Food Hygiene and Safety Science (Shokuhin Eiseigaku Zasshi)
Online ISSN : 1882-1006
Print ISSN : 0015-6426
ISSN-L : 0015-6426
Volume 51, Issue 1
Displaying 1-8 of 8 articles from this issue
Originals
  • Koichi INOUE, Yukiko YOSHIMI, Tomoaki HINO, Hisao OKA
    2010 Volume 51 Issue 1 Pages 1-9
    Published: February 25, 2010
    Released on J-STAGE: March 06, 2010
    JOURNAL FREE ACCESS
    An LC/ESI (positive-mode)-MS/MS method was developed for simultaneous quantification of 8 macrocyclic lactones (abamectin B1a, abamectin 8,9-Z isomer B1a, emamectin benzoate B1a, emamectin benzoate 8,9-Z isomer B1a, ivermectin, eprinomectin B1a, doramectin and moxidectin) in animal tissues, egg, milk and honey. The separation was achieved on a TSK-GEL ODS 100 V column (2.0×50 mm, 3 μm) with a mobile phase consisting of 0.1% formic acid in acetonitrile, and 0.1 mM ammonium formate-0.1% formic acid in water, at a flow rate of 0.2 mL/min with gradient elution. Linear calibration plots were obtained with high correlation coefficients (r=0.998-0.999). The LOQ and LOD ranged from 0.02-1.5 ng/mL and 0.1-5 ng/mL, respectively. Average recoveries were in the range of 70.8-117.1% with associated RSD values<15% (n=10) for repeatability and reproducibility. The spiking levels for recoveries and RSDs met the validation criteria for Japanese maximum residue limits (MRLs). Based on these results, the proposed analytical method has been proven to be highly efficient and suitable for routine determinations of macrocyclic lactones in animal food matrices.
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  • Mihoko MURATA, Sumi SUGIYAMA, Aiko UEDA, Masataka ISHINAGA
    2010 Volume 51 Issue 1 Pages 10-18
    Published: February 25, 2010
    Released on J-STAGE: March 06, 2010
    JOURNAL FREE ACCESS
    The contents of nitrate and nitrite in menus containing more than 350 g of vegetables per day were investigated. The amounts of vegetables in menu A developed by female students and menu B taken from a recipe book were 350±2 g and 457±77 g, respectively. The average content of the nitrate was 321.0±139.3 mg (104.2-636.9 mg) in menu A, and 245.7±90.7 mg (140.1-507.3 mg) in menu B. Sixteen and thirteen samples exceeded the ADI in menus A and B, respectively. This may be because menu A contained more raw vegetables than menu B (menu A; 120±58 g, menu B; 72±71 g). The contents of nitrite in menu A and B were 1.2±0.3 mg (0.7-1.8 mg) and 2.8±0.9 mg (1.3-4.6 mg), respectively, and 6 samples in menu B exceeded the ADI. Intake of 350 g of vegetables or more in a day may reguire careful consideration of selection, frequency of use and cooking method, especially for vegetables with high nitrate content. A questionnaire to female students showed that 80% or more of students recognized that vegetables containing high contents of nitrate, such as spinach and komatsuna, should be boiled before eating them.
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  • Naoki SUGIMOTO, Atsuko TADA, Takako SUEMATSU, Kazunori ARIFUKU, Takesh ...
    2010 Volume 51 Issue 1 Pages 19-27
    Published: February 25, 2010
    Released on J-STAGE: March 06, 2010
    JOURNAL FREE ACCESS
    A quantitative NMR (qNMR) method was applied for the determination of carminic acid. Carminic acid is the main component in cochineal dye that is widely used as a natural food colorant. Since several manufacturers only provide reagent-grade carminic acid, there is no reference material of established purity. To improve the reliability of analytical data, we are developing quantitative nuclear magnetic resonance (qNMR), based on the fact that the intensity of a given NMR resonance is directly proportional to the molar amount of that nucleus in the sample. The purities and contents of carminic acid were calculated from the ratio of the signal intensities of an aromatic proton on carminic acid to nine protons of three methyl groups on DSS-d6 used as the internal standard. The concentration of DSS-d6 itself was corrected using potassium hydrogen phthalate, which is a certified reference material (CRM). The purities of the reagents and the contents of carminic acid in cochineal dye products were determined with SI-traceability as 25.3-92.9% and 4.6-30.5% based on the crystalline formula, carminic acid potassium salt trihydrate, which has been confirmed by X-ray analysis. The qNMR method does not require a reference compound, and is rapid and simple, with an overall analysis time of only 10 min. Our approach thus represents an absolute quantitation method with SI-traceability that should be readily applicable to analysis and quality control of any natural product.
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