Narrow Particle Size Distribution Research Articles

Self-supply of hydrogen peroxide by a bimetal-based nanocatalytic platform to enhance chemodynamic therapy for tumor treatment

The tumor microenvironment (TME) is characterized by low pH, hypoxia, and overexpression of glutathione (GSH). Owing to the complexity of tumor pathogenesis and the heterogeneity of the TME, achieving satisfactory efficacy with a single treatment method is difficult, which significantly impedes tumor treatment. In this study, composite nanoparticles of calcium-copper/alginate-hyaluronic acid (HA) (CaO2-CuO2@SA/HA NC) with pH and GSH responsiveness were prepared for the first time through a one-step synthesis using HA as a targeting ligand. Nanoparticles loaded with H2O2can enhance the chemodynamic therapy effects. Simultaneously, Cu2+can generate oxygen in the TME and alleviate hypoxia in tumor tissue. Cu2+and H2O2undergo the Fenton reaction to produce cytotoxic hydroxyl radicals and Ca2+ions, which enhance the localization and clearance of nanoparticles in tumor cells. Additionally, HA and sodium alginate (SA) were utilized to improve the targeting and biocompatibility of the nanoparticles. Fourier transform infrared, x-ray diffraction, dynamic light scattering, SEM, transmission electron microscope, and other analytical methods were used to investigate their physical and chemical properties. The results indicate that the CaO2-CuO2@SA/HA NC prepared using a one-step method had a particle size of 220 nm, a narrow particle size distribution, and a uniform morphology. The hydrogen peroxide self-supplied nanodrug delivery system exhibited excellent pH-responsive release performance and glutathione-responsive •OH release ability while also reducing the level of reactive oxide species quenching.In vitrocell experiments, no obvious side effects on normal tissues were observed; however, the inhibition rate of malignant tumors HepG2 and DU145 exceeded 50%. The preparation of CaO2-CuO2@SA/HA NC nanoparticles, which can achieve both chemokinetic therapy and ion interference therapy, has demonstrated significant potential for clinical applications in cancer therapy.

Assessing the Drying Sensitivity of Alkali-Activated Binders Through Mechanical Reliability: Effect of Particle Size and Packing

Despite the steady progress of research on the alkali activation of wastes or subproducts from established industrial processes, the brittleness of the hardened alkali-activated materials frequently results in questionable mechanical reliability, particularly in industrial applications beyond construction materials. This work used a 33 factorial Design of Experiments to examine the effect of three different particle size distributions on the compressive strength and mechanical reliability (Weibull modulus) of a sodium silicate-activated blast-furnace slag under the same processing conditions. As expected, curing temperature and time were strongly correlated, and the corresponding response surfaces showed that, for all studied particle sizes, compressive strengths above 60 MPa with mechanical reliability above 5.0 could be obtained by curing at ~60 °C for ~40 h. The particle size differences caused no significant changes in the extent of alkali activation, as seen in the infrared-spectroscopy results. However, the intersection of the response surfaces showed that a coarser and narrower particle size distribution extended the working area (time × temperature) and favored mechanical reliability. Thus, the precursor’s particle size distribution, which governs particle packing and viscosity during processing, also determines the permeability of the set binder, which affects water removal during drying and the dried binder’s mechanical performance.

Cerium doped superparamagnetic Mn-Zn ferrite as a promising material for self-regulated magnetic hyperthermia

Recently, cubic ferrites (CF) have been widely explored in biomedical applications, especially those that display superparamagnetism behavior due to the desirable absence of remanent field. In this study, we report the self-stabilization of the magnetic fluid hyperthermia (MFH) temperature in the cancer therapy range (42 - 48 ºC) by Ce3+ substitution in superparamagnetic Mn0.8Zn0.2Fe2-xCexO4 ferrite with x = 0.0; 0.015; 0.030; 0.050 and 0.100. A comprehensive characterization was performed in order to investigate the influence of this replacement on the magnetic and structural properties of the ferrite. The samples were synthesized by the sol-gel auto-combustion method and the properties were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), selected area electron diffraction (SAED), Raman spectroscopy (RS), Mössbauer spectroscopy (MS), vibrational sample magnetometry (VSM), and ferromagnetic resonance (FMR). Magnetic hyperthermia essays were used to obtain the heat induction curves and calculate energy dissipation. We refined the XRD data by the Rietveld method to determine the cation distribution and calculate interionic parameters. Magnetic characterization confirms the superparamagnetic behavior at 300 K, which is expected from the TEM results that show a narrow distribution of particle sizes, with a mean size of about 6.5 nm for all samples. The VSM results show a consistent decrease in magnetization saturation with cerium content that result in a weaker self-heating induction capacity for the cerium-doped samples. FMR results also show a smaller relaxation time T2 for these samples, suggesting a slower energy dissipation rate. These conclusions are confirmed by the heat induction curves and the values of the specific absorption rate (SAR), which are smaller for cerium-doped samples. For the a field with an amplitude of 35.33 kA/m and a frequency of 222 kHz, the temperature of the cerium-doped samples saturates in the optimum interval for cancer treatment, between 42 and 48 ºC. These results suggest that Ce3+ is a promising doping ion to optimize the heating rate behavior of Mn-Zn ferrite for cancer treatment by hyperthermia.

Jet cavitation-enhanced hydration method for the preparation of magnesium hydroxide

During the preparation of magnesium hydroxide via the hydration method, in-situ growth and agglomeration often inhibit the reaction. This study used active magnesium oxide as the raw material and employed jet cavitation technology to enhance the hydration process. Based on the growth process of magnesium hydroxide, the mechanism of jet-enhanced hydration was analyzed. The effects of reaction temperature (T), reaction time (t), solid-liquid ratio (s), and cavitation number (σ) on the hydration rate were investigated. An L25(54) orthogonal experiment explored the significance of each factor's impact on the hydration rate. The hydration products were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), and a specific surface area analyzer. Results indicate that the factors affecting the hydration rate, in order of significance, are cavitation number > reaction temperature > solid-liquid ratio > reaction time. The optimal process parameters were determined to be a reaction temperature of 70 °C, reaction time of 80 min, solid-liquid ratio of 1:12, and cavitation number of 0.42. Under these conditions, the hydration rate reached 94.87 %, producing well-dispersed lamellar magnesium hydroxide with a narrow particle size distribution (median particle size D50 = 4.511 μm) and a BET specific surface area of 11.345 m²/g.

A new process for preparing ultrafine WC-Co cemented carbide by doping yttrium within the ammonium metatungstate solution

Ultrafine WC-Co cemented carbide has superior performance of high strength and high hardness, which is widely used in industrial fields. In the traditional process, high temperature carburization method is used to prepare tungsten carbide, and solid-phase mechanical milling method is used to mix grain growth inhibitor (Cr3C2) and tungsten carbide, which easily lead to large WC particle size and uneven WC grain size distribution in WC-Co cemented carbide, thus affecting mechanical properties of the alloy. In the new process, based on the genetic relationship between the particle size of ammonium paratungstate and tungsten carbide, ultrafine ammonium paratungstate uniformly doped with yttrium was firstly obtained by adding a certain amount of ammonia and yttrium oxide into the ammonium metatungstate solution. Then the ammonium paratungstate was calcined to obtain yttrium-doped tungsten trioxide, which was then converted into yttrium-doped ultrafine tungsten carbide powders by introducing carbon monoxide at a low temperature. Finally, the ultrafine WC-Co cemented carbide was prepared by pressure sintering. During the neutralization and crystallization process of ammonium metatungstate solution, the yttrium-doped ultrafine ammonium paratungstate (Fischer particle size 8.4 μm) with narrow particle size distribution and regular morphology was prepared. The yttrium-doped ammonium paratungstate was calcined at 500 °C for 90 min in air atmosphere to obtain yttrium-doped tungsten trioxide powder with a Fischer particle size of 4.5 μm and narrow size distribution. Then the yttrium-doped tungsten trioxide and carbon monoxide gas were reacted at 920 °C for 3h to obtain yttrium-doped ultrafine tungsten carbide powder with a Fischer particle size of 0.32 μm and a specific surface area of 4.44 m2/g, and ultrafine WC-Co cemented carbide with tungsten carbide grain size of 0.28 μm was obtained by pressure sintering. The yttrium uniform distributed effectively inhibited the abnormal growth of tungsten carbide grains. Compared with the WC-Co cemented carbide prepared by solid-phase mechanically mixing tungsten carbide powder and chromium carbide, the yttrium-doped WC-Co cemented carbide had a smaller average tungsten carbide grain size and a more homogeneous microstructure. The prepared yttrium-doped WC-Co cemented carbide had a hardness (HRA) of 94.6, a bending strength of 4841 M, and a coercive force of 42.3 KA/c.

Structural Modification of Ru‐Bi Catalysts and its Impact on One‐Pot Synthesis of 2,3,5‐trimethyl‐1,4‐benzoquinone with Hydrogen Peroxide

AbstractOxidative transformation of phenols is an efficient route towards the production of moieties for naturally occurring quinones with a wide range of biological activities. Silica supported Ru−Bi catalysts were prepared by microwave‐assisted loading (MW) and deposition (DP) methods. The as‐prepared catalysts were characterized by XRD (X‐ray diffraction), N2 physisoption, SEM (Scanning electron microscopy), TEM (Transmission electron microscopy) and XPS (X‐ray photoelectron spectrometry) techniques. Catalysts with low Bi loading, 5 %Ru‐1 %Bi, have narrow particle size distributions that correspond to an average particle size of 2.21–2.59 nm. 5 %Ru‐5 %Bi catalysts consist of Ru−Bi nanochains. The outcome of the catalytic oxidation of 2,3,5‐trimethylhydroquinone (TMHQ, 1) to 2,3,5‐trimethyl‐1,4‐benzoquinone (TMBQ, 2) depends on the catalyst preparation method, promoter loading, solvent and temperature used. MW‐5Ru1Bi is the most active catalyst with conversions that range between 99–100 % at both room temperature (r.t) and under refluxing MeNO2 and MeOH. The highest yields of TMBQ (100 %) were obtained over MW‐5 %Ru‐1 %Bi and DP‐5 %Ru‐5 %Bi catalysts.

Improving the Stability, Water Solubility, and Antioxidant Activity of α-Tocopherol by Encapsulating It into Niosomes Modified with Cationic Carbamate-Containing Surfactants.

The low solubility of α-tocopherol in water and its susceptibility to photodegradation make it difficult for biological systems to absorb this natural antioxidant. To overcome these limitations, α-tocopherol was encapsulated in low-toxicity nanocontainers, namely, niosomes based on Tween 80 and cholesterol. The niosomes were modified with cationic surfactants containing a carbamate fragment. The size and charge of the particles were determined and their stability was assessed using dynamic and electrophoretic light scattering methods. It was found that the introduction of cationic surfactants to niosome formulations significantly improved their physicochemical properties and increased stability due to a positive charge of up to +40 mV being generated. Modified niosomes loaded with α-tocopherol were characterized by a hydrodynamic diameter of 100-120 nm, a narrow particle size distribution, and a high encapsulation efficiency of more than 90%. Testing the photochemical stability of α-tocopherol using a spectrophotometric method demonstrated that niosomes were able to protect this substance from UV irradiation. Luminescence analysis showed that the inclusion of α-tocopherol in niosomes increased their antioxidant activity by 30%. An acute toxicity study has demonstrated the safety of the systems. The LD50 value for niosomes modified with carbamate-containing surfactants and loaded with α-tocopherol exceeded 10,000 mg·kg-1 (mice, intraperitoneal and oral administration).

Microfluidic Precision Manufacture of High Performance Liquid Chromatographic Microspheres

A key bottleneck in developing chromatographic material is the chemically entangled control of morphology, pore structure, and material chemistry, which holds back precision material manufacture in order to pursue advanced separation performance. In this work, a precision manufacture strategy based on droplet microfluidics was developed, for production of highly efficient chromatographic microspheres with independent control over particle morphology, pore structure and material chemistry. The droplet‐synthesized microspheres display extremely narrow particle size distribution (CV<3%), enabling a 100% production yield due to complete elimination of sieving steps. More importantly, the size of the droplet‐synthesized microspheres is freely adjustable without the need for re‐optimizing chemical recipes or reaction conditions. The resulting materials exhibit excellent separation efficiencies, achieving a reduced plate height of hmin​=1.67. This precision manufacture strategy also allows for flexible pore design and continuous pore size adjustment across three orders of magnitudes, providing a novel vehicle for resolution fine‐tuning targeting protein separation. Besides traditional silica, organic‐inorganic hybrid silica, zirconia, and titania microspheres can also be precisely synthesized on the same platform, supporting various separation applications and operating conditions. Powered by precision manufacture, super‐throughput production, and versatile chemistry, the high‐performance droplet‐synthesized separation material will pave the way towards green and precision chromatographic industry.

Microfluidic Precision Manufacture of High Performance Liquid Chromatographic Microspheres.

A key bottleneck in developing chromatographic material is the chemically entangled control of morphology, pore structure, and material chemistry, which holds back precision material manufacture in order to pursue advanced separation performance. In this work, a precision manufacture strategy based on droplet microfluidics was developed,for production of highly efficient chromatographic microspheres with independent controloverparticle morphology, pore structureand material chemistry.The droplet-synthesized microspheres display extremely narrow particle size distribution (CV<3%), enabling a 100% production yield due to complete elimination of sieving steps. More importantly, the size of the droplet-synthesized microspheres is freely adjustable without the need for re-optimizing chemical recipes or reaction conditions. The resulting materials exhibit excellent separation efficiencies, achieving a reduced plate height of hmin​=1.67. This precision manufacture strategy also allows for flexible pore design and continuous pore size adjustment across three orders of magnitudes, providing a novel vehicle for resolution fine-tuning targeting protein separation. Besides traditional silica, organic-inorganic hybrid silica, zirconia, and titania microspheres can also be precisely synthesized on the same platform, supporting various separation applications and operating conditions. Powered by precision manufacture, super-throughput production, and versatile chemistry, the high-performance droplet-synthesized separation material will pave the way towards green and precision chromatographic industry.

Hyperbranched Organosilicon Surfactants as Emulsifiers for the Emulsion Polymerization of Methyl Methacrylate

This report is devoted to the investigation of the emulsion polymerization of methyl methacrylate in the presence of PEGylated hyperbranched polymethylethoxysiloxane as an emulsifier. It is shown that its use in the amount of 1–5 wt % affords stable 25–50% poly(methyl methacrylate) dispersions with the controlled particle sizes from 300 to 800 nm and a narrow particle size distribution.

Lyotropic liquid crystal and self-emulsifying drug delivery systems nanoparticles as artesunic acid and praziquantel carriers: An innovative approach for formulation of anti-malaria and schistosomicidal drugs

Praziquantel (PZQ) is the drug of choice for treating cestode and trematode infections, and it is currently the only option against schistosomiasis. Artesunic acid (AcART) is effective against several parasites and has emerged as an alternative for schistosomiasis treatment. However, AcART and PZQ have limited bioavailability due to poor water solubility, low permeability, and rapid cell clearance. To address these challenges, this study aimed to develop self-emulsifying drug delivery systems to develop SEDDS and NPs-LLC to overcome the low water solubility affecting AcART and PZQ bioavailability. The study involved validating the HPLC analytical methodology for AcART, SEDDS, and NPs-LLC formulations, and conducting physicochemical characterization and ex-vivo intestinal permeation assays. The composition of formulations was determined by the solubility balance of AcART and PZQ. The drug content ranged between 83 and 90 %. The anionic zeta potential was attributed to Myverol®, and the particle diameter increased slightly after the drug incorporation, while the polydispersity index indicated the relatively narrow particle size distribution. Additionally, the DSC thermogram confirmed that PZQ and AcART are in solution within SEDDS and NPs-LLC. The FTIR analysis suggests that components of SEDDS and NPs-LLC and drugs do not react to form new chemical species. The selection of specific compound formulations was based on achieving the best solubility balance. The nanostructures were stable and exhibited a surface charge favorable to mucosal permeation, with slightly superior performance for SEDDS. The innovative formulations, SEDDS and NPs-LLC, are suitable and effective carriers for AcART and PZQ.

Microstructure and mechanical properties of Fe–30Mn–9Al–C–3Ni low-density steel manufactured by selective laser melting

Low-density Fe–Mn–Al–C steels are widely used in the automotive and aerospace industries as advanced lightweight materials. In this study, highly spherical Fe–30Mn–9Al–C–3Ni powder with a narrow particle-size distribution, low oxygen content, and good flowability was prepared using the plasma rotating electrode process (PREP). Furthermore, Fe–30Mn–9Al–C–3Ni low-density alloy steel was manufactured for the first time using the selective laser melting (SLM) molding technique. Laser power was found to significantly impact the microstructure and mechanical properties of SLM-printed Fe–30Mn–9Al–C–3Ni alloys. The Fe–30Mn–9Al–C–3Ni alloy prepared at a laser power of 110 W (denoted as P-110) exhibited the best mechanical properties, including a yield strength of 887.1 MPa, tensile strength of 1076.8 MPa, elongation of 40.80%, and a maximum hardness value of 294 HV. This study highlights the potential of SLM molding for fabricating low-density Fe–Mn–Al–C steels with complex geometrical shapes and outstanding comprehensive mechanical properties.

Preparation and performance evaluation of CNF‐enhanced polyether‐modified polysiloxane defoamer

AbstractIn this article, polyether‐modified polysiloxanes were synthesized by the reaction of poly(methyl hydrogen siloxane) (PMHS) with Allyl alcohol polyether B‐400. FT‐IR, laser particle size analysis, hydrophilic–lipophilic balance (HLB) value test, and surface tension measurements were used to characterize its structures and properties. The results show that the control law for the HLB value of polyether‐modified polysiloxanes was obtained as follow: the HLB value increases with increasing hydrogen content of PMHS. When the polyether‐modified polysiloxanes were used to emulsify the polysiloxane, at the HLB value of 10.5, the average particle size of the emulsion was about 0.23 μm with a narrow particle size distribution. The emulsion has good emulsifying and dispersing properties, as well as excellent foam elimination and foam inhibition performance. When the cellulose nanofibrils (CNF) was used as a protective agent for the preparing of the polysiloxane defoamer, the stability of the emulsion does not affect, but its foam elimination and foam inhibition of emulsion can be further improved at the presence of CNF. The lowest surface tension of CNF‐enhanced polyether‐modified polysiloxane defoamer is about 22.4 mN m−1, which has good surface property. When the concentration of CNF‐enhanced polyether‐modified polysiloxane defoamer was 0.1 g L−1, the foam elimination time and foam inhibition time were 5.8 s and 38 min, respectively, at the temperature (80°C) and alkali environment (pH 13).

Preparation of spherical HMX@PDA-based PBX by co-axial droplet microfluidic technology: Enhancing the interfacial effect and safety performance of composite microspheres

Surface engineering plays a crucial role in improving the performance of high energy materials, and polydopamine (PDA) is widely used in the field of energetic materials for surface modification and functionalization. In order to obtain high-quality HMX@PDA-based PBX explosives with high sphericity and a narrow particle size distribution, composite microspheres were prepared using co-axial droplet microfluidic technology. The formation mechanism, thermal behavior, mechanical sensitivity, electrostatic spark sensitivity, compressive strength, and combustion performance of the microspheres were investigated. The results show that PDA can effectively enhance the interfacial interaction between the explosive particles and the binder under the synergistic effect of chemical bonds and the physical "mechanical interlocking" structure. Interface reinforcement causes the thermal decomposition temperature of the sample microspheres to move to a higher temperature, with the sensitivity to impact, friction, and electrostatic sparks (for S-1) increasing by 12.5%, 31.3%, and 81.5% respectively, and the compressive strength also increased by 30.7%, effectively enhancing the safety performance of the microspheres. Therefore, this study provides an effective and universal strategy for preparing high-quality functional explosives, and also provides some reference for the safe use of energetic materials in practical applications.

Micelles as nanocarriers of fluorescent and magnetic dendrimers for potential bimodal imaging applications

Bimodal magnetic-fluorescent materials that integrate magnetic and fluorescent properties have attracted significant attention due to their potential applications in biomedical imaging, biosensing, and therapeutic diagnosis. Tetra-amido-TEMPO 1, a compound that combines a fluorescent oligo(styryl)benzene dendrimer core with TEMPO radicals in its four branches was synthesized and used to form micelles with CTAB in water. DLS and Cryo-TEM techniques revealed the formation of micelles exhibiting a narrow particle size distribution, with an average hydrodynamic diameter ranging from 95 to 140 nm. After micellization, the ultraviolet-visible absorption and fluorescence emission intensities of micelles increased with tetra-amido-TEMPO concentration and EPR spectroscopy demonstrated consistent three-line spectra in the micelles, with the integrated area directly proportional to the amount of tetra-amido-TEMPO present. Besides, sufficient contrast enhancement in the proton T1 relaxation time-weighted magnetic resonance images in vitro proved their ability to act as magnetic resonance imaging (MRI) contrast agents. These tetra-amido-TEMPO/CTAB micelles offer an aqueous-compatible system for this bimodal fluorescent-magnetic molecule, showcasing proof of concept of their potential for biomedical applications.

Preparation and in vitro/in vivo evaluation of uniform-sized Goserelin-loaded sustained release microspheres

Sustained release microspheres loaded with goserelin are regarded as a promising candidate for treating prostate cancer and other sex hormone diseases. However, their widespread adoption has been hindered by issues such as wide particle size distribution and unstable release characteristics. To address these challenges, we employed a combination of the solid-in-oil-in-water microspheres preparation approach (S/O/W) and innovative premix membrane emulsification technology and deeply investigated the effects of four key parameters on the loaded performance of microspheres and the microscopic mechanisms behind them. With this approach, we successfully produced goserelin-loaded sustained release microspheres of narrow particle size distribution (Span 0.642), remarkable encapsulation efficiency (DL = 4.23 %, EE = 93.98 %), low initial burst release (about 0.50 % within 2 h), and compatibility with small injection needles (23-G, inner diameter 0.33 mm, outer diameter 0.64 mm, maximal force 59 N). In the animal model(administered dose, 2.4 mg·Kg−1), goserelin long-acting sustained release microspheres sustained release for over 32 days, maintaining effective concentrations above 2 ng·mL−1, and effectively reduced serum testosterone concentrations to castration levels (<1.0 ng·mL−1) by day 4, maintaining this inhibition for up to 21 days, exhibiting comparable efficacy to the positive control group. In vivo release kinetics analysis revealed that goserelin-loaded sustained release microspheres exhibited a release pattern dominated by diffusion with corrosion assistance in vivo. In summary, the systematic and comprehensive evaluation of uniform-sized goserelin-loaded sustained release microspheres has highlighted their excellent translational potential, and the study herein may provide new strategies and ideas for the development of microsphere dosage forms.

Reactive crystallization regulation for synthesizing NCM811 precursor by different impellers

The spherical and dense precursors with a narrow particle size distribution are essential to achieve high electrochemical performance in cathode materials. Four newly designed impellers, including the punched-flow turbine (PFT), punched-flow disc turbine (PFDT), curved-inclined-blade disc turbine (CIBDT), and 6-folded-pitched turbine (FPT-6), are applied to prepare the precursors to investigate the interplay among the fluid flow state, precursors’ morphology and growth, and physicochemical properties of cathodes. The flow and mixing features of double impellers are predicted using computational fluid dynamics, indicating that the FPT-6 plays a crucial role in crystal nucleation while PFDT facilitates crystal growth. This concurrence can be corroborated by examining the performance of precursors synthesized using these four impellers. It is first found that the electrochemical performance is distinctly enhanced by utilizing different impellers to regulate the specified nucleation and growth stage. By increasing the nucleation rate with double impellers of FPT-6, the tap density and sphericity of the precursor and cathode materials are significantly improved. The discharge capacity of cooperative agitators (FPT-6+PT) is 2.1 times that of the only propeller turbine at a high current density (10 C). The later growth stage is suitably regulated by FPT-6 or PFDT; properly extended reactive time can enhance the sphericity and electrochemical performance. The dual mixed-impeller (PT/CIBDT) combines intense mixing and shear ability, attaining a dense spheroid with a highly smooth surface. The cycle retention of this cathode is increased by 10.35% after 200 cycles at 1 C compared to a commercial counterpart. A regulatory strategy for the reactive co-precipitation process to enhance precursor stability is proposed here. Furthermore, the optimal operation parameters derived from this strategy can be effectively applied to commercial cathode materials.

Sustained co-release of ciprofloxacin and dexamethasone in rabbit maxillary sinus using polyvinyl alcohol-based hydrogel microparticle

Topical delivery to paranasal sinuses through sustained-release stents is one of the new horizons in treating chronic rhinosinusitis (CRS). This study aims to introduce and evaluate sustained co-release of encapsulated ciprofloxacin (CIP) and dexamethasone (DEX) in polyvinyl alcohol-based carriers within the maxillary sinus of rabbit animals. DEX and CIP were loaded in a tyramine-substituted polyvinyl alcohol microparticle (PVATyr MP). The mechanical stability, degradability, and sustained-release patterns of both drugs as well as cellular cytocompatibility were assessed in vitro. The PVATyr MPs were then injected into the maxillary sinus of rabbits and they were monitored weekly for 21 days. Nasal endoscopy, MRI imaging, and tissue microscopy were used to follow the changes and compared them with the control condition. Also, the concentrations of drugs were evaluated in the maxillary sinus and blood samples over the study period. Produced PVA-based MPs possessed a relatively narrow particle size distribution (CV 7.7%) with proper physical stability until 30 days of incubation. The uniform-sized PVATyr MPs and their surrounding hydrogel showed sustained-release profiles for DEX and CIP for up to 32 days in vitro. The injected drugs-loaded hydrogel showed complete clearance from the maxillary sinus of rabbits within 28 days. The concentrations of DEX and CIP in mucosal remained within the therapeutic window when measured on days 7, 14, and 21, which were well above the plasma concentrations without any pathological changes in endoscopy, MRI imaging, and histological examinations. DEX/CIP loaded PVATyr MPs provided an effective, controlled, and safe sustained-drug delivery in both in vitro and in vivo analyses at therapeutic concentrations with minimal systemic absorption, suggesting a promising treatment approach for CRS.Graphical

Controlling particle size of levan in powder form with different technologies

Levan is a fructose polysaccharide with multiple applications in different fields, but its obtaining in powdered form with a narrow particle size distribution is a complicated task. Two techniques, electrospraying and supercritical antisolvent (SAS) precipitation, were used to process levan that was first obtained enzymatically. The SAS process was able to micronize the polymer (at experimental conditions far above the mixture critical point of the solvent-antisolvent system) to obtain spherical particles between 0.30 and 0.50 μm with a proper particle size distribution. In this case, the Peng-Robinson equation of state was used to theoretically determine the mixture critical point. Bigger and elongated particles were obtained with electrospraying (0.60 μm). According to solution properties, mainly rheology, solubility and conductivity, the best solvent for levan electrospraying, in order to avoid problems of solvent evaporation and jet formation, was a mixture of water and ethanol with a polymer concentration of 50 mg·cm−3. Indeed, that solution has a viscous behavior (according to the oscillatory analysis), a low degree of pseudo-plasticity (based on the shear flow analysis), and the highest value of conductivity. Therefore, the particle size distribution of levan in powdered form can be tuned depending on the technique used.

Formulation and analysis of acrylic emulsion coatings with chrome yellow, phthalocyanine blue, and red oxide pigments using high speed disperser and bead mill techniques

A major commercial problem is achieving stable and fine particle pigment dispersion, especially for aqueous pigment dispersions. It is essential to optimize dispersants in order to moisten, disperse, and stabilize pigments throughout the milling process. This study focuses on formulating acrylic emulsion coatings using chrome yellow, phthalocyanine blue, and red oxide pigment concentrates. The formulations were developed using both high-speed dispersers (HSD) and bead mills. A quality evaluation of the products from the two milling techniques was carried out. Formulations made with chrome yellow, phthalocyanine blue, and red oxide pigment concentrates in a water-based, binder-free system using bead mills, Tween-80, SLS, and cocosulphosuccinate surfactants showed narrower particle size distributions and stronger color than those made with HSD. Specifically, formulations prepared with bead mills and the aforementioned surfactants demonstrated superior color strength compared to those prepared with HSD. The color shade of acrylic emulsion coatings formulated with phthalocyanine blue and red oxide pigment concentrates, along with Tween-80 and cocosulphosuccinate surfactants using HSD, matched the standard color shade formulations prepared in bead mills. However, formulations using phthalocyanine blue pigment concentrates with SLS and oleylsulphosuccinate surfactants in HSD did not match the standard color shade prepared in bead mills.