posted on 2012-06-27, 00:00authored byLi-Qi Wang, Zhen-Ling Zeng, Yi-Juan Su, Gao-Kui Zhang, Xiu-Ling Zhong, Zheng-Peng Liang, Li-Min He
The synergistic influences of analyte concentration,
sample source,
and solid-phase extraction (SPE) type on matrix effects in the multiresidue
analyses of eight β-agonists with LC-ESI-MS/MS were evaluated.
Porcine muscle and liver extracts and urine from diverse sources were
purified by strong or mixed-mode cation exchange and molecularly imprinted
polymer SPE cartridges, respectively. Three spiked concentrations
(2, 10, and 20 ng/mL) of eight β-agonists in the purified matrices
and the different sample sources were analyzed. The results show that
for most β-agonists there are significant differences in matrix
effects between analyte concentrations or sample sources (P < 0.05), whereas there is no significant difference
in matrix effects between different SPE cartridges (P > 0.05). Results from main effects testing indicated that analyte
concentration was the main effector.