Validation of an HPLC analytical method coupled to a multifunctional clean-up column for the determination of deoxynivalenol

被引:40
|
作者
Sugita-Konsihi, Y
Tanaka, T
Tabata, S
Nakajima, M
Nouno, M
Nakaie, Y
Chonan, T
Aoyagi, M
Kibune, N
Mizuno, K
Ishikuro, E
Kanamaru, N
Minamisawa, M
Aita, N
Kushiro, M
Tanaka, K
Takatori, K
机构
[1] Natl Inst Hlth Sci, Setagaya Ku, Tokyo 1588501, Japan
[2] Tokyo Metropolitan Inst Publ Hlth, Tokyo, Japan
[3] Kobe Inst Hlth, Kobe, Hyogo, Japan
[4] Nagoya City Publ Hlth Res Inst, Nagoya, Aichi, Japan
[5] Yokohama Quarantine Stn, Yokohama, Kanagawa, Japan
[6] Kobe Quarantine Stn, Kobe, Hyogo, Japan
[7] Hokkaido Inst Publ Hlth, Hokkaido, Japan
[8] Japan Food Res Labs, Osaka Branch, Osaka, Japan
[9] Fertilizer & Feed Instpect Serv, Tokyo, Japan
[10] Japan Grain Inspect Assoc, Tokyo, Japan
[11] Fertilizer & Feed Inspect Serv, Sendai Branch, Sendai, Miyagi, Japan
[12] Natl Food Res Inst, Tokyo, Japan
关键词
deoxynivalenol (DON); HPLC; inter-laboratory study; multifunctional clean-up column; validation; wheat;
D O I
10.1007/s11046-006-0260-1
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
To evaluate a method using a multifunctional clean-up column coupled with high performance liquid chromatography as an official analytical method for the determination of deoxynivalenol in wheat used as food or feed, an inter-laboratory study was performed in 12 laboratories using four naturally contaminated wheat samples and one spiked sample. The relative standard deviations for repeatability (RSDr) and reproducibility (RSDR) of naturally contaminated wheat were in the range 5.8-11.3% and 12.0-20.7%, respectively. The HORRAT was less than 1.0 in each sample. From the spiking test, the recovery rate, RSDr, RSDR and HORRAT value were 100.0%, 11.2%, 10.3% and 0.5, respectively. The limit of quantification is 0.10 mg/kg from the range obtained in a linear calibration. Thus, it should be useful as a sensitive and validated analytical method for the determination of deoxynivalenol in wheat intended for use in food and feed.
引用
收藏
页码:239 / 243
页数:5
相关论文
共 50 条
  • [21] Survey of aflatoxins in rice from Iran using immunoaffinity column clean-up and HPLC with fluorescence detection
    Feizy, J.
    Beheshti, H. R.
    Fahim, N. Khoshbakht
    Janati, S. S. Fakoor
    Davari, G.
    FOOD ADDITIVES & CONTAMINANTS PART B-SURVEILLANCE, 2010, 3 (04): : 263 - 267
  • [22] Clean-up procedure with ion-exchange mini column in the analysis of flusulfamide in agricultural products by HPLC
    Nakamura, Y
    Ishimitsu, S
    Tsumura, Y
    Yoshii, K
    Kaihara, A
    Tonogai, Y
    JOURNAL OF THE FOOD HYGIENIC SOCIETY OF JAPAN, 2001, 42 (06): : 398 - 403
  • [23] Improved Analytical Extraction and Clean-up Techniques for the Determination of PAHs in Contaminated Soil Samples
    Oluseyi, T.
    Olayinka, K.
    Alo, B.
    Smith, R. M.
    INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH, 2011, 5 (03) : 681 - 690
  • [24] Determination of deoxynivalenol and deoxynivalenol-3-glucoside in wheat and barley using liquid chromatography coupled to mass spectrometry: On-line clean-up versus conventional sample preparation techniques
    Nathanail, Alexis V.
    Sarikaya, Ebru
    Jestoi, Marika
    Godula, Michal
    Peltonen, Kimmo
    JOURNAL OF CHROMATOGRAPHY A, 2014, 1374 : 31 - 39
  • [25] Rapid determination of tetracycline antibiotics in milk by HPLC using an on-line clean-up system
    Taguchi, S
    Yoshida, S
    Fukushima, S
    Hori, S
    JOURNAL OF THE FOOD HYGIENIC SOCIETY OF JAPAN, 1997, 38 (04): : 259 - 264
  • [26] Determination of ochratoxin A in wheat after clean-up through a DNA aptamer-based solid phase extraction column
    De Girolamo, Annalisa
    McKeague, Maureen
    Miller, J. David
    DeRosa, Maria C.
    Visconti, Angelo
    FOOD CHEMISTRY, 2011, 127 (03) : 1378 - 1384
  • [27] An HPLC determination of Trimetazidine in human plasma using liquid-liquid extraction for sample clean-up
    Jeoung, MK
    Kim, KS
    Kim, CS
    Kim, NH
    Chung, YB
    Hong, JT
    Moon, DC
    JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES, 2005, 28 (09) : 1299 - 1309
  • [28] Simultaneous determination of four aflatoxins and ochratoxin A in ginger and related products by HPLC with fluorescence detection after immunoaffinity column clean-up and postcolumn photochemical derivatization
    Wen, Jing
    Kong, Weijun
    Wang, Jian
    Yang, Meihua
    JOURNAL OF SEPARATION SCIENCE, 2013, 36 (23) : 3709 - 3716
  • [29] Determination of Tetrodotoxin in Human Urine and Plasma after Immunoaffinity Column Clean-up Using Ultra-Performanc Hydrophilic Interaction Chromatography Coupled with Triple Quadrupole Mass Spectrometry
    Zhang Xiu-Yao
    Cai Xin-Xin
    Zhang Xiao-Yi
    Li Rui-Fen
    CHINESE JOURNAL OF ANALYTICAL CHEMISTRY, 2014, 42 (11) : 1611 - 1616
  • [30] VALIDATION OF A HPLC METHOD FOR OCHRATOXIN A DETERMINATION
    Bulea, Delia
    Spac, A. F.
    Dorneanu, V.
    MEDICAL-SURGICAL JOURNAL-REVISTA MEDICO-CHIRURGICALA, 2011, 115 (02): : 595 - 600