Kumuthini Chandrasekaram

Honey is part and parcel of our daily nutrition, but in recent times it has been reported to be tainted by the presence of polar substituted phenols purported from the use of pesticides, herbicides, antimicrobial agents, etc. Honey’s viscous nature and matrix complexity often result in analytical chemists resorting to derivatization for the detection of polar analytes such as substituted phenols. This study aims to overcome the matrix effect without derivatization and offer a more sustainable solution with notable sensitivity and selectivity using dispersive membrane microextraction alongside high-performance liquid chromatography (DMME–HPLC) with sporopollenin–methylimidazolium-based mixed matrix membrane (Sp–MIM-MMM). The DMME–HPLC approach successfully determined the presence of mono- and disubstituted phenols from unspiked honey samples with concentrations ranging from 7.8 to 154.7 ng/mL. The sustainability of the proposed method was also validated using the Analytical Eco-Scale (AES) and the Analytical GREEnness Metric (AGREE) where an excellent score of 94 and the encouraging score of 0.72 were recorded, respectively.

Aromatic amines found in tobacco smoke are carcinogenic to humans. There are no doubts that they cause of cancers in the lungs, bladder, kidneys, pancreas, esophagus, larynx, pharynx, and oral cavities associated with public health. Therefore, monitoring, control, and awareness toward the smoking effects are important subjects to be conveyed. Thus, rapid, sensitive, simple and accurate analytical methods for the identification of aromatic amines and their metabolites are required to provide a clear and complete visualization for the occurrence of aromatic amines by investigating the urine of smokers and nonsmokers. This comprehensive review serves to give an overview of the previous and recent studies about the analytical trends for the determination of urinary aromatic amines. This review covers the sampling methodologies and sample preparation techniques such as solvent extraction, solid phase extraction, magnetic solid phase extraction, and solid phase microextraction couple with different separation methods including gas chromatography and liquid chromatography. To add more value to this review paper, the advantages, disadvantages, challenges, and the future prospects of these methods are discussed as well. This review is hopefully beneficial for researchers to access and monitor the level of potentially carcinogenic aromatic amines in human urine.

This study focuses on the synthesis and characterization of the inclusion complex of β-Cyclodextrin (β-CD) with dicationic ionic liquid, 3,3'-(1,4-Phenylenebis [methylene]) bis(1-methyl-1H-imidazol-3-ium) di(bromide) (PhenmimBr). The inclusion complex was prepared at room temperature utilizing conventional kneading technique. Proton (¹H) NMR and 2D (¹H–¹H) COSY NMR were the primary characterization tools employed to verify the formation of the inclusion complex. COSY spectra showed strong correlations between protons of imidazolium and protons of β-CD which indicates that the imidazolium ring of PhenmimBr has entered the cavity of β-CD. UV absorption indicated that β-CD reacts with PhenmimBr to form a 2:1 β-CD-PhenmimBr complex with an apparent formation constant of 2.61 × 10⁵ mol⁻² L². Other characterization studies such as UV, FT-IR, XRD, TGA, DSC and SEM studies were also used to further support the formation of the β-CD-PhenmimBr inclusion complex.

In the solid form of the title imidazolium-based ionic liquid salt, C(18)H(24)N(4) (2+)·2CF(3)SO(3) (-), the complete cation is generated by a crystallographic inversion centre. The five-membered imidazole ring is approximately perpendicular to the six-membered phenyl-ene ring [dihedral angle = 85.11 (11)°]. In the crystal, the components are linked by C-H⋯O interactions.