Productizing Nano-Bioactive Glass-Based Bilayer Scaffolds: A Graft for Reconstruction of Mandibular and Femoral Bone Defects.

This investigation aimed to construct a bilayer scaffold integrating alginate and gelatin with nanobioactive glass (BG), recognized for their efficacy in tissue regeneration and drug delivery. Scaffolds, namely, alginate/gelatin (AG), alginate-/actonel gelatin (AGD), alginate actenol/gelatin-45S5 BG (4AGD), and alginate-actonel/gelatin-59S BG (5AGD), were assembled using a cost-effective freeze-drying method, followed by detailed structural investigation via powder X-ray diffraction as well as morphological characterization using field emission scanning electron microscopy (FESEM). FESEM revealed a honeycomb-like morphology with distinct pore sizes for nutrient, oxygen, and drug transport. The scaffolds evidently exhibited hemocompatibility, high porosity, good swelling capacity, and biodegradability. In vitro studies demonstrated sustained drug release, particularly for scaffolds containing actonel. In vivo tests showed that the bilayer scaffold promoted new bone formation, surpassing the control group in bone area increase. The interaction of the scaffold with collagen and released ions improved the osteoblastic function and bone volume fraction. The findings suggest that this bilayer scaffold could be beneficial for treating critical-sized bone defects, especially in the mandibular and femoral regions.

Crucial Chemical Revelations in 45S5 Bioactive Glass via Sequential Precursor Integration Order.

Among the wet chemical nanoparticle fabrication techniques, the sol-gel process happens through hydrolysis and subsequent polycondensation reactions. The bioactive glass known as the 45S5 SiO2-Na2O-CaO-P2O5 quaternary system has intricate chemistry, yet its advantages benefit the biomedical field on an enormous scale. The order in which the ethanol and TEOS inclusions are exchanged was investigated in this work because it has a direct impact on the early hydrolysis process. Another strategy involves adding phosphate species to the sol before gelation, modifying the network chemistry, and interpreting the findings. Adding phosphate species before gelation in the biomaterial (E-Si-P) resulted in the formation of hydroxyapatite and other calcium silicate phases at 800 °C. Swapping ethanol and TEOS biomaterials (E-Si and Si-E) resulted in the sodium-calcium silicate phase only. Si-E with strong Si-O-Si siloxane rings demonstrated superior mechanical stability, hemocompatibility, and bioactivity. This compact Si-O-Si decreased the surface area of Si-E. XPS spectra revealed that E-Si-P has the lowest Na 1s binding energy (BE) and the highest BE for Si 2p. More Si-O-/Si-OH groups formed by E-Si make the network weak and decrease the surface area and protein adsorption. These differences significantly influenced the morphology, surface properties, mechanical studies, and compatibility test. This study has further unraveled the protocol to design a biomaterial with mechanical stability and load-bearing ability. In addition, the appropriate protocol to yield the desired property-rich biomaterial with preserved bioactivity, mechanical stability, cytocompatibility, as well and surface porosity has been elaborated in detail.

Enhancing Interplanar Spacing in V2O3/V3O7 Heterostructures to Optimize Cathode Efficiency for Zn-Ion Batteries.

The improvement of sophisticated cathode materials plays a major role in boosting the efficiency of Zn-ion batteries. These batteries have garnered considerable interest as a result of their excellent energy density and the promise of cost-effective solutions for energy storage. In this work, we present a novel approach to progress the electrochemical investigation of Zn-ion batteries by expanding the interplanar distance of layered hydrated V2O3/V3O7 heterostructure nanosheets. Electrochemical investigations were conducted to assess the effectiveness of the stacked hydrated V2O3/V3O7 heterostructure as a cathode component for Zn-ion batteries. The expanded interplanar space as a result of the introduction of water molecules facilitates the insertion/extraction of Zn ions, leading to significantly enhanced electrochemical characteristics. The layered hydrated V2O3/V3O7 heterostructure exhibited an impressive specific capacity of 330 mAh g-1 at a current density of 0.1 A g-1, maintaining a capacity retention of approximately 92.3% and a coulombic efficiency of 95.8% even after 2000 cycles.

Rapidly derived equimolar Ca: P phasic bioactive glass infused flexible gelatin multi-functional scaffolds - A promising tissue engineering.

The study aims to design and fabricate an ultra-easier multi-functional biomedical polymeric scaffold loaded with unique equimolar Ca:P phasic bioactive glass material (BG). Gelatin (G) - 45S5 bioactive glass (BG) scaffolds were synthesized via a simple laboratory refrigerator with higher biocompatibility and cytocompatibility. The results proved that BG has enhanced bio-mineralization of the scaffolds and results support that the G: BG (1:2) ratio is the more appropriate composition. Brunauer-Emmett-Teller (BET) study confirms the higher surface area for pure Gelatin and G: BG (1:2). Scanning Electron Microscopic images display the precipitation of hydroxycarbonate apatite layer over the scaffolds on immersing it in simulated body fluid. Alkaline phosphate activity proved that G: BG (1:2) scaffold could induce mitogenesis in MG-63 osteoblast cells, thus helping in hard tissue regeneration. Sirius red collagen deposition showed that higher content bioactive glass incorporated Gelatin polymeric scaffold G: BG (1:2) could induce rapid collagen secretion of NIH 3T3 fibroblast cell line that could help in soft tissue regeneration and earlier wound healing. The scaffolds were also tested for cell viability using NIH 3T3 fibroblast cell lines and MG 63 osteoblastic cell lines through methyl thiazolyl tetrazolium (MTT) assay. Thus, the study shows a scaffold of appropriate composition G: BG (1:2) can be a multifunctional material to regenerate hard and soft tissues.

Lattice distortion-driven band gap engineering and enhanced electrocatalytic activity of Mn-substituted nanostructured SrTiO3 materials: A comprehensive investigation.

The lattice distortion and electrocatalytic activity are investigated by the mono-substituent of Mn with different concentrations to generate localized states in the electronic structure of SrTiO3. The sol-gel approach has been employed to fabricate SrTiO3 and SrTi1-xMnxO3 nanostructures (NSs). The structural analysis indicates Mn incorporation into Ti sites of SrTiO3, which shifts the lattice towards a higher diffraction angle with a single-phase cubic structure. The optical absorption spectra exhibit a decrease in band gap from 3.27 to 1.89 eV and reveal the shift in band edge positions towards the visible region. XPS analysis is carried out to confirm the formation of oxygen vacancies and valence band edge position. For SrTi0.88Mn0.12O3, OER and HER have the overpotential of 445 and 157 mV at a current density of 100 and 10 mA cm-2. Hence, the substitution of Mn (x = 0.12) into SrTiO3 lattice results in lattice distortion that enhances the electrochemical performance compared to SrTiO3. The current work manifestly established the optimal Mn composition (x = 0.12) in SrTiO3 lattice as desirable materials with defective valence states for required electrocatalytic redox potential as well as the acceleration of charge transfer kinetics towards water splitting applications.

High-performance EMI shielding effectiveness of Fe3O4-3D rPC nanocomposites: a systematic optimization in the X-band region.

In this work, the microwave absorption (MWA) performance of a Fe3O4-3D reduced porous carbon nanocomposite (3D rPC NC) in the X-band region is reported. Three different shields are fabricated by altering the ratio of Fe3O4 nanoparticles (NPs) and 3D rPC and evaluating their microwave (MW) shielding performance with appropriate in-wearing instruments due to their minimum thickness. The chemical interaction between Fe3O4 NPs and 3D rPC is examined from chemical composition analysis of Fe3O4-3D rPC (1 : 2 ratio), which is confirmed by the presence of the Fe-O-C bond in the O 1s spectrum obtained from XPS analysis and subsequent analysis using FESEM images. Furthermore, it is found from N2 adsorption/desorption analysis that 3D rPC possesses a huge surface area of 787.312 m2 g-1 and showcases a type-V isotherm (mesoporous and/or microporous) behavior. The dielectric and magnetic losses of Fe3O4-3D rPC with a 1 : 2 ratio (tan δεr = 1.27 and tan δµr = 5.03) are higher than those of Fe3O4 NPs, 3D rPC and their NCs due to its magnetic and electrical conducting pathways modifying the material's polarization and dipole moment. The lightweight, polymer-free Fe3O4-3D rPC (1 : 2) NCs with minimum thickness on the order of 0.5 mm exhibited a higher total shielding effectiveness (SET = 41.285 dB), and it effectively blocked 99.9963% of the transmittance due to electric and magnetic polarization resulting from the presence of a heterogeneous interface surface.

Layered Structures of Enriched V5+ States of Vanadium Oxide as a Hybrid Cathode Material for Long-Cyclable Aqueous Zinc-Ion Batteries.

Recently, aqueous zinc-ion batteries (AZIBs) have garnered much attraction because of their ecofriendly nature, cost effectiveness, and reliability. However, there are still many challenges in developing suitable cathode materials for practical usage in ZIBs. In this work, we have synthesized a layered V5+-rich vanadium oxide (V6O13) flaky structure that provided the electrolyte with a large active surface area. In addition to that, the mixed (V4+/V5+) valence states of V have significantly improved the ionic diffusion of Zn2+, thereby improving the V6O13 electrical conductivity. Therefore, the AZIBs based on the layered structure V6O13 cathode with 1 M ZnSO4 electrolyte exhibited a very high specific capacity of 394 mAh g-1 @ 0.1 A g-1 without the addition of any additives or electrode modification. The rate capability and cycle life are investigated at the current density of 2 A g-1, where the capacity retention was found to be around 94% along with a coulombic efficiency of 96% for over 100 cycles. Such a material with high electrochemical performance can be used for portable electronic devices and electric vehicular applications.

Influence of pH in the synthesis of calcium phosphate based nanostructures with enhanced bioactivity and pro-angiogenic properties.

In synthetic fabrication, the process parameters decide the growth nucleation, phase translation, and the evolution of morphological facets of nanostructured materials. This work demonstrates the formation of different crystallographic phases of calcium phosphate by the influence of pH from acidic to alkaline conditions and also investigated their bone regeneration, protein adsorption, and pro-angiogenic properties. Present results illustrate that the alteration of pH is the crucial factor for the synthesis of calcium phosphate (CP) phases. The structural analysis reveals the monetite (CaHPO4 ) phase with a triclinic crystal system for pH 5, dual-phase of monetite combined with hydroxyapatite at the neutral pH 7, and pure phase of hydroxyapatite (Ca10 [PO4 ]6 OH2 ) with hexagonal structure at pH 10. Microscopic analysis portrays the cubic and rod-like morphologies by changing the pH values. FTIR and RAMAN spectroscopic analyses confirm the stretching, bending, and vibrational modes of dominant phosphate groups of different CP phases. Further, the biocompatibility of the prepared CP phases was examined by hemolysis assay, which showed less than 2% of lysis and enhanced cell viability. Moreover, the bioactivity study revealed rapid mineralization and a higher protein adsorption rate for the monetite CP phase (M-CP). Subsequently, the chick embryo angiogenesis assay elucidated 33% higher neovascularization for M-CP compared with the other two CP phases. The fabricated M-CP nanostructure constitutes a promising candidate for biomedical applications.

Influence of varying thermal treatment on bioactive material with equal Ca/P ratio: A local drug delivery system for bone regeneration.

Designing a biomaterial with excellent bioactivity, biocompatibility, mechanical strength, porosity, and osteogenic properties is essential to incorporate therapeutic agents in order to promote efficient bone regeneration. The work intended to prepare bioactive glass with tailor-made equal Ca/P (CP) ratio to obtain clinophosinaite (Cpt) as dominant phase. Clinophosinaite (Na3 CaPSiO7 ) is one of the rarest phases of bioactive glass (BG), which is supposed to play key role in bioactivity. The novelty of this work is to track the required sintering temperature to attain equimolar calcium phosphate-containing clinophosinaite phase and its behavior. Further, its consequent physicochemical and biological properties were analyzed. Phase transition from Rhenanite to Cpt, and later the Cpt emerged as dominant phase with increase of calcination temperature from 700 to 1000°C was studied. The quantifying evolution of Cpt with Rhenanite over increasing annealing temperature also results with the major morphological modifications. BET analysis confirmed the surface area and porosity (Type-IV mesoporous) were gradually elevated upto 900°C, which had contrary effect on mechanical strength. Formation of hydroxyl carbonate apatite (HCA) layer confirmed the bioactivity of the prepared samples at varying time intervals. The CP samples demonstrated better hemocompatibility in post-immersion (i.e., less than 1% of lysis) when compared with pre-immersion. Enhanced protein adsorption and cumulative release (85%) of Simvastatin (SIM) drug was attained at 900°C treatment.

Invigorating chronic wound healing by nanocomposites composed with bioactive materials: a comprehensive review.

Wound healing research has revealed a plethora of data regarding various techniques for treating diverse types of wounds. It is well known that chronic wounds heal slowly and are vulnerable to infection. Also, there are numerous factors like destitute blood passage, undetermined inflammation, angiogenesis, neuropathy, and cell multiplication which overhang chronic wound healing. To eliminate the speculative features of chronic wounds, we made a consecutive survey on specific categories of biomaterials like bioglass, bioactive glass, bioceramics, biopolymers, and biocompatible metal oxide nanoparticles. In particular, the bioglass or bioactive glass which is a silica matrix composed of sodium, calcium, phosphorous, etc., is used for bone-bonding ability and easily dissolved in vivo conditions to repair damaged and wounded tissues with their peculiar physiochemical (surface area, porous nature, structural formation, mechanical stability) and biological properties (biocompatible, cytocompatible, osteoinductive, angiogenesis, hemostatic, antibacterial, and anti-inflammation). Furthermore, based on the existing literature studies, we summarized the healing of diabetes wound tendency by bioactive composite materials and offer detailed information on the method, techniques, and future technologies for wound healing.

An enduring in vitro wound healing phase recipient by bioactive glass-graphene oxide nanocomposites.

Bioactive glass (BG) is an interesting topic in soft tissue engineering because of its biocompatibility and bonding potential to increase fibroblast cell proliferation, synthesize growth factors, and stimulate granulation tissue development. The proposed BG with and without sodium (Na), prepared by the sol-gel method, is employed in wound healing studies. The BG/graphene oxide (GO) and BG (Na-free)/GO nanocomposites were investigated against fibroblast L929 cells in vitro; the 45S5 BG nanocomposites exhibited desired cell viability (80%), cell proliferation (30%), cell migration (25%), metabolic activity, and wound contraction due to extracellular matrix (ECM) production and enhanced protein release by fibroblast cells. Additionally, the antioxidant assays for BG, BG (Na-free), GO, and BG/GO, BG (Na-free)/GO were evaluated for effective wound healing properties. The results showed decreased inflammation sites in the wound area, assessed by the (2,2-diphenyl-1-picryl-hydrazyl-hydrate) (DPPH) assay with ~ 80% radical scavenging activity, confirming their anti-inflammatory and improved wound healing properties.

Unscrambling the Influence of Sodium Cation on the Structure, Bioactivity, and Erythrocyte Compatibility of 45S5 Bioactive Glass.

The 45S5 bioglass uttering Class A bioactivity promotes both osteoconduction as well as osteoinduction. Though one of the higher reactive bioactive materials known with structural and physiological influence upon ionic modulation, poor mechanical properties are perceived. The possible solution to overcome the weak stability is to choose material's composition that provides retained bioactivity and improved mechanical stability. Meanwhile, primary burst out of Na+ ions increases the local pH, harms cell life, and acts as a well-known disruptive modifying species that weakens the bioactive glass network, decreasing network connectivity, showing faster degradation and lowering mechanical stability. Therefore, in this study, more detailed systematic exploration on structural influence of sodium monovalent cation and its behavior on physiological environment was genuinely studied and reported that bioactivity of the bioactive glass can be highly achieved even without Na+ ions. The result exhibits benefits of sodium free bioactive glass (denoted as No Na+ BG) over Na+ BG and exhibits improved mechanical stability and also possible degradability, having in-built apatite phase even before immersion in simulated body fluid (SBF). Also, sodium free bioglass proved as a superior candidate for erythrocyte compatibility with rapid clotting tendency on interaction with blood and a promising replacement for 45S5 bioglass in all aspects especially in mechanical stability view, which can withstand more than 5 months in phosphate buffer saline (PBS).

Role of bioglass in enamel remineralization: Existing strategies and future prospects-A narrative review.

Enamel, once formed, loses the ability to regenerate due to the loss of the formative ameloblasts. It is subjected to constant damaging events due to exposure to external agents and oral microbiomes. An enamel remineralization process targets to replenish the lost ionic component of the enamel through a multitude of methods. Enamel remineralization is highly challenging as it has a complex organized hierarchical microstructure. Hydroxyapatite nanocrystals of the enamel vary in size and orientation along alignment planes inside the enamel rod. The inability of the enamel to remodel unlike other mineralized tissues is another substantial deterrent. One of the well-known biomaterials, bioglass (BG) induces apatite formation on the external surface of the enamel in the presence of saliva or other physiological fluids. Calcium, sodium, phosphate, and silicate ions in BG become responsive in the presence of body fluids, leading to the precipitation of calcium phosphate. Studies have also demonstrated the bactericidal potential of BG against Streptococcus mutans biofilms. The anticariogenicity and antibacterial activity were found to be enhanced when BG was doped with inorganic ions such as F, Ag, Mg, Sr, and Zn. Due to the versatility of BG, it has been combined with a variety of agents such as chitosan, triclosan, and amelogenin to biomimic remineralization process. Key strategies that can aid in the development of contemporary enamel remineralization agents are also included in this review.

Pulsed laser deposition of nanostructured bioactive glass and hydroxyapatite coatings: Microstructural and electrochemical characterization.

Bioactive coatings on metallic implants promote osseointegration between bone and implant interfaces. A suitable coating enhances the life span of the implant and reduces the requirement of revision surgery. The coating process needs to be optimized such that it does not alter the bioactivity of the material. To understand this, the biocompatibility of nanostructured bioactive glass and hydroxyapatite-coated Titanium substrate by pulsed laser deposition method is evaluated. Raman and IR spectroscopic techniques based on silica and phosphate functional groups mapping have confirmed homogeneity in coatings by pulse laser deposition method. Comparative studies on nanostructured bioactive glass and hydroxyapatite on titanium surface elaborated the significance of bioactivity, hemocompatibility, and cytocompatibility of the coated surface. Notably, both hydroxyapatite and bioactive glass show good hemocompatibility in powder form. Hemocompatibility and cytocompatibility results validate the enhanced sustenance for hydroxyapatite coating. These results signify the importance of the choice of coating methodology of bioceramics towards implant applications.

New Insights for Consummate Diagnosis and Management of Oral Submucous Fibrosis Using Reactive and Reparative Fibrotic Parameter Derived Algorithm.

OBJECTIVE: Reproducibility of qualitative changes in histopathological diagnosis involving narrow variation is often challenging. This study aims to characterize the histological fibrotic events in detail so as to derive an in-depth multiparametric algorithm with individually quantified histological parameters for effective monitoring of the. disease process in oral submucous fibrosis and for potential therapeutic targets for early intervention. METHODS: Formalin fixed paraffin embedded (FFPE) blocks of oral submucous fibrosis (OSMF), were taken and sections were stained with Hematoxylin & Eosin stain and Masson Trichrome stain. Photomicrographs were assessed for various morphometric parameters with Image J software version 1.8. Linear Regression was used to model the relationship using Inflammatory Cell Count, Extent of Inflammation collagen stained area, Epithelial thickness integrated density of collagen, MVPA, Area, Perimeter, were taken as variables. RESULT: Inflammatory cell count and the extent of inflammation also decreased with increasing grades of OSMF. Collagen proportionate area, integrated collagen density and epithelial thickness were compared among different grades of OSMF. Grade IV OSMF had greatest mean collagen proportionate area , highest integrated collagen density and lowest epithelial thickness when compared to other grades of OSMF. Linear regression model revealed smaller variation between Grade I to Grade II. Whereas Grade II to Grade IV exhibited larger variation suggestive of increased growth rate and all the coefficients were found to lie within 95% confidence limits. CONCLUSION: Diagnostic algorithm with multiparametric regression model were derived and combinatorial therapeutic approaches have been suggested for more effective management of oral submucous fibrosis.

Chitosan mediated 5-Fluorouracil functionalized silica nanoparticle from rice husk for anticancer activity.

Herein, we have reported a cost-effective method of synthesizing highly efficient silica nanomaterial from rice husks for its application as a chemotherapeutic agent. Silica particle with two different sizes ~20 nm and ~40 nm were achieved from silica precursor obtained from rice husk. 5-Fluorouracil was functionalized onto the surface of silica nanoparticles by direct conjugation and chitosan mediated conjugation. Particle size analysis, zeta potential and functional analyzes were performed in systematic methodology to confirm chitosan coating and 5-Fluorouracil conjugation on silica nanoparticles. The drug loading percentage with respect to the particle size shows that ~20 nm particles have higher loading capacity. The chitosan mediated conjugation of drug shows sustained release in acidic pH and hence suitable for cancer cell-targeted delivery. The in vitro cell culture studies performed on MC3T3 fibroblast cell lines, MCF-7 and A549 cancer cell lines depicts that, compared to direct conjugation of 5-Fluorouracil, chitosan mediated drug conjugation on the surface of silica nanoparticles shows lesser toxic to fibroblast cell lines and higher toxicity towards cancer cell lines. The results of this toxicity were also confirmed from the nucleic acid spectral signature of Raman spectra treated with drug conjugated silica nanoparticles.

Electrochemical Performance of Nitrogen-Doped TiO2 Nanotubes as Electrode Material for Supercapacitor and Li-Ion Battery.

Electrochemical anodized titanium dioxide (TiO2) nanotubes are of immense significance as electrochemical energy storage devices owing to their fast electron transfer by reducing the diffusion path and paving way to fabricating binder-free and carbon-free electrodes. Besides these advantages, when nitrogen is doped into its lattice, doubles its electrochemical activity due to enhanced charge transfer induced by oxygen vacancy. Herein, we synthesized nitrogen-doped TiO2 (N-TiO2) and studied its electrochemical performances in supercapacitor and as anode for a lithium-ion battery (LIB). Nitrogen doping into TiO2 was confirmed by Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) techniques. The electrochemical performance of N-TiO2 nanotubes was outstanding with a specific capacitance of 835 µF cm-2 at 100 mV s-1 scan rate as a supercapacitor electrode, and it delivered an areal discharge capacity of 975 µA h cm-2 as an anode material for LIB which is far superior to bare TiO2 nanotubes (505 µF cm-2 and 86 µA h cm-2, respectively). This tailor-made nitrogen-doped nanostructured electrode offers great promise as next-generation energy storage electrode material.

Effect of Temperature, Solvent and Precursor Concentration on Anti-Aggregation of ZnO Nanoparticles Prepared by Polyol Method.

We have investigated the formation mechanism of ZnO microspheres in polyol medium. The synthesis conditions have been varied with respect to temperature, medium and Zn-precursor concentration. The X-ray diffraction (XRD) and Raman spectroscopy result shows that the prepared ZnO nanoparticles are hexagonal wurtzite crystal structure and quite crystalline in nature. High resolution transmission electron microscopy (HRTEM) image indicates that the microsphere consists of aggregated nanoparticles in the range of 6 nm to 15 nm. The samples prepared in ethylene glycol medium shows a characteristic ether bond vibration mode in FTIR and it is additionally confirmed by NMR analysis. Initially, the nanoparticles are self-assembled into loosely packed microsphere and then the particles are densely packed by ether bonds formed between the glycol molecules adsorbed on adjacent particles which then grow as perfect microspheres. The sample prepared in EG medium at 150 °C did not show much aggregation. This study proposes the possible mechanism for the formation of ZnO microsphere.

Conformational change results in loss of enzymatic activity of jack bean urease on its interaction with silver nanoparticle.

Urease is an enzyme produced by microbes such as bacteria, yeast and fungi. Plants also produce this enzyme. Urease action splits urea into ammonia and carbamate. This action is having important implications in agro-chemical, medicinal and environment. Therefore there is always a constant search for new and novel compounds which could inhibit this enzyme. Here we have studied the interaction of jack bean urease (JBU) with silver nanoparticle to analyze the influence of the resultant protein corona formation on the catalytic property of JBU. Several techniques like UV-Vis, gel shift assay and CD spectroscopy have been used to characterize this interaction. Urease activity assay suggests that the protein corona formation inhibits the enzymatic action of JBU. The loss of enzymatic action could be either due to the nanoparticle blocking the active site of JBU or a conformational change in the protein. The CD spectra of JBU-AgNP complexes clearly revealed significant changes in the secondary structural composition of the JBU and this could be the reason for the loss of enzymatic activity of JBU. This study revealed an interesting observation, where the interaction of AgNP with JBU resulted destabilization of hexameric nature of JBU which is otherwise highly stable. The results of the present study could be useful in the development of nanoparticle based material for inhibiting the ureolytic activity of ureases in different fields.