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| 10: Adv Exp Med Biol 2002;504:135-40 |
Roach JA, Brause AR, Eisele TA, Rupp HS.
U.S. Food and Drug Administration, CFSAN, Washington, DC 20204, USA.
The official patulin LC procedure was further examined (AOAC 995.10). Juice or
juice concentrate was extracted with ethyl acetate and cleaned up with sodium
carbonate. Patulin in the dried extract was determined by reversed-phase LC with
UV detection (280 nm) in 1% THF aqueous solution after evaporation of the ethyl
acetate. An end-capped C18 column was required to separate patulin from
hydroxymethylfurfural. Patulin was detected in approximately half of the >1000
extracts examined. Only ca 10% of the extracts contained patulin at levels
greater than 50 microg/L (50 ppb). Some presumptive findings were confirmed by
capillary gas chromatography/mass spectrometry as the trimethyl silyl derivative
using electron ionization or as underivatized patulin using negative ion
chemical ionization. Trifluoropropylmethyl polysiloxane capillary columns
provided superior gas chromatography of underivatized patulin compared to
phenyl/methyl polysiloxane and methyl polysiloxane columns.
Publication Types:
PMID: 11924597
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