Research Article

Application of an Optimized HPLC Method for the Detection of Various Phenolic Compounds in Apples from Lithuanian Cultivars

Table 1

Characteristics of the quantitative evaluation of phenolic compounds.

CompoundRetention time (min)aWavelength (nm)Confirmed linearity range (µg/mL)Calibration equationbDetermined quantitation limit (µg/mL)

Procyanidin B115.62806.25–100y = 7.33 × 103x + 5.49 × 1032.640.9998
(+)-Catechin19.72805–80y = 7.00 × 103x − 1.87 × 1032.200.9999
Chlorogenic acid20.73206.25–100y = 2.68 × 104x − 3.02 × 1042.930.9999
Procyanidin B222.92806.25–100y = 5.58 × 103x + 7.15 × 1032.860.9998
(−)-Epicatechin27.32805–80y = 7.53 × 103x + 1.19 × 1022.220.9999
Hyperoside40.03605–80y = 2.23 × 104x − 1.01 × 1042.420.9999
Isoquercitrin40.13603.125–50y = 2.66 × 104x − 2.10 × 1041.540.9999
Rutin39.53603.125–50y = 1.47 × 104x − 7.66 × 1032.790.9998
Quercitrin44.53602.5–40y = 1.77 × 104x − 5.57 × 1032.190.9998
Avicularin43.93603.125–50y = 2.32 × 104x − 1.12 × 1042.560.9998
Phloridzin47.62803.125–50y = 1.85 × 104x − 7.09 × 1032.400.9998

The mean was calculated from 6 replicates.
x in the calibration equation indicates the concentration of a compound, and y indicates a peak area.