Quantitation of hydroxyproline in bone by gas chromatography–mass spectrometry

Abstract

A validated gas chromatography (GC)–mass spectrometric (MS) method for the analysis of hydroxyproline in rat femur is reported. Hydroxyproline in bone hydrolysates was extracted with an anion exchange resin and the N(O)- tert-butyldimethylsilyl derivatives analyzed by GC–MS. The hydroxyproline concentration was estimated relative to pipecolic acid, 3,4-dehydroproline and n-tetracosane as internal standards. The mass-to-charge ratios ( m/ z) for the ions used for quantitation by single ion monitoring were 314 m/ z for hydroxyproline, 198 m/ z for pipecolic acid, 256 m/ z for dehydroproline and 57 m/ z for n-tetracosane. A coefficient of variation of 5.8% was achieved and the limit of detection was calculated to be 0.233 μmol/l bone hydrolysate.