scholarly journals Atrazine and 2, 4-D determination in corn samples using microwave assisted extraction and on-line solid-phase extraction coupled to liquid chromatography.

2018 ◽  
Vol 62 (2) ◽  
Author(s):  
Ana Susana Santos-Hernández ◽  
Laura Hinojosa-Reyes ◽  
Isabel del Carmen Sáenz-Tavera ◽  
Aracely Hernández-Ramírez ◽  
Jorge Luis Guzmán-Mar

<p>On-line sample pretreatment (clean-up and analyte preconcentration) was coupled to sequential injection chromatography for the determination of 2, 4-D (2,4-dichlorophenoxyacetic acid) and atrazine in corn samples. Prior to their analysis, microwave-assisted approach was evaluated and optimized for the extraction of 2,4-D and atrazine in corn samples. Extraction was carried out using MeOH:water (30:70 v/v) solvent at 50°C for 15 min. The on-line SPE-HPLC/UV approach combined reversed solid-phase extraction using strata X sorbent with MeOH:H<sub>2</sub>O (80:20 v/v) at 1 mL min<sup>-1</sup> as eluent for the enrichment of the analytes. C18 monolithic column with acetonitrile:10 mM acetate buffer pH 4 (20:80, v/v) was employed as mobile phase at 2 mL min<sup>-1</sup> flow rate for separation of the compounds before UV detection. Enrichment factors up to 13.4 were achieved with a 10 mL sample volume. The developed procedure showed linear response ranges from 0.07–0.70 mg kg<sup>−1 </sup>for 2,4-D and atrazine with correlation coefficients &gt;0.993. The LODs were 0.03 and 0.02 mg kg<sup>-1 </sup>for 2,4-D and atrazine, respectively with RSD ranged from 4.0 to 7.2 % at 0.07 and 0.30 mg kg<sup>-1</sup>. The recoveries of 2,4-D and atrazine in corn samples were from 82.6 and 98.2%. The proposed method showed good recoveries and reasonable precision for herbicide analysis in corn samples avoiding the time-consuming batch sample pretreatment step, thus minimizing risks of sample contamination and analyte losses.</p>

2011 ◽  
Vol 415-417 ◽  
pp. 1799-1805 ◽  
Author(s):  
Qing Sun ◽  
Zhi Xiang Xu ◽  
Li Min Zhang ◽  
Lei Xu ◽  
Jie Zhou

Solid phase extraction (SPE) is a sample pretreatment technique which is increasingly popular and widely used. However, most of the traditional SPE material has poor selectivity. Molecular imprinting is an emerging technology for the preparation of functionalized materials with molecular recognition ability. Using the imprinted polymers as new sorbent, a molecularly imprinted on-line solid phase extraction coupled with chromatography or other techniques has become one of the most interesting applications of MIP, which has not only the extraction efficiency of SPE but also the high selectivity of imprinted polymers. This paper focuses on the recent states, advantages and outlooks of molecularly imprinted on-line solid phase extraction in sample pretreatment. This mini review may promote the extensive application of MIP in food safety.


2015 ◽  
Vol 7 (4) ◽  
pp. 1563-1571 ◽  
Author(s):  
Yun-Kai Lv ◽  
Zhi-Yong Guo ◽  
Jin-Zhi Wang ◽  
Meng-Meng Guo ◽  
Lin-Kang Yu ◽  
...  

A novel RAM–HMC with superior enrichment and clean-up efficiency was prepared by an in situ method in a stainless-steel column, and used as a pre-column for on-line solid-phase extraction of sulfonamides residues from honey.


2001 ◽  
Vol 84 (5) ◽  
pp. 1383-1392 ◽  
Author(s):  
Maria Careri ◽  
Lisa Elviri ◽  
Alessandro Mangia

Abstract Alkylphenols are nonbiodegradable metabolites arising from various pathways of aerobic and anaerobic degradation of the nonionic surfactants alkylphenol ethoxylates. A method based on the use of on-line solid-phase extraction (SPE) and liquid chromatography (LC) with UV detection was developed to determine bisphenol A, octylphenol, and nonylphenol at trace levels in water. The on-line coupled SPE procedure automatically enables an approximately 300-fold preconcentration of analytes, which can be further enhanced by an increase in applied sample volume. By using C18 cartridges, recoveries of &gt;90% were obtained for all the analytes. A validation procedure was carried out with a groundwater sample to ensure the quality of the results; performance criteria such as detection limits (LODs), quantitation limits (LOQs), linearity, and precision were evaluated. LODs and LOQs in the range of 0.17–0.36 and 0.35–1.88 μg/L, respectively, were found; for all the analytes, linearity was established over 2 orders of magnitude (r2 &gt;0.997, n = 54). The intraday repeatability values expressed as relative standard deviations were &lt;5.3%; a nested analysis of variance was performed to verify the influence of 3 different factors, i.e., different days, extraction procedure, and LC replicate injection, on data precision.


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