Search Results (280)

The process of exploiting hydrocarbon deposits is subject to many complications, some of which can make exploitation very difficult or impossible. These factors include damage to the wellbore zone by drilling fluid, which impedes the flow of reservoir fluid from the production zone to the well. This article presents the results of research conducted to develop drilling fluid compositions with the best possible ability to form a tight sealing sediment on the borehole wall. In addition to traditional carbonate blockers, modern organic agents were used as bridging agents. Research was conducted on the selection of the drilling fluid composition, the rheological parameters of which would ensure the suspension of the solid phase in the form of various types of blockers. After preparing the base drilling fluid, its composition was modified by adding different configurations of blockers. The sets of blockers added to the fluid varied in both chemical structure and particle size. Such modified fluids were then subjected to tests of technological properties, such as rheological parameters, API filtration, and pH. In the next stage, sealing tests of the filter cake formed by the tested fluids were carried out on the surface of the rock core using the PPT—Pore Pressure Transmission Test. Based on the obtained results, it can be concluded that the new type of organic blockers used allows the rapid formation of a tight filter cake on the borehole wall, and thus significantly reduces drilling fluid filtration. During PPT, the sediment formation time (t_pmax) for OB2 was 45 min; for the combination of OB1 and the carbonate inhibitor, it was 8 min; and for the carbonate inhibitor alone, it was 150 min. Full article

Microbial hydrocarbon degradation mediated by natural/modified clay minerals represents an eco-friendly and economically viable remediation strategy for hydrocarbon contamination. However, its effects are not always positive as they depend on multiple factors, including clay mineral types, modification methods, microbial species, and hydrocarbon substrates. This review systematically synthesizes existing fragmented studies concerning the impacts of natural clay minerals, modified clay minerals (acid/alkali/thermal/organic/metal ion), and clay minerals containing composite materials on microbial hydrocarbon biodegradation. Based on current findings, future research should prioritize the following recommendations: (1) avoid using concentrated strong acids in acid activation; (2) exclude metal cations that induce strong adsorption (reducing hydrocarbon bioavailability) or trigger excessive interlayer hydrolysis (some trivalent cations) in metal cation modification; (3) eliminate biologically toxic agents during organic modification; and (4) expand understanding of alkali/thermally modified clay minerals and clay mineral-containing composite materials in this direction. Natural/modified clay mineral-mediated microbial degradation is a highly promising remediation technology for hydrocarbon contamination and poised to advance and achieve breakthroughs through continuous synthesis of knowledge and innovation. Full article

Background: Aryl hydrocarbon receptor (AhR) is a transcription factor that is involved in the regulation of immunity. AhR inhibits T cell activation in tumors, which induces immune suppression in the blood and solid tumors. We identified effective small-molecule AhR antagonists for cancer immunotherapy. Methods: A new series of pyrazolopyrimidine derivatives was synthesized and evaluated for AhR antagonistic activity. Results: Compound 7k exhibited significant antagonistic activity against AhR in a transgenic zebrafish model. In addition, 7k exhibited good AhR antagonist activity, with a half-maximal inhibitory concentration (IC₅₀) of 13.72 nM. Compound 7k showed a good pharmacokinetic profile with an oral bioavailability of 71.0% and a reasonable half-life of 3.77 h. Compound 7k selectively exerted anti-proliferative effects on colorectal cancer cells without affecting normal cells, concurrently suppressing the expression of AhR-related genes and the PD-1/PD-L1 signaling pathway. Compound 7k exhibited potent antitumor activity in syngeneic colorectal cancer models. Importantly, the combination of anti-PD1 and compound 7k enhanced antitumor immunity by augmenting cytotoxic T lymphocyte (CTL)-mediated activity. Conclusions: Collectively, a new pyrazolopyrimidine derivative, 7k, shows promise as a potential therapeutic agent for treating colorectal cancer. Full article

Air pollutants pose a growing public health concern in Puerto Rico (PR), particularly from rapid industrialization, military activities, environmental changes and natural disasters. A total of 193 pollutants, comprising the 187 hazardous air pollutants and the 6 criteria air pollutants—including particulate matter (PM), carbon monoxide (CO), volatile organic compounds (VOC), and heavy metals—coincide with rising respiratory disease rates (e.g., lung cancer) documented in national and regional health registries. This study aimed to review major air pollutants in PR, their molecular carcinogenic mechanisms (mostly focused on respiratory-related cancers), and the geographic areas impacted significantly. We conducted an extensive literature search utilizing peer-reviewed scientific articles (PubMed and Web of Science), governmental reports (EPA, WHO, State of Global Air), public health registries, (Puerto Rico Central Cancer Registry and International Agency for Research on Cancer) and local reports. Data on pollutant type, source, molecular pathways, and carcinogenic properties were extracted and synthesized. Our analysis identified ethylene oxide (EtO), polycyclic aromatic hydrocarbons, and PM from industrial sites as key pollutants. The municipalities of Salinas and Vieques, hubs of industrial activity and military exercises, respectively, emerged as critical hotspots where high concentrations of monitored pollutants (e.g., EtO, formaldehyde, 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and diesel PM) are associated with a significant prevalence of cancer and respiratory diseases. These agents, known to induce genomic instability and chromosomal aberrations, were correlated with elevated local cancer incidence. Our findings underscore the urgent need for targeted public health interventions and support a multi-pronged strategy that includes: (1) enhanced regulatory oversight of EtO and other hazardous air pollutant emissions; (2) community-based biomonitoring of high-risk populations; and (3) investment in public health infrastructure and a transition to cleaner energy sources. Integrating rigorous environmental science with public health advocacy is essential to strengthen PR’s cancer-control continuum and foster resilience in its most vulnerable communities. Full article

Volatile organic compounds (VOCs) are critical indicators of the metabolic status of whole-plant maize silage (WPMS). However, the impact of inoculating various strains of fermentation agents on VOC changes has not been systematically explored. This study aimed to determine how inoculation with Lactiplantibacillus plantarum and Lentilactobacillus buchneri modulates the VOC profile and odor of WPMS after 90 days. VOCs were extracted by headspace solid-phase microextraction and analyzed by gas chromatography-mass spectrometry (HS-SPME-GC-MS). Key VOCs were screened using the variable importance in projection (VIP) and substantiated by relative odor activity values (rOAV) and odor descriptions. A total of 82 compounds were identified, including 22 esters, 19 alcohols, 3 acids, 9 aldehydes, 2 ethers, 6 hydrocarbons, 4 ketones, 10 phenols, and 8 terpenoids. L. plantarum enhanced green/fruity odors while strain L. buchneri significantly reduced undesirable phenolic and aldehydic compounds. Six key VOCs influencing the odor of WPMS were selected: 4-ethyl-2-methoxyphenol and benzaldehyde, which contribute smoky, bacon, and bitter almond aromas, and (E)-3-hexen-1-ol, benzyl alcohol, (E, E)-2,4-heptadienal and methyl salicylate, which impart green, fruity, and nutty aromas. These findings highlight the effects and contributions of various strain additives on VOCs in WPMS, providing new theoretical insights for regulating the flavor profile of WPMS. Full article

Currently, the potential environmental concerns around the world for polycyclic aromatic hydrocarbon carcinogenic (PAHCs) contamination as carcinogenic compounds in industrial soils (automobile industry) are rising day by day. At present, the technology of treating contaminated soils using photocatalysts is commonly used; however, this study tested photolysis and photocatalysis through ultraviolet light (306 nm) due to its high treatment efficiency. FeCl₃ (0.3, 0.4 M) was used as an iron catalyst for each treatment in the presence of H₂O₂ (10%, 20%) as an oxidizing agent. The impact of light treatment on soils that contained various concentrations of PAHCs like naphthalene (NAP), chrysene (CRY), benzo(a) pyrene (BaP), indeno (1,2,3-cd) pyrene (IND) was investigated. The QuEChERS method was used to extract PAHCs, and a gas chromatograph mass spectrometer (GCMSMS) was used to determine concentration. The concentrations of PAHCs were measured for soils at intervals of every 2 h after exposure to ultraviolet rays. The results showed a decrease in PAHCs concentrations with increased exposure to UV irradiation, as the initial values were 26.8 ng/g (NAP), 97 ng/g (CRY), 9.1 ng/g (BaP) and 9.7 ng/g (IND), which decreased to 2.17 ng/g (NAP), 3.14 ng/g (CRY), 0.33 ng/g (BaP) and 0.46 ng/g (IND) at 20, 40, 30 and 40 h of UV exposure; moreover, with an increase in concentration of the catalyst (0.4 M FeCl₃ with 20% H₂O₂), NAP, CRY, BaP and IND became undetectable at 8, 26, 14 and 20 h, respectively. It was concluded that a significant effect of ultraviolet rays on the photolysis of PAHCs, along with Photovoltaic at 306 nm wavelength, was observed while using FeCl₃ (0.4 M) combined with H₂O₂ (20%) produced better results in a shorter time compared to FeCl₃ (0.3 M) with H₂O₂ (10%). Full article

Bulbine species (Asphodelaceae) are routinely used in many African communities to treat various dermatological disorders, including wounds, due to their relative accessibility, affordability, safety records, and reported efficacies. However, these reported biological activities lack robust empirical evidence and well-validated cellular mechanisms for plausible applications. Hence, this review was aimed at investigating the bioactive compounds of Bulbine species linked to their cellular wound healing attributes, their toxicity, and cytotoxicity. A detailed literature search was conducted using Web of Science, Google scholar, and PubMed, followed by Scopus and VOSviewer (version 1.6.20) bibliographic analyses. Bulbine frutescens (L.) Willd. and Bulbine natalensis Baker safely mediate tissue healing and coagulation cascade as adaptogens and cytotoxic agents. The wound healing activities of the Bulbine species were linked to the synergistic wound healing or tissue repair properties of bioactive compounds (such as saponins, terpenoids, luteolin, and apigenin) via the expression of collagen type-I, alpha-2 (COL1A2) gene, collagen III, increase in the wound tensile strength, and anti-cytokine interleukin-10 (IL-10) mRNA. Bulbine species were also reported to contain specialised biomarker compounds (such as naphthoquinones, bulbine-emodin, and aloe-emodin) which mediate the activation of hydroxyproline, Aryl Hydrocarbon Receptor, transforming growth factor beta—β1 (TGFβ1), and the suppressor of mothers against decapentaplegic proteins (SMAD), which ultimately induce tissue granulation, myofibroblast differentiation, re-epithelialization, higher protein complexes, and scar tissue formations. These findings give credence to the wound healing therapeutic potential of Bulbine species. However, additional clinical studies are necessary to further ascertain the reported efficacies of Bulbine species’ bioactive principles, their overall safety, and the underlying cellular mechanisms involved in the wound healing process and carcinogenesis. Full article

Liposomes, nanoscale vesicles with distinct structural and functional properties, are widely utilized in drug delivery due to their biocompatibility and ability to encapsulate diverse therapeutic agents. Effective sterilization is essential to ensure the safety and efficacy of liposomal formulations in biomedical applications, yet its impact on liposome integrity and functionality remains inadequately studied. This work systematically evaluates the effects of three sterilization methods: autoclaving, UV radiation, and filtration—on liposomes composed of dipalmitoylphosphatidylcholine (DPPC) and distearoylphosphatidylcholine (DSPC), two phospholipids differing in lipid chain length. Sterilization altered liposome properties in a lipid chain length-dependent manner, affecting particle size, zeta potential, and phospholipid content. Filtration caused significant hydrocarbon loss, confirmed by Fourier-transform infrared spectroscopy (FTIR) and Raman spectroscopy, and led to a higher reduction in phospholipid content in DPPC liposomes compared to DSPC liposomes. Biological evaluations showed that autoclaved and UV-irradiated DPPC liposomes exhibited higher cytotoxic and lower stability than their DSPC counterparts. While autoclaving and UV irradiation resulted in minimal chemical alterations, both methods significantly influenced biological properties. Filtration, although less disruptive to biocompatibility, also reduced key liposomal integrity and efficacy. This study underscores the critical importance of post-sterilization evaluation to optimize liposomal formulations for clinical and biomedical use. Full article

The growing accumulation of waste lubricating oil presents serious environmental issues, calling for sustainable management solutions. This research discusses the creation of FeNi/TiO₂ nanocatalysts that were synthesized through an eco-friendly method utilizing grape seed extract (GSE) as a natural reducing agent for the catalytic pyrolysis of waste lubricating oil. The nanocatalyst was produced using the microemulsion technique and refined via Response Surface Methodology (RSM) to optimize its catalytic performance. Pyrolysis was carried out at 400 °C, leading to a significant conversion of waste oil into valuable fuel. The FeNi/TiO₂ nanocatalyst exhibited exceptional capabilities in facilitating the breakdown of heavy hydrocarbons into lighter fuel fractions while reducing unwanted byproducts. GC-MS analysis demonstrated the prevalence of C6–C20 hydrocarbons in the pyrolysis oil, underscoring its potential as a high-quality alternative fuel similar to traditional diesel. This study aids in the progress of environmentally sustainable waste-to-energy technologies, offering a promising pathway for effective fuel production and hazardous waste management. Full article

The emissions from biomass combustion systems have recently been the subject of increased attention. In addition to elevated concentrations of particulate matter and hydrocarbons (HCs) in the flue gas, significant levels of NO_x emissions occur depending on the used fuel, such as biogenic residues. In response to legal requirements, owners of medium-sized plants (≈100 kW) are now also forced to minimize these emissions by means of selective catalytic reduction systems (SCR). The implementation of a selective sensor is essential for the efficient dosing of the reducing agent, which is converted to ammonia (NH₃) in the flue gas. Preliminary laboratory investigations on a capacitive NH₃ sensor based on a zeolite functional film have demonstrated a high sensitivity to ammonia with minimal cross-influences from H₂O and NO_x. Further investigations concern the application of this sensor in the real flue gas of an ordinary wood-burning stove and of combustion plants for biogenic residues with an ammonia dosage. The findings demonstrate a high degree of agreement between the NH₃ concentration measured by the sensor and an FTIR spectrometer. Furthermore, the investigation of the long-term stability of the sensor and the poisoning effects of SO₂ and HCl are of particular relevance to the laboratory measurements in this study, which show promising results. Full article

Petroleum-contaminated soils are a major environmental concern worldwide. In Ecuador, extensive oil spills in the Amazon have led to widespread hydrocarbon pollution, threatening ecosystems and posing health risks to nearby communities. Conventional remediation techniques are resource-intensive and may render soil unsuitable for future use. In contrast, mycoremediation—using fungi to degrade toxic contaminants—offers a sustainable alternative. White-rot fungi, known for their ligninolytic enzyme systems such as laccases and peroxidases, are capable of degrading a wide range of organic pollutants, including petroleum hydrocarbons. This study assessed the enzymatic activity of 16 fungal strains from the phyla Ascomycota and Basidiomycota isolated in the Ecuadorian Amazon. Plate-based screening and quantitative laccase activity assays confirmed positive enzymatic activity in all strains. The five strains with the highest enzymatic activity were Ganoderma cf. parvulum QCAM7791, Trametes menziesii QCAM7783, Trametes menziesii QCAM7788, Trametes menziesii QCAM7790, and Trametes meyenii QCAM7785, which were selected for a 60-day soil microcosm experiment under controlled laboratory conditions. These strains removed over 96% of total petroleum hydrocarbons from contaminated soil, demonstrating high biodegradation efficiency. These results highlight the promise of native fungal strains as bioremediation agents for petroleum-contaminated soils. Further studies should focus on evaluating their performance under field conditions and their potential integration into large-scale remediation strategies. Full article

The plants from the Ocimum genus, belonging to the Labiatae family, serve as important bioresources of essential oils (EOs) rich in biologically active secondary metabolites, widely used in medicine, food, and cosmetics. This study explored the volatile composition, enantiomeric distribution, and in vitro biological activities of EOs from three Ocimum species native to Nepal: O. tenuiflorum L., O. basilicum L., and O. americanum L. EOs were extracted via hydro-distillation and analyzed using gas chromatography–mass spectrometry (GC-MS) for chemical profiling and chiral GC-MS for enantiomeric composition. Hierarchical cluster analysis was performed for major chemotypes. Antioxidant activity was assessed using DPPH and ABTS assays. Antimicrobial efficacy was evaluated using the microbroth dilution method, and cytotoxicity was tested on NIH-3T3 (normal) and MCF-7 (breast cancer) cell lines via the Cell Counting Kit-8 assay. EO yield was highest in O. tenuiflorum (1.67 ± 0.13%) during autumn and lowest in O. americanum (0.35 ± 0.02%) during winter among all Ocimum spp. The major compounds identified in O. tenuiflorum were eugenol (32.15–34.95%), trans-β-elemene (29.08–32.85%), and β–caryophyllene (19.85–21.64%). In O. americanum, the major constituents included camphor (51.33–65.88%), linalool (9.72–9.91%), germacrene D (7.75–1.83%), and β–caryophyllene (6.35–3.97%). For O. basicilum, EO was mainly composed of methyl chavicol (62.16–64.42%) and linalool (26.92–27.05%). The oxygenated monoterpenes were a dominant class of terpenes in the EOs except for O. tenuiflorum (sesquiterpene hydrocarbon). A hierarchical cluster analysis based on the compositions of EOs revealed at least three different chemotypes in Ocimum species. Chiral GC-MS analysis revealed β-caryophyllene and germacrene D as enantiomerically pure, with linalool consistently dominant in its levorotatory form. O. tenuiflorum exhibited the strongest antimicrobial activity, particularly against Candida albicans, and showed notable anticancer activity against MCF-7 cells (IC₅₀ = 23.43 µg/mL), with lower toxicity to normal cells. It also demonstrated the highest antioxidant activity (DPPH IC₅₀ = 69.23 ± 0.10 µg/mL; ABTS IC₅₀ = 9.05 ± 0.24 µg/mL). The EOs from Ocimum species possess significant antioxidant, antimicrobial, and cytotoxic properties, especially O. tenuiflorum. These findings support their potential application as natural agents in medicine, food, and cosmetics, warranting further validation. Full article

Background/Objectives: Resistance of pathogenic microorganisms to antibiotics poses a serious threat to public health and often leads to devastating consequences. In this context, one of the pressing challenges in pharmacochemistry is the search for new, effective antibiotics to combat severe human diseases. Cyclic lipopeptides have emerged as some of the most promising candidates and have been widely studied. These compounds are a class of microbial secondary metabolites produced by various microorganisms, and they possess significant medical and biotechnological importance. The defining structural feature of these compounds is the presence of both a hydrophobic fragment, primarily a hydrocarbon tail of varying length, and a hydrophilic cyclic peptide moiety. This hydrocarbon tail confers amphiphilic properties to the lipopeptides, which are essential for their broad spectrum of biological activities. Their mechanism of action involves disruption of the cell membrane, and in many cases, the formation of ion-permeable defects has also been shown. Results: This review summarizes the data on cyclic lipopeptides produced by Pseudomonas spp., Streptomyces spp., and Bacillus spp. that modify membrane permeability through the formation of ion channels. The main emphasis is on understanding how the structure of the CLP can be related to the probability and mode of pore formation. Conclusions: The findings can contribute to expanding the arsenal of effective antimicrobial agents with a mechanism of action that reduces the risk of developing resistance. Full article

Syzygium oleosum (F.Muell.) B.Hyland is an Australian native species whose essential oil (EO), known commercially as “Mango Myrtle,” is gaining popularity in aromatherapy, yet remains poorly studied. This work provides the first comprehensive pharmacognostic investigation of S. oleosum. Anatomical and micromorphological analyses revealed numerous secretory cavities and calcium oxalate druses in both leaves and twigs. GC-MS analysis identified 16 components in the EO, predominantly hydrocarbon monoterpenes, with terpinolene (30.79%), β-pinene (26.79%), α-pinene (10.69%), and γ-terpinene (9.86%) as major constituents. In vitro assays showed moderate antioxidants (IC₅₀ ≤ 4.95 mg/mL) and anti-inflammatory effects (IC₅₀ ≤ 5.93 mg/mL), with specific monoterpenes contributing differentially to each activity. The EO displayed weak inhibitory activity against acetylcholinesterase (IC₅₀ 19.4 mg/mL) and butyrylcholinesterase (IC₅₀ 15.9 mg/mL), and no effect on GABA transaminase. Microelectrode array recordings on primary cortical neurons demonstrated a concentration-dependent inhibition of network activity (0.059–1.19 mg/mL) without affecting cell viability, indicating a neuromodulatory property. These results provide new insights into the pharmacological potential of S. oleosum EO and support its further evaluation as a neuroactive and anti-inflammatory agent. Full article

Atopic dermatitis (AD) is a chronic, relapsing inflammatory skin disorder characterized by immune dysregulation and epidermal barrier dysfunction. Advances in understanding the interplay of genetic predisposition, cytokine signaling, and environmental triggers have led to the emergence of targeted therapies. Although biologic agents such as dupilumab, tralokinumab, and lebrikizumab have revolutionized AD management, their high costs, injectable administration, and limited global accessibility highlight the need for alternative options. Small molecule therapies are gaining momentum as they target intracellular pathways central to AD pathogenesis and offer oral or topical administration routes. This review provides a comprehensive analysis of key agents including Janus kinase (JAK) inhibitors (upadacitinib, abrocitinib, baricitinib, ruxolitinib, delgocitinib), phosphodiesterase 4 (PDE4) inhibitors (crisaborole, difamilast, roflumilast, apremilast), as well as STAT6 degraders (KT621, NX3911), aryl hydrocarbon receptor modulators, histamine H4 receptor antagonists (adriforant, izuforant), and sphingosine-1-phosphate receptor modulators (etrasimod, BMS-986166). We summarize their mechanisms of action, pharmacological profiles, and pivotal clinical trial data, emphasizing their potential to address unmet therapeutic needs. Finally, we discuss safety concerns, long-term tolerability, and future directions for integrating small molecule therapies into precision treatment strategies for moderate-to-severe AD. Full article