Food Hygiene and Safety Science (Shokuhin Eiseigaku Zasshi)
Online ISSN : 1882-1006
Print ISSN : 0015-6426
ISSN-L : 0015-6426
Volume 42, Issue 4
Displaying 1-14 of 14 articles from this issue
Originals
  • Mihoko MURATA, Masataka ISHINAGA
    2001 Volume 42 Issue 4 Pages 215-219
    Published: August 25, 2001
    Released on J-STAGE: March 25, 2009
    JOURNAL FREE ACCESS
    Daily intakes of nitrate and nitrite of middle-aged men (30-59 years of age, n=100) in Hiroshima Prefecture were estimated directly by the duplicate portion method. The daily intake of nitrate was 190.8±128.5 mg. The daily intake of nitrate/kg body weight was 2.87±2.00 mg, which is about 78% of the acceptable daily intake (ADI). The daily intake of nitrate tended to increase with increasing age. The daily intake of nitrite was 3.837±3.647 mg. The daily intake of nitrite/kg body weight was 0.057±0.050 mg, which is about 95% of the ADI. In the case of nitrite, there was no age-related difference. The proportions of men, whose daily intakes of nitrate and nitrite were above the ADI, were 27% and 34%, respectively. The proportion of men above the ADI of both nitrate and nitrite was 10%.
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  • Kazuo EGOSHI, Hiroshi NAKAOKA, Terumi OKA, Kouji ABO
    2001 Volume 42 Issue 4 Pages 220-225
    Published: August 25, 2001
    Released on J-STAGE: March 25, 2009
    JOURNAL FREE ACCESS
    To study of the behavior of Trp-P-1 and its metabolites in rat feces and urine, rats were orally administered with Trp-P-1 (750, 1,500 and 2,500 μg/rat), and excreted Trp-P-1 was analyzed using HPLC assay and bacterial mutagenicity assay. The extraction of Trp-P-1 from urine was performed by using the chloroform extraction method, and blue rayon was used for the extraction from feces.
    When Trp-P-1 was added to rat feces and urine, the recoveries of Trp-P-1 were 85.9±3.9% and 91.3±3.7%, respectively. The extracts of feces and urine from rats administered with Trp-P-1 were individually fractionated by thin layer chromatography on C18 gel. The major mutagenic zone corresponding to Trp-P-1 was found at Rf 0.09 in both extracts, while the feces extract gave two additional mutagenic zones at Rf 0.15 and 0.20. More than 97% of the fecal mutagenic activity was due to unchanged Trp-P-1.
    In rats administered with 750 μg of Trp-P-1, the amount of extracted Trp-P-1 and the number of His+ colonies induced by whole excreta were 81.6±7.1 μg (n=6) and (432±77)×104 for feces, and 28.7±4.9 μg and (171±28)×104 for urine. The recoveries of Trp-P-1 in the feces and urine were 10.8±0.9% and 3.8±0.7% by HPLC analysis, and 11.1±2.0% and 4.4±0.7% by mutagenicity assay respectively. The results of the two assays seemed to show similar patterns of recovery.
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  • Shuzo TAGUCHI, Seisaku YOSHIDA, Yukio TANAKA, Shinjiro HORI
    2001 Volume 42 Issue 4 Pages 226-230
    Published: August 25, 2001
    Released on J-STAGE: March 25, 2009
    JOURNAL FREE ACCESS
    A simple and rapid analytical method was established for detection of anabolic agents, zeranol and α-trenbolone and β-trenbolone residues in cattle muscle and liver.
    This method consisted of aqueous acetonitrile extraction and successive solid-phase extraction with a tandem connected octadecyl (C18)-aminopropyl (NH2) cartridge, followed by on-line clean-up using multidimensional HPLC with EC and UV detection.
    On-line clean-up was performed by a three-column switching technique, the first column being a Diol size exclusion column (SEC), the second, an internal surface reversed phase trapping column (TC) and the third, a C18 analytical column (AC). Sample solution from solid-phase extraction was injected into the SEC. The anabolic agents eluted from the SEC were introduced into a TC, and the anabolic agents trapped in the TC were rapidly loaded onto an analytical column after changing the eluent. Zeranol in the eluate from the analytical column was detected at 700 mV ECD and α- and β-trenbolone were detected at UVD 350 nm. SEC and TC were washed and conditioned to the initial state just after the loading of the desired fraction on the AC.
    Recoveries from muscle fortified at a level of 0.002 mg/L (maximal residue limits, MRLs) averaged 86.1% for zeranol and 77.0% for β-trenbolone, and recoveries from liver at a level of 0.010 mg/kg (MRLs) averaged 74.3% for zeranol and 73.1% for α-trenbolone. The quantitation limits for all of them were 0.001 mg/kg in muscle and 0.002 mg/kg in liver.
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  • Yukihiro GODA, Takuya ASANO, Masaaki SHIBUYA, Akihiro HINO, Masatake T ...
    2001 Volume 42 Issue 4 Pages 231-236
    Published: August 25, 2001
    Released on J-STAGE: March 25, 2009
    JOURNAL FREE ACCESS
    A method using polymerase chain reaction (PCR) was developed to detect the genetically modified (GM) papaya (55-1 line), of which the mandatory safety assessment has not been finished in Japan because of insufficient data. The papaya intrinsic papain gene was used as an internal control. The results of PCR amplification of the papain gene segment indicated that a commercial silica membrane type kit (QIAGEN DNeasy plant mini) was useful for extraction of DNA from papaya fruit, but not for extraction from canned papaya fruit. On the other hand, a commercial ion-exchange type kit (QIAGEN Genomic-tip) provided enough purified DNA for PCR from canned papaya fruit. Compaired with the parental line and other commercial non-GM papayas, the DNA from GM papaya fruit provided specific amplification bands in PCR with five primer pairs (Nos. 2∼6) including β-glucuronidase and neomycin phosphotransferase II gene-specific ones. On the other hand, the primer pairs recognizing these genes showed false-positive results when we used DNAs from canned papaya. Therefore, we recommend that the primer pairs (Nos. 5 and 6) recognizing the sequences derived from two different species of organism should be used in order to detect specifically the GM papaya in canned fruits.
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  • Susumu HIRANO, Tsuruzo SHIMA, Tomoko SHIMADA
    2001 Volume 42 Issue 4 Pages 237-242
    Published: August 25, 2001
    Released on J-STAGE: March 25, 2009
    JOURNAL FREE ACCESS
    Moldy and split peanut kernels were separated from peanuts exported from Brazil, Sudan, India and Taiwan by visual inspection. The remaining peanuts from Brazil, Sudan and India were roasted lightly and the skins were removed. Stained peanuts were separated from the others. Aflatoxin was detected in moldy and stained peanuts. There was a positive correlation between % of aflatoxin-contaminated peanut kernels and aflatoxin B1 concentration in whole samples. Aflatoxin concentration of moldy peanuts was higher than that of stained peanut kernels.
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