Food contaminants: Impact of food processing, challenges and mitigation strategies for food security.

Food preparation involves the blending of various food ingredients to make more convenient processed food products. It is a long chain process, where each stage posing a risk of accumulating hazardous contaminants in these food systems. Protecting the public health from contaminated foods has become a demanding task in ensuring food safety. This review focused on the causes, types, and health risks of contaminants or hazardous chemicals during food processing. The impact of cooking such as frying, grilling, roasting, and baking, which may lead to the formation of hazardous by-products, including polycyclic aromatic hydrocarbons (PAHs), heterocyclic amines (HCAs), acrylamide, advanced glycation end products (AGEs), furan, acrolein, nitrosamines, 5-hydroxymethylfurfural (HMF) and trans-fatty acids (TFAs). Potential health risks such as carcinogenicity, genotoxicity, neurotoxicity, and cardiovascular effects are emerging as a major problem in the modern lifestyle era due to the increased uptakes of contaminants. Effects of curing, smoking, and fermentation of the meat products led to affect the sensory and nutritional characteristics of meat products. Selecting appropriate cooking methods include temperature, time and the consumption of the food are major key factors that should be considered to avoid the excess level intake of hazardous contaminants. Overall, this study underscores the importance of understanding the risks associated with food preparation methods, strategies for minimizing the formation of harmful compounds during food processing and highlights the need for healthy dietary choices to mitigate potential health hazards.

Unraveling the impact of nanopollution on plant metabolism and ecosystem dynamics.

Nanopollution (NPOs), a burgeoning consequence of the widespread use of nanoparticles (NPs) across diverse industrial and consumer domains, has emerged as a critical environmental issue. While extensive research has scrutinized the repercussions of NPs pollution on ecosystems and human health, scant attention has been directed towards unraveling its implications for plant life. This comprehensive review aims to bridge this gap by delving into the nuanced interplay between NPOs and plant metabolism, encompassing both primary and secondary processes. Our exploration encompasses an in-depth analysis of the intricate mechanisms governing the interaction between plants and NPs. This involves a thorough examination of how physicochemical properties such as size, shape, and surface characteristics influence the uptake and translocation of NPs within plant tissues. The impact of NPOs on primary metabolic processes, including photosynthesis, respiration, nutrient uptake, and water transport. Additionally, this study explored the multifaceted alterations in secondary metabolism, shedding light on the synthesis and modulation of secondary metabolites in response to NPs exposure. In assessing the consequences of NPOs for plant life, we scrutinize the potential implications for plant growth, development, and environmental interactions. The intricate relationships revealed in this review underscore the need for a holistic understanding of the plant-NPs dynamics. As NPs become increasingly prevalent in ecosystems, this investigation establishes a fundamental guide that underscores the importance of additional research to shape sustainable environmental management strategies and address the extensive effects of NPs on the development of plant life and environmental interactions.

Conservation linkages of endangered medicinal plant and exploration of phytochemicals, pharmaceutical screening and in silico validation against diabetics using in vivo wild and in vitro regenerated plant Boucerosia diffusa Wight.

Boucerosia diffusa Wight. is an important endangered medicinal plant belonging to the family Asclepiadaceae. In this study, an efficient protocol has been developed for B. diffusa using nodal explants for callus induction and direct organogenesis. The optimal callus induction (83.7%) was observed on 0.6 mg/L 2,4-dichlorophenoxyacetic acid (2,4-D) in Murashige and Skoog medium. The shoot regeneration was observed on different concentrations and combinations of 6-benzylaminopurine (BAP) and 2,4-D using shoot induction (88.5%) was observed on 0.5 mg/L BAP and 0.6 mg/L 2,4-D. Maximum root induction frequency (85.6%) was obtained on 0.6 mg/L α-naphthalene-acetic acid (NAA) and 0.5 mg/L BAP. The fully developed plants were acclimatized (98.86% survival rate) and transferred to natural photoperiod conditions. The phytochemical and pharmacological activity was determined in in vitro-regenerated plants (IRP) and was compared to in vivo wild plants (IWP). The primary and the secondary metabolite contents of bioactive compounds were significantly higher in the methanolic extract of IRP. A comparative antioxidant activity study shows IRP exhibited better scavenging activity. The antidiabetic activity of α- amylase (IC50 - 71.56 ± 15.4 µg/mL) and α-glucosidase (IC50 - 82.94 ± 12.84 µg/mL) inhibitor activity also exhibited maximum in methanolic extract of IRP. Furthermore, chemical composition was analyzed using gas chromatography-mass spectroscopy (GC-MS). Antibacterial activity against human pathogenic bacteria, IRP methanolic extracts showed a maximum zone of inhibition (75 µg/mL) observed against Salmonella typhi (23.5 ± 0.5 mm) compared to the IWP. Molecular docking analysis of B. diffusa inhibition of antidiabetic activity showed better affinity in ß-Sitosterol. Supplementary Information: The online version contains supplementary material available at 10.1007/s13205-023-03645-5.

Updated Progress of the Copper-Catalyzed Borylative Functionalization of Unsaturated Molecules.

Borylation has become a powerful method to synthesize organoboranes as versatile building blocks in organic synthesis, medicinal chemistry, and materials science. Copper-promoted borylation reactions are extremely attractive due to the low cost and non-toxicity of the copper catalyst, mild reaction conditions, good functional group tolerance, and convenience in chiral induction. In this review, we mainly updated recent advances (from 2020 to 2022) in the synthetic transformations in C=C/C≡C multiple bonds, and C=E multiple bonds mediated by copper boryl systems.

Organosulfur Compound Identified from Striga angustifolia (D. Don) C.J. Saldanha Inhibits Lung Cancer Growth and Induces Apoptosis via p53/mTOR Signaling Pathway.

The Striga angustifolia (D. Don) C.J. Saldanha was used as an Ayurvedic and homeopathic medicine for cancer by the tribal peoples of the Maruthamalai Hills, Coimbatore, India. Hence, the traditional use that has been proven to be effective lacks convincing scientific references. This present study was conducted to investigate the presence of potentially bioactive compounds from S. angustifolia and provides a scientific basis for the ethnobotanical utility. The organosulfur compound 5,5'-dithiobis(1-phenyl-1H-tetrazole) (COMP1) was isolated from S. angustifolia extracts, and the structures of COMP1 were elucidated and characterized by using 13C and 1H nuclear magnetic resonance (NMR) and single crystal X-ray powder diffraction (XRD). Our findings showed that COMP1 significantly reduced cell proliferation of breast and lung cancer cells, but not that of non-malignant epithelial cells. Further analysis revealed that COMP1 promoted cell cycle arrest and apoptosis of lung cancer cells. Mechanistically, COMP1 facilitates p53 activity and inhibits mammalian target of rapamycin (mTOR) signaling, thereby inducing cell cycle arrest and apoptosis of lung cancer cells by inhibiting cell growth. Our findings suggest that COMP1 may serve as a potential drug for lung cancer through the regulation of p53/mTOR pathways.

Exploration of phytochemicals and probing potential effects of Priva cordifolia active extract on PACAP 38 and its nociceptor in the human trigeminovascular system.

Several tribal medicinal systems assert anti-migraine and common headache-remedying properties in all parts of Priva cordifolia (L.f.) Druce. Therefore, there are no clear scientific references to the validated traditional use of this plant. The present study provides a scientific basis for the ethnobotanical utility of P. cordifolia whose whole-plant extracts were evaluated against target proteins (PACAP 38 and PAC1-R) that cause migraine. Understanding the polarity-based distribution and oxidative stress scavenging ability was reported higher in ethyl acetate extracts due to the moderate distribution of secondary metabolites. Based on the preliminary analysis anti-migraine activity in the wet and dry lab experiments was compared with a commercial drug Sumatriptan. The GC-MS analysis revealed that two lead volatile compounds Bicyclo(3.2.1)oct-3-en-2-one,3,8-Dihydroxy-1-methoxy-7-(7-methoxy-1,3- and -Hexyl-2-nitrocyclohexane, present in the ethyl acetate extract showed favourable in silico anti-migraine efficiency. Notably, the ex-vivo results also showed considerable downregulation of the extract-induced mRNA expression of PACAP38. The conclusion of our study justifies that P. cordifolia has valuable plant metabolites that portray it as an efficient anti-oxidant and anti-migraine source. Supplementary Information: The online version contains supplementary material available at 10.1007/s13205-023-03462-w.

Enhancing Ethylene Polymerization of NNN-Cobalt(II) Precatalysts Adorned with a Fluoro-substituent.

Unsymmetrical 2-(1-(2,4-dibenzhydryl-6-fluorophenylimino)ethyl)-6-(1-alkylphenyl-imino)ethyl)pyridine compounds (Ar = 2,6-Me2C6H3 in L1; 2,6-Et2C6H3 in L2; 2,6- i Pr2C6H3 in L3; 2,4,6-Me3C6H2 in L4; 2,6-Et2-4-Me-C6H2 in L5) were prepared and characterized. The treatment of CoCl2 with the compounds L1-L5 afforded the corresponding cobalt complexes Co1-Co5 in excellent yields. The molecular structures of Co3 and Co4 were determined by single-crystal X-ray diffraction, revealing the distorted-square-pyramidal geometry with three nitrogen atoms and two chlorine atoms around the cobalt center. Compared with previous bis(imino)pyridylcobalt analogues, all of the cobalt precatalysts displayed exceptionally higher activities toward ethylene polymerization with 1.32 × 107 g (PE) mol-1 (Co) h-1 at 60 °C in the presence of a co-catalyst MAO or MMAO. These cobalt catalysts produced highly linear polyethylene (PE) waxes with vinyl end groups and low molecular weight (M w up to 8.23 kg mol-1) along with a relatively lower melting point (all-round T ms < 128 °C). The narrow dispersity of resultant polyethylenes indicated the single-site active species of the catalytic system.

Unifying Molecular Weights of Highly Linear Polyethylene Waxes through Unsymmetrical 2,4-Bis(imino)pyridylchromium Chlorides.

By dealing CrCl3∙3THF with the corresponding ligands (L1-L5), an array of fluoro-substituted chromium (III) chlorides (Cr1-Cr5) bearing 2-[1-(2,4-dibenzhydryl-6-fluoro- phenylimino)ethyl]-6-[1-(arylimino)ethyl]pyridine (aryl = 2,6-Me2Ph Cr1, 2,6-Et2Ph Cr2, 2,6-iPr2Ph Cr3, 2,4,6-Me3Ph Cr4, 2,6-Et2-4-MePh Cr5) was synthesized in good yield and validated via Fourier Transform Infrared (FT-IR) spectroscopy and elemental analysis. Besides the routine characterizations, the single-crystal X-ray diffraction study revealed the solid-state structures of complexes Cr2 and Cr4 as the distorted-octahedral geometry around the chromium center. Activated by either methylaluminoxane (MAO) or modified methylaluminoxane (MMAO), all the chromium catalysts exhibited high activities toward ethylene polymerization with the MMAO-promoted polymerizations far more productive than with MAO (20.14 × 106 g (PE) mol-1 (Cr) h-1 vs. 10.03 × 106 g (PE) mol-1 (Cr) h-1). In both cases, the resultant polyethylenes were found as highly linear polyethylene waxes with low molecular weights around 1-2 kg mol-1 and narrow molecular weight distribution (MWD range: 1.68-2.25). In general, both the catalytic performance of the ortho-fluorinated chromium complexes and polymer properties have been the subject of a detailed investigation and proved to be highly dependent on the polymerization reaction parameters (including cocatalyst type and amount, reaction temperature, ethylene pressure and run time).

Sterically and Electronically Modified Aryliminopyridyl-Nickel Bromide Precatalysts for an Access to Branched Polyethylene with Vinyl/Vinylene End Groups.

A series of 2-((arylimino)ethyl)pyridine derivatives (L1-L5), each containing N-2,4-bis(dibenzocycloheptyl) groups with variations in the steric/electronic properties of the ortho-substituent in the aryl ring, and the corresponding nickel bromide precatalysts [2-N{2,4-(C15H13)-6-R-C6H2}C7H7N]NiBr2 (R = Me (Ni1), Et (Ni2), i-Pr (Ni3), Cl (Ni4), or F (Ni5)), have been prepared in high yield. All the precatalysts are air-stable and characterized by Fourier transform infrared spectroscopy and elemental analysis. The molecular structures of Ni2 and Ni5 were proved through single-crystal X-ray diffraction analysis. The steric/electronic impact of the catalysts on ethylene polymerization and the resulting polymer properties were studied. Upon activation with either MAO or EASC, all the complexes displayed higher activities (up to 7.93 × 106 g of PE (mol of Ni)-1 h-1 with MAO) in ethylene polymerization and produced moderate to highly branched unsaturated polyethylene with a molecular weight of up to 16.55 kg/mol with narrow dispersities (1.6-2.4). Significantly, the generated polyethylenes are branched and unsaturated with a major class of internal double bond (-CH=CH-) as compared to the terminal double bond (-CH=CH2) (vinylene/vinyl = 9.8:1 to 1.8:1). Notably, their catalytic activities, types of unsaturation, and branches are highly affected by the nature of the ortho-substituent and reaction temperature. Moreover, the precatalysts Ni4 and Ni5 (with N-ortho = Cl and F) exhibited lower catalytic activities, produced low-molecular-weight polyethylene with a high melt temperature and the least number of branches with an increased level of terminal double bonds.

Highly linear polyethylenes tailored with 2,6-bis[1-(p-dibenzo-cycloheptylarylimino)ethyl]pyridylcobalt dichlorides.

A novel family of 2,6-bis[1-(p-dibenzocycloheptylarylimino)ethyl]pyridylcobalt dichlorides Co1-Co4 were synthesized and fully characterized by FT-IR, 1H NMR, and elemental analysis as well as X-ray diffraction analysis. The 1H NMR spectra of these paramagnetic cobalt complexes Co1-Co3 showed similar spectra with one set of signals, while Co4 possessed two sets of signals due to the different conformations caused by different substituents on the ortho-position of the N-aryl group. Crystal structures of Co1, Co2 and Co4 revealed similar square-pyrimidal geometry around the cobalt ion, in which two dibenzocycloheptyl groups adapted as cis-conformers, whereas Co3 possessed bistrigonal geometry and the two dibenzocycloheptyl groups were adapted as trans-conformers. On activation with methylaluminoxane (MAO) or modified MAO (MMAO), all these cobalt complexes displayed high catalytic activities towards ethylene polymerization (up to 1.21 × 107 g (PE) mol-1 (Co) h-1) and produced polyethylenes with narrow molecular distributions (PDI ≈ 2.0). Co3 bearing bulkier isopropyl substituents on the ortho-position gave much higher molecular weight of resultant polyethylene than the other cobalt complexes reported herein. The microstructure analysis of the PEs demonstrated that they are highly linear and contain a vinyl end group as the major group and saturated methyl as the minor group, in which the content of the unsaturated polymer chain relied on the ortho-substituent of the N-aryl group.

Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand.

Six examples of 2-(1-arylimino)ethyl-9-arylimino-5,6,7,8-tetrahydrocycloheptapyridine-cobalt(II) chloride complexes, [2-(1-ArN)C2H3-9-ArN-5,6,7,8-C5H8C5H3N]CoCl2, (Ar = 2-(C5H9)-6-MeC6H3 Co1, 2-(C6H11)-6-MeC6H3 Co2, 2-(C8H15)-6-MeC6H3 Co3, 2-(C5H9)-4,6-Me2C6H2 Co4, 2-(C6H11)-4,6-Me2C6H2 Co5, and 2-(C8H15)-4,6-Me2C6H2 Co6), were synthesized by the direct reaction of the corresponding ortho-cycloalkyl substituted carbocyclic-fused bis(arylimino)pyridines (L1⁻L6) and cobalt(II) chloride in ethanol with good yields. All the synthesized ligands (L1⁻L6) and their corresponding cobalt complexes (Co1⁻Co6) were fully characterized by FT-IR, ¹H/13C-NMR spectroscopy and elemental analysis. The crystal structure of Co2 and Co3 revealed that the ring puckering of both the ortho-cyclohexyl/cyclooctyl substituents and the one pyridine-fused seven-membered ring; a square-based pyramidal geometry is conferred around the metal center. On treatment with either methylaluminoxane (MAO) or modified methylaluminoxane (MMAO), all the six complexes showed high activities (up to 4.09 × 106 g of PE mol-1 (Co) h-1) toward ethylene polymerization at temperatures between 20 °C and 70 °C with the catalytic activities correlating with the type of ortho-cycloalkyl substituent: Cyclopentyl (Co1 and Co4) > cyclohexyl (Co2 and Co5) > cyclooctyl (Co3 and Co6) for either R = H or Me and afforded strictly linear polyethylene (Tm > 130 °C). The narrow unimodal distributions of the resulting polymers are consistent with single-site active species for the precatalyst. Furthermore, compared to the previously reported cobalt analogues, the titled precatalysts exhibited good thermo-stability (up to 70 °C) and possessed longer lifetime along with a higher molecular weight of PE (Mw: 9.2~25.3 kg mol-1).

Dialkylaluminum 2-substituted 6,6-dimethylcyclopentylpyridin-7-oxylates toward structural-differentiation of the ring-opening polymerization of ε-caprolactone and l-lactides.

Herein, a series of dialkylaluminum 2-substituted 6,6-dimethylcyclopentyl pyridin-7-oxylates Al1-Al7 were synthesized and characterized by 1H- and 13C-NMR spectroscopy and elemental analysis. The molecular structure of Al3 was proven to be a dimer of an aluminum complex. These aluminum complexes could efficiently initiate the ring-opening polymerization (ROP) of ε-caprolactone (CL), and the structural differentiations of the resultant PCL were strongly dependent on the amount of BnOH (PhCH2OH) used. In the absence of BnOH, the resultant PCL showed a cyclic structure, whereas BnO-capped linear PCL was obtained in the presence of >2.0 equivalents of BnOH; the resultant PCL was a mixture of linear and cyclic PCLs in the presence of 1.0 equivalent of BnOH. Moreover, these aluminum complexes exhibited high efficiency towards the ROP of l-lactide (LLA); however, the activities were lower than those for the ROP of ε-CL. Without BnOH, the resultant PLLA showed a highly linear structure with the alkyl-end group from aluminum complexes; on the other hand, PLLA displayed a major cyclic structure and minor BnO-capped linear PLLA if 1.0 equivalent of BnOH was employed, and the percentage of BnO-capped linear PLLA was increased by increasing the amount of BnOH.

Conversion of Arylboronic Acids to Tetrazoles Catalyzed by ONO Pincer-Type Palladium Complex.

A convenient synthesis of a library of tetrazoles through a novel and operationally simple protocol effecting the direct conversion of arylboronic acids catalyzed by a new ONO pincer-type Pd(II) complex under mild reaction conditions using the readily available reagents is reported. The palladium complex was reused up to four cycles in an open-flask condition.