Determination of pamidronate in urine by ion-pair liquid chromatography after derivatization with 1-naphthylisothiocyanate

J Chromatogr B Biomed Sci Appl. 1997 Aug 15;696(1):137-44. doi: 10.1016/s0378-4347(97)00226-0.

Abstract

A sensitive method for the determination of pamidronate disodium [(3-amino-1-hydroxypropylidene)bisphosphonate, APD] in urine has been developed and validated. The procedure involves a triple co-precipitation with calcium phosphate, solid-phase extraction on a quaternary ammonium column, derivatization with 1-naphthylisothiocyanate and ion-pair liquid-liquid extraction. From the two reaction products, naphthylthiocarbamyl-APD is converted into the other, naphthylcarbamyl-APD, by an oxidative desulphuration with hydrogen-peroxide prior to analysis by ion-pair HPLC and fluorescence detection at 285/390 nm. The method has a coefficient of variation of 7% for the intra-assay precision of 99 ng ml-1 APD and 11% for the inter-assay precision. The lower limit of quantification is 3 ng ml-1 APD in 2.5 ml of human urine.

Publication types

  • Comparative Study

MeSH terms

  • 1-Naphthylisothiocyanate / chemistry*
  • Calibration
  • Chemical Precipitation
  • Chromatography, High Pressure Liquid / methods*
  • Circadian Rhythm
  • Diphosphonates / chemistry
  • Diphosphonates / urine*
  • Humans
  • Osmolar Concentration
  • Pamidronate
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Spectrometry, Fluorescence

Substances

  • Diphosphonates
  • 1-Naphthylisothiocyanate
  • Pamidronate