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 |
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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 |
GPC - GC – MS, Organochlorine, Pesticide Residues, Milk Powder
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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
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
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
@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} }
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 -