6. AOACSPIFANMethods-2018Awards
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2 D RAHER & W HITE : J OURNAL OF AOAC I NTERNATIONAL V OL . 101, N O . nnn , 2017
Table 2017.03A. Tryptophan SLV data: precision
SPIFAN code a
No. of replicates b
Mean, g/100 g RTF c
Sample type
RSD r
RSD iR
SRM 1849a
CLC10-B
12 12 12 12 12 12 12 12 12 12 12 12 12 12
20.1 25.3 18.3 25.7 24.1 21.4 23.7 32.2 23.2 19.5 18.3 22.4 70.6 91.3
0.37 0.56 4.95 0.82
1.51 0.97 6.92 2.02 1.82 1.33 1.56 2.42 1.69 2.27 1.79 3.68 1.91 1.7
Infant formula powder, partially hydrolyzed milk-based Infant formula powder, partially hydrolyzed soy-based
410057652Z 410457651Z 4052755861 4044755861 00859RF00
Toddler formula powder, milk-based Infant formula powder, milk-based
0.2 0.9
Adult nutritional powder, low-fat
Child formula powder
00866RF00
0.94 0.24
Infant elemental powder
00795RF
Infant formula powder, FOS/GOS-based Infant formula powder, milk-based Infant formula powder, soy-based
50350017W1
2
K16NTAV
0.31
E10NWZC
0.2
Infant formula, RTF milk-based
EV4H2R
0.45 1.86
Adult nutritional, RTF high-protein
00730RF00 00729RF00
Adult nutritional, RTF high-fat
0.3
a Materials from the SPIFAN Sample Kit. b Duplicates on each of 6 days performed by one laboratory. c RTF = Ready-to-feed.
hydrolysis of all sample types. (Although many samples are fully hydrolyzed within 6 h, some have been found to require longer; thus, a 16 h minimum is recommended for full applicability.) After hydrolysis, the sample – enzyme mixture is diluted to 50 mL with methanol – water and filtered. The sample is injected into a C8 column with reference standards and enzyme blank preparations and the analytes of interest detected and quantified fluorometrically. (a) HPLC system. — Equipped with an autosampler, column oven to maintain 30°C, fluorescence detector, binary or quaternary HPLC pump with degasser, and HPLC peak area integrator or chromatography data processor. (b) Analytical column. — YMC PACK C8; 3 µm particle, 3 × 50 mm (YMC America, Inc.; Product No. OC12S03-0503WT). (c) Analytical balance. — Readable to 0.001 mg. (d) Oven. — Constant-temperature oven capable of maintaining 50 ± 1°C. B. Apparatus and Materials
either at the N-terminal end (amino peptidases) or at the C terminus (carboxypeptidases; 5, 6). The protein is thus attacked on different sites simultaneously, releasing Trp in a relatively short period of time. Following proteolysis, Trp is quantitated by reversed-phase isocratic HPLC and fluorescence detection, which provides for a selective and specific determination of Trp in nutritional products. The enzymes in the pronase self-digest to produce background Trp in the absence of a sample. Consequently, the enzyme system is nonspecific for the Trp sample, and a blank subtraction is mandatory. Using this approach, recoveries of free Trp spikes as well as Trp from Bovine Serum Albumin (BSA) spikes are found to be essentially equivalent, indicating near-comparable self-digestion rates with and without sample. Sample preparation consists of adding a weighed sample, the enzyme solution, internal standard (5-methyl- DL -tryptophan), and Trizma buffer into a tube. A small amount of methanol is added as a bactericidal agent. The preparation is mixed and incubated at 50°C for 16 h (overnight) to ensure complete
Table 2017.03B. Tryptophan SLV data: accuracy
50% overspike
100% overspike
Spiking material
Native Trp level, g/100 g
Avg. recovery, %
RSD, %
Avg. recovery, %
RSD, %
SPIFAN code
No. of replicates a
Sample type
SRM 1849a
CLC10-B
12 12
BSA BSA
20.06 25.28
99.9
1.83
100.9 104.1
2.4
Infant formula powder, partially hydrolyzed milk-based Infant formula powder, partially hydrolyzed soy-based
410057652Z
104.3
3.3
2.71
410457651Z
11
BSA
18.33
103.7
8.6
101.5
4.8
Adult nutritional powder, low-fat
00859RF00
12 10 12 12 12
BSA BSA BSA BSA BSA
21.39 32.22 19.51 18.27
96.2
5.2 2.5
99.5
3.9 2.7
Infant elemental powder
00795RF
100.7 100.5
102.4 101.7
Infant formula powder, milk-based Infant formula powder, soy-based
K16NTAV
2.99 5.09
1.99 3.53
E10NWZC
93.8
99.5
Adult nutritional, RTF high-fat
00729RF00
91.3
104.8
1.6
104.9
1.3
a Samples spiked in duplicate with two levels of spikes over 3 days. Samples with <12 replicates contained data points that were confirmed outliers.
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