Determination of ganciclovir in human plasma by ultra performance liquid chromatography-UV detection.

Abstract

OBJECTIVES Implement a sensitive UHPLC method for the assay of ganciclovir in human plasma. DESIGN AND METHODS We developed and validated a chromatographic method coupled to ultraviolet detection for quantification of ganciclovir, with a short run time using a small volume of human plasma. Comparison of system performance was made with respect to analysis time, efficiency and sensitivity. RESULTS Correlation coefficients (r) of the calibration curves ranged from 0.999744 to 0.999784. Within-day and between-day imprecision and inaccuracy, specificity and recovery were also evaluated for validation. The method was precise and accurate and the retention time was 0.7 min. The calibration curves were linear between 0.5 and 30 μg/mL. There was a good correlation between HPLC and UHPLC techniques. CONCLUSIONS We developed a method that is currently applied in a clinical study assessing GCV plasma concentration variability after ganciclovir and valganciclovir administration.

DOI: 10.1016/j.clinbiochem.2011.12.014

Cite this paper

@article{Padulls2012DeterminationOG, title={Determination of ganciclovir in human plasma by ultra performance liquid chromatography-UV detection.}, author={Ariadna Padull{\'e}s and Helena Colom and Yolanda Armend{\'a}riz and Gema Cerezo and Anna Cald{\'e}s and Leonor Pou and Jaume Torras and Josep Mar{\'i}a Grinyo and N{\'u}ria Lloberas}, journal={Clinical biochemistry}, year={2012}, volume={45 4-5}, pages={309-14} }