Polymeric ionic liquid sorbent coatings in thin film microextraction: Insight into sorbent selectivity for pesticides and cannabinoids.

Polymeric ionic liquid (PIL) sorbent coatings consisting of polymerizable cations and anions were employed as sorbent coatings in thin film microextraction (TFME) for the extraction of pesticides and cannabinoids. The blades consisted of a thin film of PIL sorbents chemically bonded to vinyltrimethoxysilane-functionalized nitinol sheets. The imidazolium- or ammonium-based PIL sorbents contained aromatic benzyl moieties as well as polar hydroxyl groups or aliphatic functional groups within the chemical structure of the IL monomer. The chemical structure of the IL crosslinkers of the PILs were kept constant across each sorbent, except for the anion, which consisted of either bis[(trifluoromethyl)sulfonyl]imide ([NTf2-]), p-styrenesulfonate ([SS-]), or 3-sulfopropyl acrylate ([SPA-]). Temperature, salt content, and methanol content were optimized as extraction conditions to maximize pesticide-cannabinoid selectivity using Doehlert design of experiments (DOE). Effects of these three factors on selectivity and extraction efficiency are discussed. The optimal extraction conditions consisting of sample temperature (31°C), sodium chloride (30% w/v), and methanol content (0.25% v/v) are compared to initial sorbent screening conditions at a sample temperature of 40°C, 15% (w/v) sodium chloride, and 2.5% (v/v) methanol content. PIL sorbent swelling behavior at different salt and methanol content conditions and its effect on extraction efficiency are hypothesized. Selectivity factors for the sorbents indicated that aromatic moieties within the IL monomer may enhance pesticide-cannabinoid selectivity under optimized conditions, but the extraction efficiency of pesticides that are known to coelute with cannabinoids in the chromatographic separation may be enhanced by employing sorbent coatings with [SPA-] anions.

Understanding the influence of polymeric ionic liquid sorbent coating substituents on cannabinoid and pesticide affinity in solid-phase microextraction.

To understand factors that drive pesticide-cannabinoid selectivity in solid-phase microextraction (SPME), eight new polymeric ionic liquid (PIL) sorbent coatings were designed and compared to four previously reported PIL sorbent coatings for the extraction of pesticides. The four PIL sorbent coatings consisted of either vinylimidazolium or vinylbenzylimidazolium ILs with long alkyl chain substituents (i.e., -C8H17 or -C12H25) and bis[(trifluoromethyl)sulfonyl]imide ([NTf2-]) anions, from which the eight new PIL sorbent coatings were adapted. Modifications to the chemical structure of IL monomers and crosslinkers included incorporation of polymerizable p-styrenesulfonate or 3-sulfopropyl acrylate anions, the addition of aromatic moieties, and/or the addition of polar functional groups (i.e., -OH or -O- groups). A total of ten commonly regulated pesticides and six cannabinoids were examined in this study. The effect of salt on the solubility of pesticides and cannabinoids in aqueous solutions was assessed by determining their extraction efficiencies in the presence of varied methanol content. Differences in their solubilities appear to play a dominant role in enhancing pesticide-cannabinoid selectivity. The selectivity, represented as the ratio of pesticide total peak areas to cannabinoid total peak areas, also exhibited a moderate correlation to the affinity of the sorbent coatings towards both the pesticides and the cannabinoids. A positive correlation was observed for the pesticides and a negative correlation was observed for the cannabinoids, suggesting that selectivity was driven by more than the presence of salt in the samples. The sorbent coatings' affinity towards each class of analytes were examined to determine specific interactions that might influence selectivity. The two main structural modifications increasing pesticide-cannabinoid selectivity included the absence of aromatic moieties and the addition of hydrogen bond donor functional groups. Extractions of simple aromatic molecules as probes were performed under similar extraction conditions as the cannabinoids and confirmed the influence of hydrogen bonding interactions on sorbent coating affinity.

Selective isolation of pesticides and cannabinoids using polymeric ionic liquid-based sorbent coatings in solid-phase microextraction coupled to high-performance liquid chromatography.

The high abundance of cannabinoids within cannabis samples presents an issue for pesticide testing as cannabinoids are often co-extracted with pesticides using various sample preparation techniques. Cannabinoids may also chromatographically co-elute with moderate polarity pesticides and inhibit the ionization of pesticides when using mass spectrometry. To circumvent these issues, we have developed a new approach to isolate commonly regulated pesticides and cannabinoids from aqueous samples using tunable, crosslinked imidazolium polymeric ionic liquid (PIL)-based sorbent coatings for direct immersion solid-phase microextraction (DI-SPME). The selectivity of four PIL sorbent coatings towards 20 pesticides and six cannabinoids, including cannabidiol and Δ9-THC, was investigated and compared against a commercial PDMS/DVB fiber. Extraction and desorption conditions, including salt content, extraction temperature, pH, extraction time, desorption solvent, and desorption time, were optimized using high-performance liquid chromatography (HPLC) with ultraviolet (UV) detection. Under optimized conditions, the PIL fiber consisting of 1-vinylbenzyl-3-octylimidazolium bis[(trifluoromethyl)sulfonyl]imide ([VBIMC8+][NTf2-]) and 1,12-di(3-vinylbenzylimidazolium)dodecane dibis[(trifluoromethyl)sulfonyl]imide ([(VBIM)2C122+]2[NTf2-]) sorbent coating provided the best selectivity towards pesticides compared to other PILs and the PDMS/DVB fibers and was able to reach limits of detection (LODs) as low as 1 µg/L. When compared to a previously reported PIL-based SPME HPLC-UV method for pesticide analysis, the amount of cannabinoids extracted from the sample was decreased 9-fold while a 4-fold enhancement in the extraction of pesticides was achieved. Additionally, the PIL-based SPME method was applied to samples containing environmentally-relevant concentrations of pesticides and cannabinoids to assess its feasibility for Cannabis quality control testing. Relative recoveries between 95% and 141% were obtained using the PIL sorbent coating while recoveries ranging from 50% to 114% were obtained using the PDMS/DVB fiber.

Comparing the extraction performance of cyclodextrin-containing supramolecular deep eutectic solvents versus conventional deep eutectic solvents by headspace single drop microextraction.

A headspace single drop microextraction (HS-SDME) method coupled with high performance liquid chromatography was developed to compare the extraction of eighteen aromatic organic pollutants from aqueous solutions using cyclodextrin-based supramolecular deep eutectic solvents (SUPRADESs) and alkylammonium halide-based conventional deep eutectic solvents (DESs). Different derivatives of beta-cyclodextrin (ß-CD) were employed as hydrogen bond acceptors (HBA) in SUPRADESs and the extraction performance investigated. SUPRADES comprised of the 20 wt% native ß-CD HBA provided the highest enrichment factors of analytes compared to SUPRADESs comprised of other derivatives of ß-CD (random methylated ß-cyclodextrin, heptakis(2,3,6-tri-O-methyl)-ß-cyclodextrin, and 2-hydroxypropyl ß-cyclodextrin). In addition, native ß-CD and its derivatives were dissolved in the neat DESs and their effect on the extraction of analytes examined. Dissolution of 20 wt% native ß-CD in the choline chloride ([Ch+][Cl-]):2Urea DES resulted in a significant increase in the extraction efficiencies of target analytes compared to the neat [Ch+][Cl-]:2Urea DES. Under optimum conditions, the extraction method required a solvent microdroplet of 6.5 µL, 1000 rpm stir rate, 30% (w/v) salt concentration, and a temperature of 40 °C. The tetrabutylammonium chloride: 2 lactic acid DES resulted in the highest enrichment factors while the [Ch+][Cl-]:2Urea DES had the lowest for most of the analytes among the evaluated solvents. The method provided limits of detection (LODs) down to 35 µg L-1. Furthermore, the developed method was applied for the analysis of spiked tap and lake water, where relative recoveries ranging from 83.7% ̶ 119.7% and relative standard deviations lower than 19.2% were achieved.

Quantification of the α2-6 Sialic Acid Linkage in Branched N-Glycan Structures with Capillary Nanogel Electrophoresis.

Sialylation and sialic acid linkage in N-glycans are markers of disease but are analytically challenging to quantify. A capillary electrophoresis method is reported that integrates a unique combination of enzymes and lectins to modify sialylated N-glycans in real time in the capillary so that N-glycan structures containing α2-6-linked sialic acid are easily separated, detected, and quantified. In this study, N-glycans were sequentially cleaved by enzymes at the head of the separation capillary so that the presence of α2-6-linked sialic acids corresponded to a shift in the analyte migration time in a manner that enabled interpretation of the N-glycan structure. Following injection, only afucosylated N-glycan structures were passed through enzyme zones that contained α2-3 sialidase, followed by ß1-3,4 galactosidase, which cleaved any terminal α2-3-linked sialic acid and underlying galactose yielding a terminal N-acetyl glucosamine. With this treatment complete, a third zone of α2-3,6,8 sialidase converted the remaining α2-6-linked sialic acid to terminal galactose. With these enzyme processing steps the α2-6-linked sialic acid residues on an N-glycan correlated directly to the number of terminal galactose residues that remained. The number of terminal galactose residues could be interpreted as a stepwise decrease in the migration time. Complex N-glycans from α-1-acid glycoprotein were analyzed using this approach, revealing that a limited number of α2-6-linked sialic acids were present with biantennary, triantennary, and tetraantennary N-glycans of α-1-acid glycoprotein generally containing 0 or 1 α2-6-linked sialic acid.