2002
DOI: 10.1016/s0731-7085(02)00352-7
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Stability of the constituents of Calendula, Milk-thistle and Passionflower tinctures by LC-DAD and LC-MS

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Cited by 69 publications
(43 citation statements)
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“…5 In the literature, milk thistle phenolic composition is characterized by the presence of a mixture of flavonolignans (silymarin), which are known to be normally present in its seeds. [33][34][35][36][37][38][39][40][41][42][43] [ ) flavonolignans (silymarin), assigned based on their UV spectra (λ max around 286-290 nm), the observation of the ion at m/z 481 and a very characteristic fragmentation pattern observed in many studies. [33][34][35][36][37][38][39][40][41][42][43] Nevertheless, due to the lack of commercial standards and difficulty in interpreting fragmentation, the complete identification of these compounds was not possible, and therefore they were characterized as silymarin derivatives.…”
Section: Food and Function Papermentioning
confidence: 99%
“…5 In the literature, milk thistle phenolic composition is characterized by the presence of a mixture of flavonolignans (silymarin), which are known to be normally present in its seeds. [33][34][35][36][37][38][39][40][41][42][43] [ ) flavonolignans (silymarin), assigned based on their UV spectra (λ max around 286-290 nm), the observation of the ion at m/z 481 and a very characteristic fragmentation pattern observed in many studies. [33][34][35][36][37][38][39][40][41][42][43] Nevertheless, due to the lack of commercial standards and difficulty in interpreting fragmentation, the complete identification of these compounds was not possible, and therefore they were characterized as silymarin derivatives.…”
Section: Food and Function Papermentioning
confidence: 99%
“…Separation of the silymarin compounds was accomplished using a Symmetry® (Waters, Milford, MA, USA) C 18 Data Analysis The first order degradation rate constants (k) were determined from plots of the experimental data using the natural log of the ratio of the compound concentration to its initial concentration as a function of time, while activation energies (E) were calculated from the slope of a plot of the natural log of k as a function of the inverse absolute temperature. Compound half-lives were calculated as the time required for the silymarin concentrations to decrease to half of their initial values, in accordance with the first order rate constants.…”
Section: Methodsmentioning
confidence: 99%
“…Peak purity was checked by examination of the mass spectra and/or by use of HPLC with diode-array detection (UV spectra of the peaks were compared with those of authentic reference samples). Table 5 shows the comparison of LC-MS data obtained from Cissus verticillata tincture to those from Passiflora incarnata which allows the characterization of the compounds listed therein (BILIA et al, 2002). Peaks A, B, C, D, G and H show very similar retention time in both chromatograms (Figure 17).…”
Section: Characterization Of Flavonoid Glycosides As Potential Markermentioning
confidence: 99%