Active Agents Research Articles

Green adsorption of quinoline as basic N-compounds from liquid fuel using mesoporous and Fe-functionalized walnut shell-activated carbon

Removing nitrogenous compounds from liquid fuels is essential, and adsorption de-nitrogenation is a new process for this goal. This work has the purpose of investigating quinoline adsorption using Iron functionalized Activated carbon (IFAC) mesoporous nanocomposite. The mesoporous nanocomposite was synthesized in a one-step process by chemical activation of the walnut shell using Iron chloride as the activation and modification agent. The IFAC mesoporous nanocomposite was utilized to remove quinoline from isooctane as the liquid fuel via a discontinuous (batch) process by examining the effect of initial concentration, contact time, and temperature. The effect of contact time on the adsorption ability of IFAC for quinoline was well described by the pseudo-second-order model. The Langmuir model described the equilibrium manner of the process well, and the adsorbent could retain 344.82 mg/g of quinoline (37.37 mg N/g). The thermodynamic parameters show the endothermic (ΔH°= +30.070 kJ/mol) and spontaneity of the adsorption process. The regeneration experiments indicated that functionalized AC’s adsorption ability for quinoline adsorption decreased by 23% after five cycles. The obtained data indicate that the functionalization of activated carbon surface with iron particles leads to improving its adsorption ability toward N-containing compounds from liquid fuels.

Chemical composition, cytotoxicity, antimicrobial, antibiofilm, and anti-quorum sensing potential of Mentha Piperita essential oil against the oral pathogen Streptococcus mutans

ABSTRACT Dental caries is a highly prevalent oral disease affecting billions of individuals globally. The disease occurs chemically as a result of breakdown of the tooth surface attributed to metabolic activity in colonizing biofilm. Biofilms, composed of exopolysaccharides and proteins, protect bacteria like Streptococcus mutans, which is notable for its role in tooth decay due to its acid-producing abilities. While various antimicrobial agents may prevent biofilm formation, these drugs often produce side effects including enamel erosion and taste disturbances. This study aimed to examine utilization of the Mentha piperita essential oil as a potential antibiofilm activity agent against S. mutans. M. piperita oil significantly (1) reduced bacterial biofilm, (2) exhibited a synergistic effect when combined with chlorhexidine, and (3) did not induce cell toxicity. Chemical analysis identified the essential oil with 99.99% certainty, revealing menthol and menthone as the primary components, constituting approximately 42% and 26%, respectively. Further, M. piperita oil eradicated preformed biofilms and inhibited biofilm formation at sub-inhibitory concentrations. M. piperita oil also interfered with bacterial quorum sensing communication and did not produce any apparent cell toxicity in immortalized human keratinocytes (HaCaT). M. piperita represented an alternative substance for combating S. mutans and biofilm formation and a potential combination option with chlorhexidine to minimize side effects. An in-situ performance assessment requires further studies.

Evaluation of Quantamatrix dRASTTM system for rapid antimicrobial susceptibility testing of bacterial isolates from positive blood cultures, in comparison with commercial Micronaut broth microdilution system

Antimicrobial susceptibility testing (AST) from blood culture (BC) may take several days, limiting the eventual impact on antimicrobial stewardship. Hence, rapid AST systems represent a valuable support in shorting the time-to-response. In this work, the Quantamatrix dRASTTM system (dRAST) was evaluated for rapid AST on 100 monomicrobial BCs (50 Gram-negatives and 50 Gram-positives), including several isolates with clinically relevant resistance mechanisms. AST results were provided in 6-hours, on average. Compared to Micronaut (Merlin) system based on broth microdilution, dRAST exhibited an overall categorical agreement of 92.5 %, essential agreement of 89.0 %, and mean bias of 15.9 %. Category overestimation (potentially leading to unnecessary high-dosage treatment or to exclude active agents) and category underestimation (potentially leading to underdosing or using ineffective agents) were observed in 4.3 % and 3.1 % of cases, respectively. Even though several issues were reported, results confirmed the potential contribution of dRAST to shorten the BCs clinical microbiology workflow and management.

Bacillus velezensis HN-2: a potent antiviral agent against pepper veinal mottle virus.

Pepper veinal mottle virus (PVMV) belongs to the genus Potyvirus within the family Potyviridae and is a major threat to pepper production, causing reduction in yield and fruit quality; however, efficient pesticides and chemical treatments for plant protection against viral infections are lacking. Hence, there is a critical need to discover highly active and environment-friendly antiviral agents derived from natural sources. Bacillus spp. are widely utilized as biocontrol agents to manage fungal, bacterial, and viral plant diseases. Particularly, Bacillus velezensis HN-2 exhibits a strong antibiotic activity against plant pathogens and can also induce plant resistance. The experimental subjects employed in this study were Bacillus velezensis HN-2, benzothiadiazole, and dufulin, aiming to evaluate their impact on antioxidant activity, levels of reactive oxygen species, activity of defense enzymes, and expression of defense-related genes in Nicotiana benthamiana. Furthermore, the colonization ability of Bacillus velezensis HN-2 in Capsicum chinense was investigated. The results of bioassays revealed the robust colonization capability of Bacillus velezensis HN-2, particularly in intercellular spaces, leading to delayed infection and enhanced protection against PVMV through multiple plant defense mechanisms, thereby promoting plant growth. Furthermore, Bacillus velezensis HN-2 increased the activities of antioxidant enzymes, thereby mitigating the PVMV-induced ROS production in Nicotiana benthamiana. Moreover, the application of Bacillus velezensis HN-2 at 5 dpi significantly increased the expression of JA-responsive genes, whereas the expression of salicylic acid-responsive genes remained unchanged, implying the activation of the JA signaling pathway as a crucial mechanism underlying Bacillus velezensis HN-2-induced anti-PVMV activity. Immunoblot analysis revealed that HN-2 treatment delayed PVMV infection at 15 dpi, further highlighting its role in inducing plant resistance and promoting growth and development. These findings underscore the potential of Bacillus velezensis HN-2 for field application in managing viral plant diseases effectively.

A Comprehensive on Synthesis and Antimicrobial Evaluation of Substituted-Arylideneamino-5-(5-Chlorobenzofuran-2-yl)-1, 2, 4-Triazole-3-Thiol Derivatives/ Schiff Bases.

Schiff bases are well known and popular classes of organic compounds containing imine (R2C = NH) group that are widely used as catalysts and intermediates in numerous organic transformations. Schiff bases are medicinally very important because they exhibit antimicrobial like antibacterial, antiviral and anticancer activities. Benzofuran based Schiff bases have been found as interesting scaffolds for the synthesis and design of biologically active agents. Moreover, they possess a wide range of biological activities against fungal, bacterial, malarial, inflammatory and viral diseases. In this reviw, substituted-arylideneamino-5-(5-chlorobenzofuran-2-yl)-1,2,4-triazole-3-thiols have been synthesized by using efficient synthetic protocols. The synthesized derivatives are also evaluated against different bacterial strains.

Improving Clinical Communication: a qualitative study on the Informed Consent

In the context of the Patient-Centred Care paradigm (Epstein et al., 2005; Suojanen et al., 2012) and the shift toward the psychobiological model (Dean & Street, 2015; Muñoz & García-Izquierdo, 2020), there is a growing demand for the patient to be an active agent in the management of their health. Clinical communication should be conveyed accurately and empathetically (Bellés Fortuño & García-Izquierdo, forthcoming), especially in complex legal genres such as the Informed Consent (IC). The research carried out by the Gentt research group up-to-date has revealed that there is no specific monitoring with the use of IC protocols in clinical practice. In this paper, we present the results of a qualitative pilot study with a group of practitioners from the Valencian Community (Spain). A focus group was conducted where the articulation of communication with patients was analyzed. The study tries to define the practical insights of using the IC to draw conclusions that can improve clinical communication. Results show that MPs generally consider that the IC process needs improvement, especially when considering closeness with patients to enhance communication.

Fabrication and characterization of hydroquinone in liposomal gel for transdermal drug delivery

This study aimed to formulate a gel for hydroquinone dermal therapy using liposomes to maintain the active agents' concentration in the skin's deepest layers. Cholesterol was incorporated to enhance the liposome's bilayer characteristics, increasing microviscosity, membrane stability, and blister rigidity. Various methods for liposome preparation exist, but the film hydration method, being the most common, was utilized here. Results for formulation HL6, which had lower levels of Lecithin Cholesterol and rotation speed, revealed a vesicle size of 180.4 nm, a Zeta potential of -37.5 mV, and an entrapment efficiency of 69.10±1.52%. In-vitro drug release data for formulations F1, F2, and F3 within 30 minutes showed hydroquinone release rates of 97.75±0.28%, 98.92±0.56%, and 94.45±0.36%, respectively. The order of drug release was F2 > F1 > F3, with F2 demonstrating the maximum release rate. The study concludes that liposomal gel is an effective transdermal drug delivery system for therapeutic molecules. Lipid vesicles, such as liposomes, are among the best mechanisms for delivering medications to their intended locations while minimizing their dissemination to non-target tissues. This liposomal gel-based formulation shows significant potential for effectively treating acne by maintaining high concentrations of active agents in the skin's deepest layers and ensuring a controlled and sustained drug release.

Hypoxia-Responsive Prodrug of ATR Inhibitor, AZD6738, Selectively Eradicates Treatment-Resistant Cancer Cells.

Targeted therapy remains the future of anti-cancer drug development, owing to the lack of specificity of current treatments which lead to damage in healthy normal tissues. ATR inhibitors have in recent times demonstrated promising clinical potential, and are currently being evaluated in the clinic. However, despite the considerable optimism for clinical success of these inhibitors, reports of associated normal tissues toxicities remain a concern and can compromise their utility. Here, ICT10336 is reported, a newly developed hypoxia-responsive prodrug of ATR inhibitor, AZD6738, which is hypoxia-activated and specifically releases AZD6738 only in hypoxic conditions, in vitro. This hypoxia-selective release of AZD6738 inhibited ATR activation (T1989 and S428 phosphorylation) and subsequently abrogated HIF1a-mediated adaptation of hypoxic cancers cells, thus selectively inducing cell death in 2D and 3D cancer models. Importantly, in normal tissues, ICT10336 is demonstrated to be metabolically stable and less toxic to normal cells than its active parent agent, AZD6738. In addition, ICT10336 exhibited a superior and efficient multicellular penetration ability in 3D tumor models, and selectively eradicated cells at the hypoxic core compared to AZD6738. In summary, the preclinical data demonstrate a new strategy of tumor-targeted delivery of ATR inhibitors with significant potential of enhancing the therapeutic index.

Communities in ecosystem restoration: The role of inclusive values and local elites' narrative innovations

Abstract Ecosystem restoration practices are gaining prominence in coping with the crisis of ecosystem degradation. To improve the long‐term effectiveness of restoration activities, community engagement in restoration projects needs to be strengthened. In communities where traditional and local values drive adaptation to environmental changes, a community‐engaged restoration approach requires the integration of restoration techniques and local value systems. In two pastoral communities on the Qinghai‐Tibetan Plateau, we used the Q method to explore pastoralists' attitudes towards grassland degradation and restoration and to understand different levels of community engagement in grassland restoration activities. Through this study, we aim to promote an understanding of the value‐based approach of local communities to enable better community engagement for the long‐term effectiveness of ecosystem restoration projects and contribute to the achievement and synergy of global Sustainable Development Goals (SDGs). The study revealed eight types of pastoralists with different attitudes in two communities, with the type of Active Agents leverages transformative restoration action through creating value‐inclusive narratives of grassland restoration in the community with a higher level of engagement in restoration practices. Alongside this, we explored the pastoralists' perspectives of biodiversity in restoration and the importance of local elites in facilitating multiple‐actor cooperation in restoration projects. We recommend that decision‐makers recognize the significance of local worldviews and values in facilitating environmental adaptations, as well as the irreplaceable role played by local people in developing value‐inclusive narratives that align with the local cultural context. Open dialogues and sufficient communication between multiple stakeholders are needed to build mutual trust and accumulate social capital for driving transformative actions in traditional communities. Such approaches are essential to foster community engagement and gain better momentum in ecosystem management initiatives. Read the free Plain Language Summary for this article on the Journal blog.

Antimicrobial Polymer Films with Grape Seed and Skin Extracts for Food Packaging.

The development of antimicrobial food packaging is a very important and current goal, but it still difficult to implement in practice. Reducing microbial contamination and preserving food quality are very important tasks for food manufacturers as the use of antimicrobial packaging can preserve the health of consumers. On the other hand, the difficulty of degrading packaging materials, leading to environmental pollution, is also an important problem. These problems can be solved by using biodegradable biopolymers and antimicrobial agents in the production of food packaging. Very suitable antimicrobial agents are grape seed and skin extracts as they have high antioxidant and antimicrobial capacity and are obtained from grape pomace, a waste product of winemaking. The present review presents the valuable bioactive compounds contained in grape seeds and skins, the methods used to obtain the extracts, and their antimicrobial and antioxidant properties. Then, the application of grape seed and skin extracts for the production of antimicrobial packaging is reviewed. Emphasis is placed on antimicrobial packaging based on various biopolymers. Special attention is also paid to the application of the extract of grape skins to obtain intelligent indicator packages for the continuous monitoring of the freshness and quality of foods. The focus is mainly placed on the antimicrobial properties of the packaging against different types of microorganisms and their applications for food packaging. The presented data prove the good potential of grape seed and skin extracts to be used as active agents in the preparation of antimicrobial food packaging.

Magnetically controlled bacterial turbulence

Concentrated active agents can exhibit turbulent-like flows reminiscent of hydrodynamic turbulence. Despite its importance, the influence of external fields on active turbulence remains largely unexplored. Here we demonstrate the ability to control the swimming direction and active turbulence of Bacillus subtilis bacteria using external magnetic fields. The control mechanism leverages the magnetic torque experienced by the non-magnetic, rod-shaped bacteria in a magnetizable medium containing superparamagnetic nanoparticles. This allows aligning individual bacteria with the magnetic field, leading to a nematically aligned state over millimetric scales with minute transverse undulations and flows. Turning off the field releases the alignment constraint, leading to directly observable hydrodynamic instability of the dipole pushers. Our theoretical model predicts the intrinsic length scale of this instability, independent of the magnetic field, and provides a quantitative control strategy. Our findings suggest that magnetic fields and torques can be excellent tools for controlling non-equilibrium phase transitions in active systems.

Assessing the forecasting power of mean-field approaches for disease spreading using active systems

The forecasting of the temporal evolution of real-world diseases is systematically performed via mean-field, compartmental models, such as the SIR model and its various variants. Here, we investigate the spreading of SIR dynamics over a system of interacting, active agents – whose dynamics generate random contacts among the agents, as well as temporal and spatial correlation and fluctuations – to assess whether mean-field-like SIR models are able to accurately describe the temporal evolution of an epidemics. We find that such models display temporal dynamics that are intrinsically and fundamentally different from the ones obtained in active agent simulations. Specifically, we numerically prove that no effective mean-field SIR model is consistent with the dynamics that emerge in agent-based simulations. Our results call into question the use of such models to forecast the evolution of real-world epidemics, independently of the method used to estimate the basic reproduction number.

Биоактивные вещества геропротекторной направленности

People are constantly exposed to adverse environmental factors that affect their health. If combined with hereditary predisposition, they may lead to gerontological changes that reduce healthy and working life expectancy. Some measures can prevent premature aging, e.g., a balanced diet or biologically active anti-aging substances also called geroprotectors. This article reviews biologically active geroprotectors with a view to select promising components for novel biologically active additives and functional foods. The review covered five years of Russian research articles and patents on biologically active anti-aging agents indexed in the National Center for Biotechnology Information, ScienceDirect, eLIBRARY.RU, and the database of the Federal Institute of Industrial Property. The domestic market demonstrates a growing demand for biologically active supplements: in 2023, it increased by 10% in value terms as consumers’ interest in a healthy and long life continues to grow. The review also included quality criteria for biologically active anti-ageing agents, e.g., such plant metabolites as vitamins, polyphenols, antioxidants, adaptogens, peptides, etc. Thymalin, epithalamin, dasatinib, and epithalon are available on the domestic market. The list of potential anti-aging agents includes ethylamine, carnosine, glutathione, ubiquinone, curcumin, rutin, quercetin, resveratrol, senolytics, and sirutins. These biologically active substances prevent oxidative stress, accumulation of lipofuscin, and senescent cells. The most effective anti-aging agents come from Vitis amurensis, Rhodiola rosea, Schisandra chinensis, Galega officinalis, Eleutherococcus senticosus, Withania somnifera, and Panax ginseng.

Antimicrobial Effect of Cinnamomum verum Leaf Extract on Fungus and MDR Bacteria

Multi-drug resistance is a major concern to medical science across the globe. The inability of most drugs to destroy different pathogenic bacteria and fungi demands the use of natural products like phytochemicals to treat various infections. At this juncture, Cinnamomum verum is an active agent against various bacteria and fungi. C. verum or true cinnamon is widely used as a spice. It has several medicinal values and is widely accepted as traditional medicine. Cinnamaldehyde is the most active compound of C. verum that is responsible for its antimicrobial activity. In this study, the minimum inhibitory concentration (MIC) of C. verum leaf ethanolic extract was determined against different bacteria and fungi along with ethanol as a control. The extract showed remarkable antifungal action on Candida albicans and antibacterial action against Pseudomonas aeruginosa with a MIC value of only 0.039 mg/ml. The MIC value against other microorganisms ranges from 0.78 mg/ml to 25mg/ml. C. verum leaf extract can be used as an effective antimicrobial agent in fungal and bacterial infections.

Leaven of Dough, Ferment of Gold: The Breadmaking Analogy in Medieval Metallic Transmutation

This paper traces the analogy between the making of bread with ferment (leaven or yeast) and theories of metallic transmutation throughout the Middle Ages. For this purpose it surveys several medieval alchemical writings, including Hortulanus’s influential Commentary on the Emerald Tablet. In this work, the ferment, an essential ingredient of the philosophers’ stone, is portrayed less as an active agent and more as the passive, nutritive earth (terra nutrix) which combines with the soul (anima) in order to yield the stone (lapis). I argue that the background of these theories has both a practical and a medical-theoretical dimension. The practical aspect derives from historical everyday practices of making bread from sourdough, and using old yeast “starter” as a kind of inoculum to speed up the fermentation of a new batch of fresh dough. The medical-theoretical framework for the understanding of ferment action was likely provided by the widely influential Galenic idea of whole substance action (Gr. καθ᾽ὅλην τὴν οὐσίαν, Lat. tota substantia), initially developed by Galen in pharmacology and later imported into alchemy via Arabic medicine. Together, these aspects converge into a successful model of “inoculation-emergence,” which underlies many medieval and early modern theories of fermentation, both medical and alchemical.

Fire, Vulcanus, Archeus, and Alchemy: A Hybrid Close-Distant Reading of Paracelsus’s Thought on Active Agents

The Swiss physician and philosopher Theophrastus von Hohenheim, called Paracelsus (1493-1541) is known for his strong advocacy of medical alchemy. That his natural philosophy was tied to medical alchemy is perhaps uncontroversial, but just how it was so is less straightforward. This article provides an insight into the connection between the two by means of Paracelsus’s concept of active agents, with an emphasis on fire, its master Vulcanus, and the associated term Archeus. I will show how these evolved in the thought of Paracelsus by taking an evolutionary view of his works. The complexity of his views comes to light as a result of employing the method of hybrid reading, which integrates the traditional close reading technique with the much more novel one of distant reading. The latter is part of the emerging field of digital and computational humanities, and involves the analysis of corpora by means of digital tools, including computer programming (Python). In the article, I will attempt to combine distant and close reading and showcase how such hybrid reading approaches may provide new insights into historical corpora.

P-Stereogenic Phosphorus Ligands in Asymmetric Catalysis.

Chiral phosphorus ligands play a crucial role in asymmetric catalysis for the efficient synthesis of useful optically active compounds. They are largely categorized into two classes: backbone chirality ligands and P-stereogenic phosphorus ligands. Most of the reported ligands belong to the former class. Privileged ones such as BINAP and DuPhos are frequently employed in a wide range of catalytic asymmetric transformations. In contrast, the latter class of P-stereogenic phosphorus ligands has remained a small family for many years mainly because of their synthetic difficulty. The late 1990s saw the emergence of novel P-stereogenic phosphorus ligands with their superior enantioinduction ability in Rh-catalyzed asymmetric hydrogenation reactions. Since then, numerous P-stereogenic phosphorus ligands have been synthesized and used in catalytic asymmetric reactions. This Review summarizes P-stereogenic phosphorus ligands reported thus far, including their stereochemical and electronic properties that afford high to excellent enantioselectivities. Examples of reactions that use this class of ligands are described together with their applications in the construction of key intermediates for the synthesis of optically active natural products and therapeutic agents. The literature covered dates back to 1968 up until December 2023, centering on studies published in the late 1990s and later years.

Synthesis and Investigation of Biological Activity of New Betulonic Acid Derivatives Containing 1,2,3-Triazole Fragments.

The results of this study showed that the compounds synthesized by the authors have significant potential due to their antibacterial and cytotoxic properties. The apparent antibacterial activity demonstrated by the compounds suggests that they are active antimicrobial agents against common microbial pathogens that cause various socially significant infectious diseases. Compound 6 showed pronounced antimicrobial activity against the Gram-positive test strain Staphylococcus aureus ATCC 6538, and compound 7 demonstrated pronounced antimicrobial activity against the Gram-negative test strain Escherichia coli ATCC 25922 (MIC = 6.3 µg/mL). This allowed us to consider these compounds to have great potential.

Removal of tetracycline from the aquatic environment using activated carbon: A comparative study of adsorption performance based on the activator agents

This research focus endeavour to compare the remediation of tetracycline (TC) through activated carbon (AC), crafted utilizing two distinct chemical activators: zinc chloride (ACZ), and potassium hydroxide (ACK), using pine cone biowaste as an effective carbon precursor, followed by microwave-assisted activation. The impact of TC removal by ACZ and ACK adsorbents was thoroughly examined. The influence of pH, adsorbent mass, adsorption isotherms, kinetics, and inclusive thermodynamics were studied. Our results revealed that the interaction between TC and ACZ or ACK adsorbents aligned well with the model of pseudo-second-order kinetics, whilst the Langmuir model fitted the adsorption isotherm data of ACZ and ACK. The ACZ have a maximum adsorption capacity of 327.87 mg/g compared to that of the ACK (283.29 mg/g). Adsorption of TC was facilitated by the suitable pore volume, abundant microporous, and mesoporous structure of these adsorbents. The ACZ adsorbent is abundant in oxygen-containing functional groups, compared to ACK with minimized reactive sites, in bonding with the TC molecules through hydrogen bonding, for faster removal of TC. Our finding from this work further highlights that the synthesized ACZ from pine cones evidenced significant environmental potentials in the elimination of antibiotics from aqueous solution, to promote clean application perspectives.

Synthesis and characterization of Azo-Azomethine derivatives bearing thiazole moiety: In vitro antimicrobial, in vitro and in vivo anti-inflammatory, and cytotoxicity assessment, accompanied by computational molecular docking, RDG, ELF, DFT, and MEP analysis

In this study, a novel series of Azo-azomethine derivatives incorporating thiazole moieties (5a-h) were synthesized and thoroughly characterized using NMR (1H and 13C), FT-IR spectroscopy, and ESI-MS methods. The synthesized compounds underwent screening for their antimicrobial, anti-inflammatory (both in vitro and in vivo), and cytotoxic activities. Notably, compound 5d exhibited significant activity against S. aureus and S. epidermidis, with minimum inhibitory concentration (MIC) values as low as 20 μg/L. Additionally, compound 5d demonstrated the most potent anti-inflammatory activity both in vitro (84.72%) and in vivo. Furthermore, molecular analyses including RDG, ELF, DFT, and MEP were conducted to investigate molecular interactions, electron distribution, electronic configuration, and electrostatic potential, thus facilitating a deeper understanding of the molecular characteristics and aiding in the refinement and design of these molecules. Moreover, the compounds' efficacy against bacterial proteins was assessed through molecular docking calculations. Utilizing the PASS and pkCSM platforms, an examination of the compounds' bioactivity regulation and physicochemical attributes was conducted, highlighting their potential as prospective novel active agents.