4.7 Article

Validation and application of sub-2 μm core-shell UHPLC-UV-ESI-Orbitrap MS for identification and quantification of β-carotene and selected cleavage products with preceding solid-phase extraction

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 406, 期 12, 页码 2909-2924

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-014-7725-8

关键词

beta-Carotene; Apo-carotenals; Cellculturemedia; Solid-phase extraction; Core-shell particles; UHPLC-UV-MS; Validation

资金

  1. Austrian Science Fund (FWF) [P20096-B05]
  2. Austrian Science Fund (FWF) [P20096] Funding Source: Austrian Science Fund (FWF)

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A validated ultrahigh-performance liquid chromatography method using 1.7 mu m core-shell particles is presented for the identification and quantification of beta-carotene (BC) and related cleavage products (CPs) in primary cell culture media. Besides BC, apo-4'-, apo-8'-, apo-10'-, and apo-12'-carotenals, as well as 5,6-epoxy-beta-carotene, were selected as target analytes. Detection was performed via an 80-Hz diode array detector and an electrospray ionization-linear quadrupole ion trap-Orbitrap XL mass spectrometer, both hyphenated in series. Total analysis time was below 6 min with peak widths < 12 s. Addition of trifluoroacetic acid and tetrahydrofuran to the mobile phase allowed for the mass spectrometric detection of BC and related CPs and reduced peak tailing due to improved solubility of hydrophobic analytes. Intra-day and inter-day precision for UV and mass spectrometric detection were a parts per thousand currency sign1.5 % for retention times and a parts per thousand currency sign5.1 % for peak areas. Instrumental linearity was confirmed by Mandel's fitting test between 0.25 (or 1.00 mu g/mL) and 5.00 mu g/mL for UV detection. The higher sensitivity of mass spectrometric detection allowed for the coverage of three concentration domains between 0.025 and 5.00 mu g/mL in linearity testing. Homoscedasticity was confirmed between 0.10 and 5.00 mu g/mL for Orbitrap XL MS. The limits of quantification were between 52.6 and 889.4 ng/mL for UV detection and between 19.3 and 102.4 ng/L for mass spectrometric detection. Offline solid-phase extraction from culture media fortified with BC and CPs provided intra- and inter-day recoveries between 65.8 and 102.4 % with coefficients of variation a parts per thousand currency sign6.2 %. Primary rat hepatocyte cultures treated with BC and subjected to different oxidative stress conditions contained 5,6-epoxy-BC and apo-4'-carotenal besides residual BC. Apparently, 5,6-epoxy-BC was formed in the medium via autoxidation of BC by ambient oxygen.

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