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Table 1 Method validation

From: A stable isotope dilution method for a highly accurate analysis of karrikins

Compound

Calibration curve

Determinated spiked KARs content [pmol]

Method precision [RSD%]

Method accuracy [%bias]

1

5

10

1

5

10

1

5

10

KAR1

Cal 1

1.27 ± 0.03

5.60 ± 0.05

11.09 ± 0.49

2.4

1.0

4.5

27.1

12.0

10.9

Cal 2

1.58 ± 0.04

6.89 ± 0.07

13.57 ± 0.60

2.4

1.0

4.4

58.0

37.7

35.7

Cal 3

1.08 ± 0.03

5.39 ± 0.06

11.29 ± 0.54

2.6

1.0

4.8

8.2

7.7

12.9

KAR2

Cal 1

2.79 ± 0.12

10.50 ± 0.28

20.72 ± 0.74

4.2

2.6

3.6

178.8

110.1

107.2

Cal 2

1.72 ± 0.08

7.39 ± 0.21

15.61 ± 0.61

4.6

2.9

3.9

71.5

47.8

56.1

Cal 3

1.06 ± 0.05

4.47 ± 0.13

9.34 ± 0.36

4.5

2.9

3.9

6.0

− 10.6

− 6.6

  1. Analytical precision (RSD%) and accuracy (%bias) of whole procedure shown for different amounts of karrikins (1, 5 and 10 pmol). The extract of 10 mg (FW) Arabidopsis sample was spiked from 1 to 10 pmol of authentic KAR standards, purified by SPE and analysed by UHPLC-MS/MS. Concentrations of KARs were quantified using the standard isotope dilution method combined with calibration curves without (Cal 1) and with (Cal 2 and 3) plant matrix. Values are means ± SD (n = 3)