| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1213521 | Journal of Chromatography B | 2013 | 6 Pages |
A sensitive, selective, and quantitative method for the determination of urea has been developed and validated in human epithelial lining fluid (ELF; the supernatant from bronchoalveolar lavage). The method employs a simple derivatization of urea with camphanic chloride to improve the chromatographic retention and separation. The derivatization was performed after drying an aliquot of ELF (20 μL) without prior sample clean-up. Ultra High Performance Liquid Chromatography (UHPLC) on a HSS-T3 stationary phase column with 1.8 μm particle size was used for chromatographic separation coupled to tandem mass spectrometry. The method was validated over the concentration range of 8.78–103.78 μg/mL, however the dynamic range can be further lowered if needed. The results from assay validation show that the method is rugged, precise, accurate, and well-suited to support analysis of urea in ELF samples. In addition, the relatively small sample volume (20 μL) and a run time of 1.5 min facilitate automation and allow for high-throughput analysis. This derivatization method was compared to a commercially available colorimetric assay kit, and it was used in a preclinical non-GLP mouse study where urea measurements were used as marker of bronchoalveolar lavage fluid dilution.
► Derivatization with improved chromatographic retention and separation. ► The derivatization was performed without prior sample clean-up. ► The method was validated over the concentration range of 8.78–103.78 μg/mL. ► This method was compared to a commercially available colorimetric assay kit. ► The method can also be adapted for determination of urea in plasma samples.
