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. Author manuscript; available in PMC: 2020 Aug 17.
Published in final edited form as: J Chromatogr A. 2019 Apr 1;1599:66–74. doi: 10.1016/j.chroma.2019.03.066

Table 2.

Validation data for target analytes in water and fish tissue.

Linear Range Correlation Recovery (%, CV) Precision (%, CV) Detection Limits (pg) MDL
Analyte (ngmL−1) Coefficient (r2) Water Fish Water Fish LOD LOQ Water (ng L−1) Fish (μg kg−1)
ANA 0.1–20 0.999 97 (1.2) 103 (1.3) 1.9 3.4 4.0 10 0.08 0.14
CLD 0.5–100 0.998 90 (2.6) 90 (1.8) 5.0 8.2 70 230 0.43 0.12
SAX 0.1–20 0.995 53 (2.7) 45 (4.4) 1.6 5.6 10 40 0.22 0.04
M-LA 0.5–100 0.998 97 (1.8) 96 (5.7) 0.8 5.7 20 70 0.60 0.61
M-LR 0.1–100 0.998 94 (2.4) 97 (5.1) 0.6 5.1 40 130 0.38 0.31
M-LY 0.5–100 0.998 73 (7.3) 75 (7.1) 7.2 4.7 40 140 0.83 0.35
M-RR 0.1–100 0.999 97 (3.0) 90 (5.9) 2.4 6.3 60 220 0.91 0.28
M-YR 0.5–100 0.999 93 (4.6) 77 (4.7) 3.9 1.2 80 280 0.80 0.70
NOD 0.5–100 0.996 98 (3.1) 90 (7.9) 2.9 4.7 50 180 0.96 0.57

Limit of detection (LOD) was defined as LOD = (3σ/b) where σ is the standard deviation of the quantified value from replicate blank samples (n=8), and b is the slope of the calibration for the target analyte. Limit of quantification (LOQ) was defined as LOQ = (10σ/b). Method detection limits (MDL) were defined as MDL = t (n-1,0.99) × SD, where t (n-1,0.99) is the one-sided Student’s t-statistic at the 99% confidence limit for n-1 degrees of freedom, (2.998 for n = 8), and SD is the standard deviation of replicate spiked matrix sample (spiking level ≤ 10 × MDL).