2012
DOI: 10.1016/j.foodchem.2011.11.030
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Antioxidant anthocyanins screening through spectrum–effect relationships and DPPH-HPLC-DAD analysis on nine cultivars of introduced rabbiteye blueberry in China

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Cited by 69 publications
(31 citation statements)
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“…DPPH-HPLC is a simple and rapid screening method that aids in the rapid selection of target components in complex extracts and has been widely used in many studies. [25][26][27] HSCCC is a unique separation technique based on the liquid-liquid partition chromatography without any solid support matrix. Therefore, it prevents the loss of sample observed in the conventional adsorption chromatography.…”
Section: Introductionmentioning
confidence: 99%
“…DPPH-HPLC is a simple and rapid screening method that aids in the rapid selection of target components in complex extracts and has been widely used in many studies. [25][26][27] HSCCC is a unique separation technique based on the liquid-liquid partition chromatography without any solid support matrix. Therefore, it prevents the loss of sample observed in the conventional adsorption chromatography.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, acetic acid-induced writhing test was used to evaluate analgesic activity of AT roots, with aspirin as positive drug. The higher the correlation coefficient is, the higher the contribution of the corresponding peak to analgesic activity of AT roots extract is [20]. The results (Table 5: correlation coefficient A) revealed that the contributions of 16 common peaks to analgesic activity of AT roots extract were in the order: peak 12 (atropine) > 8 (scopolamine) > 13 > 7 (scopolin) > 9 (anisodamine) > 11 > 10 > 4 > 2 (anisodine) > 5 > 15 > 6 (fabiatrin) > 1 (caffeoylputrescine) > 16 > 14 > 3.…”
Section: Discussionmentioning
confidence: 99%
“…The peak areas of antioxidants decreased or disappeared in the HPLC chromatogram after spiked with radicals, while for those without antioxidant activities, there was almost no change in their peak areas. The difference of the reduction of peak areas (PA) for radicals between the control sample and the experiment sample was used to evaluate radical scavenging activity of the sample according to the following equation [17][18][19] In this equation, PA control is the peak area of the control sample, and PA exp is the peak area of the experimental sample.…”
Section: Evaluation Of Radical Scavenging Capacitymentioning
confidence: 99%