The phenolic compounds confirmation analysis by HPLC (1260 Infinity ll, Agilent Technologies, Santa Clara, CA, USA) was accomplished by Agilent ZORBAX Eclipse Plus C18 column (250 × 4.6 mm, 5 μm). The phenolic compounds were separated under gradient conditions with a flow rate of 0.8 mL/min. Column temperature was 35 °C and volume injection was 10 µL. The wavelength was 280 nm. The solvents used in the elution process were an aqueous solution of 100% methanol (phase A) and 0.02% (v/v) formic acid (phase B). The samples were eluted according to the linear gradient, the phase-time program was as follows: 0–10% A (0–5 min), 10–20% A (5–10 min), 10–35% A (10–20 min), 35–40% (20–35 min), 40–75% A (35–40 min), 75–10% A (40–45 min). The peak areas of the samples were compared with those of the internal standards and quantified [26 (link)].
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