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1.
Shokuhin Eiseigaku Zasshi ; 49(2): 100-5, 2008 Apr.
Artigo em Japonês | MEDLINE | ID: mdl-18503246

RESUMO

Methods using high-performance liquid chromatography with fluorescence detection (HPLC-FL) and using liquid chromatography with tandem mass spectrometry (LC/MS/MS) were developed for simultaneous determination of ochratoxin A (OTA), ochratoxin B (OTB) and citrinin (CIT) in cereal, fruit, and coffee products. The samples were extracted with ethyl acetate under an acidic condition, and then cleaned up with liquid-liquid separation. The test solutions were analyzed by reverse-phase HPLC-FL and LC/MS/MS. Mass spectral acquisition was performed in positive ion mode by applying multiple reaction monitoring. The performances of both detectors were almost equivalent. The recoveries of OTA and OTB were 87-111%, and that of CIT were 70-88%. The limits of quantification (S/N> or =10) of OTA, OTB and CIT was 0.1 mug/kg or less. These methods were considered to be useful for the determination of the three mycotoxins at low levels (0.1 microg/kg).


Assuntos
Cromatografia Líquida de Alta Pressão/métodos , Cromatografia Líquida/métodos , Citrinina/análise , Análise de Alimentos/métodos , Contaminação de Alimentos/análise , Ocratoxinas/análise , Espectrometria de Massas em Tandem/métodos , Café/química , Grão Comestível/química , Frutas/química
2.
Shokuhin Eiseigaku Zasshi ; 49(2): 111-5, 2008 Apr.
Artigo em Japonês | MEDLINE | ID: mdl-18503248

RESUMO

Ochratoxin A (OTA), ochratoxin B (OTB) and citrinin (CIT) in commercial foods were simultaneously determined and confirmed with high-performance liquid chromatography (HPLC) and liquid chromatography coupled with tandem mass spectrometry (LC/MS/MS). The samples examined were made up of cereal, fruit, coffee, and cacao products. The limits of quantification (S/N> or =10) of OTA, OTB and CIT were 0.1 microg/kg or less. Aflatoxins (AF), deoxynivalenol (DON) and fumonisins were also surveyed. Of 157 samples examined, 44 were contaminated with OTA at levels of 0.11 to 4.0 microg/kg. At least 2 positive samples were labeled as domestics. In most positive samples, the OTA level was low, less than 1 microg/kg. The highest incidence of OTA was observed in cacao powder (10/12), followed by instant coffee (5/7), cocoa (5/8) and raisin (6/13). OTB was found in fruit and cacao products containing relatively high levels of OTA. Co-occurrence of OTA, CIT and DON was found in cereal products, and co-occurrence of OTA and AF was found in cacao products. Approximately 30% of naturally contaminated OTA in roasted coffee bean moved into the extract solution when brewed with paper filter.


Assuntos
Citrinina/análise , Análise de Alimentos/métodos , Contaminação de Alimentos/análise , Ocratoxinas/análise , Aflatoxinas/análise , Cacau/química , Cromatografia Líquida de Alta Pressão , Cromatografia Líquida , Café/química , Grão Comestível/química , Frutas/química , Fumonisinas/análise , Espectrometria de Massas em Tandem , Tricotecenos/análise
3.
Shokuhin Eiseigaku Zasshi ; 48(3): 77-82, 2007 Jun.
Artigo em Japonês | MEDLINE | ID: mdl-17658001

RESUMO

The content of potato glycoalkaloid (PGA) was investigated in 27 cultivars of raw potatoes and 31 potatoes in commercial foods with peel. The investigation of the 27 cultivars of potatoes showed different contents of glycoalkaloids. "May queen" and "Sherry" showed high contents of PGA (180 mg/kg and 320 mg/kg, respectively) among the raw potatoes of middle size (ca. 100 g). On the other hand, "Inca red" showed the lowest content of 21 mg/kg. Higher contents of PGA were found in smaller potatoes in this study. The content of PGA varied in the range of 48-350 mg/kg in the potatoes in commercial foods with peel.


Assuntos
Alcaloides de Solanáceas/análise , Solanum tuberosum/química , Solanina/análogos & derivados , Solanina/análise
4.
Shokuhin Eiseigaku Zasshi ; 44(2): 110-3, 2003 Apr.
Artigo em Japonês | MEDLINE | ID: mdl-12846158

RESUMO

A simple and rapid determination of anticoccidial drug residues, diclazuril (DCZ) and nicarbazin (NCZ), in chicken tissues has been developed. DCZ and NCZ were extracted with acetonitrile from chicken liver, muscle, and fat. The extract was rinsed with n-hexane saturated with acetonitrile and then evaporated. The residue was dissolved in 1.4 mL of acetonitrile-methanol (1:1), then 1.0 mL of n-hexane saturated with acetonitrile-methanol (1:1) was added, and the mixture was partitioned by the addition of 0.6 mL of water. DCZ and NCZ in the aqueous layers were determined by HPLC on an Xterra RP-18 column with acetonitrile-0.5% ammonium acetate containing 0.01 mol/L tetra-n-butylammonium hydrogen sulfate (43:57) as the mobile phase. The mean recoveries (n = 5) of DCZ and NCZ spiked in chicken tissues at the maximum residue levels were 92.0-95.6% (CV 2.4-3.0%) and 87.3-89.4% (CV 1.7-2.8%), respectively. The detection limits of DCZ and NCZ were 0.01 and 0.004 microgram/g, respectively.


Assuntos
Cromatografia Líquida de Alta Pressão/métodos , Coccidiostáticos/análise , Carne/análise , Nicarbazina/análise , Nitrilas/análise , Resíduos de Praguicidas/análise , Triazinas/análise , Animais , Galinhas
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