2017
DOI: 10.1111/ijfs.13359
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Determination of antioxidant activity and phenolic compounds of Muntingia calabura Linn. peel by HPLCDAD and UPLCESIMS/MS

Abstract: Summary Antioxidant activity in Muntingia calabura Linn. peel was evaluated by DPPH radical, ORAC, ABTS cation radical, FRAP assays and total phenolic contents by different extraction conditions. In addition, a method for determination of phenolic compounds in calabura peel samples harvested in Brazil using methanol:water and magnetic stirring as the extraction method, HPLC‐DAD and UPLC‐ESI‐MS/MS analysis were developed. Calabura peel showed antioxidant activity for all extraction conditions and assays evaluat… Show more

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Cited by 30 publications
(18 citation statements)
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References 47 publications
(73 reference statements)
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“…However, for individual identification and quantification, chromatographic techniques based on liquid chromatography coupled to ultraviolet-visible spectrophotometry (UV-Vis) and mass spectrometry detectors have been widely used. 25,[30][31][32] The extraction step also plays a crucial role in the individual identification and quantification of phenolic compounds. Currently, there is a trend in the use of sample preparation techniques that are easier to perform, faster, inexpensive and that promote clean-up of the sample extract.…”
Section: Introductionmentioning
confidence: 99%
“…However, for individual identification and quantification, chromatographic techniques based on liquid chromatography coupled to ultraviolet-visible spectrophotometry (UV-Vis) and mass spectrometry detectors have been widely used. 25,[30][31][32] The extraction step also plays a crucial role in the individual identification and quantification of phenolic compounds. Currently, there is a trend in the use of sample preparation techniques that are easier to perform, faster, inexpensive and that promote clean-up of the sample extract.…”
Section: Introductionmentioning
confidence: 99%
“…The mobile phase was composed of solvent A (water acidified with 0.1% formic acid) and solvent B (methanol). The following gradient was used and the organic solvent (B) percentage was changed linearly as follows: 0 min, 30; 0.33 min, 60; 1 min, 60; 1.33 min, 50; 2.33 min, 50; 2.67 min, 30; and 4 min, 30% (Rotta, Haminiuk, Maldaner, & Visentainer, 2017) The ESI Xevo Acquity ® (Waters, Milford, MA) source parameters were as follows: 3.0 kV capillary voltage, 50 L hour -1 cone gas flow, 700 L h -1 desolvation gas flow, 550°C desolvation temperature, and 130°C source temperature. The mass spectrometer was operated in MS/MS mode using multiple reaction monitoring (MRM) and a 30 ms dwell time.…”
Section: Uplc-esi-ms/ms Analysismentioning
confidence: 99%
“…The results were expressed as a percentage inhibition. The ABTS test was carried out according to the technique described by Rotta, Haminiuk, Maldaner, and Visentainer (2017), with some modifications: 50 μL of extract was diluted with 1450 μL of ABTS, 30 min after was measured the absorbance to 732 nm.…”
Section: Evaluation Of Antioxidant Activitymentioning
confidence: 99%