Search Results (99)

Mid-high-frequency ultrasound (375 kHz) and anodic oxidation at low current intensity (<50 mA, NaCl as the supporting electrolyte) were employed to treat sulfonamide antibiotics (sulfamethoxazole—SMX and sulfacetamide—SAM). The sonodegradation involved HO•, while electrogenerated HClO was mainly responsible for the antibiotics’ elimination in the electrochemical process. A comparison of the processes evidenced that the degradation of SMX by ultrasound was faster due to its higher hydrophobicity. In contrast, in the electrochemical system, the SAM degradation was more efficient, which was associated with a higher reactivity of its acetamide moiety toward HClO. Interestingly, SMX was selectively sonodegraded in synthetic hospital wastewater and seawater, whereas the matrix components strongly accelerated the electrochemical degradation but affected the process performance in the hospital wastewater. On the other hand, theoretical analyses of atomic charge indicated that the central S-N bond, the N and aromatic ring in the aniline moiety, the C=C bond, and methyl groups in the isoxazole groups on SMX are the most susceptible moieties to the attacks by HO• and HClO. Furthermore, for the typical byproducts, calculations of the probability of being active against bacteria were slightly lower than that of the parent pharmaceutical, even being much lower for the byproducts from the electrochemical treatment. Full article

Triple-negative breast cancer (TNBC) remains one of the most aggressive breast cancer subtypes and is associated with limited therapeutic options, underscoring the urgent need for novel treatment strategies. In this study, a library of seventeen 1,3,5-triazine derivatives potentially targeting TNBC was developed using an activity-based approach. Compounds were synthesized via an ultrasound-assisted protocol, providing an efficient and environmentally friendly methodology. The synthesized library was evaluated in vitro against the human TNBC cell lines MDA-MB-468, MDA-MB-231, and Hs578T, as well as the non-tumorigenic epithelial cell line MCF10A. Compounds 9 and 17 exhibited the most promising antiproliferative activity against TNBC cell lines (MDA-MB-468: IC₅₀ = 36.62 µM for 9 and 38.29 µM for 17; MDA-MB-231: IC₅₀ = 37.32 µM for 9 and 32.86 µM for 17; Hs578T: IC₅₀ = 57.26 µM for 9 and 34.87 µM for 17), while maintaining acceptable selectivity toward non-cancerous cells. The lead compounds were further assessed in vivo using a Danio rerio model to evaluate general toxicity and cardiotoxicity. In addition, ADME parameters were predicted for all compounds using biomimetic chromatography. Overall, compounds 9 and 17 emerged as promising small-molecule candidates for TNBC treatment, requiring further toxicological evaluation in more human-relevant in vivo models. Full article

Carbon nanocomposites have gained interest due to the rapid development of nanotechnology. The graphite-based composites have been demonstrated to possess unique mechanical, electrical, and thermal properties. This paper presents a facile one-step sonochemical synthesis of antimony sulfoiodide (SbSI)/graphite nanocomposite. The weight concentrations of graphite in the prepared material varied from 0% to 33.3%. The morphology and chemical composition of the SbSI/graphite nanocomposites are studied with scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS), respectively. SEM examination shows that SbSI/graphite nanocomposite consists of one-dimensional SbSI nanostructures and graphite microparticles. The influence of graphite concentration on the energy band gap of SbSI/graphite nanocomposite is investigated using diffuse reflectance spectroscopy (DRS). The prepared materials are cold-pressed to obtain the bulk samples. They are characterized by direct current (DC) electrical measurements and thermoelectric examination. The increase in the graphite concentration in the SbSI/graphite nanocomposite resulted in a significant reduction in the electrical resistivity of the material. The Seebeck coefficients of the pristine SbSI nanowires and SbSI/graphite nanocomposite are determined for the first time. The investigations of the thermoelectric effect reveal that these nanomaterials exhibited p-type electrical conductivity. The thermoelectric power factor of the SbSI/graphite nanocomposite is examined as a function of the graphite concentration. The presented work demonstrates the comprehensive optical, electrical, and thermoelectric characterization of novel hybrid SbSI/graphite nanocomposites, which has not been studied before. Full article

This overview is intended to shed light on the current state of knowledge on highly efficient cavitation reactors, which are used in industry yet often remain undisclosed. The development of ultrasound (US) and hydrodynamic cavitation (HC) reactors requires a thorough understanding and precise engineering to ensure the efficacy of cavitation processes in larger industrial settings. Successful scaling-up must maintain a high energy density and ensure a homogeneous distribution of cavitation. Industrial reactor designs for both US and HC are typically optimised for continuous flow operations, though some configurations operate in a loop system. This review provides a concise examination of various reactor setups, with examples of relevant chemical and environmental applications, focusing on energy consumption and scalability challenges. Despite the similarities in the effects of acoustic and hydrodynamic cavitation, US and HC are best regarded as complementary technologies in industrial applications. This work presents our direct experience in designing novel cavitation reactors for specific applications, incorporating recent advances from the literature and insights from industry. Notably, the synergistic effects of hybrid technologies are gaining attention, particularly the integration of HC with cold plasma, which is emerging as one of the most effective techniques for treating polluted water. These technologies play a crucial role in modern process engineering, and continued advancements in their design and understanding will further expand their industrial applications in chemical processing. Full article

Estrogen deficiency is a primary cause of osteoporosis, compromising bone mineral density that may impair peri-implant healing. Given the compromised bone environment associated with estrogen deficiency, strategies such as particle reduction via sonochemistry are promising approaches to enhance regenerative outcomes. However, its effects in promoting bone formation remain insufficiently explored. Therefore, this study evaluated the potential of two sonicated biomaterials to improve peri-implant repair in ovariectomized rats. Fifty female rats were allocated into five groups: blood clot (CLOT), Biogran^® (BGN), sonicated Biogran^® (BGS), Bio-Oss^® (BON), and sonicated Bio-Oss^® (BOS). Tibial peri-implant defects were created 30 days after ovariectomy and analyzed 28 days later by removal torque, microcomputed tomography, and confocal microscopy. BGS exhibited the highest removal torque (6.28 Ncm), followed by BON (5.37 Ncm), BOS (3.92 Ncm), BGN (3.15 Ncm), and CLOT (2.58 Ncm). Micro-CT revealed bone volume fraction (BV/TV) values of 8.07% (CLOT), 6.47% (BOS), 6.02% (BGS), 5.55% (BGN), and 2.84% (BON). For the trabecular number (Tb.N), BGS (1.11 mm⁻¹) showed a significant increase compared with BGN (0.69 mm⁻¹), p < 0.05. These findings show that sonochemically modified bioactive glass improves mechanical stability and trabecular microarchitecture under estrogen-deficient conditions. However, further studies are needed to standardize sonication parameters for different biomaterials and expand their translational applicability. Full article

This study quantifies radical pathways and the influence of process variables in a 425 kHz sonoreactor through a coupled calorimetric and multidosimetric approach during Sunset Yellow FCF degradation. Reactive oxygen species were mapped with four complementary dosimeters. Potassium iodide (KI) tracked interfacial hydroxyl radicals (^•OH). KI with ammonium heptamolybdate (AHM) captured ^•OH radicals together with hydrogen peroxide (H₂O₂). Bulk H₂O₂ accumulation integrated the recombination branch. Hydroxylation of 4-nitrophenol to 4-nitrocatechol acted as a selective near-interface ^•OH probe. Calorimetry showed that acoustic power density increased with set power and decreased with liquid height. All four dosimeters rose coherently with this variable, indicating that stronger driving elevated ^•OH generation while channeling a larger fraction into H₂O₂ through recombination. Process studies linked energy delivery to performance across operating conditions. Higher power accelerated pseudo-first order dye decay. Increasing initial dye concentration reduced fractional removal at fixed power, consistent with a radical-limited regime. Acidic media enhanced degradation by maintaining a stronger hydroxyl radical to water redox couple and by improving H₂O₂ persistence. Near neutral and alkaline media exhibited carbonate and bicarbonate scavenging of hydroxyl radicals and faster peroxide loss. Dissolved gas identity strongly modulated activity. Oxygen and argon outperformed air and carbon dioxide due to the combined thermophysical and chemical roles of the bubble gas. The calorimetry anchored and multidosimetric protocol provides a general route to compare reactors, optimize conditions, and support scale-up based on delivered energy density. Ultrasonication-driven degradation is a robust, practical technology for advanced treatment of dye-laden waters. Full article

This study investigates the formation of hydroxyl radicals (OH radicals) in cavitation bubble plasma-treated water (CBPTW) using a chemical probe method. CBPTW samples were prepared with different electrode materials (W, Fe, Cu, and Ag), and the chemical scavenger was added two minutes after the completion of cavitation and plasma treatments. The concentrations of metal ions and hydrogen peroxide (H₂O₂) generated in the CBPTW were also measured over time. This study reveals a novel mechanism whereby metal nanoparticles and ions released from electrodes catalyze the continuous generation of hydroxyl radicals in CBPTW, which has not been fully addressed in previous studies. The results suggest a continuous generation of OH radicals in CBPTW prepared with W, Fe, and Cu electrodes, with the amount of OH radicals produced in the order Cu > Fe > W. The study reveals a correlation between OH radical production and electrode wear, suggesting that the continuous generation of OH radicals in CBPTW results from the catalytic decomposition of H₂O₂ by metal nanoparticles or ions released from the electrodes. It should be noted that cavitation bubble plasma (CBP) is fundamentally different from sonochemistry. While sonochemistry utilizes ultrasound-induced cavitation to generate radicals, CBP relies on plasma discharge generated inside cavitation bubbles. No ultrasound was applied in this study; therefore, all observed radical formation is attributable exclusively to plasma processes rather than sonochemical effects. However, the precise mechanism of continuous OH radical formation in CBPTW remains unclear and requires further investigation. These findings provide new insights into the role of electrode materials in continuous OH radical generation in cavitation bubble plasma treated water, offering potential applications in water purification and sterilization technologies. Full article

Isoxazole-based molecules constitute a crucial category of heterocyclic compounds with wide-ranging applications across pharmaceutical development, advanced materials, and pesticide synthesis. Traditional synthetic approaches for isoxazole derivatives frequently encounter challenges such as extended reaction periods, severe operating conditions, and reliance on toxic solvents. As an eco-friendly alternative, sonochemistry has emerged as a promising approach for organic synthesis, offering enhanced reaction efficiency, reduced energy consumption, and improved yields. In this context, this review introduces the recent advancements in ultrasound-assisted strategies for the synthesis of isoxazole-scaffolds and their derivatives. Various methodologies are discussed, including multi-component reactions, catalytic systems, and solvent-free protocols. The integration of ultrasound not only accelerates reaction kinetics but also minimizes byproduct formation and enables the use of green solvents or catalysts. Key advantages such as shorter reaction durations, higher atom economy, and operational simplicity are emphasized. This work underscores the potential of sonochemical techniques to revolutionize isoxazole-based molecule synthesis, aligning with the principles of sustainable and green chemistry. Full article

Date pits are considered waste, and micronized date pit powder could be developed for use in foods and bio-products. In this study, micronized date pit powders were extracted by alcoholic sedimentation after ultrasound treatment. The control was considered untreated, i.e., without sonication. Six micronized fractions (i.e., three from control and three from treated) were prepared by three stages of alcoholic sedimentation. In the case of untreated date pit powder, the average particle size of the fractionated date pit powder (i.e., residue) from three stages of alcoholic sedimentation varied from 89 to 164 µm, while ultrasonic treatment showed variation from 39 to 65 µm. The average particle size of the supernatant fractions of untreated date pit powder varied from 22 to 63 µm, while ultrasonic treatment showed variation from 18 to 44 µm. Ultrasound treatment produced smaller particles. In all cases, Scanning Electron Microscopy (SEM) showed that supernatant fractions contained lumped particles compared to the residue fractions. Transmission Electron Microscopy (TEM) showed the presence of nanoparticles in all extracted fractions. Two glass transitions were observed in all fractions except for the residue from the first sedimentation stage. In addition, higher levels of degradation in the fractionated date pits could be achieved by ultrasonic treatment, as is evident from the Fourier Transform Infrared (FTIR) analysis. Full article

Colorectal cancer (CRC) remains a major global health challenge, necessitating the development of more effective and environmentally sustainable treatments. This study presents a novel green synthetic protocol for 1,3,5-triazine derivatives with anticancer potential, employing both microwave-assisted and ultrasound-assisted methods. The synthesis was optimized using 4-chloro-N-(2-chlorophenyl)-6-(morpholin-4-yl)-1,3,5-triazin-2-amine as the key intermediate, with sodium carbonate, TBAB, and DMF providing optimal yields under microwave conditions. To enhance sustainability, a modified sonochemical method was also developed, enabling efficient synthesis in aqueous media with a minimal use of organic solvents. A series of nine morpholine-functionalized derivatives were synthesized and evaluated for cytotoxic activity against SW480 and SW620 colorectal cancer cell lines. Compound 11 demonstrated superior antiproliferative activity (IC₅₀ = 5.85 µM) compared to the reference drug 5-fluorouracil, while compound 5 showed promising dual-line activity. In silico ADME analysis supported the drug likeness of the synthesized compounds, and biomimetic chromatography analysis confirmed favorable physicochemical properties, including lipophilicity and membrane affinity. These results underscore the potential of the developed protocol to produce bioactive triazine derivatives through an efficient, scalable, and environmentally friendly process, offering a valuable strategy for future anticancer drug development. Full article

A sonochemical synthesis of SnS₂ quantum dots using acetone as a solvent is investigated. Two different tin sources (SnCl₂∙2H₂O or SnCl₄∙5H₂O) as well as two different sulfur sources (thioacetamide or Na₂S₂O₃) were applied. The sonication time was also varied between 60 and 120 min. Resulting products of syntheses were characterized with the following techniques: powder X-ray diffraction, electron microscopy (SEM and HR-TEM), Raman and FT-IR spectroscopies, the Tauc method, and X-ray photoelectron spectroscopy. Obtained SnS₂ nanostructures were in the form of quantum dots in the case of synthesis lasting 60 min (size of crystallites in the range of 3.5–7 nm) and in the form of elongated nanorods of length ca. 25–30 nm and width of 5–6 nm in the case of synthesis lasting 120 min. XPS analyses revealed that the surface of the obtained products contained a significant amount of tin at the second oxidation state (i.e., SnS). The quantum dots produced in the synthesis lasting 60 min showed a value of energy bandgap of 2.7 eV indicating potential applications in photocatalysis. Full article

Sonochemical synthesis is becoming a popular method of preparing various nanomaterials, including metals, carbons, oxides, and chalcogenides. This method is relatively cheap and responds to the challenges of green chemistry as it typically does not involve high temperatures, high pressures, inert atmospheres, or long reaction times in comparison to other conventional methods. The utilization of ultrasound in synthesis makes the elimination of toxic solvents possible, as well as the execution of the synthesis without the use of reducing and stabilizing agents, while receiving products with the same or even better properties. The application of ultrasound allows for the synthesis of various nanomaterials with different properties for use in fields such as catalysis, electrochemistry, medicine, and biosensors. The final product is influenced by multiple variables such as temperature, pH, reagents, capping agents, time of reaction, and the addition of dopants. Full article

The serotonin 5-HT₆ receptor (5-HT₆R), expressed almost exclusively in the brain, affects the Cdk5 signaling as well as the mTOR pathway. Due to the association of 5-HT₆R signaling with pathways involved in cancer progression, we decided to check the usefulness of 5-HT₆R ligands in the treatment of CNS tumors. For this purpose, a new group of low-base 5-HT₆R ligands was developed, belonging to arylsulfonamide derivatives of cyclic arylguanidines. The selected group of molecules was also tested for their antiproliferative activity on astrocytoma (1321N1) and glioblastoma (U87MG, LN-229, U-251) cell lines. Some of the molecules were subjected to ADMET tests in vitro, including lipophilicity, drug binding to plasma proteins, affinity for phospholipids, drug–drug interaction (DDI), the penetration of the membrane (PAMPA), metabolic stability, and hepatotoxicity as well as in vivo cardiotoxicity in the Danio rerio model. Two antagonists with an affinity constant K_i < 50 nM (PR 68 K_i = 37 nM) were selected. These compounds were characterized by very high selectivity. An analysis of pharmacokinetic parameters for the lead compound PR 68 confirmed favorable properties for administration, including passive diffusion and acceptable metabolic stability (metabolized in 49%, MLMs). The compound did not exhibit the potential for drug–drug interactions. Full article

Plastics have become indispensable in modern society; however, the proliferation of their waste has become a problem that can no longer be ignored as most plastics are not biodegradable. Depolymerization/degradation through sustainable processes in the context of the circular economy are urgent issues. The presence of multiple types of plastic materials makes it necessary to study the specific characteristics of each material. This mini-review aims to provide an overview of technological approaches and their performance for the depolymerization and/or degradation of one of the most widespread plastic materials, polypropylene (PP). The state of the art is presented, describing the most relevant technologies focusing on advanced oxidation technologies (AOT) and the results obtained so far for some of the approaches, such as ozonation, sonochemistry, or photocatalysis, with the final aim of making more sustainable the PP depolymerization/degradation process. Full article

Cellulose is used widely in antimicrobial packaging due to its abundance in nature, biodegradability, renewability, non-toxicity, and low cost. However, how efficiently and rapidly it imparts high antimicrobial activity to cellulose-based packaging materials remains a challenge. In this work, Ag NPs were deposited on the surface of carboxymethyl cellulose/starch/N’N Methylenebisacrylamide film using ultrasonic radiation. Morphology and structure analysis of as-prepared films were conducted, and the antibacterial effects under different ultrasonic times and reductant contents were investigated. These results showed that Ag NPs were distributed uniformly on the film surface under an ultrasonic time of 45 min. The size of Ag NPs changes as the reducing agent content decreases. The composite film demonstrated a slightly better antibacterial effect against E. coli than against S. aureus. Therefore, this work can provide valuable insights for the research on antimicrobial packaging. Full article