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  1. C. 医薬保健学域; 医学類・薬学類・医薬科学類・保健学類
  2. c 10. 学術雑誌掲載論文(医・保健)
  3. 2.査読済論文(薬)

Characterization of fumonisin A-series by high-resolution liquid chromatography-orbitrap mass spectrometry

http://hdl.handle.net/2297/44800
http://hdl.handle.net/2297/44800
3480a814-334f-48b1-afaa-77688fb57e95
名前 / ファイル ライセンス アクション
PH-PR-TAMURA-M-2580.pdf PH-PR-TAMURA-M-2580.pdf (1.1 MB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-04
タイトル
タイトル Characterization of fumonisin A-series by high-resolution liquid chromatography-orbitrap mass spectrometry
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Tamura, Masayoshi

× Tamura, Masayoshi

WEKO 27231

Tamura, Masayoshi

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Mochizuki, Naoki

× Mochizuki, Naoki

WEKO 27232

Mochizuki, Naoki

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Nagatomi, Yasushi

× Nagatomi, Yasushi

WEKO 27233

Nagatomi, Yasushi

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Harayama, Koichi

× Harayama, Koichi

WEKO 27234

Harayama, Koichi

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Toriba, Akira

× Toriba, Akira

WEKO 66
e-Rad 50313680
金沢大学研究者情報 50313680
研究者番号 50313680

Toriba, Akira

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書誌情報 Toxins

巻 6, 号 8, p. 2580-2593, 発行日 2014-08-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 2072-6651
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 10.3390/toxins6082580
出版者
出版者 MDPI AG
抄録
内容記述タイプ Abstract
内容記述 Fumonisin A-series (FAs) in a reference material of corn sample that was naturally contaminated with fumonisins was characterized using high-resolution liquid chromatography-Orbitrap mass spectrometry (LC-Orbitap MS). Peaks for fumonisin B1 (FB1), fumonisin B2 (FB2), and fumonisin B3 (FB3), in addition to three peaks corresponding to unknown compounds I, II, and III, were detected in the chromatogram for the corn sample. Fragment ion analysis for FB1, FB2, and FB3 showed that while the ions formed at m/z values of 200-800 were similar to those formed by the cleavage of the tricarballylic acids and the hydroxyl groups, the fragmentation patterns at m/z values of 50-200 varied depending on the hydroxyl group locations in the compounds. Fragment ion analysis of compounds I-III revealed structural similarities to FBs, only differing by an additional C<inf>2</inf>H<inf>2</inf>O in the unknown compounds. Using these results and by comparing the product ion mass spectra of compound I with fumonisin A1 (FA1) synthesized from FB1 standards, compounds I-III were hypothesized to be N-acetyl analogs of FBs: fumonisins A1 (FA1), A2 (FA2), and A3 (FA3). The method for determining concentrations was validated with FA1, FB1, FB2, and FB3 standards and applied to analyze the reference material. The FB1, FB2, and FB3 analytical levels were within acceptance limits and the amount of FA1 in the material was ~15% of FB1 amount at 4.2 mg/kg. © 2014 by the authors; licensee MDPI, Basel, Switzerland.
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
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