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. 2012 Feb 22;60(11):2778–2784. doi: 10.1021/jf204777m

Table 2. Results of Method Validation for Selected Compounds.

    aspartamea
           
  caffeine light sample zero sample acesulfame-K cyclamate benzoate E150D vanillin HMF
LOD (mg/L) 1.7 4.6 2.9 0.75 1.6 0.97 41 0.6 0.7
LOQ (mg/L) 5.3 18.0 8.8 2.5 4.7 3.4 140 2.1 2.4
precision intraday (%)                  
standard solutionb 4.2 (108) 0.8 (240) 1.0 (240) 2.2 (160) 1.2 (242) 0.7 (210) 2.7 (2.00) 1.9 (20) 18 (4.0)
authentic sampleb 1.6 (100) 5.4 (240) 8.8 (390) 2.8 (160) 2.6 (253) 2.2 (146) 6.8 (2.05) 1.9 (16) 19 (4.7)
precision interday (%)                  
standard solution 4.0 1.2 2.3 2.9 0.8 0.9 2.6 5 18
authentic sample 1.5 6.3 6.7 3.1 3.7 2.8 6.5 3.1 17
recovery range: at two concentrationsb 100 (101) 103 (100) 107 (100) 94 (100) 102 (242) 99 (84) 99 (500) 140 (20) 67 (6.3)
  103 (51) 103 (50) 97 (50) 96 (50) 106 (133) 96 (42) 103 (250) 164 (10) 91 (3.1)
a

Two signals were used depending of the amount of citric acid: for the light sample, the doublet between 2.73 and 2.76 ppm was integrated, and for zero samples, the multiplet between 3.03 and 3.11 ppm was integrated.

b

Concentrations used for validation are given in parentheses (expressed in mg/L).