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Studies on the antioxidant activity of the essential oil and methanol extract of Marrubium globosum subsp. globosum (lamiaceae) by three different chemical assays

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dc.contributor.author Sarikurkcu, C en
dc.contributor.author Tepe, B en
dc.contributor.author Daferera, D en
dc.contributor.author Polissiou, M en
dc.contributor.author Harmandar, M en
dc.date.accessioned 2014-06-06T06:48:41Z
dc.date.available 2014-06-06T06:48:41Z
dc.date.issued 2008 en
dc.identifier.issn 09608524 en
dc.identifier.uri http://dx.doi.org/10.1016/j.biortech.2007.08.058 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/4238
dc.subject β-carotene en
dc.subject Antioxidant activity en
dc.subject DPPH en
dc.subject Marrubium globosum subsp. globosum en
dc.subject Reducing power en
dc.subject.other Enzyme inhibition en
dc.subject.other Extraction en
dc.subject.other Methanol en
dc.subject.other Scavenging en
dc.subject.other Antioxidant activity en
dc.subject.other Marrubium globosum subsp. globosum en
dc.subject.other Reducing power en
dc.subject.other Enzyme activity en
dc.subject.other 1,1 diphenyl 2 picrylhydrazyl en
dc.subject.other antioxidant en
dc.subject.other beta carotene en
dc.subject.other bicyclogermacrene en
dc.subject.other caryophyllene en
dc.subject.other caryophyllene oxide en
dc.subject.other essential oil en
dc.subject.other germacrene D en
dc.subject.other linoleic acid en
dc.subject.other phenol derivative en
dc.subject.other spathulenol en
dc.subject.other Enzyme activity en
dc.subject.other Enzyme inhibition en
dc.subject.other Extraction en
dc.subject.other Methanol en
dc.subject.other Scavenging en
dc.subject.other antioxidant en
dc.subject.other carotenoid en
dc.subject.other enzyme activity en
dc.subject.other essential oil en
dc.subject.other gas chromatography en
dc.subject.other herb en
dc.subject.other inhibition en
dc.subject.other methanol en
dc.subject.other antioxidant activity en
dc.subject.other article en
dc.subject.other drug isolation en
dc.subject.other gas chromatography en
dc.subject.other Marrubium globosum en
dc.subject.other mass spectrometry en
dc.subject.other medicinal plant en
dc.subject.other phytochemistry en
dc.subject.other priority journal en
dc.subject.other Antioxidants en
dc.subject.other beta Carotene en
dc.subject.other Biotechnology en
dc.subject.other Biphenyl Compounds en
dc.subject.other Chromatography, Gas en
dc.subject.other Flavonoids en
dc.subject.other Gas Chromatography-Mass Spectrometry en
dc.subject.other Hydrazines en
dc.subject.other Lamiaceae en
dc.subject.other Linoleic Acid en
dc.subject.other Marrubium en
dc.subject.other Methanol en
dc.subject.other Oils, Volatile en
dc.subject.other Phenol en
dc.subject.other Plant Extracts en
dc.subject.other Lamiaceae en
dc.subject.other Marrubium en
dc.title Studies on the antioxidant activity of the essential oil and methanol extract of Marrubium globosum subsp. globosum (lamiaceae) by three different chemical assays en
heal.type journalArticle en
heal.identifier.primary 10.1016/j.biortech.2007.08.058 en
heal.publicationDate 2008 en
heal.abstract This study is designed to examine the chemical composition and in vitro antioxidant activity of the essential oil and sub-fractions of the methanol extract of Marrubium globosum subsp. globosum. The GC and GC-MS analysis of the essential oil were resulted in the determination of 84 components representing 88.2% of the oil. The major constituents of the oil were spathulenol (15.8%), β-caryophyllene (9.0%), caryophyllene oxide (7.9%), germacrene D (6.5%), and bicyclogermacrene (3.1%). Antioxidant activities of the samples were determined by three different test systems namely DPPH, β-carotene/linoleic acid and reducing power assay. In DPPH system, the weakest radical scavenging activity was exhibited by the essential oil (1203.38 ± 7.18 μg ml-1). Antioxidant activity of the polar sub-fraction of methanol extract was superior to the all samples tested with an EC50 value of 157.26 ± 1.12 μg ml-1. In the second case, the inhibition capacity (%) of the polar sub-fraction of methanol extract (97.39% ± 0.84) was found the strongest one, which is almost equal to the inhibition capacity of positive control BHT (97.44% ± 0.74). In the case of reducing power assay, a similar activity pattern was observed as given in the first two systems. Polar sub-fraction was the strongest radical reducer when compared with the non-polar one, with an EC50 value of 625.63 ± 1.02 μg ml-1. The amount of the total phenolics was highest in polar sub-fraction (25.60 ± 0.74 μg/mg). A positive correlation was observed between the antioxidant activity potential and total phenolic level of the extracts. On the other hand, total flavonoid content was found equal for the both sub-fractions. © 2007 Elsevier Ltd. All rights reserved. en
heal.journalName Bioresource Technology en
dc.identifier.issue 10 en
dc.identifier.volume 99 en
dc.identifier.doi 10.1016/j.biortech.2007.08.058 en
dc.identifier.spage 4239 en
dc.identifier.epage 4246 en


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