The [DPPH●/DPPH-H]-HPLC-DAD Method on Tracking the Antioxidant Activity of Pure Antioxidants and Goutweed (<i>Aegopodium podagraria</i> L.) Hydroalcoholic Extracts
The 2,2-diphenyl-1-picrylhydrazyl (DPPH)-reverse phase (RP)-HPLC-diode array detector (DAD) method was tested on standard antioxidants (AOs), i.e., reduced glutathione (GSH), ascorbic acid (vitamin C), and alcoholic extracts of <i>A. podagraria</i> L. An elaborated HPLC procedure enabled...
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doaj-f94f42b44c894af4907d1ebf87d9f2c62020-12-19T00:05:44ZengMDPI AGMolecules1420-30492020-12-01256005600510.3390/molecules25246005The [DPPH●/DPPH-H]-HPLC-DAD Method on Tracking the Antioxidant Activity of Pure Antioxidants and Goutweed (<i>Aegopodium podagraria</i> L.) Hydroalcoholic ExtractsJolanta Flieger0Michał Flieger1Department of Analytical Chemistry, Medical University of Lublin, Chodźki 4a (Collegium Pharmaceuticum), 20-093 Lublin, PolandFaculty of Medicine, Medical University of Lublin, Aleje Racławickie 1, 20-059 Lublin, PolandThe 2,2-diphenyl-1-picrylhydrazyl (DPPH)-reverse phase (RP)-HPLC-diode array detector (DAD) method was tested on standard antioxidants (AOs), i.e., reduced glutathione (GSH), ascorbic acid (vitamin C), and alcoholic extracts of <i>A. podagraria</i> L. An elaborated HPLC procedure enabled the simultaneous measurement of the redox couple DPPH-R (2,2-diphenyl-1-picrylhydrazyl radical)/DPPH-H (2,2-diphenyl-1-picrylhydrazine). Both forms were fully separated (R<sub>s</sub> = 2.30, <i>α</i> = 1.65) on a Zorbax Eclipse XDB-C18 column eluted with methanol–water (80:20, <i>v</i>/<i>v</i>) and detected at different wavelengths in the range of 200–600 nm. The absorbance increases of the DPPH-H as well as the DPPH-R peak inhibition were measured at different wavelengths in visible and UV ranges. The chromatographic method was optimized, according to reaction time (slow, fast kinetics), the linearity range of DPPH radical depending on the detection conditions as well as the kind of the investigated antioxidants (reference chemicals and the ground elder prepared from fresh and dry plants). The scavenging capacity was expressed by the use of percentage of peak inhibition and the IC<sub>50</sub> parameters. The evaluated extracts displayed antioxidant activity, higher than 20% inhibition against 350 µM DPPH free radical. The results show that extract prepared from dry plants in the ultrasonic bath exhibits the highest antioxidant potential (IC<sub>50</sub> = 64.74 ± 0.22 µL/mL).https://www.mdpi.com/1420-3049/25/24/6005<i>Aegopodium podagraria</i> L.goutweedantioxidant activityDPPHRP-HPLC |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jolanta Flieger Michał Flieger |
spellingShingle |
Jolanta Flieger Michał Flieger The [DPPH●/DPPH-H]-HPLC-DAD Method on Tracking the Antioxidant Activity of Pure Antioxidants and Goutweed (<i>Aegopodium podagraria</i> L.) Hydroalcoholic Extracts Molecules <i>Aegopodium podagraria</i> L. goutweed antioxidant activity DPPH RP-HPLC |
author_facet |
Jolanta Flieger Michał Flieger |
author_sort |
Jolanta Flieger |
title |
The [DPPH●/DPPH-H]-HPLC-DAD Method on Tracking the Antioxidant Activity of Pure Antioxidants and Goutweed (<i>Aegopodium podagraria</i> L.) Hydroalcoholic Extracts |
title_short |
The [DPPH●/DPPH-H]-HPLC-DAD Method on Tracking the Antioxidant Activity of Pure Antioxidants and Goutweed (<i>Aegopodium podagraria</i> L.) Hydroalcoholic Extracts |
title_full |
The [DPPH●/DPPH-H]-HPLC-DAD Method on Tracking the Antioxidant Activity of Pure Antioxidants and Goutweed (<i>Aegopodium podagraria</i> L.) Hydroalcoholic Extracts |
title_fullStr |
The [DPPH●/DPPH-H]-HPLC-DAD Method on Tracking the Antioxidant Activity of Pure Antioxidants and Goutweed (<i>Aegopodium podagraria</i> L.) Hydroalcoholic Extracts |
title_full_unstemmed |
The [DPPH●/DPPH-H]-HPLC-DAD Method on Tracking the Antioxidant Activity of Pure Antioxidants and Goutweed (<i>Aegopodium podagraria</i> L.) Hydroalcoholic Extracts |
title_sort |
[dpph●/dpph-h]-hplc-dad method on tracking the antioxidant activity of pure antioxidants and goutweed (<i>aegopodium podagraria</i> l.) hydroalcoholic extracts |
publisher |
MDPI AG |
series |
Molecules |
issn |
1420-3049 |
publishDate |
2020-12-01 |
description |
The 2,2-diphenyl-1-picrylhydrazyl (DPPH)-reverse phase (RP)-HPLC-diode array detector (DAD) method was tested on standard antioxidants (AOs), i.e., reduced glutathione (GSH), ascorbic acid (vitamin C), and alcoholic extracts of <i>A. podagraria</i> L. An elaborated HPLC procedure enabled the simultaneous measurement of the redox couple DPPH-R (2,2-diphenyl-1-picrylhydrazyl radical)/DPPH-H (2,2-diphenyl-1-picrylhydrazine). Both forms were fully separated (R<sub>s</sub> = 2.30, <i>α</i> = 1.65) on a Zorbax Eclipse XDB-C18 column eluted with methanol–water (80:20, <i>v</i>/<i>v</i>) and detected at different wavelengths in the range of 200–600 nm. The absorbance increases of the DPPH-H as well as the DPPH-R peak inhibition were measured at different wavelengths in visible and UV ranges. The chromatographic method was optimized, according to reaction time (slow, fast kinetics), the linearity range of DPPH radical depending on the detection conditions as well as the kind of the investigated antioxidants (reference chemicals and the ground elder prepared from fresh and dry plants). The scavenging capacity was expressed by the use of percentage of peak inhibition and the IC<sub>50</sub> parameters. The evaluated extracts displayed antioxidant activity, higher than 20% inhibition against 350 µM DPPH free radical. The results show that extract prepared from dry plants in the ultrasonic bath exhibits the highest antioxidant potential (IC<sub>50</sub> = 64.74 ± 0.22 µL/mL). |
topic |
<i>Aegopodium podagraria</i> L. goutweed antioxidant activity DPPH RP-HPLC |
url |
https://www.mdpi.com/1420-3049/25/24/6005 |
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