Evaluation of different strategies to minimize the matrix effects on LC-MS/MS analysis of multiple lipophilic shellfish toxins in both acidic and alkaline chromatographic conditions

Toxicon ◽  
2020 ◽  
Vol 188 ◽  
pp. 16-26
Author(s):  
Jiangbing Qiu ◽  
Huidan Chen ◽  
Ying Ji ◽  
Tianshen Li ◽  
Aifeng Li
2010 ◽  
Vol 93 (1) ◽  
pp. 306-314 ◽  
Author(s):  
Anneli Kruve ◽  
Koit Herodes ◽  
Ivo Leito

Abstract The matrix effects in HPLC/electrospray ionization (ESI)-MS analysis are difficult to compensate for because of their large variability. It is, therefore, often more practical to include uncertainty due to the matrix effect into the uncertainty budget rather than try to compensate. This work presents an empirical approachthe matrix effect graph approachfor estimating the uncertainty due to the matrix effect in HPLC/ESI-MS analysis of pesticide residues in fruits and vegetables. At certain time intervals (1 month), a calibration graph using extracts of different fruits/vegetables as calibration solutions is prepared, and a regression line is fitted through these data. These fruits/vegetables may be either from the commodity group of the samples or from different commodity groups. The relative residuals of the calibration point peak areas are calculated and plotted against the measurement time. We term the resulting graph the matrix effect graph. The root mean square of the relative residuals is calculated and used as the estimate of relative uncertainty of the sample peak areas caused by the matrix effect. The matrix effect graph obtained over fruits/vegetables from different commodity groups can also be used to identify fruits/vegetables with extreme matrix effects. The matrix effect graph approach was used for determination of thiabendazole, aldicarb, imazalil, and methiocarb and was validated with tomato, cucumber, and sweet corn matrixes at the 0.5 mg/kg concentration level. When different commodity groups were used to compile the matrix effect graph, results of analysis of all samples agreed with the spiked concentrations within the expanded uncertainties (at k = 2 level). When the matrix effect graph was compiled using fruits from the same commodity group as the analyzed samples (fruiting vegetables in this case), agreement was found in 98 of the cases.


2021 ◽  
Author(s):  
Shiva Emami ◽  
Ameer Y Taha

Several validated methods exist for the quantitation of antibiotics in seafood with ultra-high pressure liquid chromatography coupled with tandem spectrometry (UPLC-MS/MS). To our knowledge, none have explored the effects of co-eluting matrix components on the accuracy of quantitation. Such matrix effects could disproportionally change the ionization of analytes and their respective surrogate/internal standards during UPLC-MS/MS analysis, resulting in over- or under-estimation of antibiotic values. In this study, we measured matrix effects, alongside extraction recoveries for 30 antibiotics and their respective class-specific surrogate standards in Sockeye, King and Ivory (non-pigmented) salmon extracted using the QUEChERS method. A modified QUEChERS method involving dispersive or hydrophilic-lipophilic balance (HLB) solid phase extraction (SPE) was also tested on Sockeye salmon. Despite acceptable extraction recoveries for most antibiotics extracted using the QUEChERS method, significant matrix effects were observed for most antibiotic standards. Dispersive or HLB SPE clean-up did not improve analyte recoveries from Sockeye salmon, and in some cases, increased matrix effects. Accuracy and sensitivity were reduced when matrix effects were high. Our results demonstrate that matrix components in salmon cause matrix effects on antibiotics during UPLC-MS/MS analysis which could impact the accuracy and sensitivity of the analysis.


2019 ◽  
Vol 6 (1) ◽  
pp. 30-41
Author(s):  
Ranjith Arimboor ◽  
Karunkara Ramakrishna Menon ◽  
Natarajan Ramesh Babu ◽  
Haneesh Chandran

Background:Increased consumer demand for curry leaves free from pesticides demands fast and reliable analytical methods for the analysis of pesticide residues.Objective:The optimization of a QuEChERS based sample preparation technique with improved analytical accuracy by removing interfering matrix components for LC-MS/MS analysis of pesticide residues from curry leaves.Methods:A modified QuEChERS solid phase extraction method was developed and validated for the analysis of 26 pesticides in fresh and dried curry leaves. The effects of the sample preparation steps and column retention time on the matrix suppression of analyte ions were also evaluated.Results:Validation parameters were found within an acceptable range. The matrix effect evaluation studies showed that the QuEChERS sample preparation was able to minimize the ion suppression of analytes due to co-eluting matrix of components and that a d-SPE clean up step had major role in reducing matrix effect. The gradient mobile phase with longer retention time for analytes resulted in comparatively lesser matrix effects than the isocratic mobile phase of non-polar nature. Even after the clean up, a considerable number of compounds had more than 20% reduction in their MS response in the gradient mobile phase.Conclusion:This study emphasized the need of proper sample clean up before a LC-MS/MS analysis and the usage of matrix matched standards and mobile phase that ultimately results in an appropriate analyte separation in reasonable retention times.


2014 ◽  
Vol 240 (4) ◽  
pp. 488-497 ◽  
Author(s):  
Nianbai Fang ◽  
Shanggong Yu ◽  
Martin JJ Ronis ◽  
Thomas M Badger

1998 ◽  
Vol 217 (1-2) ◽  
pp. 51-60 ◽  
Author(s):  
Claire L. Morgan ◽  
David J. Newman ◽  
Jacky M. Burrin ◽  
Christopher P. Price

2014 ◽  
Vol 29 (5) ◽  
pp. 903 ◽  
Author(s):  
Jitka Míková ◽  
Jan Košler ◽  
Michael Wiedenbeck

Author(s):  
Ji Chen ◽  
Kaiping Zhan ◽  
Qingzhou Li ◽  
Zhiyang Tang ◽  
Chenwei Zhu ◽  
...  

The quantification accuracy of laser-induced breakdown spectroscopy was limited due to matrix effects. In this work, a method named unsupervised-clustering-based quantification (UCQ) was proposed to reduce the matrix effects by...


Author(s):  
Beena Sunilkumar ◽  
S. B. Singh

A simple method has been developed for the determination of trace toxic elements like arsenic, lead and chromium in titanium dioxide pigment samples by ICP OES attached with a Concomitant Metals Analyser. Open mineral acid decomposition was used for sample dissolution employing a mixture of nitric and hydrofluoric acids. The continuous online generation of hydrides into the plasma was achieved through a concomitant metals analyser. The recovery of arsenic, lead and chromium and the matrix effects of titanium on these elements have been studied with spiking experiments. The proposed method has been successfully applied to the determination of arsenic and other elements in titanium pigment samples. The continuous hydride generating system, Concomitant Metals Analyser (CMA) improved the sensitivity of analysis nearly five times in pigment samples. The precision of the measurements was found to be less than 10% RSD.


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