Development and applications of solid-phase extraction and liquid chromatography-mass spectrometry methods for quantification of microcystins in urine, plasma, and serum

被引:29
|
作者
Palagama, Dilrukshika S. W. [1 ]
Baliu-Rodriguez, David [1 ]
Lad, Apurva [2 ]
Levison, Bruce S. [3 ]
Kennedy, David J. [2 ]
Hailer, Steven T. [2 ]
Westrick, Judy [4 ]
Hensley, Kenneth [5 ]
Isailovic, Dragan [1 ]
机构
[1] Univ Toledo, Coll Nat Sci & Math, Dept Chem & Biochem, Toledo, OH 43606 USA
[2] Univ Toledo, Med Ctr, Dept Med, Hlth Sci Campus, Toledo, OH 43614 USA
[3] Univ Toledo, Med Ctr, Dept Physiol & Pharmacol, Hlth Sci Campus, Toledo, OH 43614 USA
[4] Wayne State Univ, Coll Liberal Arts & Sci, Dept Chem, Detroit, MI 48202 USA
[5] Arkansas Coll Osteopath Med, Dept Biochem Cellular & Mol Biol, Ft Smith, AR 72916 USA
关键词
Solid-phase extraction; Biofluids; Microcystins; Quantification; LC-MS; MS/MS; BLUE-GREEN-ALGA; CYANOBACTERIAL TOXINS; BIOLOGICAL EVIDENCE; EXPOSURE; WATER; LR; EXCRETION; TOXICITY; LIVER; PEPTIDE;
D O I
10.1016/j.chroma.2018.08.023
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The protocols for solid-phase extraction (SPE) of six microcystins (MCs; MC-LR, MC-RR, MC-LA, MC-LF, MC-LW, and MC-YR) from mouse urine, mouse plasma, and human serum are reported. The quantification of those MCs in biofluids was achieved using HPLC-orbitrap-MS in selected-ion monitoring (SIM) mode, and MCs in urine samples were also quantified by ultra-HPLC-triple quadrupole-tandem mass spectrometry (UHPLC-QqQ-MS/MS) in multiple reaction monitoring (MRM) mode. Under optimal conditions, the extraction recoveries of MCs from samples spiked at two different concentrations (1 mu g/L and 10 mu g/L) ranged from 90.4% to 104.3% with relative standard deviations (RSDs) <= 4.7% for mouse urine, 90.4-106.9% with RSDs <= 6.3% for mouse plasma, and 90.0-104.8% with RSDs <= 5.0% for human serum. Matrix-matched internal standard calibration curves were linear with R-2 >= 0.9950 for MC-LR, MC-RR and MC-YR, and R-2 >= 0.9883 for MC-LA, MC-LF, and MC-LW. The limits of quantification (LOQs) in spiked urine samples were similar to 0.13 mu g/L for MC-LR, MC-RR, and MC-YR, and similar to 0.50 mu g/L for MC-LA, MC-LF, and MC-LW, while the LOQs in spiked plasma and serum were similar to 0.25 mu g/L for MC-LR, MC-RR, and MC-YR, and similar to 1.00 mu g/L for MC-LA, MC-LF, and MC-LW. The developed methods were applied in a proof-of-concept study to quantify urinary and blood concentrations of MC-LR after oral administration to mice. The urine of mice administered 50 mu g of MC-LR per kg bodyweight contained on average 1.30 mu g/L of MC-LR (n = 8), while mice administered 100 mu g of MC-LR per kg bodyweight had average MC-LR concentration of 2.82 mu g/L (n = 8). MC-LR was also quantified in the plasma of the same mice. The results showed that increased MC-LR dosage led to larger urinary and plasma MC-LR concentrations and the developed methods were effective for the quantification of MCs in mouse biofluids. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:66 / 77
页数:12
相关论文
共 50 条
  • [21] Fast determination of paraquat in plasma and urine samples by solid-phase microextraction and gas chromatography-mass spectrometry
    Gao, Lina
    Liu, Junting
    Wang, Chunyuan
    Liu, Guojie
    Niu, Xiaodong
    Shu, Cuixia
    Zhu, Juan
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2014, 944 : 136 - 140
  • [22] Determination and Validation of a Solid-phase Extraction Gas Chromatography-mass Spectrometry for the Quantification of Methadone and Its Principal Metabolite in Human Plasma
    Chiadmi, Fouad
    Schlatter, Joel
    [J]. ANALYTICAL CHEMISTRY INSIGHTS, 2015, 10 : 17 - 22
  • [23] Determination of Antofloxacin in Human Plasma by Solid Phase Extraction-Liquid Chromatography-Mass Spectrometry
    Wei Min-Ji
    Zhao Cai-Yun
    Mao Long-Qing
    Kang Zi-Sheng
    Li Tian-Yun
    Lu Yuan
    [J]. CHINESE JOURNAL OF ANALYTICAL CHEMISTRY, 2012, 40 (05) : 787 - 790
  • [24] Method development for fingerprinting of biodiesel blends by solid-phase extraction and gas chromatography-mass spectrometry
    Yang, Zeyu
    Hollebone, Bruce P.
    Wang, Zhendi
    Yang, Chun
    Landriault, Mike
    [J]. JOURNAL OF SEPARATION SCIENCE, 2011, 34 (22) : 3253 - 3264
  • [25] Enrichment and quantification of monoacylglycerols and free fatty acids by solid phase extraction and liquid chromatography-mass spectrometry
    Chu, Boon-Seang
    Nagy, Kornel
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2013, 932 : 50 - 58
  • [26] Development and validation of a solid-phase extraction method using anion exchange sorbent for the analysis of cannabinoids in plasma and serum by gas chromatography-mass spectrometry
    Gasse, Angela
    Pfeiffer, Heidi
    Koehler, Helga
    Schuerenkamp, Jennifer
    [J]. INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 2016, 130 (04) : 967 - 974
  • [27] Development and validation of a solid-phase extraction method using anion exchange sorbent for the analysis of cannabinoids in plasma and serum by gas chromatography-mass spectrometry
    Angela Gasse
    Heidi Pfeiffer
    Helga Köhler
    Jennifer Schürenkamp
    [J]. International Journal of Legal Medicine, 2016, 130 : 967 - 974
  • [28] Quantification of sofalcone in human plasma and urine by high performance liquid chromatography-mass spectrometry
    Wang, Ling
    Song, Lin
    Jiang, Xuehua
    [J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2011, 55 (05) : 1179 - 1185
  • [29] Factorial design for the development of automated solid-phase extraction in the 96-well format for determination of tesaglitazar, in plasma, by liquid chromatography-mass spectrometry
    Svennberg, H
    Bergh, S
    Stenhoff, H
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2003, 787 (02): : 231 - 241
  • [30] Online solid-phase extraction liquid chromatography-mass spectrometry of hair cortisol using a surrogate analyte
    Kostolanska, Katarina
    Novotna, Lucie
    Taborska, Eva
    Pes, Ondrej
    [J]. CHEMICAL PAPERS, 2019, 73 (01): : 151 - 158