Determination of trace levels of triazines in corn matrices by bar adsorptive microextraction with a molecularly imprinted polymer.

This manuscript addresses the determination of triazines (ametryn, atrazine, simazine, and terbutryn) in corn matrices using bar adsorptive microextraction coated with a selective molecularly imprinted polymer phase following microliquid desorption and high-performance liquid chromatography with diode array detection. The molecularly imprinted polymer was synthesized using atrazine as a template and methacrylic acid as a functional monomer. Assays performed in 25 mL of ultrapure water samples spiked at 8.0 µg/L yielded 80-120 % recoveries under the evaluated experimental conditions. The method showed an accuracy (0.2 < bias < 17.9%), precision (relative standard deviation <17.4%), convenient detection (0.2 µg/L), and quantification (0.7 µg/L) limits, as well as linear dynamic ranges (0.8-24.0 µg/L) with remarkable determination coefficients (R(2) > 0.9926). The proposed analytical method was applied to monitor triazines in three types of corn matrices using the standard addition methodology. Experiments performed in corn samples spiked with triazines at the trace level (8.0 µg/kg of each analyte) gave rise to recoveries (81.0-119.4%) with good reproducibility and robustness. The proposed methodology is also easy to implement and showed to be a good analytical alternative to monitor triazines in complex matrices, when compared with other sorption-based microextraction techniques.

Biological Activities and Chemical Composition of Methanolic Extracts of Selected Autochthonous Microalgae Strains from the Red Sea.

Four lipid-rich microalgal species from the Red Sea belonging to three different genera (Nannochloris, Picochlorum and Desmochloris), previously isolated as novel biodiesel feedstocks, were bioprospected for high-value, bioactive molecules. Methanol extracts were thus prepared from freeze-dried biomass and screened for different biological activities. Nannochloris sp. SBL1 and Desmochloris sp. SBL3 had the highest radical scavenging activity against 1,1-diphenyl-2-picrylhydrazyl, and the best copper and iron chelating activities. All species had potent butyrylcholinesterase inhibitory activity (>50%) and mildly inhibited tyrosinase. Picochlorum sp. SBL2 and Nannochloris sp. SBL4 extracts significantly reduced the viability of tumoral (HepG2 and HeLa) cells with lower toxicity against the non-tumoral murine stromal (S17) cells. Nannochloris sp. SBL1 significantly reduced the viability of Leishmania infantum down to 62% (250 µg/mL). Picochlorum sp. SBL2 had the highest total phenolic content, the major phenolic compounds identified being salicylic, coumaric and gallic acids. Neoxanthin, violaxanthin, zeaxanthin, lutein and ß-carotene were identified in the extracts of all strains, while canthaxanthin was only identified in Picochlorum sp. SBL2. Taken together, these results strongly suggest that the microalgae included in this work could be used as sources of added-value products that could be used to upgrade the final biomass value.

First report of the in vitro antileishmanial properties of extremophile plants from the Algarve Coast.

This work reports for the first time the in vitro anti Leishmania infantum activity of acetone and dichloromethane (DCM) extracts from 25 extremophile plants from Southern Portugal. DCM extracts from Inula chritmoides and Spergularia rubra were active against axenic promastigotes and intracellular amastigotes, had anti-inflammatory properties on lipopolysaccharide (LPS)-stimulated macrophages, inhibited acetylcholinesterase and had no haemolytic activity on human erythrocytes. Eleven phenolics were identified by high-performance liquid chromatography with diode-array detection (HPLC-DAD) in I. crithmoides and one phenolic in S. rubra. Isolation and identification of the active molecules is in progress.

Determination of Trace Levels of Irgarol in Estuarine Water Matrices by Bar Adsorptive Microextraction.

Bar adsorptive microextraction (BAµE), using selective sorbent phases, followed by liquid desorption in combination with large volume injection-gas chromatography coupled to mass spectrometry (BAµE-LD/LVI-GC-MS), is proposed for the determination of trace levels of irgarol in estuarine water matrices. While we compared several polymers and activated carbons, one of the latter coatings showed much higher selectivity through BAµE. Assays performed on 25 mL of ultra-pure water sample fortified at 0.6 µg/L levels of irgarol yielded recoveries of 74.5 ± 8.6%, under optimized experimental conditions. The proposed analytical procedure showed convenient detection limits (16.0 ng/L) and good linear dynamic range (0.2-16.0 µg/L), with determination coefficients of 0.9982. Good precision was also achieved with RSD lower than 12.0%. The application of the present analytical approach on estuarine water samples by using the standard addition methodology revealed good sensitivity and linearity. The proposed methodology, using nanostructured sorbents and operating under the floating sampling technology, proved to be a suitable analytical alternative to monitor irgarol in estuarine water matrices. Moreover, it is easy to implement, reliable, sensitive, require low sample volume and have the possibility to choose the most selective sorbent coating according to the target compound involved.