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. 2017 Feb 25;9(3):76. doi: 10.3390/toxins9030076

Table 1.

Method validation parameters including accuracy and precision determined at two different concentrations levels and recovery with standard deviation (STD, n = 3).

Compounds a Accuracy (RE %) Intraday (RSD %) Interday (RSD %) Recovery (%) R2 Linearity Range (µg∙g−1) MDL (µg∙g−1) MQL (µg∙g−1)
L H L H L H L H
1 MMPB b,c 8 6 7 9 12 12 79 (9) 85 (10) 0.9988 0.6–20 0.2 0.6
ANA-a b 6 5 6 7 11 13 95 (7) 92 (8) 0.9987 0.8–20 0.3 0.8
2 ANA-a 9 7 5 5 8 9 89 (7) 90 (8) 0.9995 0.1–20 0.04 0.1
MC-RR 7 8 7 3 11 8 86 (9) 89 (8) 0.9993 0.03–20 0.01 0.03
MC-YR 8 4 5 2 12 9 85 (7) 90 (6) 0.9992 0.07–20 0.02 0.07
MC-LR 6 3 7 6 9 7 91 (10) 95 (10) 0.9995 0.06–20 0.02 0.06
MC-LA 6 4 5 1 9 11 92 (7) 91 (9) 0.9990 0.03–20 0.01 0.03
MC-LY 7 6 8 5 7 9 87 (8) 92 (8) 0.9995 0.1–20 0.03 0.1
MC-LW 10 7 9 4 9 10 96 (7) 94 (9) 0.9993 0.05–20 0.02 0.05
MC-LF 8 5 10 2 11 8 93 (9) 90 (7) 0.9992 0.1–20 0.03 0.1
3 CYN 11 10 11 9 15 12 88 (10) 85 (7) 0.9990 0.1–20 0.04 0.1
STX 12 10 12 8 13 13 83 (11) 86 (9) 0.9989 0.3–20 0.1 0.3
BMAA 8 7 8 8 10 12 97 (6) 94 (5) 0.9993 0.08–20 0.02 0.08

a Validation results are divided between the three methods. L (low concentration) and H (high concentrations) are respectively set as the follow: 1 and 10 µg∙g−1 (1), 0.1 and 10 µg∙g−1 (2), and 0.5 and 10 µg∙g−1 (3). b Analysis using LDTD-APCI-HRMS detection. c Results reported as total MCs equivalent.