María Marina

The increasing demand for food to feed an exponentially growing population, the fast evolution of climate changes, how global warming affects soil productivity, and the erosion of arable lands, create enormous pressure on the food chain. This problem is particularly evident for fresh fruits and vegetables that have a short shelf life. For this reason, food safety precautions are not always a priority and they are often overused to increase the productivity and shelf life of these food commodities, causing concerns among consumers and public authorities. In this context, this review discusses the potential of microextraction in comparison to conventional extraction approaches as a strategy to improve the survey of food safety requirements. Accordingly, selected examples reported in the literature in the last five years will focus on the detection and quantification of pesticides, antibiotics, hormones, and preservatives in fresh fruits and vegetables using different extraction approaches. Overall, the use of microextraction techniques to survey the presence of contaminants in the food chain is very advantageous, involving simpler and faster protocols, reduced amounts of solvents and samples, and consequently, reduced waste produced during analysis while conserving a high potential for automation. Additionally, this higher greener profile of the microextraction techniques will boost a progressive substitution of conventional extraction approaches by microextraction processes in most analytical applications, including the survey of food chain safety.

The nano‐LC technique is increasingly used for both fast studies on enantiomeric analysis and test beds of novel stationary phases due to the small volumes involved and the short conditioning and analysis times. In this study, the enantioseparation of 10 drugs from different families was carried out by nano‐LC, utilizing silica with immobilized amylose tris(3‐chloro‐5‐methylphenylcarbamate) column. The effect on chiral separation caused by the addition of different salts to the mobile phase was evaluated. To simultaneously separate as many enantiomers as possible, the effect of buffer concentration in the mobile phase was studied, and, to increase the sensitivity, a liquid–liquid microextraction based on the use of isoamyl acetate as sustainable extraction solvent was applied to pre‐concentrate four chiral drugs from tap and environmental waters, achieving satisfactory recoveries (>70%).