Amide Groups Research Articles

Discovery of a CB2 and 5-HT1A receptor dual agonist for the treatment of depression and anxiety

Cannabinoid CB2R agonists have gained considerable attention as potential novel therapies for psychiatric disorders due to their non-psychoactive nature, in contrast to CB1R agonists. In this study, we employed molecular docking to design and synthesize 23 derivatives of cannabidiol (CBD) with the aim of discovering potent CB2R agonists rather than CB2R antagonists or inverse agonists. Structure-activity relationship (SAR) investigations highlighted the critical importance of the amide group at the C-3′ site and the cycloalkyl group at the C-4′ site for CB2R activation. Interestingly, three CBD derivatives, namely 2o, 6g, and 6h, exhibited substantial partial agonistic activity towards the CB2 receptor, in contrast to the inverse agonistic property of CBD. Among these, 2o acted as a CB2R and 5-HT1AR dual agonist, albeit with some undesired antagonist activity for CB1R. It demonstrated significant CB2R partial agonism while maintaining a level of 5-HT1AR agonistic and CB1R antagonistic activity similar to CBD. Pharmacokinetic experiments confirmed that 2o possesses favorable pharmacokinetic properties. Behavioral studies further revealed that 2o elicits significant antidepressant-like and anxiolytic-like effects while maintaining a good safety profile.

Enhancing floc size and strength with a hybrid polymer of zinc oxide, acrylamide, and tannin in textile wastewater.

This study involved synthesising new hybrid polymers called ZOPAT, made up of zinc oxide, acrylamide, and tannin, using a blended technique. The effectiveness of ZOPAT in treating textile wastewater was then tested by measuring floc growth rate, flocculation index, strength factor, and recovery factor under optimised conditions. The study also identified the zeta potential, morphology, elemental composition, and functional groups of the polymers. Response surface methodology determines the optimal pH and ZOPAT dose, resulting in 93% colour, 80% chemical oxygen demand (COD), 100% turbidity, and suspended solids (SS) removal at pH 9.22 and 737 mg/L ZOPAT. The study found that ZOPAT was more effective than commercial Polyaluminium chloride in reducing colour and COD, producing larger and stronger flocs, and requiring a shorter coagulation time of 17.5 min. ZOPAT was also easy to homogenise and operate due to its one-unit dosing system. The study attributes the success of ZOPAT to the presence of Zn, N, and K, which create electrostatic attraction with opposite charged particles, and the formation of dye-particle-dye with amide, hydroxyl, and carboxyl groups in ZOPAT, which remove colour, turbidity, COD, and SS. Overall, the study concludes that ZOPAT has significant potential for textile wastewater treatment.

Tuning of the Anion Affinity and Selectivity of Tripyrromethane‐Based Receptors by Simple Structural Modification

AbstractTripyrromethane‐based tripodal compounds 1–3 were synthesized as anion receptors. It was revealed by 1H NMR spectroscopic analyses carried out in CDCl3 that tripyrromethane 1 with an ester group was capable of recognizing F−, Cl−, Br−, and H2PO4− with relatively high selectivity for F−. By contrast, receptor 2 having an additional hydrogen bond donor of an amide group binds F− and H2PO4− with much improved affinity relative to receptor 1. On the other hand, receptor 3 bearing formyl groups on its two pyrrole subunits showed markedly enhanced selectivity for F− presumably due to the increased acidity of the pyrrolic NHs and the resulting strengthened intermolecular hydrogen bonds. In addition, tripodal receptors 1–3 were found to bind H2PO4−, a tetrahedral oxyanion, more efficiently than 2‐dimensional macrocyclic calix[4]pyrrole 4.

Hydro thermal carbonization (HTC) of sewage sludge: process optimization through RSM and assessing its energy potential

Sewage sludge is a by-product of municipal wastewater treatment, and its production is increasing with population growth and urbanization. Hydrothermal carbonization (HTC) is a promising method for managing sewage sludge due to its applicability and cost-effectiveness. The HTC process produces hydrochar, a stabilized carbon material derived from sewage sludge. In this study, sewage sludge was subjected to HTC at optimized conditions of 200 °C and 6 h using the response surface methodology (RSM) statistical tool. The structural morphology of the hydrochar was analyzed using Scanning Electron Microscopy and Transmission Electron Microscopy, which revealed a fluffy and coarse surface with deeper fragments, indicating the presence of carbon microspheres. Fourier Transform Infrared (FTIR) spectra showed that the hydrochar retained similar functional groups as the original sewage sludge, such as hydroxyl, aliphatic methyl, amino, ketonic, amide, and ether groups, with minimal shifts and reductions in vibrational peaks. The higher heating value (HHV) of the sewage sludge increased from 16.24 to 19.41 MJ kg−1 after HTC, indicating energy densification with a factor of 1.07. However, when hydrochar was blended with coal, the HHV gradually decreased. Thermo-gravimetric analysis was performed to assess the co-combustion effectiveness, and it showed that a blend of 50% coal and 50% sewage sludge-derived hydrochar exhibited extended heat generation with minimal reduction in HHV compared to other blends, reaching a value of 23.16 MJ kg−1. These findings suggest that hydrochar produced from sewage sludge through HTC could serve as an alternative energy source in industries, reducing the reliance on coal. Furthermore, the combustion behavior of hydrochar was significantly altered after the HTC process, highlighting its potential for energy generation. By utilizing hydrochar, the industry can contribute to the sustainable management of sewage sludge while reducing greenhouse gas (GHG) emissions associated with coal combustion.

Hydrogen‐Bonded Organic Frameworks Based on Endless‐Stacked Amides for Iodine Capture and Detection

AbstractRecently, hydrogen‐bonded organic frameworks (HOFs) have emerged as a rapidly advancing class of porous materials with significant potential for applications in the absorption and detection of various chemicals. Here, the unique ability of amide groups to form endless‐stacking H‐bonds is implemented in the design of HOFs. Starting from benzene‐1,3,5‐tricarboxamide and amide‐containing tribenzocyclynes as foundational building blocks, a diverse range of HOFs featuring 1D, 2D, or 3D hydrogen‐bonded frameworks has been synthesized. Among those, all three porous HOFs, HOF_B‐Hex, HOF_T‐Pr and HOF_T‐Hex exhibited permanent porosity, thereby demonstrating the effectiveness of amide‐based HOFs strategy. Notably, HOF_T‐Hex stands out with a 42% pore volume and an impressive iodine capture efficiency of 6.4 g g−1. The iodine capture capacity is influenced not only by pore volume but also by the presence of accessible π‐electrons within the material (i.e., electrons not engaged in a π–π stacking interaction. Furthermore, some of these HOFs exhibited fluorescent responses to iodine positioning them as highly promising materials for both the capture and sensing of iodine.

Dielectric Analysis of Blended Polysulfone/Polyethylenimine Membrane Contactors for CO2 Capture.

Polysulfone membranes, used as contactors for CO2 capture, are blended with two different hyperbranched polyethyleneimines modified with benzoyl chloride (Additive 1) and phenyl isocyanate (Additive 2) in different percentages. Fourier-transformed infrared spectra evidence the presence of urea and amide groups, whereas the field emission scanning electron microscopy images show differences in the microstructure of the blended membranes. Dielectric spectra determine the motions of the side and backbone chains, which can facilitate the diffusion of CO2 . The spectra consist of six dielectric processes; three of them are due to the polysulfone (γPSf , βPSf , and αPSf ), whereas the rest are characteristic of the additive (γHPEI , βHPEI , and αHPEI ). The benzoyl chloride and phenyl isocyanate functional groups introduce variations in molecular mobility and modify the relaxations associated with the hyperbranched polyethyleneimine (HPEI). The additives also increase the conductivity of the blended membranes, which can compromise the performance of the membranes, specifically in the case of Additive 1. Ion hopping is found to be the prevailing charge transport mechanism while both relaxations, αHPEI and αPSf , are actives. These results, together with the final morphology of the membranes, may explain the greater absorption capacity of the membranes prepared with the hyperbranched polyethyleneimine modified with Additive 2.

A Small Change in Structure, a Big Change in Flexibility.

Studies of the rotational barrier energy of the amide bond using quantum computing and nuclear magnetic resonance (NMR) are focused mainly on its use as a model of the peptide bond. The results of these studies are valuable not only in terms of the fundamental conformational properties of amide bonds, but also in the design of molecular machines, which have recently attracted interest. We investigate the fluxionality of the amide and enamide bonds of compound 3-[(E)-(dimethylamino)methylidene]-1,1-dimethylurea using advanced dynamic NMR experiments and a theoretical evaluation of the density functional theory (DFT) calculation. The dynamic NMR study shows restricted rotation around the amide group (16.4 kcal/mol) and a very high barrier around the enamine group (18.6 kcal/mol). In a structurally similar compound, (E)-3-(dimethylamino)-N,N-dimethylacrylamide (N atom is replaced by CH), the amide barrier is 12.4 kcal/mol and the enamine barrier is 11.7 kcal/mol. The DFT studies of both compounds reveal the electronic origin of this phenomenon. Theoretical calculations reveal the origin of the higher enamine barrier. The better delocalization of the lone pair of electrons on the end nitrogen atom into the antibonding orbital of the neighboring C-N double bond leads to the better stabilization of the ground state, and this leads to a greater increase in the enamine barrier.

Application of autochthonous extremophilic Bacillus xiamenensis in remediation of groundwater- A sorption-based metal cleaning approach

Surface water and groundwater used for drinking and agricultural purposes are contaminated due to anthropogenic and geogenic activities. Escalated metal concentrations, xenobiotic pollutants, competitive ions, and reusability issues are main hindrances towards decontamination of water. Moreover, the expensive purification technology brings obstacles to the underdeveloped community from availing clean water. In this context, the present work offers a sustainable cost-effective approach by providing an effective and sustainable sorption-based purification method by novel polyextremophilic bacteria Bacillus xiamenensis ISIGRM16 isolated from metal-rich industrial waste, red mud. Batch adsorption study revealed that the bacterium can remove Cd2+(>99%), Ni2+(>85%), and Cr6+(>40%) from aqueous solution. The optimum parametric conditions for the removal of Cd2+ and Ni2+ were observed at a temperature of 30 °C and a pH of 6, while for Cr6+ removal, the optimal conditions were a temperature of 45 °C and a pH of 2. The adsorption process of Cd2+ was best explained by Freundlich isotherm (R2 ≥ 0.95), revealing multilayer adsorption. Ni2+ and Cr6+ followed the Langmuir isotherm, indicated adsorption onto the monolayer surface. The interaction mechanism was determined to be following 2nd order kinetics, with both exothermic (Cd2+, Ni2+) and endothermic (Cr6+) characteristics. The maximum adsorption capacities were found to be 31.42, 29.30, and 15.21 mg g−1 for Cd2+, Ni2+, and Cr6+ respectively. In the ternary system, the adsorption capacity followed the order Ni2+ > Cd2+ > Cr6+, as confirmed by both their relative adsorption capacity and from analysis visual MINTEQ. Microscopic and spectroscopic analyses revealed, altered cell morphology, metal deposition on the bacterial cell surface, and the involvement of hydroxyl, carboxyl, and amide groups in the elimination of Cd2+, Ni2+, and Cr6+. Further the sequential adsorption-desorption study confirmed a significantly preserved removal efficacy (p < 0.05), indicating the advantageous use of the bacterium as a biosorbent.

Towards nanomaterials with tubular pores: synthesis and self-assembly of bis-pillar[5]arene

Recently, materials obtained using supramolecular chemistry approaches, and, in particular, spatially preorganized macrocyclic compounds, have attracted close attention of the researchers. Pillar[n]arenes are of special interest due to their tubular spatial structure and macrocyclic cavity. A similar tubular structure is retained in the supramolecular packaging of pillar[5]arene crystals, forming pores. In this study, we developed a block synthetic approach for the preparation of bis-pillar[5]arene containing amide groups. The ability of the synthesized bis-pillar[5]arene to form stable self-associates in solvents of different polarity (CHCl3 and CH3OH) was demonstrated by the DLS method. In trichloromethane at concentration of 1·10–3 M, monodisperse associates with average hydrodynamic diameter of 227 nm (PDI = 0.28) are formed; in methanol, stable associates (1·10–6 M) have an average hydrodynamic diameter of 136 nm (PDI = 0.21). The results obtained can be used to create new supramolecular systems, molecular machines, or capture and detect various organic molecules.

Combined spectroscopic and quantum chemical study to explore the effect of hydrogen bonding in hydrochlorothiazide-nicotinamide cocrystal

The present work focuses on the study of structural, vibrational, chemical properties and the effect of hydrogen bonding interaction in the formation of a cocrystal of hydrochlorothiazide (HCTZ, a diuretic drug) with nicotinamide (NCT) using vibrational spectroscopy (FT-IR and FT-Raman) and density functional theory. HCTZ being a BCS class IV drug, has low permeability and solubility; therefore, its cocrystal is studied. Monomer, dimer and trimer of HCTZ-NCT cocrystal were studied to understand hydrogen bonding interactions. The shifting in the wavenumber and the elongation in bond lengths of the amide (NH2) group of HCTZ and carbonyl (C = O) group of NCT were observed in all the models of HCTZ-NCT cocrystal due to the hydrogen bonding interaction. The importance of hydrogen bonding were also explored by natural bond orbital (NBO) analysis in support of the quantum theory of atom in molecules (QTAIM). The chemical reactivity of HCTZ, NCT and HCTZ-NCT cocrystal was examined by MEPS map, FMOs, global electronic reactivity descriptor, ECT descriptors, and molar refractivity. The lesser value of the HOMO-LUMO energy gap in the cocrystal than API reflects that the chemical reactivity of the cocrystal was better than API itself. The comparison between API(HCTZ) and cocrystal (HCTZ-NCT) implies that pharmaceutical cocrystals may be a better option to improve and enhance the pharmacological properties of drugs.

Protolytic Equilibrium of Glycine and Glycylglycine: Structure of Ionic Forms and Solvent Effect on the Thermodynamic Parameters of Processes

Quantum-chemical calculations of the structure of the molecular forms of glycine and glycylglycine and conjugate ionic forms have been performed. Our own and published data on the thermodynamic characteristics of the reactions of acid–base interactions of glycine and glycylglycine in aqueous organic solutions are summarized, and the influence of the composition of mixed solvents on the acid dissociation constant of the amide group in the copper(II) peptide complex is considered.

Fabrication of self-assembly iguratimod prodrug into polymeric nanoparticles delivery for the care of breast cancer therapy

Based on occurrence, death and prevalence in 2019, GLOBOCAN reports 36 forms of cancer in 185 countries. At the moment, chemotherapy is the furthermost commonly utilized cancer management by resistant systems, gene and hormone therapeutics. Herein, we define a precise straightforward and cost-effective method that therapeutically incorporates drug reconstruction, macromolecular nano-assembled and specific tumor targeting to overcome the various experiments modelled via the distribution of the potential anticancer Iguratimod (IGU) drug. The IGU drugs were empowered to instinctually assembly into admirable, stable nanoparticles on the conjugations covalent interactions of hydrophobic linoleic acid bonded with an amide group of ∼100 nm. Various microscopic methods have proven synthesized IGU-NP morphology. Following effective fabrication, the IGU and IGU-NP anti-cancer properties of MCF-7 (breast carcinoma) and 4T1 (breast carcinoma) cell lines were assessed. Additional studies include AO-EB (acridine bromide orange ethidium), nuclear staining. In contrast with IGU, the IGU-NPs showed excellent cytocompatibility, this investigation explained that IGU-NPs are a healthy and encouraging solution in breast cancer chemotherapy and are worthy of further clinical assessment.

Umpolung Isomerization in Radical Copolymerization of Benzyl Vinyl Ether with Pentafluorophenylacrylate Leading to Degradable AAB Periodic Copolymers

AbstractThis study revealed that benzyl vinyl ether (BnVE) shows a peculiar isomerization propagation in its radical copolymerization with an electron‐deficient acrylate carrying a pentafluorophenyl group (PFA). The co‐monomer pair inherently exhibits the cross‐over propagation feature due to the large difference in the electron density. However, the radical species of PFA was found to undergo a backward isomerization to the penultimate BnVE pendant giving a benzyl radical species prior to propagation with BnVE. The isomerization brings a drastic change in the character of the growing radical species from electrophilic to nucleophilic, and thus the isomerized benzyl radial species propagates with PFA. Consequently, the two monomers were consumed in the order AAB (A: PFA; B: BnVE) and the unique periodic consumption was confirmed by the pseudo‐reactivity ratios calculated by the penultimate model: r11=0.174 and r21=6600 for PFA (M1) with BnVE (M2). The pentafluorophenyl ester groups of the resulting copolymers are transformed into ester and amide groups by post‐polymerization alcoholysis and aminolysis modifications. The unique isomerization in the AAB sequence allowed the periodic introduction of a benzyl ether structure in the backbone leading to efficient degradation under acid conditions.

Umpolung Isomerization in Radical Copolymerization of Benzyl Vinyl Ether with Pentafluorophenylacrylate Leading to Degradable AAB Periodic Copolymers.

This study revealed that benzyl vinyl ether (BnVE) shows a peculiar isomerization propagation in its radical copolymerization with an electron-deficient acrylate carrying a pentafluorophenyl group (PFA). The co-monomer pair inherently exhibits the cross-over propagation feature due to the large difference in the electron density. However, the radical species of PFA was found to undergo a backward isomerization to the penultimate BnVE pendant giving a benzyl radical species prior to propagation with BnVE. The isomerization brings a drastic change in the character of the growing radical species from electrophilic to nucleophilic, and thus the isomerized benzyl radial species propagates with PFA. Consequently, the two monomers were consumed in the order AAB (A: PFA; B: BnVE) and the unique periodic consumption was confirmed by the pseudo-reactivity ratios calculated by the penultimate model: r11 =0.174 and r21 =6600 for PFA (M1 ) with BnVE (M2 ). The pentafluorophenyl ester groups of the resulting copolymers are transformed into ester and amide groups by post-polymerization alcoholysis and aminolysis modifications. The unique isomerization in the AAB sequence allowed the periodic introduction of a benzyl ether structure in the backbone leading to efficient degradation under acid conditions.

One-Dimensionally Arranged Quantum-Dot Superstructures Guided by a Supramolecular Polymer Template.

Colloidal quantum dots (QDs) exhibit important photophysical properties, such as long-range energy diffusion, miniband formation, and collective photoluminescence, when aggregated into well-defined superstructures, such as three-dimensional (3D) and two-dimensional (2D) superlattices. However, the construction of one-dimensional (1D) QD superstructures, which have a simpler arrangement, is challenging; therefore, the photophysical properties of 1D-arranged QDs have not been studied previously. Herein, we report a versatile strategy to obtain 1D-arranged QDs using a supramolecular polymer (SP) template. The SP is composed of self-assembling cholesterol derivatives containing two amide groups for hydrogen bonding and a carboxyl group as an adhesion moiety on the QDs. Upon mixing the SP and dispersed QDs in low-polarity solvents, the QDs self-adhered to the SP and self-arranged into 1D superstructures through van der Waals interactions between the surface organic ligands of the QDs, as confirmed by transmission electron microscopy. Furthermore, we revealed efficient photoinduced fluorescence resonance energy transfer between the 1D-arranged QDs by an in-depth analysis of the emission spectra and decay curves.

One‐Dimensionally Arranged Quantum‐Dot Superstructures Guided by a Supramolecular Polymer Template

AbstractColloidal quantum dots (QDs) exhibit important photophysical properties, such as long‐range energy diffusion, miniband formation, and collective photoluminescence, when aggregated into well‐defined superstructures, such as three‐dimensional (3D) and two‐dimensional (2D) superlattices. However, the construction of one‐dimensional (1D) QD superstructures, which have a simpler arrangement, is challenging; therefore, the photophysical properties of 1D‐arranged QDs have not been studied previously. Herein, we report a versatile strategy to obtain 1D‐arranged QDs using a supramolecular polymer (SP) template. The SP is composed of self‐assembling cholesterol derivatives containing two amide groups for hydrogen bonding and a carboxyl group as an adhesion moiety on the QDs. Upon mixing the SP and dispersed QDs in low‐polarity solvents, the QDs self‐adhered to the SP and self‐arranged into 1D superstructures through van der Waals interactions between the surface organic ligands of the QDs, as confirmed by transmission electron microscopy. Furthermore, we revealed efficient photoinduced fluorescence resonance energy transfer between the 1D‐arranged QDs by an in‐depth analysis of the emission spectra and decay curves.

A Monoanionic Pincer Ligand with Pendant Phosphazene Arms: Stabilization of Main‐Group and Transition Metal Complexes

AbstractAn unprecedented anionic pincer ligand with pendant phosphazene arms [2,6‐(MesN=PPh2)2C5H4N]− (LH) has been synthesized through a facile reaction of a bis(iminophosphoranyl)‐pyridine ligand with K‐selectride. LH can stabilize main‐group and transition metal complexes LHGeCl, LHSnCl, LHZnCl, and LHCdI. X‐ray diffraction analysis and theoretical study show that the phosphazene arms of LH strongly coordinate to the metal centers, while the central amide group alternatively donates one or two pairs of electrons to bind with different metal centers.

Comparative study of the structure and mechanical properties of starch aerogels fabricated from air-classified and isolated pulse starches

Significant amounts of starch and protein are generated as co-products during fractionation of pulse seeds. While pulse proteins (PP) have garnered a lot of interest in numerous applications, little attention is shown to pulse starch (PS). The creation of novel materials such as bioplastics could revolutionize the use of pulse starches. In this study, we investigated the prospects of air-classified and isolated pea, lentil, and faba bean starches as a precursor for fabricating pulse starch bioaerogels (PSBs) via freeze-drying technique. The results evidenced ultra-low densities (<0.1 m2/g), mesopore sizes (2−50 μm), high porosities (∼99 %), low surface areas (SBET = ∼4−18 m2/g) for all the aerogels. The adsorption isotherm showed typical Type II and III profiles, while the thermogravimetric analysis showed more weight loss (74.39−78.12 %) in aerogels mostly developed from isolated starches. Microstructural studies showed a unique distribution of pores within the developed aerogels. FTIR and XPS studies confirmed the presence of an amide (I, II, III) at different absorption bands range (∼1600–1200 cm−1) and functional groups (carboxylic group and the amide group), respectively. All the PSBs became stiffer with a corresponding increase in load, and a reversible deformation in the linear region was identified at <5 % strain. Comparatively, saturated PSBs from air-classified starch at a relative humidity of 95 % showed a drastic reduction in their compressive moduli (CM), while PSBs from isolated starch experienced markedly high CM. Moisture saturation was achieved at 72 h for all the samples. This study provides crucial information that could spark a keen interest in the use of non-conventional starch for the creation of novel and sustainable biobased products with expanded applications.

Highly Stable Amide-Functionalized Zirconium-Organic Frameworks: Synthesis, Structure, and Methane Storage Capacity.

With the development of crystalline porous materials toward methane storage, the stability issue of metal-organic framework (MOF) materials has caused great concern despite high working capacity. Considering the high stability of zirconium-based MOFs and effective functions of amide groups toward gas adsorption, herein, a series of UiO-66 type of Zr-MOFs, namely, Zr-fcu-H/F/CH3/OH, were successfully designed and synthesized by virtue of amide-functionalized dicarboxylate ligands bearing distinct side groups (i.e., -H, -F, -CH3, and -OH) and ZrCl4 in the presence of trifluoroacetic acid as the modulator. Single-crystal X-ray diffraction and topology analyses reveal that these compounds are archetypal fcu MOFs encompassing octahedral and tetrahedral cages, respectively. The N2 sorption isotherms and acid-base stability tests demonstrate that the materials possess not only relatively high surface areas, pore volumes, and appropriate pore sizes but also great hydrolytic stabilities ranging pH = 3-11. Furthermore, the volumetric methane storage working capacities of Zr-fcu-H, Zr-fcu-F, Zr-fcu-CH3, and Zr-fcu-OH at 298/273 K and 80 bar are 187/217, 175/193, 167/187, and 154/171 cm3 (STP) cm-3, respectively, which indicate that the zirconium-based crystalline porous materials are capable of storing relatively high amounts of methane.

A chitin-based magnetic hyper-cross-linked polymer for highly efficient enrichment of neonicotinoids in lemon juice and tomatoes

A chitin-based magnetic hyper-cross-linked polymer (labeled as Ch-MHCP) has been successfully synthesized and utilized for highly-effective solid-phase extraction of neonicotinoid insecticides (NEOs). The extraction capability of Ch-MHCP for four common NEOs is higher than that of four commercial sorbents including octadecyl-silane C18, oasis hydrophilic/lipophilic balanced sorbent, oasis mixed anion sorbent and poly-phenylacetic mixed anion sorbent. The large number of hydroxyl and amide groups as well as benzene rings in Ch-MHCP allow the H-bond and π-π* interaction to be the principal adsorption mechanism of Ch-MHCP for NEOs. Besides, polar interaction was also involved in the adsorption process. In combination of Ch-MHCP based extraction technique with high-performance liquid chromatography, a novel analytical method for sensitive detection of NEOs in lemon juice and tomatoes has been established. At optimal conditions, wide linear ranges were obtained to be 0.20–100 ng mL−1 for lemon juice and 0.80–1000 ng g−1 for tomatoes. The detection limits were 0.06–0.12 ng mL−1 for lemon juice and 0.24–0.60 ng g−1 for tomatoes. This work not only provides a powerful tool for simultaneously detecting four NEOs in lemon juice and tomatoes, but also offers a new insight into the preparation of bio-based magnetic sorbents for adsorption/removal of pollutants.