Literature DB >> 3125145

Optimum conditions for formation of aflatoxin M1-trifluoroacetic acid derivative.

R D Stubblefield1.   

Abstract

Because thin-layer chromatographic (TLC) confirmation of identity and reverse-phase liquid chromatographic (LC) determination with fluorescence detection of aflatoxin M1 both require the derivative formed in the reaction of M1 and trifluoroacetic acid (TFA), various reaction conditions were studied to obtain complete derivative formation. Of the various organic solvents tested, the reaction between M1 and TFA proceeded best in the nonpolar solvents hexane and isooctane. Other parameters investigated were reaction temperature and time, aflatoxin M1 concentration, and solvent volume. The following procedure is considered optimum: 200 microL each of hexane and trifluoroacetic acid are mixed with M1 standard in a silylated glass vial or with milk residue in a regular glass vial with a Teflon-lined screw cap and heated 10 min at 40 degrees C. The mixture is evaporated to dryness under N2, and the derivative is saved for TLC or LC. No unreacted aflatoxin M1 was detected by reverse-phase LC after this procedure was incorporated for analysis of milk samples.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3125145

Source DB:  PubMed          Journal:  J Assoc Off Anal Chem        ISSN: 0004-5756


  3 in total

1.  Study of aflatoxin B1 production by Aspergillus parasiticus in bee pollen of Greek origin.

Authors:  Maria Pitta; Panagiota Markaki
Journal:  Mycotoxin Res       Date:  2010-06-29       Impact factor: 3.833

2.  Situation of mycotoxins in milk, dairy products and human milk in Egypt.

Authors:  A El-Sayed Abd Alla; A Neamat-Allah; S E Aly
Journal:  Mycotoxin Res       Date:  2000-06       Impact factor: 3.833

3.  Human exposure to mycotoxins in Egypt.

Authors:  Am Abdalla El-Sayed; E Aly Soher; Aa Neamat-Allah
Journal:  Mycotoxin Res       Date:  2002-03       Impact factor: 3.833

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.