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Quantitative Analysis of Iridoid Compounds

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The content of iridoid compounds was determined in three repetitions according to the method of Duan et al. [11] (link). with own modifications. The mobile phase of the flow rate of 1 mL/min was: H3PO4 (0.1 %) - reagent A and methanol (100 %) - reagent B. The results were recorded at a wavelength of 210 nm. Luna 5 µm C18(2), 250x4.6 mm column (Phenomenex, Torrance, California, USA) and PDA detector were used for chromatographic separation. The gradient program varied linearly: 0–4 min 0–25 % B, 4–10 min 25–35 % B, 10–22 min 35–40 % B, 22–27 min 40–0 % B, 27–42 min 0 % B. The amounts of iridoids were calculated based on standards of loganic acid (ChromaDex), loganin (Sigma-Aldrich), secologanin (ChromaDex) and sweroside (ChromaDex) and the total iridoids (TI) was calculated (mg/100 mL) as a sum of identified iridoids.
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2

Characterization of Medicinal Plant Compounds

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Maltodextrin (MD) ) was provided from Davisco Foods International (Le Sueur, MN, USA), whey protein (WP) was provided from Polmlek (Raciąż, Poland), pectin was provided from CPKelco (Großenbrode, Germany), and corn starch was supplied from Production sector of the Institute for Medicinal Plants Research Dr. Josif Pančić. Gelatin was produced by Aleva, Novi Kneževac. Folin-Ciocalteu reagent, gallic acid, orthophosphoric acid, and sodium carbonate were purchased from Sigma-Aldrich Chemie GmbH (Munich, Germany). Ultra-pure water was prepared using a Milli-Q purification system (Millipore, France), and HPLC-grade acetonitrile was obtained from Merck (Darmstadt, Germany). Standards swertiamarin, sweroside, and gentiopicroside were purchased from ChromaDex, USA, isoorientin and isovitexin were from Extrasynthese (Cedex, France), and isogentisin was purchased from Phytolab (Germany).
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