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Determination of 19 Organochlorine Pesticides Residues in Milk Powder by GPC-GC-MS

Received: 5 June 2018     Accepted: 22 June 2018     Published: 17 July 2018
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Abstract

To establish the GPC - GC - MS detection method for determination of organochlorine pesticide residues in milk powder. After simple processing samples, concentration with multi-position concentrator, and online cleaning with GPC-GC-MS, injection into the mass spectrometer for analysis. Results showed that in the linear range of 5~100 ug/L, the correlation coefficient were >0.998, and the method detection limits (MDLs) were <0.5 ug/kg. The spiked recoveries at three levels of 10, 50, 100 ug/kg were in the range of 70 ~ 95%, the relative standard deviations (RSDs) (n=6) were<10%. This method had advantages of good accuracy and precision, simple operation, rapid, and was suitable for routine analysis.

Published in International Journal of Nutrition and Food Sciences (Volume 7, Issue 4)
DOI 10.11648/j.ijnfs.20180704.13
Page(s) 129-133
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2018. Published by Science Publishing Group

Keywords

GPC - GC – MS, Organochlorine, Pesticide Residues, Milk Powder

References
[1] Fu Yao, Yu Chao, Xu Chen, et al. Research progress on determination methods of organochlorine pesticide residues in food [J]. Beijing Agriculture, 2014, 12 (4): 9~11.
[2] Wu minglai. Exploration of pretreatment methods for detection of organochlorine and pyrethroid pesticide residues in vegetables [J]. Anhui Agricultural Science Bulletin, 2012, 18 (13): 197~198.
[3] Liu Yi, Zheng Guocan, Wang Jing, et al. Determination of 20 Organochlorine Pesticides Residues in Milk by Gas Chromatography-Tandem Mass Spectrometry [J]. Journal of Inspection and Quarantine, 2012, 4 (22): 38~45.
[4] Deng Xiaojuan, Li Wenbin, Jin Lichuan, et al. Determination of 24 Organochlorine and Pyrethroid Pesticide Residues in Milk by Modified QuEChERS Method and Gas Chromatography [J]. Food Science, 2016, 18 (37): 141~145.
[5] GB/T 23210—2008, Determination of 511 pesticides and related chemicals residues in milk and milk powder GC-MS method [S].
[6] GB/T 23211-2008, Determination of 493 pesticides and related chemicals residues in milk and milk powder LC-MS-MS method [S].
[7] Yan Hui, Zhang Wen-li, Jiang Jia-xiao, et al. Determination of 20 organochlorine pesticides in soils using gas chromatography-tandem mass spectrometry combined with accelerated solvent extraction and gel permeation chromatography [J]. Chinese Journal of Analysis Laboratory, 2015, 34(6): 722~726.
[8] Su Jian-feng, Zhong Mao-sheng, Chen Jing, et al. Multi-residue Determination of 295 Pesticides in Tea and Its Products by Gas Chromatography-Mass Spectrometry and Gas Chromatography [J]. Journal of Instrumental Analysis, 2015, 34 (6): 625~638.
[9] Wang Bo, Li Xian-liang, Zhang Lei, et al. Simultaneous Determination of Organochlorine and Pyrethroid Pesticide Residues in Hotpot Condiment by Gas Chromatography [J]. Chinese Journal of Analytical Chemistry, 2010, 38 (10): 1433~1438.
[10] Zhang Yuan, Zhang Qi, Wang Xian-qin. SPE-GC/MS determination of 19 organophosphorus pesticide residues and organochlorine pesticide residues in Rhizoma Curcumae [J]. Chin J Pharm Anal, 2012, 32(1): 95~98.
[11] Fu Wenwen, Luo Tong, Zhu Ying, et al. Determination of Organochlorine Pesticides and Polychlorinated Biphenyls in Milk by QuEChERS-Gas Chromatography-Tandem Mass Spectrometry [J]. Food Science, 2018, 8(39): 309~313.
[12] Xue Haiquan, Cui Zhaojie, Du Shi-yong. Determination of organochlorine pesticides and polychlorinated biphenyls in wheat by gas chromatography with accelerated solvent extraction and gel permeation chromatography cleanup [J]. Journal of Shandong University (Natural Science), 2011, 46(1): 11~15.
[13] Du Juan, Lv Bing, Zhu Pan. et al. Determination of 30 organochlorine pesticides in animal-originated food products using combined purification by gel permeation chromatography and solid-phase extraction coupled with gas chromatography-mass spectrometry [J]. Chinese Journal of Chromatography, 2013, 31(8): 739~746.
[14] Chen Meiyu. Study and Application of Analytical Method for Pesticide Residue in Food by Gas Chromatography-Mass Spectrometry and Gas Chromatography-Tandem Mass Spectrometry [D]. Xiamen: Xiamen University, 2007.
[15] Zheng Junhong. Determination of multiple pesticides residue in milk and milk powder by LC-MS/MS [D]. Shandong: Shandong Agricultural University, 2009.
[16] Chu Chun, Wang Bin. Detection of plasticizer in oil-bearing samples by gel chromatography purification system [A]. 7th chromatography symposium in northwest China 12th annual chromatography conference in Gansu province [C]. Beijing: Beijing Polytech Instrument co., LTD., 2012. 183~185
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Cite This Article
  • APA Style

    Zhaofeng Wu, Xiaoyan Peng, Sheng Chen, Zhanteng Zeng. (2018). Determination of 19 Organochlorine Pesticides Residues in Milk Powder by GPC-GC-MS. International Journal of Nutrition and Food Sciences, 7(4), 129-133. https://doi.org/10.11648/j.ijnfs.20180704.13

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    ACS Style

    Zhaofeng Wu; Xiaoyan Peng; Sheng Chen; Zhanteng Zeng. Determination of 19 Organochlorine Pesticides Residues in Milk Powder by GPC-GC-MS. Int. J. Nutr. Food Sci. 2018, 7(4), 129-133. doi: 10.11648/j.ijnfs.20180704.13

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    AMA Style

    Zhaofeng Wu, Xiaoyan Peng, Sheng Chen, Zhanteng Zeng. Determination of 19 Organochlorine Pesticides Residues in Milk Powder by GPC-GC-MS. Int J Nutr Food Sci. 2018;7(4):129-133. doi: 10.11648/j.ijnfs.20180704.13

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  • @article{10.11648/j.ijnfs.20180704.13,
      author = {Zhaofeng Wu and Xiaoyan Peng and Sheng Chen and Zhanteng Zeng},
      title = {Determination of 19 Organochlorine Pesticides Residues in Milk Powder by GPC-GC-MS},
      journal = {International Journal of Nutrition and Food Sciences},
      volume = {7},
      number = {4},
      pages = {129-133},
      doi = {10.11648/j.ijnfs.20180704.13},
      url = {https://doi.org/10.11648/j.ijnfs.20180704.13},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijnfs.20180704.13},
      abstract = {To establish the GPC - GC - MS detection method for determination of organochlorine pesticide residues in milk powder. After simple processing samples, concentration with multi-position concentrator, and online cleaning with GPC-GC-MS, injection into the mass spectrometer for analysis. Results showed that in the linear range of 5~100 ug/L, the correlation coefficient were >0.998, and the method detection limits (MDLs) were <0.5 ug/kg. The spiked recoveries at three levels of 10, 50, 100 ug/kg were in the range of 70 ~ 95%, the relative standard deviations (RSDs) (n=6) were<10%. This method had advantages of good accuracy and precision, simple operation, rapid, and was suitable for routine analysis.},
     year = {2018}
    }
    

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  • TY  - JOUR
    T1  - Determination of 19 Organochlorine Pesticides Residues in Milk Powder by GPC-GC-MS
    AU  - Zhaofeng Wu
    AU  - Xiaoyan Peng
    AU  - Sheng Chen
    AU  - Zhanteng Zeng
    Y1  - 2018/07/17
    PY  - 2018
    N1  - https://doi.org/10.11648/j.ijnfs.20180704.13
    DO  - 10.11648/j.ijnfs.20180704.13
    T2  - International Journal of Nutrition and Food Sciences
    JF  - International Journal of Nutrition and Food Sciences
    JO  - International Journal of Nutrition and Food Sciences
    SP  - 129
    EP  - 133
    PB  - Science Publishing Group
    SN  - 2327-2716
    UR  - https://doi.org/10.11648/j.ijnfs.20180704.13
    AB  - To establish the GPC - GC - MS detection method for determination of organochlorine pesticide residues in milk powder. After simple processing samples, concentration with multi-position concentrator, and online cleaning with GPC-GC-MS, injection into the mass spectrometer for analysis. Results showed that in the linear range of 5~100 ug/L, the correlation coefficient were >0.998, and the method detection limits (MDLs) were <0.5 ug/kg. The spiked recoveries at three levels of 10, 50, 100 ug/kg were in the range of 70 ~ 95%, the relative standard deviations (RSDs) (n=6) were<10%. This method had advantages of good accuracy and precision, simple operation, rapid, and was suitable for routine analysis.
    VL  - 7
    IS  - 4
    ER  - 

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Author Information
  • China Customs Guangdong Inspection and Quarantine Technology Center, Guangzhou, China

  • China Customs Guangdong Inspection and Quarantine Technology Center, Guangzhou, China

  • China Customs Guangdong Inspection and Quarantine Technology Center, Guangzhou, China

  • China Customs Guangdong Inspection and Quarantine Technology Center, Guangzhou, China

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