Fruit and Cereal Bioactives 2011
DOI: 10.1201/b10786-25
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High Pressure Processing Technology on Bioactives in Fruits and Cereals

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Cited by 6 publications
(5 citation statements)
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References 72 publications
(91 reference statements)
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“…The extract also contained the acetyl derivative of the peonidin hexoside (5). The ion at m/z 505 gave the MS 2 fragment ion at m/z 301, identifiable in peonidin aglycone [23]. The loss of a 204 (42+162) Da residue allowed us to hypothesize the presence of an acetylhexoside moiety.…”
Section: Resultsmentioning
confidence: 99%
“…The extract also contained the acetyl derivative of the peonidin hexoside (5). The ion at m/z 505 gave the MS 2 fragment ion at m/z 301, identifiable in peonidin aglycone [23]. The loss of a 204 (42+162) Da residue allowed us to hypothesize the presence of an acetylhexoside moiety.…”
Section: Resultsmentioning
confidence: 99%
“…The CHCA-SA mixture has a main ion at about 414 Da that was removed from the MALDI-TOF mass spectrum in order to highlight anthocyanins signals profiles were acquired; ion gate has been set to corresponding mass range of the each compound mass, as given in Table 5, to allow the anthocyanins aglycon characterisation. The fragmentation of 531, 573 and 677 ions generated a common fragment (369) that derived from carboxy-pyrano compounds, this being reported even by Stefova and Ivanova (2011). In the MALDI-TOF mass spectrum of the samples was noticed the presence of Vitisin A (561 Da) and Vitisin B (517 Da); the 399 and 355 fragment ions are also due to the pyranoderivatives (Flamini and Traldi 2010).…”
Section: Maldi Analysismentioning
confidence: 84%
“…The identification of the anthocyanidins and anthocyanins occurring in the analysed samples were per- Fig. 4), and compared to other published data (He et al 2012;Castañeda-Ovando et al 2012;Ivanova et al 2011;Grant and Helleur 2008;Stefova and Ivanova 2011) that confirmed the ascription of the fragments.…”
Section: Maldi Analysismentioning
confidence: 96%
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“…MS data were assigned to metabolites on the basis of accurate mass, isotopic distribution and fragmentation pattern in both positive and negative ion modes. Assignments were confirmed after comparison with literature data (see for instance Cantos, Espín, & Tomás-Barberán, 2002;Cavaliere et al, 2008;Cejudo-Bastante, Pérez-Coello, & Hermosín-Gutiérrez, 2010;Flamini, 2013;Guerrero et al, 2009;Gómez-Romero, Segura-Carretero, & Fernández-Gutiérrez, 2010;Kajdžanoska, Gjamovski, & Stefova, 2010;Kneknopoulos, Skouroumounis, Hayasaka, & Taylor, 2011;Rodríguez-Medina, Segura-Carretero, & Fernández-Gutiérrez, 2009;Sonni et al, 2011;Stalmach, Edwards, Wightman, & Crozier, 2011;Stefova & Ivanova, 2011) and with on-line public metabolite databases (PubChem <http://pubchem. ncbi.nlm.nih.gov/>, Metlin <http://metlin.scripps.edu/> and Chemspider <http://www.chemspider.com>).…”
Section: High Resolution Mass Spectrometrymentioning
confidence: 98%