HPLC determination of aflatoxin M1 in liquid milk and milk powder using solid phase extraction on OASIS HLB

Food Control ◽  
2012 ◽  
Vol 28 (1) ◽  
pp. 131-134 ◽  
Author(s):  
Yutang Wang ◽  
Xuebo Liu ◽  
Chunxia Xiao ◽  
Zhouli Wang ◽  
Jianguo Wang ◽  
...  
2017 ◽  
Vol 100 (5) ◽  
pp. 1559-1564 ◽  
Author(s):  
Yang Zheng ◽  
Xiuli Xu ◽  
Fei Yuan ◽  
Meiyi Yao ◽  
Shunli Ji ◽  
...  

Abstract A sensitive, high-throughput analytical method based on a GC-MS method was established for the simultaneous quantitative determination of two categories of harmful coumarins: simple coumarins (coumarin, 6-methylcoumarin, 7-methoxycoumarin, 3,4-dihydrocoumarin, and 7-ethoxy-4-methylcoumarin) and furocoumarines (psoralen, 8-methoxypsoralen, 5-methoxypsoralen, and trioxysalen). The nine analytes were extracted with ethyl acetate, purified with Oasis HLB solid-phase extraction (SPE) cartridges, and identified and quantitatively determined by GC-MS in selected-ion monitoring mode. The LODs and LOQs of these compounds were in the ranges of 12.5–21.2 and 41.6–70.0 μg/kg, respectively. Average recoveries for the nine analytes ranged from 72.7 to 86.6% atLOQ, 1.5× LOQ, and 2× LOQ spike levels, with RSDs that were typically lower than 5.1%. TheSPE-GC-MS method developed in this study was initially applied to research coumarins in cigarette samples; it proved to be accurate, sensitive, convenient, and practical.


2009 ◽  
Vol 32 (17) ◽  
pp. 3020-3028 ◽  
Author(s):  
Michela Sturini ◽  
Andrea Speltini ◽  
Luca Pretali ◽  
Elisa Fasani ◽  
Antonella Profumo

RSC Advances ◽  
2014 ◽  
Vol 4 (63) ◽  
pp. 33497-33506 ◽  
Author(s):  
Mahdi Hashemi ◽  
Zohreh Taherimaslak

A new and sensitive method based on magnetic solid phase extraction (MSPE) with antibody-free modified magnetic nanoparticles (MMNPs) followed by high performance liquid chromatography with post-column derivatization and fluorescence detection (HPLC-PCD-FD) has been developed for the separation and determination of aflatoxin M1 (AFM1) in liquid milk.


2019 ◽  
Vol 95 (11) ◽  
pp. 1099-1104 ◽  
Author(s):  
I. V. Bragina ◽  
Natalia E. Fedorova ◽  
V. N. Volkova ◽  
O. E. Egorchenkova ◽  
L. P. Mukhina ◽  
...  

In the work there are considered results of the development of the multicomponent method of measurement of concentration of herbicides of various chemical nature under their joint presence in the water. There was justified the optimality of application of HPLC-DAD (the working wavelength of 240 nm) for the determination of levels of 10 active ingredients of herbicides of class of sulfonylurea (metsulfuron-methyl, nikosulfuron, sulfometuron-methyl, thifensulfuron-methyl, triflusulfuron-methyl), imidazolinone (imazapyr, imazethapyr), 2,6-Bis[(4,6-dimethoxy-2- pyrimidinyl)oxy]benzoic acid (bispyribac acid), triazol-pyrimidines (Penoxsulam), a benzoylpyrazole compound (Topramenzone). For the concentrating and cleaning of samples of water there were used cartridges for solid-phase extraction of Oasis HLB - the macro porous copolymer made on the basis of the balanced ratio of 2 monomers - lipophilic divinylbenzene and hydrophilic N-vinylpirrolidone. The range of the detected concentrations in water was volatile between 0.0005 and 0.005 mg/L, values of standard deviation vary in the range of 1.8-3.9%. Chlorine-containing acidic herbicides were analyzed by the method of GC-ECD and GC-MS (IE) after preliminary converting of compounds into flying derivatives with the use of diazomethane. Satisfactory extraction of substances from a water sample may be achieved by classical extraction in the system “liquid-liquid” with the application of Methyl tert-butyl ester. For cleaning of the derivatized sample there were used cartridges for solid-phase extraction on the basis of silica gel. The range of the determination of 9 active ingredients referring to classes of phenoxy-acetic acid (2,4- D, MCPA), pyridinecarboxylic (aminopyiralid, picloram, clopyralid), benzoic acids (dicamba), benzothiadiazinone (bentazone), biphenyl ester (acifluorfen) and a chloroacetamide (acetochlor) - 0.0001-0.001 mg/L, SD values vary in the range of 1.8-33%.


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