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Plant-based hard capsules have gained considerable attention because of their great properties. Accordingly, designing and developing of these kinds of capsules will be a difficult task. Herein, an innovative pullulan-based hard capsule formulation was prepared for the first time. A series of characterization approaches, including Fourier transform infrared, field emission scanning electron microscope, and rheology analysis, were utilized to figure out the straightforward preparation of a designed hard capsule. Many tests and experiments were performed to achieve the optimum capsule formulation. Based on the obtained results, specifications such as uniform downfall and non-desirable adhesion, and other ideal characteristics of the capsule display the critical function. The gelling promoter of divalent cationic salts is more beneficial than its single-valent counterparts. With respect to the key role of gelling promoter, the presence of chosen MgSO4.7H2O salt and the source of selected carrageenan are important parameters to achieve optimal formulation. Moreover, field emission scanning electron microscope images illustrate that the weight ratio of 3.5 (gelling agent to salt) displays uniform surface morphology without any impurities or other foreign materials. Likewise, the outcomes of the rheology test also illustrated that the weight ratio of 3.5 is preferable. Considering the different weight ratios, the benefits of a weight ratio of 3.5 outweigh the other investigated ratios. Overall, the current research addresses substantial information about developing pullulan-based hard capsules for target usage.

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Modification surface of chitosan nanoparticles using ZnO nanoparticles is important interest in drug delivery because of the beneficial properties. In this study, we proposed a chitosan/ZnO nanocomposite for the targeted delivery of antibacterial peptide (LL37). Synthesized LL37-loaded chitosan/ZnO nanocomposite (CS/ZnO/LL37-NCs) was based on the ionotropic gelation method. The antibacterial activity of the synthesized platform versus Methicillin-resistant Staphylococcus aureus (MRSA) was determined by the microdilution method in 10 mM sodium phosphate buffer. The biofilm formation inhibitory was also evaluated using microtiter plate method. In addition, the ability of CS/ZnO/LL37-NCs on the icaA gene expression level was assessed by the Real-Time PCR. The loading and release investigations confirmed the suitability of CS/ZnO-NCs for LL37 encapsulation. Results showed 6 log10 CFU/ml reduction in MRSA treated with the CS/ZnO/LL37-NPs. Moreover, CS/ZnO/LL37-NCs showed 81 % biofilm formation inhibition than LL37 alone. Also, icaA gene expression decreased 1-fold in the face of CS/ZnO/LL37-NCs. In conclusion, the modification surface of chitosan nanoparticles with ZnO nanoparticles is a suitable chemical platform for the delivery of LL37 that could be used as a promising nanocarrier for enhancing the delivery of antibacterial peptide and improving the antibacterial activity of LL37.

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In recent years, water contamination has become a significant crisis, and it is crucial to find new materials that can efficiently eliminate these contaminants. The current work presents the Sm2CuO4 nanophotocatalyst for the decolorization of different water-soluble organic contaminants. The fabrication of Sm2CuO4 nanostructures was achieved using a simple and rapid sonochemical pathway, resulting in an optical bandgap of 1.62 eV as determined by diffuse reflectance spectroscopy. Several factors, including different organic contaminants, organic contaminant concentrations, Sm2CuO4 dosages, and the pH of the media, were scrutinized to achieve the best efficiency. The results manifested that Sm2CuO4 was highly effective in removing different organic contaminants from water. For example, when 30 mg of Sm2CuO4 was used with 20 mg L-1 methyl orange under visible irradiation for 100 min, 91.4% of the methyl orange was destroyed. Further investigation revealed that holes (h+) were primarily responsible for pollutant photodegradation when using Sm2CuO4 as a photocatalyst. This finding suggests that Sm2CuO4 could be an excellent candidate for developing new materials to effectively remove water contaminants.

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Capsules are popular oral dosage forms because of their ease of production. They are widespread pharmaceutical products. Hard capsules are preferred dosage forms for new medicines undergoing clinical tests because they do not require expansive formulation development. Functional capsules with built-in gastroresistance, aside from the traditional hard-gelatin or cellulose-based vegetarian capsules, would be beneficial. In this research, the effect of polyethylene glycol-4000 (PEG-4000) was investigated on the formulation of uncoated enteric hard capsules based on hypromellose phthalate (HPMCPh) and gelatin. Three different formulations based on HPMCPh, gelatin, and PEG-4000 were tested to achieve the optimal formulation for the industrial production of hard enteric capsules with desired physicochemical and enteric properties. The results reveal that the capsules containing HPMCPh, gelatin, and PEG-4000 (F1) are stable in the stomach environment (pH = 1.2) for 120 min, and during this time, no release happens. The outcomes also demonstrate that PEG-4000 blocks the pores and improves enteric hard capsule formulation. In this research, we present a specific procedure for manufacturing uncoated enteric hard capsules on an industrial scale that does not require an extra coating step for the first time. The industrial-scale validated process can considerably reduce the cost of manufacturing standard enteric-coated dosage forms.

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Thulium vanadate (TmVO4) nanorods were successfully prepared by a simple sonochemical approach using Schiff-base ligands. Additionally, TmVO4 nanorods were employed as a photocatalyst. The most optimal crystal structure and morphology of TmVO4 have been determined and optimized by varying Schiff-base ligands, the molar ratio of H2Salen, the sonication time and power, and the calcination time. A Eriochrome Black T (EBT) analysis revealed that the specific surface area was 24.91 m2/g. A bandgap of 2.3 eV was determined by diffuse reflectance spectroscopy (DRS) spectroscopy, which makes this compound suitable for visible photocatalytic applications. In order to assess the photocatalytic performance under visible light, two anionic dyes (EBT) and cationic dyes (Methyl Violet (MV)) were used as models. A variety of factors have been studied in order to improve the efficiency of the photocatalytic reaction, including dye type, pH, dye concentration, and catalyst loading. Under visible light, the highest efficiency was achieved (97.7%) when 45 mg TmVO4 nanocatalysts were present in 10 ppm Eriochorome Black T at pH = 10.

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In this paper, the oscillation patterns and characteristics of gyroscopic reaction to rotation-induced Coriolis force and phase relations are reviewed by examining the main principles of operation of Coriolis vibratory gyroscopes based on the dynamic relations and proposed improvements in performance using parameter changes. Coriolis vibratory gyroscopes (CVGs) are among the most modern applicable gyroscopes in position detection that have replaced traditional gyroscopes due to some great features of the design of vibrating proof mass and elastic suspension. Given the key characteristics of capacitive versus piezoelectric excitation technologies for determining the vibration type in sensors, their operating principles and equations have completely changed. Therefore, two-dimensional finite element analysis is required to evaluate their optimal performance. Since the sensor space is constantly vibrating, a general equation is presented in this paper to explain the impact of parameters on the frequency of different operating modes. The main purposes of building vibrating gyroscopes are replacing the constant spinning of the rotor with a vibrating structure and utilizing the Coriolis effect, based on which the secondary motion of the sensitive object is generated according to the external angular velocity.

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Medicine/nanotechnology as a new and applicable technique according to drug delivery systems has gained great consideration for cancer treatment. Polysaccharides including, cellulose, ß-cyclodextrin and sodium carboxymethyl cellulose and chitosan as natural bio-materials, are appropriate candidates for designing and formulations of these nanosystems because of the exceptional advantages such as bio-compatibility, bio-degradability, non-toxicity, and gelling characteristics. An intelligent drug delivery platform based on these hybrids nowadays is developed, which can be used for dual-responsive dual-drug delivery. Nanotechnology accompany with biological molecules has been carefully considered to decrease the drawbacks of conventional cancer treatments. Consequently, this review is intended to state and investigate on the latest development on the combination treatment of platforms based on the hybrids of anticancer drugs/nanoparticles/Polysaccharides in the fields of biomedical therapeutics and cancer therapy owing to the bio-compatibility, great surface area, good chemical and mechanical features, the challenges and future perspectives are reported as well.

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Attempts are continuing to discover novel and efficient solutions to promote water grade and industrial sewage treatment. For the first time, we present a novel Cs2HgI4 photocatalyst functional below visible radiation. Cs2HgI4 nano photocatalyst has been prepared via an accelerated sonochemical approach to examine its photocatalytic progression. Several construction circumstances, including variations of power and time of sonication and performance of different surfactant types, were conducted to produce fine particles with uniform morphology. FESEM images attested that the presence of surfactant had an adverse and destructive effect on the morphology of products. The bandgap for Cs2HgI4 nanostructures was determined to be approximately 2.3 eV, making these nanostructures desirable for photocatalytic applications. The photocatalytic data confirmed that Cs2HgI4 could destroy acidic coloring agents greater than basic ones. The highest photodegradation was observed for methyl orange with 76.8%.

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Stem cell treatment is promising in the various disorders treatment, but its effect is confined by the adverse conditions in the damaged tissues. The utilization of hydrogels has been suggested as a procedure to defeat this issue by developing the engraftment and survival of injected stem cells. Specifically, injectable hydrogels have drawn much attention due to their shape adaptability, ease of use, and the capability to reach body parts that are hard to access. In this study, the thermosensitive injectable hydrogels based on oxidized alginate, gelatin, and carbon nitride quantum dots (CNQDs) have been fabricated for tissue engineering. The mechanical characteristics of the nanocomposite hydrogels were investigated by rheology analysis. The results show that increasing the amount of CNQDs improve the mechanical strength of the nanocomposite hydrogels. The Cross-section morphology of freeze dried hydrogels comprising 0.25, 1.5, and 3.0% CNQDs indicate porous structure with interrelated pores. Besides, the result of in vitro degradation reveals that the hydrogels comprising CNQDs are more durable than the one without CNQDs. A reduction in the biodegradation and swelling ratio is perceived with the addition of CNQDs. The cell viability and attachment show that the nanocomposite hydrogels are biocompatible (>88%) with great cell adhesion to osteosarcoma cell line MG63 depending on the presence of CNQDs.

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The photocatalytic process is an environmentally-friendly procedure that has been well known in the destruction of organic pollutants in water. The multiple semiconductor heterojunctions are broadly applied to enhance the photocatalytic performances in comparison to the single semiconductor. Polymeric semiconductors have received much attention as inspiring candidates owing to their adjustable optical absorption features and simply adaptable electronic structure. The shortcomings of the current photocatalytic system, which restricts their technical applications incorporate fast charge recombination, low-utilization of visible radiation, and low immigration capability of the photo-induced electron-hole. This paper indicates the novel fabrication of new CuI/g-C3N4 nanocomposite by hydrothermal and ultrasound-assisted co-precipitation methods. The structure, shape, and purity of the products were affected by different weight percentages and fabrication processes. Electron microscope unveils that CuI nanoparticles are distributed on g-C3N4. The bandgap of pure carbon nitride is estimated at 2.70 eV, and the bandgap of the nanocomposite has increased to 2.8 eV via expanding the amount of CuI. The CuI/C3N4 nanocomposite has a great potential to degrade cationic and anionic dyes in high value because of its appropriate bandgap. It can be a great catalyst for water purification. The photocatalytic efficiency is affected by multiple factors such as types of dyes, fabrication methods, the light sources, mass ratios, and scavengers. The fabricated CuI/C3N4 nanocomposite exposes higher photocatalytic performance than the pure C3N4 and CuI. The photocatalytic efficiency of nanocomposite is enhanced by enhancing the amount of CuI. Besides, the fabricated CuI/C3N4 revealed remarkable reusability without the obvious loss of photocatalytic activity. The antibacterial activity of the specimens reveals that the highest antimicrobial activities are revealed against P. aeruginosa and E. coli. These results prove that the nanocomposite possesses high potential for killing bacteria, and it can be nominated as a suitable agent against bacteria.

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Visible photocatalytic procedures exhibit encouraging potential in water purification by increasing the photocatalytic performance. Therefore, the improvement of low-cost and efficient photocatalysts for environmental remediation is an increasing demand, and photocatalysts based on semiconductors have gained considerable attention due to their superior stability and activity. In the current study, novel Rb2HgI4 nanostructures were prepared via a simple, low-cost, and low-temperature solid-state method. The effects of different parameters such as type of surfactants, reaction temperature, and reaction time were studied on the structure, crystallinity, particle size, and shape of nanostructures. This new compound has a suitable band gap (2.6 eV) in the visible region. The photocatalytic performance of Rb2HgI4 was examined for the removal of coloring agents under visible light irradiation and it was found that this compound could degrade and eliminate acid black 1 by about 72.1%.

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Porous substrates composed of biodegradable polymers and nanoparticles have found extensive use as three-dimensional (3D) scaffolds to regenerate damaged tissues through the incorporation of cells or growth factors. Here, injectable thermally responsive hydrogels based on SiO2 nanoparticles (NPs), alginate, and gelatin biopolymers, with possible utilization for cartilage tissue engineering, are introduced. The nanocomposites contain different amounts of SiO2 NPs for reinforcement and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC)/N-hydroxysuccinimide (NHS) for chemical crosslinking of polymer chains in the 3D hydrogel network. The cross-sectional structure of the hydrogels containing 0.25, 1.5, and 3.0% SiO2 NPs was observed by FE-SEM, confirming porous morphology with interconnected pores. Based on the rheometer analyses, by increasing the amount of SiO2 NPs, the mechanical strength of the gels can be found. In addition, in vitro biodegradation studies show that the hydrogels without SiO2 are more unstable than the hydrogels containing SiO2 NPs. In vitro biocompatibility of the products tested by MTT assay indicates that cell viability and attachment depend on the presence of SiO2 NPs.

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Efforts to find new and practical solutions to improve water quality and treatment of industrial effluents are ongoing. In this study, Tl4HgI6/HgI2 nanocomposites were synthesized by a rapid ultrasonic method to investigate their photocatalytic and antibacterial activity. Various synthesis conditions such as changes in the ratio of precursors, use of surfactants, and changes in the power and time of sonication to achieve particles with optimal size and morphology were performed. X-ray diffraction (XRD) and energy dispersive spectroscopy (EDS) analysis confirmed the purity and formation of the nanocomposite. Optimal nanoparticles in terms of size and morphology were selected by examining the images obtained from scanning electron microscopy (SEM) analysis. The nanocomposites obtained in the presence of PVP (polyvinylpyrrolidone) as a surfactant (sample no. 8) were selected as the optimal sample. Transmission electron microscopy (TEM), differential reflectance spectroscopy (DRS), Raman, N2 adsorption/desorption analyzes were performed for the optimal sample to evaluate the properties of nanocomposites. The band-gap for Tl4HgI6/HgI2 nanocomposites was calculated to be about 2.3 eV for HgI2 and 3.1 eV for Tl4HgI6. The optimal sample was used to evaluate the photocatalytic activity for decolorizing an aqueous solution of six different organic dyes. Finally, for rhodamine B, the decolorization was about 80%. Also, Tl4HgI6/HgI2 nanocomposite showed a significant inhibition zone in the antibacterial test. The maximum inhibition diameter of 50 mm was obtained against Streptococcus pyogenes. The results showed that Tl4HgI6/HgI2 nanocomposites have good potential for many industrial applications.

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Hybrid injectable and biodegradable hydrogels based on oxidized alginate/gelatin and containing nitrogen-doped carbon dots (NCDs) as a reinforcement have been fabricated and crosslinked by 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC)/N-hydroxysuccinimide (NHS) as the chemical crosslinking agents in the hydrogel system. The idea of composite hydrogels relies on the assumption that they supply a microenvironment that is convenient for the exchange of nutrients via a porous structure and cell proliferation and have mechanical characteristics that approximately match natural tissue. The effect of the NCD content on the morphology structure, mechanical strength, swelling ratio, and biodegradation has been investigated. The results indicate that nanocomposite hydrogels containing a higher content of NCDs have smaller pore sizes and higher mechanical properties. The in vitro biodegradation and swelling behavior demonstrated that increasing the amount of NCDs up to 0.06% decreased the swelling ratio and weight loss of the hydrogels. The composite hydrogels are biocompatible, as verified by the MTT assay of MG-63 cells. The N-doped graphene quantum dots considerably affect degradation and interaction within the cells and hydrogels.

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Recently, nanocomposite photocatalysts based on semiconductors have drawn consideration due to their suitable bandgap. Combination of tow of several semiconductors can slow down the electron-hole recombination. For this purpose, we have introduced DyMnO3/Fe2O3 nanocomposite as a novel and efficient catalyst for water purification. For this regard, DyMnO3/Fe2O3 nanocomposite has been fabricated by a simple and green sol-gel auto-combustion technique. The impact of calcination temperature, time, and types of fuel was investigated on morphology, structure, and purity of the products. The samples were identified by XRD, FTIR, FESEM, HRTEM, BET, and DRS. The bandgap was calculated by DRS to be 3.20 and 3.28 eV for Fe2O3 and DyMnO3. Due to the appropriate bandgap, DyMnO3/Fe2O3 degraded 80% of methylene blue under UV light. The future aspects of the DyMnO3/Fe2O3 application can be applied in thermoelectric materials, solid fuel cells, electrochemical gas sensors, and electrochemical biosensors.

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Silver iodide/graphitic carbon nitride nanocomposites have been successfully fabricated through sonication-assisted deposition-precipitation route at room temperature and hydrothermal method. Varied mass ratios and preparation processes can modify the structure, purity, shape, and scale of specimens. The purity of the product was confirmed by Energy Dispersive X-Ray Spectroscopy (EDS) and X-ray crystallography. The morphology and size of specimens could be observed with transmission electron microscopy (TEM) and field emission scanning electron microscopy (FESEM). The bandgap was evaluated around 2.82 eV for pure g-C3N4. The bandgap has reduced to 2.70 eV by increasing the quantity of silver iodide in the nanocomposites. The photocatalytic activity of AgI/C3N4 has been studied over the destruction of rhodamine B (RhB) and methyl orange (MO) through visible radiation due to their suitable bandgap. The as-prepared AgI/C3N4 nanocomposites photocatalyst revealed better photocatalytic behavior than the genuine AgI and C3N4 which ascribed to synergic impacts at the interconnection of C3N4 and AgI. Furthermore, these nanocomposites have great potential for being a great antibacterial agent.

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In the current paper, the main aim is to fabricate the BaMnO3 nanostructures via the sonochemical route. The various factor, including precursors, reaction time and power of sonication can affect the shape, size, and purity of the samples. We utilized X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), and X-ray energy dispersive spectroscopy (EDS) to characterize the BaMnO3 nanostructures. The optical property of BaMnO3 nanostructures was explored by Ultraviolet-visible spectroscopy (UV-vis) and the energy gap was suitable for catalytic activity (about 2.75 eV). Changing the precursor can affect the size, nanoparticle shape, architectures, and uniformity of the samples. We employed the BaMnO3 nanostructures for O2 evolution reaction as catalysts. It can observe that increasing the homogeneity of the catalysts can increase the efficiency of the Oxygen evolution reaction. The maximum amount of the O2 evolution and the highest TOF and TON are related to nanoplate disc using barium salicylate as a precursor of barium. As a result, we can nominate the BaMnO3 nanostructures as an effective and novel catalyst for water-splitting reaction.

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In the present study, Tl4CdI6 nanostructures were synthesized via a facile sonochemical method. The effect of molar ratio of TlI to CdI2, reaction time, power of sonication, and the capping agents was investigated on morphology, size, and purity of the products. The as-prepared nanomaterials were characterized by X-ray diffraction, X-ray energy dispersive spectroscopy, field emission scanning, transmission electron microscopy, and Raman spectroscopy. The optical property of Tl4CdI6 nanoparticles was investigated by ultraviolet-visible spectroscopy (UV-vis), and the band gap was estimated about 2.82 eV. The photocatalytic behaviors of the nanoparticles were investigated by removal and degradation of different organic dyes under the UV irradiation. The results indicated a highest degradation for acid black 1 of 85.7% in 110 min. This sample was selected as an optimum sample for photocatalytic application.