2017
DOI: 10.1016/j.jpba.2017.03.007
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Development and validation of a HILIC-ELSD method for simultaneous analysis of non-substituted and acetylated xylo-oligosaccharides

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Cited by 16 publications
(2 citation statements)
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“…In particular, in AXOS analysis, it has been observed that the position of substituent arabinose affects the retention time, and that some of these AXOS can elute simultaneously, which complicates their identification [137]. Furthermore, according to some scholars, HPAEC-PAD could perhaps lead to epimerization and OS degradation when an aqueous solution with a high concentration of sodium hydroxide is used as the mobile phase [138]. Several studies have also tried to establish a method for OS structural identification by relying on liquid chromatography, coupled with different detectors.…”
Section: Characterization Of Obtained (A)xosmentioning
confidence: 99%
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“…In particular, in AXOS analysis, it has been observed that the position of substituent arabinose affects the retention time, and that some of these AXOS can elute simultaneously, which complicates their identification [137]. Furthermore, according to some scholars, HPAEC-PAD could perhaps lead to epimerization and OS degradation when an aqueous solution with a high concentration of sodium hydroxide is used as the mobile phase [138]. Several studies have also tried to establish a method for OS structural identification by relying on liquid chromatography, coupled with different detectors.…”
Section: Characterization Of Obtained (A)xosmentioning
confidence: 99%
“…One limitation of MS is that it alone cannot discriminate between hexose isomers or pentose isomers, since they all have the same molecular formula and therefore the same mass [145]. Pu et al proposed another method to characterize XOS, based on hydrophilic interaction liquid chromatography with evaporative light scattering detection (HILIC-ELSD), without the need for derivatization [138]. The coupling of HILIC with ELSD and with the MSn detector can give important structural information, such as the presence of acetyl groups, and allows the characterization and quantification of many OS with different structures; however, isomeric structures tend to coelute, leading to overlapping peaks [146].…”
Section: Characterization Of Obtained (A)xosmentioning
confidence: 99%