Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2009 Jul 27;14(8):2717-28.
doi: 10.3390/molecules14082717.

Headspace, volatile and semi-volatile organic compounds diversity and radical scavenging activity of ultrasonic solvent extracts from Amorpha fruticosa honey samples

Affiliations

Headspace, volatile and semi-volatile organic compounds diversity and radical scavenging activity of ultrasonic solvent extracts from Amorpha fruticosa honey samples

Igor Jerković et al. Molecules. .

Abstract

Volatile organic compounds of Amorpha fruticosa honey samples were isolated by headspace solid-phase microextraction (HS-SPME) and ultrasonic solvent extraction (USE), followed by gas chromatography and mass spectrometry analyses (GC, GC-MS), in order to obtain complementary data for overall characterization of the honey aroma. The headspace of the honey was dominated by 2-phenylethanol (38.3-58.4%), while other major compounds were trans- and cis-linalool oxides, benzaldehyde and benzyl alcohol. 2-Phenylethanol (10.5-16.8%) and methyl syringate (5.8-8.2%) were the major compounds of ultrasonic solvent extracts, with an array of small percentages of linalool, benzene and benzoic acid derivatives, aliphatic hydrocarbons and alcohols, furan derivatives and others. The scavenging ability of the series of concentrations of the honey ultrasonic solvent extracts and the corresponding honey samples was tested by a DPPH (1,1-diphenyl-2-picrylhydrazyl) assay. Approximately 25 times lower concentration ranges (up to 2 g/L) of the extracts exhibited significantly higher free radical scavenging potential with respect to the honey samples.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Representative TIC chromatogram of A. fruticosa honey headspace VOCs isolated by HS-SPME. Numbers refer to the compounds listed in Table 1.
Figure 2
Figure 2
Representative TIC chromatogram of A. fruticosa honey VOCs isolated by USE. Numbers refer to the compounds listed in Table 2.
Figure 3
Figure 3
DPPH reduction percentage against increasing concentration of A. fruticosa USE extracts (a) and the honey samples (b) Results are expressed as mean values ± SD.

Similar articles

Cited by

References

    1. Bertelli D., Papotti G., Lolli M., Sabatini A.G., Plessi M. Development of an HS-SPME-GC method to determine the methyl anthranilate in Citrus honeys. Food Chem. 2008;108:297–303. doi: 10.1016/j.foodchem.2007.10.019. - DOI
    1. de la Fuente E., Valencia-Barrera R.M., Martïnez-Castro I., Sanz J. Occurrence of 2-hydroxy-5-methyl-3-hexanone and 3-hydroxy-5-methyl-2-hexanone as indicators of botanic origin in eucalyptus honeys. Food Chem. 2007;103:1176–1180. doi: 10.1016/j.foodchem.2006.10.020. - DOI
    1. Guyot C., Bouseta A., Scheirman V., Collin S. Floral origin markers of chestnut and lime tree honeys. J. Agric. Food Chem. 1998;46:625–633. doi: 10.1021/jf970510l. - DOI - PubMed
    1. Castro-Vázquez, Díaz-Maroto M.C., González-Viñas M.A., Pérez-Coello M.S. Differentiation of monofloral citrus, rosemary, eucalyptus, lavender, thyme and heather honeys based on volatile composition and sensory descriptive analysis. Food Chem. 2009;112:1022–1030. doi: 10.1016/j.foodchem.2008.06.036. - DOI
    1. Guyot C., Scheirman V., Collin S. Floral origin markers of heather honeys: Calluna vulgaris and Erica arborea. Food Chem. 1999;64:3–11. doi: 10.1016/S0308-8146(98)00122-8. - DOI

Publication types

MeSH terms

LinkOut - more resources