2007
DOI: 10.1016/j.jpba.2007.08.003
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α-Lipoic acid in dietary supplements: Development and comparison of HPLC-CEAD and HPLC-ESI-MS methods

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Cited by 43 publications
(39 citation statements)
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“…Liquid chromatography-ESI-MS measurements, in negative mode, were carried out for the quantification of ALA in plasma, and the observed peak at m/z 205.0 was attributed to [ALA-H] À [26]. In the present work, ESI-MS measurements, in negative mode, of ALA showed: i) the principal peak at m/z of 205.04; ii) a peak at m/z of 411.09, which could be attributed to the dimmer of ALA; iii) a third signal at m/z of 171.06, which seems to correspond to the fragment ion [ALA-H 2 S-H] À , as it was reported elsewhere [27]. The three peaks were observed in all series of spectra obtained for ALA and for Hg 2þ :ALA at different proportions.…”
Section: Resultssupporting
confidence: 80%
“…Liquid chromatography-ESI-MS measurements, in negative mode, were carried out for the quantification of ALA in plasma, and the observed peak at m/z 205.0 was attributed to [ALA-H] À [26]. In the present work, ESI-MS measurements, in negative mode, of ALA showed: i) the principal peak at m/z of 205.04; ii) a peak at m/z of 411.09, which could be attributed to the dimmer of ALA; iii) a third signal at m/z of 171.06, which seems to correspond to the fragment ion [ALA-H 2 S-H] À , as it was reported elsewhere [27]. The three peaks were observed in all series of spectra obtained for ALA and for Hg 2þ :ALA at different proportions.…”
Section: Resultssupporting
confidence: 80%
“…However, it was found the tissue LA is essentially protein bound, and thus complicated sample preparation steps including protease digestion and solvent extraction are required until liberated free LA is detected by high sensitive methods even at the picomole range such as HPLC with various detection systems such as ultraviolet (UV), fluorescence (FL) and electrochemical (EC) detectors [22][23] . For example, Durrani et al 24) developed a method for the determination of LA in dietary supplements based on high performance liquid chromatography coupled with a coulometric electrode array detector (CEAD) and an electrospray ionization mass spectrometer (ESI-MS). In this method, LA was first extracted with methanol by sonication, following chromatographic separation by isocratic elution using an ACE 3-C-18 column, and then LA was detected by means of a CEAD against palladium reference electrodes.…”
Section: Determination Of Protein Bound Lamentioning
confidence: 99%
“…The extracts were analyzed using a previous proposed LC/MS/MS method and all MS experiments were performed using electrospray ionization (ESI) mode; we were only able to measure the relative amount of parent drug IBU (data not shown) [27,28].…”
Section: S1mentioning
confidence: 99%