J. Jastrebova et al., ONLINE DEOXYGENATION FOR REDUCTIVE ELECTROCHEMICAL DETECTION OF ARTEMISININ AND DIHYDROARTEMISININ IN LIQUID-CHROMATOGRAPHY, Analyst, 123(2), 1998, pp. 313-317
A straightforward method for the deoxygenation of mobile phases and sa
mples required for reductive detection in liquid chromatography is des
cribed, The method, which is based on the use of a commercially availa
ble on-line deoxygenator placed between the column and the detector, e
liminates the problems associated with separate deoxygenations of the
mobile phase and samples and restrictions imposed by work in an oxygen
-free environment, The method is compatible with determinations of art
emisinin and its main metabolite, dihydroartemisinin, and also artelin
ate, in liquid samples, With the deoxygenator, efficiencies of the ord
er of 4000-10 000 theoretical plates mere obtained for artemisinin usi
ng 3.0, 4.0 and 4.6 mm diameter columns, The extra-column band broaden
ing due to the deoxygenator was not found to be a limiting factor, Amp
erometric detection with a gold electrode gave rise to lower backgroun
d currents and better peak current reproducibilities than that with gl
assy carbon and gold amalgam electrodes, The relative standard deviati
ons in the peak current for 10 injections of 100 pmol of artemisinin,
dihydroartemisinin and artelinate were 3.0, 1.4 and 3.3%, respectively
, The peak currents for the compounds depended linearly on the amount
injected in the range 10-200 pmol and the detection limits for artemis
inin and dihydroartemisinin were calculated to be 2 and 3 pmol, respec
tively.