Polyvinylpyrrolidone Research Articles

Microwave-assisted synthesis of highly uniform Prussian Blue@Carbon cathode materials for sodium-ion batteries

Prussian blue (PB) and its analogues (PBAs) as cathode material for sodium-ion batteries suffer from poor cycling stability because of crystal defects and sluggish ion diffusion kinetics. Composite with carbon materials is an effective solution to alleviate this problem. However, this is typically achieved through simple physical mixing or encapsulation, which relies heavily on the compatibility between carbon and PB, often resulting in composites that are neither stable nor uniform. Herein, we have developed a facile strategy that utilizes microwave radiation to anchor PB onto the surface of polyvinylpyrrolidone (PVP) functionalized graphene oxide (GO-PVP) through stable, uniform covalent bonds via the amide groups in PVP, in order to obtain an excellent composite material with Prussian blue and carbon materials for sodium-ion batteries. The as-prepared composite materials exhibit lower content of crystallization water and higher crystal integrity, delivering a high initial specific capacity of 165.2 mAh g−1 at 1 C rate and maintaining a capacity of 120.1 mAh g−1 after 500 cycles. This composite approach offers novel insights into the creation of uniform and stable PB/carbon materials as the cathode of sodium-ion batteries.

An inorganic-organic hybrid CQDs@PVP lubricant additive: Achieving low friction and wear in PEG and water

High-temperature lubrication has always been a hot topic in the lubricant and grease industry, and is also an essential concern in the high-end equipment sector to be addressed. Carbon quantum dots (CQDs) are an emerging material widely applied in the field of lubrication, owing to their exceptional lubricity and high load-bearing capacity. However, the vulnerability of CQDs to oxidation in air and reduced stability dramatically restrict their high-temperature application capability. In this study, a nanocomposite of amphiphilic polyvinyl pyrrolidone (PVP) homopolymer with excellent lubricating properties and thermal stability, which is hydrogen bonded to CQDs (CQDs@PVP), was designed to achieve low friction and wear of lubricants at high temperatures. The CQDs@PVP are consistently dispersed in both PEG400 and water, and exhibit superior lubricity compared to unmodified CQDs at high temperatures (ranging from 200–150 °C and 90.50 °C). Meanwhile, the dense carbon film on the wear surface and the chemically reactive film of iron compounds directly contribute to the enhanced lubrication performance. These analytical results demonstrate the powerful candidacy of CQDs@PVP as a lubrication additive and promote future high-temperature applications of CQDs in industrial production.

Fabrication of polysulfone-cellulose acetate based TiO2 @SiO2-CuS and Fe3O4 @XG membrane and its application in wastewater treatment

Membrane technology emerged as a preferred method for wastewater treatment due to its efficiency, and low energy consumption, particularly in pharmaceutical industries. In this study, two types of membranes were developed and compared: cellulose acetate with dimethyl sulfoxide, glycerol, and polysulfone with dimethylformamide, and polyvinyl pyrrolidone. These membranes were augmented with nanocomposites, such as Fe3O4 @XG and TiO2 @SiO2-CuS, to enhance performance. Experimental investigations involved doping membranes with nanocomposites at varying concentrations (0.1 wt%, 0.5 wt%, and 1.0 wt%). Atomic force microscopy revealed that increasing nanocomposite content led to smoother surfaces and improved anti-fouling properties. Incorporating nanocomposites reduced the contact angle, with 1.0 wt% PSF/TiO2 @SiO2-CuS exhibiting the lowest angle at 33.134°. Physical property assessments, including density, viscosity, pH, and porosity, were conducted to evaluate the impact of nanocomposites. Under 4 atm pressure, 1.0 wt% CA-TiO2 @SiO2-CuS demonstrated a maximum pure water flux of 3300 ± 50 lit/m2.hr compared to the pure membrane. Furthermore, biodegradability tests indicated a significant weight loss of the nanocomposite membranes, with a 13.89 % increase in CA membrane weight loss compared to a 0.20 % increase in PSF membrane weight loss. The study highlights the potential of these membranes for diverse applications, particularly in wastewater treatment, underscoring their efficiency and suitability for pharmaceutical industry use.

The effect of recompression and concentration of polyvinylpyrrolidone (PVP) K-30 on the quality of paracetamol tablets

The effect of recompression and concentration of polyvinylpyrrolidone (PVP) K-30 on the quality of paracetamol tablets

Pd octahedra nanocubes mediated photo-fenton catalytic performance for sustainable degradation of methylene blue

This research utilized a typical solvothermal approach, by employing Na2PdCl4 as the synthetic precursor, L-ascorbic acid (AA) as the reductant agent, and polyvinylpyrrolidone (PVP) as the practical surfactant, palladium (Pd) octahedra was finally effectively synthesized by the hydrothermal and solvothermal methods. Subsequently, characterizations of Pd octahedra were conducted by using TEM, XPS, XRD, and other analytical methods. Whereafter, Pd octahedra displayed a consistent shape and size, featuring a distinctive tip-shaped structure, which conferred upon them outstanding optical absorption properties within the near-infrared (NIR) region. Consequently, under NIR laser exposure, Pd octahedra could elevate local reaction temperature via in-situ photothermal conversion, thereby stimulating the formation of active sites of Fenton catalysts. The Photo-Fenton catalytic activity of Pd octahedra was investigated by using methylene blue (MB) as a model pollutant. The degradation efficiency of MB reached 94.8 % within 35 min under 808 nm laser irradiation, and the removal rate of MB by Pd octahedra could still reach more than 90 % after five cycles of use. All the results manifest that Pd octahedra exhibit excellent purification performance for MB dyestuff wastewater.

Innovative enhancements in polymer nanocomposites: Integrating ZnO nanorods into Hydroxypropyl methylcellulose/Polyvinyl pyrrolidone blend for advanced energy storage devices

Polymer nanocomposites are promising for various industrial and scientific applications due to their flexibility, diverse functionalities, and unique properties. In this study, zinc oxide nanorods (ZnO NRs) were incorporated into a blend of polymers (Hydroxypropyl methylcellulose - HPMC and Polyvinyl pyrrolidone - PVP) using a solution-casting technique, with concentrations varying from 2 % to 8 % by weight. Transmission electron microscopy (TEM) revealed that the ZnO NRs had an average diameter of 140 nm and a length of 3.22 μm. X-ray diffraction (XRD) analysis showed reduced crystallinity in the samples as the ZnO NR content increased. Fourier-transform infrared spectroscopy (FTIR) indicated changes in vibrational peaks due to interactions between functional groups in the blend and the nanorods. The addition of ZnO NRs significantly influenced the optical bandgap energies and UV/visible light absorption spectra of the samples. The bandgap of the nanocomposites significantly decreased upon ZnO NR incorporation, with direct and indirect bandgaps ranging from 5.19 to 4.70 eV and 4.74–3.66 eV, respectively. Electrical conductivity and dielectric characteristics were assessed across frequencies ranging from 0.1 to 10 MHz, revealing increasing AC conductivity, dielectric permittivity, and dielectric loss with higher ZnO NR content. Notably, at 10 Hz, the electrical conductivity increased from 3.5 × 10⁻12 S/m to 3.62 × 10⁻10 S/m upon loading with ZnO NR. The combination of adjustable optical bandgaps, frequency-dependent AC conductivity, and a wide range of tunable permittivity highlights the potential of these HPMC/PVP-ZnO NR nanocomposites for developing flexible optoelectronic and energy storage devices.

PVP-assisted in-situ self-assembly hierarchical BiOCl with oxygen vacancies for efficient photocatalytic oxidation of cyclohexane under air in solvent-free conditions

Cyclohexane (CHA) selective oxidation reactions are crucial in designing advanced organic intermediates but suffering from very challenges as the products of KA oil (cyclohexanol and cyclohexanone) are more readily oxidized to CO2. Herein, we report that a polyvinylpyrrolidone (PVP) coating of fluffy self-assembled morphology of BiOCl by nanosheets with exposed {001} facets are synthesized via the solvothermal method. Moreover, the as-synthesized hierarchical BiOCl exhibits a significant presence of in-situ produced oxygen vacancies during photocatalysis, thereby facilitating efficient CHA oxidation to KA oil with air as an oxidant in solvent-free at room temperature. The crystallinity, micromorphology, and electronic structure of BiOCl can be significantly influenced by the concentration of NH4Cl and PVP. In the photocatalytic oxidation, oxygen vacancies act as traps to inhibit electrons and holes recombination and adsorb-activate the oxygen molecule, producing h+ and ·O2− radical to achieve 466.7 μmol of KA oil (340.8 μmol of cyclohexanone and 125.9 μmol of cyclohexanol) with a selectivity of 93.9 %. The ∙OH radicals play a predominant role in the production of CHA-one. After conducting 5 experimental cycles, a consistent yield of 92 % towards KA oil and unchanged selectivity can still be maintained. The excellent photocatalytic performance can be attributed to the enhanced photo-absorption and narrow energy gap, abundant oxygen vacancies, high exposed {001} facets, smaller size and large specific surface area, and efficient electron-hole separation. The present work sheds light on the synergistic effect of PVP coating and in-situ formed oxygen vacancies on enhancing photocatalytic activity of Bi-based materials.

Water-Soluble Lead Sulfide Nanoparticles: Direct Synthesis and Ligand Exchange Routes.

Colloidal semiconductor nanoparticles (NPs) represent an emergent state of matter with unique properties, bridging bulk materials and molecular structures. Their distinct physical attributes, such as bandgap and photoluminescence, are intricately tied to their size and morphology. Ligand passivation plays a crucial role in shaping NPs and determining their physical properties. Ligand exchange (LE) offers a versatile approach to tailoring NP properties, often guided by Pearson's Hard-Soft Acid-Base theory. Lead sulfide (PbS), a semiconductor of considerable interest, exhibits size-dependent tunable bandgaps from the infrared to the visible range. Here, we present two methods for synthesizing water-soluble, polyvinylpyrrolidone (PVP)-coated PbS NPs. The first involves direct synthesis in an aqueous solution while utilizing PVP as the surfactant for the formation of nano-cubes with a crystal coherence length of ~30 nm, while the second involves LE from octadecylamine-coated PbS truncated nano-cubes to PVP-coated PbS NPs with a crystal coherence length of ~15 nm. Multiple characterization techniques, including X-ray diffraction, transmission electron microscopy, Fourier-transform infrared spectroscopy, and thermal gravimetric analysis, confirmed the results of the synthesis and allowed us to monitor the ligand exchange process. Our findings demonstrate efficient and environmentally friendly approaches for synthesizing PVP-coated PbS NPs.

Emerging Two-Dimensional Ti3C2-BiOCl Nanoparticles for Excellent Antimicrobial and Antioxidant Properties.

Introduction MXenes (Ti3C2) represent a group of two-dimensional inorganic compounds, produced through a top-down exfoliation method. They comprise ultra-thin layers of transition metal carbides, or carbonitrides, and exhibit hydrophilic properties on their surfaces. Utilizing Ti3C2 BiOCl nanoparticles for their antimicrobial and antioxidant attributes involves enhancing synthesis, processing, and characterization techniques. Materials and method To prepare Ti3C2 MXene, dissolve 1.6 g of LiF in 20 ml of 9M HCl. Slowly add 1 g of Ti3AlC2(titanium aluminum carbide) powder to the solution while stirring. Etch at 35°C for 24 h to remove Al layers from Ti3AlC2, leaving Ti3C2 layers. Wash the mixture with distilled water and ethanol until the pH is around 6. Collect the washed sediment by centrifugation and sonicate it in distilled water for 1 h. Centrifuge to remove unexfoliated particles. For BiOCl synthesis, dissolve 2 mmol of Bi(NO3)3·5H2O (bismuth nitrate pentahydrate) in 10 ml of 2M HCl (hydrochloric acid) with 0.5 g of PVP (polyvinylpyrrolidone). Transfer the solution to a Teflon-lined autoclave, fill it with distilled water up to 80%, and heat at 160°C for 24 h. Collect the precipitate by centrifugation, wash, and dry at 60°C for 12 h. Disperse BiOCl nanoparticles in distilled water, sonicate for 30 min, add Ti3C2 MXene dispersion, stir for 2 h, collect, wash, dry, and calcine at 400°C for 2 h. Result The Scanning Electron Microscope (SEM) utilizes electrons, rather than light, to generate highly magnified images. Energy Dispersive X-ray Spectroscopy (EDS) complements SEM by analyzing the X-ray spectrum emitted when a solid sample is bombarded with electrons, enabling localized chemical analysis. In SEM imaging, incorporating an X-ray spectrometer allows for both element mapping and point analysis. The SEM image of the prepared samples reveals accordion-like multilayer structures in BiOCl, characterized by thin sheet-like structures with numerous pores. EDS, relying on X-ray emissions from electron bombardment, facilitates detailed chemical analysis at specific locations within the sample. Conclusion Our research has shed light on the synthesis and characterization processes of two-dimensional Ti3C2 BiOCl nanoparticles, revealing their remarkable antimicrobial and antioxidant properties.

Fabrication and characterization of Ecklonia cava phlorotannin‐loaded PVA/PVP blend electrospun nanofibers as a potential diabetic wound dressing biomaterial

AbstractDiabetic wound healing remains a challenging issue, necessitating advanced dressings with active therapeutic agents to reduce inflammation and promote healing. Ecklonia cava phlorotannin (ECP) possesses therapeutic potential for wound healing including anti‐microbial, antioxidant, and anti‐inflammatory properties. Our previous study demonstrates the therapeutic efficacy of ECP‐loaded nanofibers in an in vitro hyperglycemic wound model. The present paper focuses on the detailed characterization of the polyvinyl alcohol (PVA)/polyvinylpyrrolidone (PVP) blend nanofiber incorporated with ECP. The ideal ratio, PVA80:PVP20, is selected to incorporate with ECP via the blend electrospinning method. To confirm the successful loading of ECP (0.5% and 1%), physicochemical characterization is conducted using scanning electron microscopy, Fourier‐transform infrared spectroscopy, and thermal analysis. Functionality assays are performed to evaluate their applicability as dressing biomaterials. Physicochemical analyses confirm the successful loading of ECP into the nanofibers. Overall, the ECP‐loaded PVA/PVP nanofiber membranes exhibit favorable wound dressing criteria, which attributed to high water absorption capacity (200%–400%), sufficient water vapor transmission rate (1550–1650 g/m2/d), high loading efficiency and slow release. Bioactivity tests indicate that the ECP's effectiveness is unaffected by the electrospinning process. Importantly, these membranes exhibit biocompatibility and nontoxicity to human dermal fibroblasts, indicating their potential as good diabetic wound dressings.

Experimental study on the effect of PVP, NaCl and EG on the methane hydrates formation and dissociation kinetics

The problem of hydrate plug, low efficiency of hydrate dissociation and short production time in hydrate exploitation processes have significantly hindered the commercial viability of gas hydrate extraction. This study investigated the inhibitory effects of ethylene glycol (EG), EG + polyvinyl pyrrolidone (PVP), and EG + PVP + sodium chloride (NaCl) on methane hydrate formation through experiment. The hydrate inhibitory performance is evaluated by using differential of pressure curve, the amount of hydrate, and pressure drop values, and the effects of different temperatures, pressures, inhibitors, and injection time on hydrate dissociation are further studied. The experiment results indicate that the rank of inhibitors combination in terms of effectiveness is 5%EG + 0.5 wt%PVP + 3 wt%Nacl > 10%EG + 1 wt%PVP > 30% EG. At low-temperature conditions, 30% EG exhibits good inhibition of hydrate synthesis but poor dissociation efficiency. As temperature increases, the hydrates dissociation rate with 30% EG also increases. For the combination inhibitor system of EG, PVP, and NaCl, PVP will reduce the dissociation efficiency of hydrates, while EG and Nacl will improve the hydrate dissociation performance. For low production pressure, it is found that 10% EG + 10% NaCl have a good promotion effect on hydrate dissociation, whereas under high production pressure, 20% EG + 10% NaCl is more effective. Furthermore, injecting the inhibitors earlier enhances the dissociation of hydrates more effectively.

Development of AgNPs-PVP/TPU based flexible strain sensors for structural health monitoring of composite structures

Real-time in-stu structural health monitoring (SHM) of composite structure developed through highly sensitive and flexible smart sensors based on colloidal solution of Silver Nano Particles (AgNPs). Synthesis of AgNPs through chemical reduction method by citrate and then in Haxen phase transferred by using surfactant Cetyltrimethylammonium bromide (CTAB). Colloidal solution of AgNPs-Haxen and Polyvinylpyrrolidone (PVP) - Haxen has been followed by mixed, calcined and deposited that thick paste on flexible Thermoplastic Polyurethane (TPU) film. These sensors become more sensitive than metallic foil made sensors and farther this sensor pasted on polymer composite for monotonic loading like tensile loading. The data extracted from sensors was monitored effectively by data acquisitioning technique using Keithley KUSB-3100. This research based on chemical synthesis of metallic nanoparticles like silver, its functionalization, protection of these nanoparticles from environment by capping agents and by creating inert atmosphere respectively. Then these functionalized capped nanoparticles are embedded on the surface of thermoplastic Urethane (TPU) film to make piezo resistive semi conductive strips which serve as flexible strain gauge/smart sensor. One other technique is also being used to make sensor is that colloidal solution of metallic Nanoparticles sprays over TPU substrate using Connective Self Assembly (CSA) method. The sensor then properly attached to Glass fabric reinforced polymer (GFRP) composite and calibrated using data acquisitioning (DAQ) under different mode of testing.

Mass Transfer Limitation within Molecular Crowding Electrolyte Reorienting (100) and (101) Texture for Dendrite‐Free Zinc Metal Batteries

AbstractAqueous zinc metal batteries are emerging as a promising alternative for energy storage due to their high safety and low cost. However, their development is hindered by the formation of Zn dendrites and side reactions. Herein, a macromolecular crowding electrolyte (MCE40) is prepared by incorporating polyvinylpyrrolidone (PVP) into the aqueous solutions, exhibiting an enlarged electrochemical stability window and anti‐freezing properties. Notably, through electrochemical measurements and characterizations, it is discovered that the mass transfer limitation near the electrode surface within the MCE40 electrolyte inhibits the (002) facets. This leads to the crystallographic reorientation of Zn deposition to expose the (100) and (101) textures, which undergo a “nucleation‐merge‐growth” process to form a uniform and compact Zn deposition. Consequently, the MCE40 enables highly reversible and stable Zn plating/stripping in Zn/Cu half cells over 600 cycles and in Zn/Zn symmetric cells for over 3000 hours at 1.0 mA cm−2. Furthermore, Na0.33V2O5/Zn and α‐MnO2/Zn full cells display promising capacity and sustained stability over 500 cycles at room and sub‐zero temperatures. This study highlights a novel electrochemical mechanism for achieving preferential Zn deposition, introducing a unique strategy for fabricating dendrite‐free zinc metal batteries.

Grating-Integrated Gold Nanograsses Encapsulated with ZIF-8: A Quantitative and Ultrasensitive Surface-Enhanced Raman Scattering Substrate.

We proposed and demonstrated highly sensitive hybrid surface-enhanced Raman scattering (SERS) substrates, which are grating-integrated gold nanograsses (GIGN) that are tip-selectively encapsulated by ZIF-8 nanospheres (GIGN/tip-ZIF). This unique structure is realized through the tip-selective modification of GIGN by polyvinylpyrrolidone (PVP), and then, the tips of the GIGN were encapsulated by ZIF-8 nanospheres. The ZIF-8 nanospheres can adsorb analyte molecules, resulting in the spatial overlap between the analyte molecules and the "hotspots" on the tips of GIGN. Such a unique GIGN/tip-ZIF hybrid SERS substrate exhibits high sensitivity and quantitative detection ability. The detection limits can reach as low as 10-11 M, and the relative standard deviation is 5.59% for 4-aminothiophenol (4-ATP). In a wide range of concentrations from 10-5 to 10-11 M, the SERS intensity and concentration relationship can be fitted as a sigmoidal curve with R2 = 0.988. These indicate that the GIGN/tip-ZIF hybrid SERS substrates have broad applications in detecting toxic and harmful substances in food safety, disease diagnosis, and environmental monitoring.

Mass Transfer Limitation within Molecular Crowding Electrolyte Reorienting (100) and (101) Texture for Dendrite-Free Zinc Metal Batteries.

Aqueous zinc metal batteries are emerging as a promising alternative for energy storage due to their high safety and low cost. However, their development is hindered by the formation of Zn dendrites and side reactions. Herein, a macromolecular crowding electrolyte (MCE40) is prepared by incorporating polyvinylpyrrolidone (PVP) into the aqueous solutions, exhibiting an enlarged electrochemical stability window and anti-freezing properties. Notably, through electrochemical measurements and characterizations, it is discovered that the mass transfer limitation near the electrode surface within the MCE40 electrolyte inhibits the (002) facets. This leads to the crystallographic reorientation of Zn deposition to expose the (100) and (101) textures, which undergo a "nucleation-merge-growth" process to form a uniform and compact Zn deposition. Consequently, the MCE40 enables highly reversible and stable Zn plating/stripping in Zn/Cu half cells over 600 cycles and in Zn/Zn symmetric cells for over 3000 hours at 1.0 mA cm-2. Furthermore, Na0.33V2O5/Zn and α-MnO2/Zn full cells display promising capacity and sustained stability over 500 cycles at room and sub-zero temperatures. This study highlights a novel electrochemical mechanism for achieving preferential Zn deposition, introducing a unique strategy for fabricating dendrite-free zinc metal batteries.

Optimization of Biologically Inspired Electrospun Scaffold for Effective Use in Bone Regenerative Applications.

Human bone is composed of organic and inorganic composite materials, contributing to its unique strength and flexibility. Hydroxyapatite (HAP) has been extensively studied for bone regeneration, due to its excellent bioactivity and osteoconductivity, which makes it a highly valuable biomaterial for tissue engineering applications. For better therapeutic effects, composite nanofibers containing polyvinyl alcohol (PVA) and polyvinyl Pyrrolidone (PVP) were developed using an electrospinning technique in this study. Herein, hydroxyapatite (a major inorganic constituent of native bone) concentrations varying from 5 to 25% were reinforced in the composite, which could alter the properties of nanofibers. The as-prepared composite nanofibers were characterized by SEM, TEM, XRD, and FT-IR spectroscopy, and a bioactivity assessment was performed in simulated body fluid (SBF). The ICP-OES analysis was used to determine the concentration of Ca2+ and PO42- ions before and after SBF immersion. To optimize the material selection, the nanofibrous scaffolds were subjected to cell proliferation and differentiation in MG-63 osteoblast cell lines, but no significant toxicity was observed. In conclusion, HAP-PVA-PVP scaffolds exhibit unique physical and chemical properties and ideal biocompatibility, with great promise to serve as effective candidates for bone tissue applications.

Improved release of sulfamethoxazole from electrospun water soluble fibers

Electrospun fibers containing an active component, sulfamethoxazole, were successfully prepared from three water-soluble polymers, poly(vinyl pyrrolidone) (PVP), poly(vinyl alcohol) (PVA) and hydroxypropyl methylcellulose (HPMC). The conditions of electrospinning had to be optimized individually for the three systems. The presence of the drug did not influence fiber characteristics significantly, the diameter of the fibers increased only slightly upon the addition of the drug. Detailed investigations proved that the drug is located within the fibers in the amorphous form facilitating release. The strong pH sensitivity of the dissolution of the drug decreased considerably by encapsulation into the fibers. Drug release from the fibers is much faster than the dissolution of the neat drug and the relative amount of dissolved drug is also considerably larger (95 % vs. 30 %) from fibers encapsulating it. PVP seems to be the best selection for the preparation of electrospun fibers containing sulfamethoxazole, encapsulation is the largest (90.1 %) and drug release is the fastest from it among the three polymers. The preparation of formulations from sulfamethoxazole by electrospinning is clearly beneficial and must increase the bioavailability of this BCS IV drug.

Engineering of Silane-Pyrrolidone Nano/Microparticles and Anti-Fogging Thin Coatings.

Polyvinylpyrrolidone (PVP) exhibits remarkable qualities; owing to the strong affinity for water of its pyrrolidone group, which enhances compatibility with aqueous systems, it is effective for stabilizing, binding, or carrying food, drugs, and cosmetics. However, coating the surface of polymeric films with PVP is not practical, as the coatings dissolve easily in water and ethanol. Poly(silane-pyrrolidone) nano/microparticles were prepared by combining addition polymerization of methacryloxypropyltriethoxysilane and N-vinylpyrrolidone, followed by step-growth Stöber polymerization of the formed silane-pyrrolidone monomer. The silane-pyrrolidone monomeric solution was spread on oxidized polyethylene films with a Mayer rod and polymerized to form siloxane (Si-O-Si) self-cross-linked durable anti-fog thin coatings with pyrrolidone groups exposed on the outer surface. The coatings exhibited similar wetting properties to PVP with significantly greater stability. The particles and coatings were characterized by microscopy, contact angle measurements, and spectroscopy, and tested using hot fog. Excellent anti-fogging activity was found.

Development of itraconazole ocular delivery system using β-cyclodextrin complexation incorporated into dissolving microneedles for potential improvement treatment of fungal keratitis

Itraconazole (ITZ) is one of the broad-spectrum antifungal agents for treating fungal keratitis. In clinical use, ITZ has problems related to its poor solubility in water, which results in low bioavailability when administered orally. To resolve the issue, we formulated ITZ into the inclusion complex (ITZ-IC) system using β-cyclodextrin (β-CD), which can potentially increase the solubility and bioavailability of ITZ. The molecular docking study has confirmed that the binding energy of ITZ with the β-CD was −5.0 kcal/mol, indicating a stable conformation of the prepared inclusion complex. Moreover, this system demonstrated that the inclusion complex could significantly increase the solubility of ITZ up to 4-fold compared to the pure drug. Furthermore, an ocular drug delivery system was developed through dissolving microneedle (DMN) using polyvinyl pyrrolidone (PVP) and polyvinyl alcohol (PVA) as polymeric substances. The evaluation results of DMN inclusion complexes (ITZ-IC-DMN) showed excellent mechanical strength and insertion ability. In addition, ITZ-IC-DMN can dissolve rapidly upon application. The ex vivo permeation study revealed that 75.71% (equivalent to 3.79 ± 0.21 mg) of ITZ was permeated through the porcine cornea after 24 h. Essentially, ITZ-IC-DMN exhibited no signs of irritation in the HET-CAM study, indicating its safety for application. In conclusion, this study has successfully developed an inclusion complex formulation containing ITZ using β-CD in the DMN system. This approach holds promise for enhancing the solubility and bioavailability of ITZ through ocular administration.

Determination of vat-photopolymerization parameters for microneedles fabrication and characterization of HPMC/PVP K90 dissolving microneedles utilizing 3D-printed mold

Three-dimensional (3D) printing serves as an alternative method for fabricating microneedle (MN) patches with a high object resolution. In this investigation, four distinct needle shapes: pyramid mounted over a long cube (shape A), cone mounted over a cylinder (shape B), pyramidal shape (shape C), and conical shape (shape D) were designed using computer-aided design (CAD) software with compensated bases of 350, 450 and 550 µm. Polylactic acid (PLA) biophotopolymer resin from eSun and stereolithography (SLA) 3D printer from Anycubic technology were used to print MN patches. The 3D-printed MN patches were employed to construct MN molds, and those molds were used to produce hydroxypropyl methylcellulose (HPMC) and polyvinyl pyrrolidone (PVP) K90 dissolving microneedles (DMNs). Various printing parameters, such as curing time, printing angle, and anti-aliasing (AA), were varied to evaluate suitable printing conditions for each shape. Furthermore, physical appearance, mechanical property, and skin insertion ability of HPMC/PVP K90 DMNs were examined. The results showed that for shape A and C, the suitable curing time and printing angle were 1.5 s and 30° while for shapes B and D, they were 2.0 s and 45°, respectively. All four shapes required AA to eliminate their stair-stepped edges. Additionally, it was demonstrated that all twelve designs of 3D-printed MN patches could be employed for fabricating MN molds. HPMC/PVP K90 DMNs with the needles of shape A and B exhibited better physicochemical properties compared to those of shape C and D. Particularly, both sample 9 and 10 displayed sharp needle without bent tips, coupled with minimal height reduction (< 10%) and a high percentage of blue dots (approximately 100%). As a result, 3D printing can be utilized to custom construct 3D-printed MN patches for producing MN molds, and HPMC/PVP K90 DMNs manufactured by those molds showed excellent physicochemical properties.