6. AOACSPIFANMethods-2018Awards
102
E llingson et al .: J ournal of AOAC I nternational V ol . 99, N o . 1, 2016 207
Table 2. Choline precision summary a
Free choline
Total choline
Mean concn, mg/100 g
,
RSD INT , %
Mean concn, mg/100 g
,
RSD INT , %
RSD r
RSD r
%
%
Sample
81.3
2.1 2.3
105 2.1 1.8
SRM
1849a b,c
0.364 d
1.8 d,e
2.7 d,f
4.11 2.3 g
2.8 f
AN powder milk protein- based IF hydrolyzed milk-based IF hydrolyzed soy-based AN powder low fat Child formula powder IF elemental powder
14.4
1.7 2.7
18.8 2.1 3.5
17.8
1.7 2.7
17.8 2.0 2.9
18.1 2.4 h
2.8
15.5
1.6 3.5
4.61
1.0 1.7
5.70 2.3 2.6
Figure 2015.10B. Extracted ion chromatogram (XIC) of carnitine.
Table 2015.10B. Compound transitions
8.11
1.1 2.2
8.68 2.2 2.8
Transition (Q1/Q3)
Collision energy, V
Retention time, min
17.4 2.1 i
3.3 f
Compound
Use/type
IF powder
13.8
2.2 2.5
milk-based
Carnitine
Quantitation 162.0/103.0
25 25
1.7 1.7
IF powder
14.9
1.1 2.1
20.2 2.6 4.0
Carnitine-d3 Internal standard
165.0/103.0
soy-based
12.6 3.1 i
2.7 g
21.4 2.8 2.5
IF RTF milk- based AN RTF high protein
Carnitine Carnitine Choline
Confirmation 162.0/84.4 Confirmation 162.0/59.1 Quantitation 104.2/60.0
29 27 25 25
1.7 1.7 2.1 2.1
42.8
2.7 2.6
49.3 1.6 1.5
Choline-d4
Internal standard
108.2/60.0
AN RTF high fat
48.1
1.4 1.5
53.2 1.2 1.5
Choline
Confirmation 104.2/45.2
25
2.1
0.205 d
2.2 d
4.0 d
1.25 d
2.7 d
2.2 d
Child formula powder placebo IF elemental powder placebo AN RTF high protein placebo AN RTF high fat placebo
where R = results expressed in mg/100 g, C = concentration of the analyte in the injected solution in ng/mL, V = volume of the initial extract in mL, S = sample weight in grams, and D = dilution factor, the inverse of any dilution made. All results were calculated on a RTF or reconstituted basis of 25 g diluted to 225 g with water, except for SRM 1849a that was calculated back to powder basis.
0.118 d
6.4 d
6.4 d
0.651 d
1.8 d
3.0 d
0.491 d
1.7 d
1.9 d
6.03 3.4 3.2
0.522 d
2.8 d
2.8 d
5.10 2.7 2.5
Results and Discussion
IF RTF
5.42
1.6 2.4
13.2 2.0 2.2
Linearity was assessed from the percent deviation from the theoretical concentration across the working standard range (Table 1). The results from the validation showed an overall repeatability for free and total choline of 1.9 and 2.3% RSD r , whereas the overall intermediate precision obtained for free and total choline was 2.4 and 2.7% RSD INT , respectively (Table 2). Free and total carnitine had an overall repeatability of 2.9 and 2.7% RSD r , whereas the overall intermediate precision obtained for free and total carnitine was 3.3 and 3.1% RSD INT ,
milk-based placebo
Overall 2.3 2.7 a Samples were run in triplicate across 4 days, n = 12. Deviation is footnoted due to outliers by Grubbs’ test at a 95% confidence interval, loss of sample during preparation, or failure to prepare in triplicate. Twelve data points were still obtained for all samples. b Free choline information mass fraction value of 79.8 mg/100 g. c Total choline certified mass fraction mean and range of 109 mg/100 g and 98.0–120 mg/100 g, respectively. d Results below the SMPR-required LOQ of 2.0 mg/100 g and are not included in the calculations. e Three days of duplicates used for calculation. f Calculated across 5 days. g Two days of duplicates and 1 day of four replicates used for calculation. h One day of duplicates and 1 day of four replicates used for calculation. i One day of duplicates used for calculation. 1.9 2.4
Table 1. Linearity a
Percent deviation from theoretical concn, ng/mL
Compound 10
20
500 2000 4000 5000 Mean 2.0 2.4 1.2 2.0 2.2
Carnitine 2.9 3.0
Choline 1.4 1.1 1.0 1.7 1.9 a Average from three analyses of duplicates at each working standard level. 2.5 4.1
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