Category: Article
• ISSN: 0951-4198
• DOI: 10.1002/(sici)1097-0231(19981215)12:23<1899::aid-rcm417>3.0.co;2-i

✦ Synopsis

Sensitive, mass spectrometry based bioanalytical methods are described for the determination of the R-and S-enantiomers of the b-agonist salbutamol (albuterol) and its 4-O-sulphate metabolite in human plasma and urine. In both methods samples are prepared by 96 well format solid phase extraction using a custom built robotic system. Extracts are then analysed by liquid chromatography tandem mass spectrometry (LC-MS/ MS) using a teicoplanin-based chiral stationary phase and selected reaction monitoring. The methods are accurate (bias AE 10%), precise (%CV 11%) and sensitive, providing lower limits of quantitation (LLoQ) in plasma of 100 pg/mL and 5 ng/mL for the enantiomers of salbutamol and its 4-O-sulphate metabolite, respectively. By restricting the chiral method for plasma to the enantiomers of salbutamol only, it was possible to revalidate at an improved LLoQ of 25 pg/mL. A high throughput LC-MS/MS method has also been developed for racemic salbutamol only, which uses a similar extraction procedure but a conventional C 8 column. The method has a reduced analysis time of three minutes per sample and using a high sensitivity, triple quadrupole mass spectrometer provides an LLoQ of 5 pg/mL based on extraction of 0.5 mL of plasma.