1996
DOI: 10.1016/0308-8146(95)00149-2
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Liquid chromatographic determination of vitamins B1 and B2 in foods. A collaborative study

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Cited by 83 publications
(43 citation statements)
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“…Due to the extensive phosphorylated and protein-bound vitamins in natural foods, quantitative analysis of the entire array of B-group vitamins at endogenous levels requires vigorous sample extraction to release the free vitamins using strong acids and enzyme hydrolysis. [19][20][21][22][23][24][25][26][27][28][29][30] However, these tedious, complex and harsh methods are not necessary to extract the vitamins from vitamin-supplemented food products.…”
Section: Resultsmentioning
confidence: 99%
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“…Due to the extensive phosphorylated and protein-bound vitamins in natural foods, quantitative analysis of the entire array of B-group vitamins at endogenous levels requires vigorous sample extraction to release the free vitamins using strong acids and enzyme hydrolysis. [19][20][21][22][23][24][25][26][27][28][29][30] However, these tedious, complex and harsh methods are not necessary to extract the vitamins from vitamin-supplemented food products.…”
Section: Resultsmentioning
confidence: 99%
“…[19][20][21][22]24,25,27,30 Interference in the chromatograms and poor recovery indicate degradation of some vitamins due to the harsh acid. Organic solvents can also be used to precipitate proteins and are milder toward the samples.…”
Section: Resultsmentioning
confidence: 99%
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“…A literatura apresenta métodos analí-ticos para determinação das vitaminas nesses produtos como, por ex., a determinação das vitaminas do complexo B pode ser realizada através de métodos microbiológicos 13,14 , CLAE [15][16][17][18][19][20][21][22] , cromatografia micelar eletrocinética 23 , cromatografia gasosa 24 e por espectrofotometria, empregando sistema de análises por injeção em fluxo 25 . Entretanto, a literatura é deficiente em relação à avaliação dos níveis e da estabilidade das vitaminas em bebidas fortificadas.…”
Section: Introductionunclassified
“…10,13,[15][16][17] Ion-pairing reagents improve the chromatographic resolution and peak shape, particularly by reducing peak tailing. With these methods, the mixture of an acetate buffer with 1-octanesulfonate and organic solvents (acetonitrile and methanol) was selected as the mobile phase for the pharmaceutical analysis of thiamine in both United States Pharmacopoeia (USP) 18 and Korean Pharmacopoeia (KP) 19 monographs.…”
mentioning
confidence: 99%