Honey is a natural substance produced by bees of the genus Apis. Depending on the raw material used for its production, honey can be classified into two large groups: blossom honey, which results from the metabolization of nectar extracted from flowers; and honeydew honey, in which bees use plant or insect secretions for its production. The physicochemical characteristics are different between these two types of honey. For example, honeydew honey is darker and is characterized by a high content of phenolic acids. On the contrary, blossom honey stands out for its abundance of flavonoids. Blossom honey can be also classified based on the pollen origin. Thus, honey with more than 45% of the pollen coming from the same species can be considered monofloral; otherwise, it is considered multifloral. Honey is one of the food products with the highest level of fraudulent practices. Most of the adulterations consist of ingredient dilution, adding sweet substances, such as syrups, sugar cane, or corn syrup, among others. In the market, this was reflected in the dubious drop in prices for this product. In the last few years, several instance of honey fraud have come to light. This work aimed to develop a non-targeted ultra-high-performance liquid chromatography–high-resolution mass spectrometry (UHPLC–HRMS) fingerprinting method to address the characterization, classification, and authentication of Spanish honey samples considering their botanical and geographical origin. A total of 136 kinds of honey from different Spanish production regions belonging to different botanical varieties were analyzed, including: blossom honey (orange blossom, rosemary, thyme, eucalyptus, and heather) and honeydew honey (holm oak, forest, and mountain). A simple sample treatment was carried out, consisting of dissolving 1 g of honey in 10 mL of water, followed by a 1:1 dilution with methanol. The chromatographic separation of the obtained extracts was performed using a Kinetex
® C-18 core–shell column (100 × 4.6 mm I.D., 2.6 μm), working under gradient elution, using an aqueous solution of 0.1% formic acid and acetonitrile as the mobile phase components. HRMS acquisition was performed using electrospray in negative ionization mode (−2500 V) in an LTQ-Orbitrap working in full scan MS (
m/
z 100–1000) at a resolution of 50,000 full-width at half maximum (FWHM). The obtained non-targeted UHPLC–HRMS fingerprints (peak signals as a function of retention time and
m/
z) were considered as chemical descriptors of the analyzed honey samples for principal component analysis (PCA) and partial least squares-discriminant analysis (PLS-DA). PLS-DA revealed good discrimination between blossom and honeydew honey. Furthermore, the obtained chemometric models allowed the achievement of very good classification among the different botanical varieties under study for both blossom and honeydew honey. The discrimination of honey regarding the different Spanish climate production regions was more limited, although some trends were observed. Thus, the non-targeted UHPLC–HRMS fingerprinting approach proved to be an appropriate methodology to address honey characterization, classification, and authentication based on their different botanical origin.
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