Search Results (98)

Background/Objectives: PEGylated liposomes are widely recognized for their biocompatibility and capacity to extend systemic circulation via “stealth” properties. However, the PEG corona often limits tumor penetration and cellular internalization. Targeting matrix metalloproteinase-2 (MMP-2), frequently upregulated in breast cancer stroma, presents an opportunity to enhance tissue-specific drug delivery. In this study, we engineered MMP-2-responsive GPLGVRG peptide-modified cleavable PEGylated liposomes for targeted paclitaxel (PTX) delivery. Methods: Molecular docking simulations employed the MMP-2 crystal structure (PDB ID: 7XJO) to assess GPLGVRG peptide binding affinity. A cleavable, enzyme-sensitive peptide-PEG conjugate (Chol-PEG_2K-GPLGVRG-PEG_5K) was synthesized via small-molecule liquid-phase synthesis and characterized by ¹H NMR and MALDI-TOF MS. Liposomes incorporating this conjugate (S-Peps-PEG_5K) were formulated to evaluate whether MMP-2-mediated peptide degradation triggers detachment of long-chain PEG moieties, thereby enhancing internalization by 4T1 breast cancer cells. Additionally, the effects of tumor microenvironmental pH (~6.5) and MMP-2 concentration on drug release dynamics were investigated. Results: Molecular docking revealed robust GPLGVRG-MMP-2 interactions, yielding a binding energy of −7.1 kcal/mol. The peptide formed hydrogen bonds with MMP-2 residues Tyr A:23 and Arg A:53 (bond lengths: 2.4–2.5 Å) and engaged in hydrophobic contacts, confirming MMP-2 as the primary recognition site. Formulations containing 5 mol% Chol-PEG_2K-GPLGVRG-PEG_5K combined with 0.15 µg/mL MMP-2 (S-Peps-PEG_5K +MMP) exhibited superior internalization efficiency and significantly reduced clonogenic survival compared to controls. Notably, acidic pH (~6.5) induced MMP-2-mediated cleavage of the GPLGVRG peptide, accelerating S-Peps-PEG_5K dissociation and facilitating drug release. Conclusions: MMP-2-responsive, cleavable PEGylated liposomes markedly improve PTX accumulation and controlled release at tumor sites by dynamically modulating their stealth properties, offering a promising strategy to enhance chemotherapy efficacy in breast cancer. Full article

Background/Objectives: Currently there are very few effective oral antileishmanial treatments. In this study we evaluated a new bis(pyridine-2-carboxamidine) antileishmanial drug (JNII40_base) and its hydrochloride salt (JNII40_HCl). Methods: The characterization studies performed allowed us to determine the crystallinity, hydration water, and presence of hydrogen bonds in these drugs. Different dissolution methods were employed to predict intestinal absorption. A high-performance liquid chromatography–mass spectrophotometry (HPLC-MS/MS) method was developed for the determination of JNII40 in plasma. Results: Pharmacokinetic studies in rats of JNII40_base at 100 and 20 mg/kg, and JNII40_HCl at 20 mg/kg, showed a non-linear pharmacokinetic at high doses. An innovative biorelevant medium of phosphate buffer pH 6.8 with polysorbate 80 at 0.6% (w/v) showed high concentration values for JNII40_base at 30 min, which predicts good intestinal absorption. These results were consistent with the bioavailability data, which exhibited a significant (p < 0.05) increase in maximum plasma concentration (C_max) and a slight delay in time to maximum (T_max) compared to JNII40_HCl. Furthermore, the sustained release of JNII40_base in this biorelevant media was related to high plasma concentration values at 24 h (C_24h) observed in bioavailability studies. These plasma concentrations of JNII40_base were above the half-maximal inhibitory concentration (IC₅₀) against promastigote and amastigote forms of Leishmania donovani, which is indicative of effectiveness and should reduce the occurrence of drug resistance during treatments. Conclusions: The bioavailability and pharmacokinetic data support the consideration of this drug for further in vivo studies as an oral antileishmanial treatment. Full article

The layout of an urban waste-fired zero-emission power plant is described in this paper. The principle layout, which is based on similar coal-fired plants retrieved from the literature, integrates gasification with a power-generation section and implements two parallel conversion processes: one relies on the heat developed in the gasifier and consists of a thermoacoustic-magnetohydrodynamic (TA-MHD) generator; the other involves treating syngas to obtain almost pure hydrogen, which is then fed to fuel cells. The CO₂ derived from the oxidation of Carbon is stocked in liquid form. The novelty of the proposed layout lies in the fact that the entire conversion is performed using static equipment. The resulting plant prevents the release of any type of emissions in the atmosphere and increases mechanical efficiency, compared to traditional plants—thanks to the absence of moving parts—resolving, nonetheless, the ever-increasing waste-related pollution issue. A case study of a Union of Municipalities in Southern Lebanon is considered. The ideal cycle handles 65 tons/day of urban waste and is capable of generating 7.71 MW of electric power, with a global efficiency of 52.39%. Full article

A technique has been proposed and experimentally tested for measuring the hydrogen concentration in an inert atmosphere within a closed system. This method utilizes a metal-oxide-semiconductor field-effect capacity-type (MOSFEC) sensor under harsh conditions such as exposure to inert gases, pressure fluctuations, and varying temperatures. The measurement is performed during the thermal decomposition of metal hydrides in a liquid sodium environment. The developed measurement technique for determining hydrogen concentration released from metal hydride samples in a system with a closed gas path is cost-effective compared to standardized, resource-intensive open-volume flow measurement methods. The use of the developed MOSFEC sensor technique allows for rapid and efficient investigation of the in situ real-time dynamics of gas release from various metal hydride materials differing in their hydrogen content within a small closed volume. Additionally, this approach enables precise determination of the specific gas release temperatures. Full article

The safety performance of liquid hydrogen storage has a significant influence on its large-scale commercial application. Due to the complexity and costs of experimental investigation, computational fluid dynamics (CFD) simulations have been extensively applied to investigate the dynamic behaviors of liquid hydrogen release. The involved physical and chemical models, such as models of species thermodynamic properties and liquid–gas mass transfer, play a major role for the entire CFD model performance. However, comprehensive investigations into their impacts remain insufficient. In this study, CFD models of liquid hydrogen release were developed by using two widely used commercial simulation tools, Fluent and FLACS, and validated against experimental data available in the literature. Comparisons of the model results reveal strong discrepancies in the prediction accuracy of temperature and hydrogen volume fraction between the two models. The impact of the models of thermodynamic properties and liquid–gas mass transfer on the prediction results was subsequently explored by incorporating the FLACS sub-models to Fluent and evaluating the resulting prediction differences in temperatures and hydrogen volume fractions. The results show that the models of thermodynamic properties and liquid–gas mass transfer used in FLACS underestimate the vertical rise height and the highest hydrogen volume fraction of the cloud. Sensitivity analyses on the parameters in these sub-models indicate that the specific heats of hydrogen and nitrogen, in conjunction with the mass flow rate and outflow density of the mass transfer model, have a significant influence on model prediction of temperature. Full article

Industrial growth led to the expansion of existing environmental problems, where different kinds of pollutants can enter the environment by many known routes, particularly through wastewater. Among other contaminants, pharmaceuticals, such as diazepam, once released, pose a significant challenge related to their removal from complex environmental matrices due to their persistence and potential toxicity. For this reason, it is a great challenge to find suitable methods for the treatment of wastewater. The aim of this paper was to investigate the stability of diazepam, subjecting it to various degradation processes (hydrolysis and photolysis), focusing on photocatalysis, an advanced oxidation process commonly used for the purification of industrial wastewater. The photocatalytic system consisted of UV-A and simulated solar irradiation with titanium dioxide (TiO₂) immobilized on a glass mesh as a photocatalyst, with an additional reaction performed in the presence of an oxidizing agent, i.e., hydrogen peroxide, to improve diazepam removal from water matrices. The kinetic rate of diazepam degradation was monitored with a high-performance liquid chromatograph coupled with a photodiode array detector (HPLC-PDA). The target compound was characterized as a hydrolytically and photolytically stable compound with t_1/2 = 25 h. The presence of an immobilized TiO₂ catalyst contributed significantly to the degradation of diazepam under the influence of UV-A and simulated solar radiation, with t_1/2 in the range of 1.61–2.56 h. Five degradation products of diazepam were identified at the laboratory scale by MS analysis (m/z = 267, m/z = 273, m/z = 301, m/z = 271, and m/z = 303), while the toxicity assessment revealed that diazepam exhibited developmental toxicity and a low bioaccumulation factor. The pilot-scale process resulted in significant improvements in diazepam degradation with the fastest degradation kinetics (0.6888 h⁻¹). These results obtained at the pilot scale highlight the potential for industrial-scale implementation, offering a promising and innovative solution for pharmaceutical removal from wastewater. Full article

Gas channeling phenomena in carbonate fracture-vuggy reservoirs frequently occur, primarily in the form of negative pressure gas channeling and displacement gas channeling, with the possibility of mutual conversion between the two. This is accompanied by the risk of hydrogen sulfide (H₂S) release from the reservoir, which poses significant challenges to controlling safety. Currently, liquid bridging and gel plugging technologies are effective methods for mitigating complex issues such as downhole overflow, fluid loss, and heavy oil backflow. This paper focuses on the development and optimization of key treatment agents, including high-temperature-resistant polymers and crosslinking agents, to formulate a high-temperature chemical gel plugging agent. A gel-breaking, high-strength colloidal chemical gel plugging agent system capable of withstanding temperatures up to 150 °C was developed, and it has an apparent viscosity of about 7500 mPa·s, an energy storage modulus and a loss modulus of 51 Pa and 6 Pa, respectively, after gel formation at elevated temperatures, and an apparent viscosity retention rate of the gel of greater than 82% after aging for 9 d at a temperature of 150 °C. This system forms a stable gas isolation barrier in the wellbore, with performance remaining stable after 7 to 12 days of aging, and the degradation rate reaches 99.8% after 24 h at 150 °C. This technology is of significant importance in solving complex issues such as overflow, fluid loss, and heavy oil backflow in gas injection and recovery wells in high-temperature, high-pressure reservoir conditions. Full article

The surge in photovoltaic (PV) power generation has made it increasingly difficult to integrate the intermittent PV industry into the power grid while maintaining grid stability. The solution is to use the seasonal surplus of PV electricity to produce “green” hydrogen through water electrolysis and then use the hydrogen as an energy source or as a reactant in chemical processes in the chemical industry to produce value-added products. However, the development of advanced hydrogen storage technologies to ensure the safe handling, transportation, and distribution of H₂ is a major issue. The use of stable liquid organic hydrogen carriers (LOHCs) has emerged as a suitable technology for hydrogen storage. This review highlights prospective LOHC technologies based on reversible catalytic hydrogenation–dehydrogenation cycles of liquid organic molecules for hydrogen storage and release under mild temperature and pressure conditions. The state-of-the-art LOHC systems are critically reviewed, highlighting the most effective heterogeneous catalytic systems. Full article

Lignin is the largest renewable source of aromatic biopolymers on Earth, and it is commercially available as by-product of biorefineries and pulp/paper industries. It is mainly burned for heat and power, but pyrolysis can provide high-value-added products. In this study, the pyrolysis characteristics of alkali lignin pellets are investigated using a packed-bed reactor at a laboratory scale for heating temperatures of 800–900 K. Conversion dynamics are analyzed by means of the thermal field and the rates of gaseous species release, which is a very innovative aspect of the study. The yields of the lumped product classes do not vary significantly in the range of heating temperatures examined (biochar yields around 58–63 wt%, together with gas and liquid yields around 9–12 and 28–30 wt%, respectively). Carbon dioxide is the most abundant gaseous product, followed by methane and carbon monoxide (smaller amounts of C₂ hydrocarbons and hydrogen), while bio-oil is rich in phenolic compounds, especially guaiacols, cresols, and phenol. A comparison with the conversion dynamics of fir, beech, and straw reveals that, mainly as a consequence of softening and melting, the lignin heat- and mass-transfer rates as well as actual reaction temperatures are profoundly different. In fact, the characteristic process size becomes the diameter of the reactor rather than that of the pellets. Full article

As environmental pollution has become a global concern, regulations on carbon emissions from maritime activities are being implemented, and interest in using renewable energy as fuel for ships is growing. Hydrogen, which does not release carbon dioxide and has a high energy density, can potentially replace fossil fuels as a renewable energy source. Notably, storage of hydrogen in a liquid state is considered the most efficient. In this study, a 0.7 m³ liquid hydrogen fuel tank suitable for small vessels was designed, and a structural analysis was conducted to assess its structural integrity. The extremely low liquefaction temperature of hydrogen at −253 °C and the need for spatial efficiency in liquid hydrogen fuel tanks make vacuum insulation essential to minimize the heat transfer due to convection. A composite insulation system of sprayed-on foam insulation (SOFI) and multilayer insulation (MLI) was applied in the vacuum annular space between the inner and outer shells, and a tube-shaped supporter made of a G-11 cryogenic (CR) material with low thermal conductivity and high strength was employed. The material selected for the inner and outer layers of the tank was STS 316L, which exhibits sufficient ductility and strength at cryogenic temperatures and has low sensitivity to hydrogen embrittlement. The insulation performance was quantitatively assessed by calculating the boil-off rate (BOR) of the designed fuel tank. Structural integrity evaluations were conducted for nine load cases using heat transfer and structural analyses in accordance with the IGF code. Full article

Liquid organic hydrogen carriers (LOHCs) are recognized as promising sustainable hydrogen (H₂) carriers due to their high volumetric capacity and ability to store H₂ at ambient conditions, eliminating the need for energy-intensive liquefaction or compression processes associated with H₂ or ammonia gas. One of the main current drawbacks, however, is LOHCs’ high energy demand for H₂ release. This work presents the photo-induced liberation of H₂ from formic acid (FA) as a liquid H₂ carrier, using visible light and well-established 5 wt% palladium nanoparticles supported over carbon (Pd/C). We show that low-power light-emitting diodes (LEDs) produced higher gas flow than their thermal baseline (35 $°$C), with 27.2 mL/min and 7.72 mL/min, respectively. Further, the rate of gas evolved with light intensity, catalyst loading, and the concentration of FA. Light-induced dehydrogenation shows similar deactivation as the known thermal mechanisms, such as the decreased Pd²⁺/Pd⁰ ratio and Pd nanoparticle agglomeration. Hence, these observations suggest a photothermal mechanism, whereby the LED provides heat efficiently absorbed by the Pd/C catalyst and enhanced by Pd’s ability to absorb light, thereby driving the FA dehydrogenation reaction at ambient conditions. Full article

In the WCLL-BB liquid blanket concept, among the postulated accidental scenarios to be investigated regarding the PbLi system, a loss of liquid metal is one of the most crucial for safety purposes. As a consequence of this loss, chemical reactions might occur between lithium, air, and water. These reactions may lead to significant increases in temperature and pressure and to the formation of hydrogen inside the building; the evaluation of the impact of these events is essential to define future safety guidelines. Using MELCOR for fusion (v.1.8.6.), a first approach for investigating an out-vessel loss of PbLi was presented in this work. The temperature and pressure trends were investigated through the default MELCOR package for lithium air chemical reactions; however, this package works only with pure lithium. Therefore, a new model of the reaction was developed in this work using MELCOR Control Functions, which allows the simulation of the chemical reactions using PbLi as working fluid, in order to investigate a more realistic scenario. The results from different approaches were compared, and the limits of the code were outlined. It was found that the final pressure and temperature in the tokamak building might reach critical values at the end of the transient, if the energy released by the chemical reaction was entirely considered; however, it is important to note that, due to the assumptions and simplifications adopted, the results were very conservative in terms of temperature and pressure reached in the system, and further investigations were suggested in this work. Full article

Doxorubicin (DOX) is one of the most widely used chemotherapy drugs in the treatment of both solid and liquid tumors in patients of all age groups. However, it is likely to produce several side effects that include doxorubicin cardiomyopathy. Nanoparticles (NPs) can offer targeted delivery and release of the drug, potentially increasing treatment efficiency and alleviating side effects. This makes them a viable vector for novel drug delivery systems. Currently, DOX is commonly conjugated to NPs by non-covalent conjugation–physical entrapping of the drug using electrostatic interactions, van der Waals forces, or hydrogen bonding. The reported downside of these methods is that they provide a low drug loading capacity and a higher drug leakage possibility. In comparison to this, the covalent conjugation of DOX via amide (typically formed by coupling carboxyl groups on DOX with amine groups on the nanoparticle or a linker, often facilitated by carbodiimide reagents), hydrazone (which results from the reaction between hydrazines and carbonyl groups, offering pH-sensitive cleavage for controlled release), or disulfide bonds (formed through the oxidation of thiol groups and cleavable by intracellular reducing agents such as glutathione) is more promising as it offers greater bonding strength. This review covers the covalent conjugation of DOX to three different types of NPs—metallic, silica/organosilica, and polymeric—including their corresponding release rates and mechanisms. Full article

Hydrogen fuel cell-based UAM (urban air mobility) systems are gaining significant attention due to their advantages of higher energy density and longer flight durations compared to conventional battery-based UAM systems. To further improve the flight times of current UAM systems, various hydrogen storage methods, such as liquid hydrogen and hydrogen metal hydrides, are being utilized. Among these, hydrogen metal hydrides offer the advantage of high safety, as they do not require the additional technologies needed for high-pressure gaseous hydrogen storage or the maintenance of cryogenic temperatures for liquid hydrogen. Furthermore, because of the relatively slower dynamic response of hydrogen fuel cell systems compared to batteries, they are often integrated into hybrid configurations with batteries, necessitating an efficient power management system. In this study, a UAM system was developed by integrating a hydrogen fuel cell system with hydrogen metal hydrides and batteries in a hybrid configuration. Additionally, a state machine control approach was applied to a distribution valve for the endothermic reaction required for hydrogen desorption from the hydrogen metal hydrides. This design utilized waste heat generated by the fuel cell stack to facilitate hydrogen release. Furthermore, a fuzzy logic control-based power management system was implemented to ensure efficient power distribution during flight. The results show that approximately 43% of the waste heat generated by the stack was recovered through the tank system. Full article

A jet flame occurs when the release of flammable gas or liquid ignites, resulting in a long, intense, and highly directional flame. This type of fire is commonly associated with industrial incidents involving pipelines, storage tanks, and other pressurized equipment. Jet fires are a significant concern in the oil and gas industry due to the handling and processing of large volumes of flammable hydrocarbons under pressure. The new computational method presented here includes several aspects of hydrogen jet flame accidents and their mitigation: the CFD simulation of a hydrogen jet flame using the HyRAM code and Fire Dynamics Simulator (FDS) software 5.0 using a large eddy simulation (LES) turbulence model; the calculation of the gaseous mixture’s thermo-physical properties using the GASEQ thermochemical code; the calculation of convective and radiative heat fluxes using empirical correlation; and a heat transfer simulation on the pipe thermal barrier coating (TBC) using COMSOL Multiphysics software 4.2a during the heating phase. This method developed for the ceramic blanket was validated successfully against the previous experimental results obtained by Gravit et al. It was shown that a jet fire’s maximum temperature obtained using FDS software was similar to that obtained using GASEQ thermochemical software 0.79 and HyRAM software. The TBC’s surface temperature reached 1945 °C. The stainless steel’s maximal temperature reached 165.5 °C. There was a slight decrease in UTS at this temperature. Full article