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. 2020 Aug 24;58(6):2121–2132. doi: 10.1007/s13197-020-04722-w

Table 2.

Assay validation parameters of the proposed HPLC method for determination of trans-resveratrol

Parameter Trans-resveratrol
Accuracya (mean recovery  % ± SD) 98.78 ± 0.45
Precision
 Repeatabilityb ±0.78
 Intermediate precisionc ±1.79
Linearity
 Slope 158,164
 Intercept +4266.8
 Correlation cofficient (r) 0.9991
Range (mg L−1) 0.10–40
LODd (mg L−1) 0.03
LOQd (mg L−1) 0.10

aAverage of (n = 3), average five concentrations (0.5- 30 mg L−1) for trans-resveratrol

bThe intraday (n = 3), average of three concentrations (0.5, 10 and 30 mg L−1) for trans-resveratrol repeated three times within the day

cThe inter-day (n = 3), average of three concentrations (0.5, 10 and 30 mg L−1) for trans-resveratrol repeated three times in 3 days

dDetermined via calculations, LOD = 3.3 (SD of the response/slope), LOQ = 10 (SD of the response/slope)