2022
DOI: 10.3390/foods11182868
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Amino Acid Fingerprinting of Authentic Nonfat Dry Milk and Skim Milk Powder and Effects of Spiking with Selected Potential Adulterants

Abstract: A collaborative study was undertaken in which five international laboratories participated to determine amino acid fingerprints in 39 authentic nonfat dry milk (NFDM)/skim milk powder (SMP) samples. A rapid method of amino acid analysis involving microwave-assisted hydrolysis followed by ultra-high performance liquid chromatography-ultraviolet detection (UHPLC-UV) was used for quantitation of amino acids and to calculate their distribution. The performance of this rapid method of analysis was evaluated and was… Show more

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Cited by 3 publications
(2 citation statements)
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“…The nitrogen contents (N) of the adulterants were melamine (66.60% N), urea (46.62% N), glycine (18.65% N), and taurine (11.19% N). Due to the relative difference in nitrogen content among these adulterants, melamine and urea were used in an overall lower concentration than the amino acids (glycine and taurine), which aligns with industrial applications and previous research [1,38,44]. All the powdered samples were prepared to have the same particle size.…”
Section: Sample Acquisitionmentioning
confidence: 88%
“…The nitrogen contents (N) of the adulterants were melamine (66.60% N), urea (46.62% N), glycine (18.65% N), and taurine (11.19% N). Due to the relative difference in nitrogen content among these adulterants, melamine and urea were used in an overall lower concentration than the amino acids (glycine and taurine), which aligns with industrial applications and previous research [1,38,44]. All the powdered samples were prepared to have the same particle size.…”
Section: Sample Acquisitionmentioning
confidence: 88%
“…The above methods stipulate that the sample for determination of free amino acids in proteins should be hydrolyzed by hydrochloric acid (6 mol/L) at 110 °C for 20–24 h. In recent years, the microwave digestion method has been gradually used in the pretreatment for the determination of amino acids in proteins with the advantages of accelerating the rate of hydrolysis, simple processing, and reliable results. Importantly, there is no significant difference in the results of the determination of the content of each amino acid compared with the traditional digestion method [ 17 , 18 ].…”
Section: Introductionmentioning
confidence: 99%