scholarly journals Automatic solid-phase extraction by programmable flow injection coupled to chromatographic fluorimetric determination of fluoroquinolones

2018 ◽  
Vol 10 (18) ◽  
pp. 2180-2186 ◽  
Author(s):  
Patricia S. Peixoto ◽  
Eduarda M. P. Silva ◽  
Marcelo V. Osório ◽  
Luisa Barreiros ◽  
José L. F. C. Lima ◽  
...  

Automatic sample preparation targeting preconcentration of fluoroquinolones present in environmental waters.

2019 ◽  
Vol 15 (7) ◽  
pp. 788-800 ◽  
Author(s):  
Natasa P. Kalogiouri ◽  
Victoria F. Samanidou

Background:The sample preparation is the most crucial step in the analytical method development. Taking this into account, it is easily understood why the domain of sample preparation prior to detection is rapidly developing. Following the modern trends towards the automation, miniaturization, simplification and minimization of organic solvents and sample volumes, green microextraction techniques witness rapid growth in the field of food quality and safety. In a globalized market, it is essential to face the consumers need and develop analytical methods that guarantee the quality of food products and beverages. The strive for the accurate determination of organic hazards in a famous and appreciated alcoholic beverage like wine has necessitated the development of microextraction techniques.Objective:The objective of this review is to summarize all the recent microextraction methodologies, including solid phase extraction (SPE), solid phase microextraction (SPME), liquid-phase microextraction (LPME), dispersive liquid-liquid microextraction (DLLME), stir bar sorptive extraction (SBSE), matrix solid-phase dispersion (MSPD), single-drop microextraction (SDME) and dispersive solid phase extraction (DSPE) that were developed for the determination of hazardous organic compounds (pesticides, mycotoxins, colorants, biogenic amines, off-flavors) in wine. The analytical performance of the techniques is evaluated and their advantages and limitations are discussed.Conclusion:An extensive investigation of these techniques remains vital through the development of novel strategies and the implication of new materials that could upgrade the selectivity for the extraction of target analytes.


2008 ◽  
Vol 27 (1) ◽  
pp. 25 ◽  
Author(s):  
Aleksandra Nestorovska-Krsteska ◽  
Meri Mirčeska ◽  
Jean-Jacques Aaron ◽  
Zoran Zdravkovski

An HPLC-UVDAD method for determination of dimethoate, 2,4-dichlorophenoxy acetic acid (2,4-D), mecoprop (MCPP) and linuron in environmental waters was developed. The water samples were concentrated and extracted by a solid phase extraction (SPE) method on Bond Elut PPL cartridges. After extraction the investigated compounds were separated on Stability RP Pesticides chromatographic column using mobile phase composed of acetonitrile- water-acetic acid in volume fractions of 39:59:2 and flow rate of 0.7 mL/min. Ultraviolet absorption detection was carried out for dimethoate, 2,4-D and MCPP at 229 nm, and for linuron at 249 nm. Recoveries made from 500 mL of drinking waters using solid phase extraction ranged between 64.3–92.1 %. The method was applied to environmental waters in Macedonia that receive runoffs from agriculture lands. The levels of pesticides under study ranged between 0.31 μg/L and 7.05 μg/L, depending on the compound and sampling period.


Sign in / Sign up

Export Citation Format

Share Document