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1.
J Chromatogr B Analyt Technol Biomed Life Sci ; 879(26): 2764-71, 2011 Sep 15.
Article in English | MEDLINE | ID: mdl-21855424

ABSTRACT

Pyridinoline (Pyr), deoxypyridinoline (D-Pyr), galactosyl-pyridinoline (Gal-Pyr) and glucosyl-galactosyl pyridinoline (GluGal-Pyr) are enzymatic mature pyridinium crosslinks. Generally, only total Pyr and D-Pyr urinary amounts (free+bound forms) are evaluated by HPLC as indices of bone resorption. This report describes the validation of an HPLC-fluorescence method for the simultaneous evaluation of free Pyr and D-Pyr, together with GluGal-Pyr and Gal-Pyr, in urine of healthy women (n=20, aged 27-41) and girls (n=20, aged 5-10). The use of an unnatural D-Pyr homologue, here proposed for the first time as internal standard, and of pure Pyr, D-Pyr, GluGal-Pyr and Gal-Pyr synthesized to be used as primary calibrators, guarantees method specificity and correct crosslink quantification. Urine, spiked with IS, was solid-phase extracted prior to HPLC analysis. Total Pyr and D-Pyr amounts were also evaluated after urine hydrolysis. The HPLC method was validated for selectivity, sensitivity, linearity, precision, accuracy, recovery and stability for all measured crosslinks. Both free and total Pyr and D-Pyr as well as GluGal-Pyr and Gal-Pyr amounts were significantly higher in girls than in women (p<0.0001), indicating an increased collagen turnover rather than only bone turnover. Gal-Pyr, for the first time evaluated in girls, was under its lower quantification limit (

Subject(s)
Amino Acids/urine , Chromatography, High Pressure Liquid/methods , Galactosides/urine , Adult , Amino Acids/analysis , Amino Acids/chemistry , Bone Resorption/urine , Child , Child, Preschool , Drug Stability , Female , Galactosides/chemistry , Glycosylation , Humans , Hydrolysis , Least-Squares Analysis , Reproducibility of Results , Sensitivity and Specificity , Spectrometry, Fluorescence
2.
Chem Commun (Camb) ; 46(33): 6153-5, 2010 Sep 07.
Article in English | MEDLINE | ID: mdl-20652187

ABSTRACT

The synthesis of new pinene-derived chiral cyclopropylamines and their use in the synthesis of the first asymmetric Alkyl-BIAN ligands (Alkyl-BIAN = bis-(alkylimino)acenaphthenequinone) are reported.

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