RP-HPLC/MS/MS Analysis of the Phenolic Compounds, Antioxidant and Antimicrobial Activities of Salvia L. Species
Tarih
2016Yazar
Tohma, Hatice and Koksal, Ekrem and Kilic, Omer and Alan, Yusuf and
Yilmaz, Mustafa Abdullah and Gulcin, Ilhami and Bursal, Ercan and
Alwasel, Saleh H.
Üst veri
Tüm öğe kaydını gösterÖzet
The identification and quantification of the phenolic contents of
methanolic extracts of three Salvia L. species namely S. brachyantha
(Bordz.) Pobed, S. aethiopis L., and S. microstegia Boiss. and Bal. were
evaluated using reverse phase high performance liquid chromatography, UV
adsorption, and mass spectrometry (RP-HPLC/MS). In order to determine
the antioxidant capacity of these species, cupric ions (Cu2+) reducing
assay (CUPRAC) and ferric ions (Fe3+) reducing assay (FRAP) were
performed to screen the reducing capacity and
1,1-diphenyl-2-picrylhydrazyl (DPPH) assay was employed for evaluation
of the radical scavenging activity for both solvents. In further
investigation, the antimicrobial activities of Salvia species were
tested using the disc diffusion method against three Gram-positive and
four Gram-negative microbial species, as well as three fungi species.
The results showed that there is a total of 18 detectable phenols, the
most abundant of which was kaempferol in S. microstegia and rosmarinic
acids in S. brachyantha and S aethiopis. The other major phenols were
found to be apigenin, luteolin, p-coumaric acid, and chlorogenic acid.
All species tested showed moderate and lower antioxidant activity than
standard antioxidants such as butylated hydroxyanisole (BHA), butylated
hydroxytoluene (BHT), and ascorbic acid. The ethanolic extracts of
Salvia species revealed a wide range of antimicrobial activity. S.
brachyantha and S. microstegia showed the highest antimicrobial
activities against B. subtilis, whereas S. aethiopis was more effective
on Y. lipolytica. None of the extracts showed anti-fungal activity
against S. cerevisiae. Thus these species could be valuable due to their
bioactive compounds.
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