2012
DOI: 10.1016/j.jchromb.2011.12.011
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Optimisation of an HPLC method for the simultaneous quantification of the major sugars and organic acids in grapevine berries

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Cited by 108 publications
(70 citation statements)
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References 22 publications
(38 reference statements)
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“…Determination of organic acid profile of umezu was conducted by high performance liquid chromatography (HPLC) as previously described [9]. An Agilent 1200 series HPLC system (Agilent Technologies, Palo Alto, California, USA) equipped with VWD detector was used to analyze organic acids.…”
Section: Analysis Of Organic Acids By Hplcmentioning
confidence: 99%
See 1 more Smart Citation
“…Determination of organic acid profile of umezu was conducted by high performance liquid chromatography (HPLC) as previously described [9]. An Agilent 1200 series HPLC system (Agilent Technologies, Palo Alto, California, USA) equipped with VWD detector was used to analyze organic acids.…”
Section: Analysis Of Organic Acids By Hplcmentioning
confidence: 99%
“…The characteristic sourness of P. mume fruits is caused by the presence of free organic acids in this fruit [9,18]. Generally, the total titratable acid of P. mume fruits could be as high as 6.0-7.0% on a fresh weight basis, though its profile is diversified [2].…”
Section: Organic Acid Profilementioning
confidence: 99%
“…Typically the calibration curve generated using an ELSD is sigmoidal or exponential including fructose, sorbitol, glucose and sucrose which produced second order polynomial curves. Further, to convert the calibration curves from polynomial to linear, the log 10 of the peaks area and calibration concentrations were calculated [8]. According to the chromatographic condition in table 1, the mixed standard solution was measured and the linear equation was constructed by the quality logarithm of fructose, sorbitol, glucose and sucrose versus peak area logarithm.…”
Section: The Optimization Of Mobile Phasementioning
confidence: 99%
“…In this type of chromatography, the analytical conditions allow that part of the mobile phase to remain immobilized in the stationary phase, and the separation is due to the differences in the partitioning of the molecular solute between the solvent from the mobile phase and the solvent immobilized on the resin [43]. However, no analytical method has been described in the literature for the determination of urinary tt-MA as a BEI for benzene using HPLC with an Aminex HPX-87H column, although this analyte and other volatile organic acids have been determined in various other sample matrices using this type of column [44][45][46].…”
Section: Introductionmentioning
confidence: 99%