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Voltammetric determination of parthenolide in spiked human plasma and urine
Author(s) -
Belal F.,
Galal A. M.,
AlMajed A.,
ElFeraly F. S.
Publication year - 2001
Publication title -
phytochemical analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 72
eISSN - 1099-1565
pISSN - 0958-0344
DOI - 10.1002/pca.588
Subject(s) - chemistry , parthenolide , chromatography , polarography , diffusion , urine , relative standard deviation , analytical chemistry (journal) , detection limit , inorganic chemistry , apoptosis , biochemistry , physics , thermodynamics
The voltammetric behaviour of parthenolide, a biologically active sesquiterpene lactone, was studied using direct current (DC t ), alternating current and differential‐pulse polarography (DPP). Parthenolide developed well‐defined cathodic waves over the whole pH range in Britton–Robinson buffers. At pH 10 the diffusion current constant was 3.54 ± 0.08 (± standard deviation; n  = 8). The current vs concentration plots were rectilinear over the range 4–36 and 1–28 µg/mL in the DC t and DPP modes, respectively, with a minimum detectability of 0.06 µg/mL (about 1 × 10 −7   M ) using the latter technique. The waves were characterised as being diffusion controlled, although adsorption phenomenon played a limited role in the electrode process. The described analytical method was applied to the determination of parthenolide in spiked human urine and plasma; the percentage recoveries were 95.72 ± 0.22 and 94.0 ± 0.13 (± standard deviation; n  = 9), respectively. Copyright © 2001 John Wiley & Sons, Ltd.

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