Synthesis of strontium oxide-zinc oxide nanocomposites by Co-precipitation method and its application for degradation of malachite green dye under direct sunlight.

Photocatalysts workable under direct sunlight are the safe and cost-effective option for water purification. The nanocomposites of strontium oxide and zinc oxide (SZ NCs) were synthesized using coprecipitation method. The respective precursors of SZ NCs were subjected to alkaline hydrolysis and subsequently thermally treated to yield SZ NCs. The SZ NCs with different ZnO composition was synthesized by varying the concentration of ZnO precursor from 0.2 to 1 M. The structural properties of SZ NCs evaluated using X-Ray diffraction (XRD), Thermogravimetric analysis (TGA), and Differential thermal analysis DTA). The optical properties of SZ NCs studied using ultraviolet-visible (UV-Vis) spectroscopic study. The trend observed in the intensity of XRD peaks indicated the occurrence of Zn doping in the crystalline lattice of SrO and the formation of SrO-ZnO composite. Upon incorporation of 1 M of ZnO precursor, the grain size of the SrO was decreased from 49.3 to 27.6 nm. The weight loss in the thermal analysis indicates the removal of carbonates from the sample upon heating and shows the formation of an oxide structure. UV-Vis spectra confirmed that the presence of SrO enhanced the sunlight absorption of SZ NCs. The increase in the composition of ZnO precursors increased the bandgap of SrO (2.09 eV) to the level of ZnO (3.14 eV). SZ NCs exhibited heterostructure morphology, where the nanosized domains with varying shapes (layered and rod-like) were observed. Under direct sunlight conditions, SZ NCs prepared using 1 M/0.6 M of SrO/ZnO precursors exhibited 15-20 % higher photocatalytic efficiency than neat SrO and ZnO. In precise, 1 mg of this SZ NC was degraded 98 % of malachite green dye dissolved in water (10 ppm) under direct sunlight. Additionally, the thermal stability results showed that 18 % decomposition was obtained due to the degradation impurities in SrO/ZnO catalysts and the XRD results revealed that no structural change is obtained in SrO/ZnO photocatalysts after stability test. The SZ NCs can be effectively used as safe and economic sunlight photocatalysts for water purification in remote areas without the electricity.

Phytochemical Analysis and Antioxidant Activity of Centella Asiatica Extracts: An Experimental and Theoretical Investigation of Flavonoids.

Centella asiatica (CA) is a medicinal plant widely used in the East, with many of its phytoconstituents remaining unexplored. In this study, compounds were extracted and identified from C. asiatica to determine its medicinal properties. Phytochemical screening was conducted on shoot, callus, and cell suspension extracts, revealing the presence of tannins, flavonoids, terpenoids, saponins, and steroids in all three cultures, with no alkaloids detected. IC50 values were determined to evaluate the antioxidant activity of the extracts, with the highest value observed for cell suspension culture (20 µg/mL), followed by shoot culture (19 µg/mL), and then callus extract (10 µg/mL), with ascorbic acid as the standard at an IC50 value of 26.25 µg/mL. Finally, density functional theory was used to analyze the structure-activity relationships of the identified compounds from C. asiatica extract. The results suggest that ultrasonic-assisted extraction yielded the highest recovery and antioxidant activity, with a scavenging activity of 79%. This study provides valuable insights into the phytochemical composition and antioxidant potential of C. asiatica, which may have implications for its use in traditional medicine and future drug development.

Recent Advances in the Production of Pharmaceuticals Using Selective Laser Sintering.

Selective laser sintering (SLS) is an additive manufacturing process that has shown promise in the production of medical devices, including hip cups, knee trays, dental crowns, and hearing aids. SLS-based 3D-printed dosage forms have the potential to revolutionise the production of personalised drugs. The ability to manipulate the porosity of printed materials is a particularly exciting aspect of SLS. Porous tablet formulations produced by SLS can disintegrate orally within seconds, which is challenging to achieve with traditional methods. SLS also enables the creation of amorphous solid dispersions in a single step, rather than the multi-step process required with conventional methods. This review provides an overview of 3D printing, describes the operating mechanism and necessary materials for SLS, and highlights recent advances in SLS for biomedical and pharmaceutical applications. Furthermore, an in-depth comparison and contrast of various 3D printing technologies for their effectiveness in tissue engineering applications is also presented in this review.

Drug Delivery Application of Functional Nanomaterials Synthesized Using Natural Sources.

Nanomaterials (NMs) synthesized from natural sources have been attracting greater attention, due to their intrinsic advantages including biocompatibility, stimuli-responsive property, nontoxicity, cost-effectiveness, and non-immunogenic characteristics in the biological environment. Among various biomedical applications, a breakthrough has been achieved in the development of drug delivery systems (DDS). Biocompatibility is necessary for treating a disease safely without any adverse effects. Some components in DDS respond to the physiological environment, such as pH, temperature, and functional group at the target, which facilitates targeted drug release. NM-based DDS is being applied for treating cancer, arthritis, cardiovascular diseases, and dermal and ophthalmic diseases. Metal nanomaterials and carbon quantum dots are synthesized and stabilized using functional molecules extracted from natural sources. Polymers, mucilage and gums, exosomes, and molecules with biological activities are directly derived from natural sources. In DDS, these functional components have been used as drug carriers, imaging agents, targeting moieties, and super disintegrants. Plant extracts, biowaste, biomass, and microorganisms have been used as the natural source for obtaining these NMs. This review highlights the natural sources, synthesis, and application of metallic materials, polymeric materials, carbon dots, mucilage and gums, and exosomes in DDS. Aside from that, challenges and future perspectives on using natural resources for DDS are also discussed.

Direct sunlight induced room temperature synthesis of anticancer and catalytic silver nanoparticles by shrimp shell waste derived chitosan.

The use of marine waste derived chitosan (CS) for the synthesis of nanomaterials is considered as one of the effective routes for bio-waste management and recovering functional products. Herein, CS capped silver nanoparticles (Ag NPs-CS) with potential anticancer and dye pollutants adoption properties have been synthesized photochemically under direct sunlight. To obtain, CS, shrimp shell waste was subjected to a serious of standard demineralization, deproteinization and deacetylation processes. The electronic absorption peak (400 nm) denoting surface plasmonic resonance of Ag NPs and infrared peaks relevant to CS (3364 cm-1 of OH/NH2, 2932 cm-1 of CH, and 1647 cm-1 of -CO) exhibited peaks confirmed the formation of CS-Ag NPs. Ag NPs-CS exhibited anticancer activity against Human lung adenocarcinoma cell lines (A549), the maximum cell death noticed at the concentration of 20 µg/mL and 70 µg/mL was 20 and 52 %, respectively. An aqueous Ag NPs-CS (100 µg/mL) was degraded ≥95 % of mixed dye target solution (25 mg/mL) containing equal volume of cationic dye (Methylene blue and Rhodamine B) and anionic dye (methyl orange). Therefore, these findings suggest that the shrimp shell waste derived CS can be used for the synthesis of CS-Ag NPs with potential biomedical and environmental applications.

Gel Polymer Electrolytes: Advancing Solid-State Batteries for High-Performance Applications.

Gel polymer electrolytes (GPEs) hold tremendous potential for advancing high-energy-density and safe rechargeable solid-state batteries, making them a transformative technology for advancing electric vehicles. GPEs offer high ionic conductivity and mechanical stability, enabling their use in quasi-solid-state batteries that combine solid-state interfaces with liquid-like behavior. Various GPEs based on different materials, including flame-retardant GPEs, dendrite-free polymer gel electrolytes, hybrid solid-state batteries, and 3D printable GPEs, have been developed. Significant efforts have also been directed toward improving the interface between GPEs and electrodes. The integration of gel-based electrolytes into solid-state electrochemical devices has the potential to revolutionize energy storage solutions by offering improved efficiency and reliability. These advancements find applications across diverse industries, particularly in electric vehicles and renewable energy. This review comprehensively discusses the potential of GPEs as solid-state electrolytes for diverse battery systems, such as lithium-ion batteries (LiBs), lithium metal batteries (LMBs), lithium-oxygen batteries, lithium-sulfur batteries, zinc-based batteries, sodium-ion batteries, and dual-ion batteries. This review highlights the materials being explored for GPE development, including polymers, inorganic compounds, and ionic liquids. Furthermore, it underscores the transformative impact of GPEs on solid-state batteries and their role in enhancing the performance and safety of energy storage devices.

Synthesis and investigation on synergetic effect of activated carbon loaded silver nanoparticles with enhanced photocatalytic and antibacterial activities.

In this study, we synthesized silver nanoparticle-loaded cashew nut shell activated carbon (Ag/CNSAC). The synthesized samples were characterized by XRD, XPS, SEM with EDS, FT-IR, and BET analysis. The XRD, XPS, and EDS data provided convincing proof that Ag loaded on CNSAC is formed. The energy dispersive spectrum analysis and X-ray diffraction pattern both supported the face-centered cubic and amorphous structures of Ag/CNSAC. The SEM micrographs showed the inner surface development of Ag NPs and many tiny pores in CNSAC. The photodegradation of methylene blue (MB) dye by the Ag/CNSAC photocatalyst was investigated. This effective degradation of MB dye by Ag/CNSAC is attributed to the cooperative action of Ag as a photocatalyst and CNSAC as a catalytic support and adsorbent. In tests with gram-positive and negative bacteria including Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus), the as-synthesized Ag/CNSAC showed outstanding antibacterial efficiency. Additionally, this study demonstrates a workable procedure for creating an affordable and efficient Ag/CNSAC for the photocatalytic eradication of organic contaminants.

Encapsulation of tannic acid in polyvinylidene fluoride mediated electrospun nanofibers and its antibiofilm and antibacterial activities.

In the past 15 years or more, interest in polymer-mediated nanofibers (NFs), a significant class of nanomaterials, has grown. Although fibers with a diameter of less than 1 mm are frequently commonly referred to as NFs, and are typically defined as having a diameter of less than several hundreds of nanometers. Due to the increased antibiotic resistance of many diseases nowadays, NFs with antibacterial activity are quite important. A flexible technique for creating NFs with the desired characteristics is called electrospinning. This research article describes how to make electrospun NFs of tannic acid (TA) with polyvinylidene fluoride (PVDF) as the template. As a result, the absorbance of the obtained NFs has been raised without forming any additional peaks in the spectral ranges. The obtained NF has a gradual increase in intensity, and the FT-IR data show that the TA is present in the NFs. FE-SEM images show that the NFs are discovered to be completely bead-free. Since TA reduced the viscosity of the spinning solution while marginally increasing solution conductivity, PVDF NFs have a greater average fiber diameter (AFD) than NFs of TA with PVDF, which is likely a result of the TA solutions in it. The findings showed that TA greatly decreased S. aureus and E. coli's ability to attach. The acquired NFs created in this work may have significant potential for reducing the pathogenicity of S. aureus and E. coli as well as their ability to build biofilms.

Effect of metal doping and non-metal loading on light energy driven degradation of organic dye using ZnO nanocatalysts.

Photocatalytic degradation of azo dyes is seen as a viable technique for addressing environmental and energy concerns simultaneously. Therefore, the primary requirement is the creation of a better catalyst with adequate product selectivity for removal efficiency under solar light. Herein, pure ZnO and Cu (0.10 M) doped cotton stalk activated carbons with ZnO (Cu-doped ZnO/CSAC) were produced, and these are labelled as CZ1, CZ2, CZ3, and CZ3/CSAC, respectively. The optoelectronic and photodegradation efficiencies were examined regarding the impact of doping and loading samples. The XRD patterns confirmed that the CZ3/CSAC sample exhibited a hexagonal wurtzite structure. The XPS survey confirmed that Cu ions were incorporated into the ZnO lattice in a Cu2+ oxidation state. The band gap value (CZ3/CSAC) was reduced (2.38 eV) compared to pure ZnO and CZ3. Moreover, PL and EIS analysis proved more efficient at separating photoinduced charged carriers for CZ3/CSAC than all other samples. The CZ3/CSAC sample showed improved photocatalytic degradation efficiency (93.09%) compared to the pure ZnO and CZ3 samples using brilliant green (BG) dye under sunlight irradiation.

Synthesis, antimycobacterial screening, molecular docking, ADMET prediction and pharmacological evaluation on novel pyran-4-one bearing hydrazone, triazole and isoxazole moieties: Potential inhibitors of SARS CoV-2.

The respiratory infection tuberculosis is caused by the bacteria Mycobacterium tuberculosis and its unrelenting spread caused millions of deaths around the world. Hence, it is needed to explore potential and less toxic anti-tubercular drugs. In the present work, we report the synthesis and antitubercular activity of four different (hydrazones 7-12, O-ethynyl oximes 19-24, triazoles 25-30, and isoxazoles 31-36) hybrids. Among these hybrids 9, 10, 33, and 34, displayed high antitubercular activity at 3.12 g/mL with >90% of inhibitions. The hybrids also showed good docking energies between -6.8 and -7.8 kcal/mol. Further, most active molecules were assayed for their DNA gyrase reduction ability towards M. tuberculosis and E.coli DNA gyrase by the DNA supercoiling and ATPase gyrase assay methods. All four hybrids showed good IC50 values comparable to that of the reference drug. In addition, the targets were also predicted as a potential binder for papain-like protease (SARS CoV-2 PLpro) by molecular docking and a good interaction result was observed. Besides, all targets were predicted for their absorption, distribution, metabolism, and excretion - toxicity (ADMET) profile and found a significant amount of ADMET and bioavailability.

Construction of novel g-C3N4 coupled efficient Bi2O3 nanoparticles for improved Z-scheme photocatalytic removal of environmental wastewater contaminant: Insight mechanism.

Recently, the major environmental pollution produced by the release of wastewater in liquid type is one of the most extensive forms of foremost pollution in water ecosystems. In this article, the Bi2O3/g-C3N4 nanocomposite with a direct Z-scheme was effectively obtained by a facile hydrothermal system. The crystal structures, surface morphology, chemical composition, and the optical belongings of the as-obtained composite catalysts were examined by Power XRD, FT-IR spectra, High-resolution XPS spectra, FE-SEM images with EDX spectra, High-resolution TEM images, UV-Vis DRS, and PL spectra respectively. Furthermore, the photocatalytic performance was assessed by the degradation of aqueous Rhodamine B (Rh B) dye under visible-light exposure. The Bi2O3/g-C3N4 composite photocatalysts (PCs) showed the maximum photo-degradation efficiency through a rate constant value of 0.0149 min-1, which is 4.9 and 5.3 folds superior to Bi2O3, and GCN, respectively. The better GBO2 nanocomposite PCs showed a superior photocatalytic degradation performance (>82%) of aqueous Rh B dye after five successive recycles. Moreover, based on these outcomes of the radical scavenging test, a direct and effective Z-scheme photocatalytic charger transfer mechanism was also projected. Finally, the reusability of the as-obtained Bi2O3/g-C3N4 nanocomposite has better stability and reusability, which was a favourable applicant for wastewater handling.

Recent Advances in Biomedical Applications of Polymeric Nanoplatform Assisted with Two-Photon Absorption Process.

Polymers are well-recognized carriers useful for delivering therapeutic drug and imaging probes to the target specified in the defined pathophysiological site. The functional drug molecules and imaging agents were chemically attached or physically loaded in the carrier polymer matrix via cleavable spacers. Using appropriate targeting moieties, these polymeric carriers (PCs) loaded with functional molecules were designed to realize target-specific delivery at the cellular level. The biodistribution of these carriers can be tracked using imaging agents with suitable imaging techniques. The drug molecules can be released by cleaving the spacers either by endogenous stimuli (e.g., pH, redox species, glucose level and enzymes) at the targeted physiological site or exogenous stimuli (e.g., light, electrical pulses, ultrasound and magnetism). Recently, two-photon absorption (2PA)-mediated drug delivery and imaging has gained significant attention because TPA from near-infrared light (700-950 nm, NIR) renders light energy similar to the one-photon absorption from ultraviolet (UV) light. NIR has been considered biologically safe unlike UV, which is harmful to soft tissues, cells and blood vessels. In addition to the heat and reactive oxygen species generating capability of 2PA molecules, 2PA-functionalized PCs were also found to be useful for treating diseases such as cancer by photothermal and photodynamic therapies. Herein, insights attained towards the design, synthesis and biomedical applications of 2PA-activated PCs are reviewed. In particular, specific focus is provided to the imaging and drug delivery applications with a special emphasis on multi-responsive platforms.

Antibacterial, Antioxidant, Larvicidal and Anticancer Activities of Silver Nanoparticles Synthesized Using Extracts from Fruits of Lagerstroemia speciose and Flowers of Couroupita guianensis.

The present study aimed to analyze the in vitro antibacterial, antioxidant, larvicidal and cytotoxicity properties of green synthesized silver nanoparticles (Ag NPs) using aqueous extracts from fruits of Lagerstroemia speciosa and flowers of Couropita guinensis. Synthesized Ag NPs were characterized using UV-DRS, FTIR, XRD, DLS, and High-Resolution SEM and TEM analyses. Absorption wavelength was observed at 386 nm by UV-DRS analysis and energy band gap was calculated as 3.24 eV. FTIR analysis showed the existence of various functional groups in the aqueous extract and in the NPs. DLS analysis showed the stability and particle size of the synthesized Ag NPs. SEM analysis revealed that Ag NPs are in a face centered cubic symmetry and spherical shape with a size of 23.9 nm. TEM analysis showed particle size as 29.90 nm. Ag NPs showed antibacterial activity against both Gram-positive and Gram-negative bacteria. DPPH scavenging trait of Ag NPs was ranging from 20.0 ± 0.2% to 62.4 ± 0.3% and observed significant larvicidal activity (LC50 at 0.742 ppm and LC90 at 6.061 ppm) against Culex quinquefasciatus. In vitro cytotoxicity activity of Ag NPs was also tested against human breast cancer (MCF-7) and fibroblast cells (L-929) and found that cells viabilities are ranging (500 to 25 µg/mL) from 52.5 ± 0.4 to 94.0 ± 0.7% and 53.6 ± 0.5 to 90.1 ± 0.8%, respectively. The synthesized Ag NPs have the potential to be used in the various biomedical applications.

Structural Activity and HAD Inhibition Efficiency of Pelargonidin and Its Glucoside-A Theoretical Approach.

Anthocyanins are an important pharmaceutical ingredient possessing diet regulatory, antioxidant, anticancer, antidiabetic, anti-obesity, antimicrobial, and anti-inflammatory properties. Pelargonidin is an important anthocyanin-based orange-red flavonoid compound used in drugs for treating hypoglycemia, retinopathy, skeletal myopathy, etc. The main sources of pelargonidin are strawberries and food products with red pigmentation. There is a lack of evidence for supporting its use as an independent supplement. In the present study, pelargonidin and pelargonidin-3-O-glucoside are studied for their structural properties using quantum chemical calculations based on density functional theory. The results confirmed that the parent compound and its glycosylated derivative acted as good electron donors. Electrostatic potential, frontier molecular orbitals, and molecular descriptor analyses also substantiated their electron donating properties. Furthermore, based on the probability, a target prediction was performed for pelargonidin and pelargonidin-3-O-glucoside. Hydroxyacyl-coenzyme A dehydrogenase was chosen as an enzymatic target of interest, since the presence work focuses on glucuronidated compounds and their efficacy over diabetes. Possible interactions between these compounds and a target with nominable binding energies were also evaluated. Further, the structural stability of these two compounds were also analyzed using a molecular dynamics simulation.

Highly Durable Antimicrobial Tantalum Nitride/Copper Coatings on Stainless Steel Deposited by Pulsed Magnetron Sputtering.

Highly durable and antimicrobial tantalum nitride/copper (TaN/Cu) nanocomposite coatings were deposited on D-9 stainless steel substrates by pulsed magnetron sputtering. The Cu content in the coating was varied in the range of 1.42-35.42 atomic % (at.%). The coatings were characterized by electron probe microanalyzer, X-ray diffraction, scanning electron microscope and atomic force microscope. The antibacterial properties of the TaN/Cu coatings against gram-negative Pseudomonas aeruginosa were evaluated using a cell culture test. The peak hardness and Young's modulus of TaN/Cu with 10.46 at.% Cu were 24 and 295 GPa, respectively, which amounted to 15 and 41.67% higher than Cu-free TaN. Among all, TaN/Cu with 10.46 at.% exhibited the lowest friction coefficient. The TaN/Cu coatings exhibited significantly higher antibacterial activity than Cu-free TaN against Pseudomonas aeruginosa. On TaN, the bacterial count was about 4 × 106 CFU, whereas it was dropped to 1.2 × 102 CFU in case of TaN/Cu with 10.46 at.% Cu. The bacterial count was decreased from 9 to 6 when the Cu content increased from 25.54 to 30.04 at.%. Live bacterial cells were observed in the SEM images of TaN, and dead cells were found on TaN/Cu. Overall, TaN/Cu with 10.46 at.% Cu was found to be a potential coating composition in terms of higher antimicrobial activity and mechanical durability.

Synthesis of MoS2/Mg(OH)2/BiVO4 hybrid photocatalyst by ultrasonic homogenization assisted hydrothermal methods and its application as sunlight active photocatalyst for water decontamination.

In this work, MoS2/Mg(OH)2/BiVO4 ternary hybrid photocatalyst was synthesized by sonicated precursor mixture to the hydrothermal procedure to generate a highly efficient solar light-induced and simply recyclable photocatalyst. The obtained hybrid was confirmed by the characteristic peaks of MoS2/Mg(OH)2/BiVO4 observed in X-ray diffraction (14.31°/18.62°/28.18°), infrared spectra (465/445/679 cm-1), ultraviolet-visible spectra (636/683/639 nm) studies, and the band-gap narrowing (2.62/2.44/2.25 eV). The morphological structure of MoS2 (rod), Mg(OH)2 (particles), and BiVO4 (random aggregates) were turned into MoS2/Mg(OH)2/BiVO4 hierarchical nanosheets that coexisted with particles. The photodegradation experiments of the photocatalysts were assessed by using Congo Red (CR), Malachite Green (MG) and Textile Industry Effluent (TIE) as the model pollutant under direct sunlight. The photocatalytic efficiency of the hybrids was noticeably 2.1 to 2.3 times higher than that of the individual components. Photocurrent response test indicate that MoS2/Mg(OH)2/BiVO4 ternary hybrid nanocomposites photocatalysts had a more effective electron/hole pair separation than individual and binary composite photocatalysts. The mechanism of photodegradation of MoS2/Mg(OH)2/BiVO4ternary hybrid photocatalysts was investigated and discussed.

Dextran Sulfate Nanocarriers: Design, Strategies and Biomedical Applications.

Dextran sulfate (DXS) is a hydrophilic, non-toxic, biodegradable, biocompatible and safe biopolymer. These biomedically relevant characteristics make DXS a promising building block in the development of nanocarrier systems for several biomedical applications, including imaging and drug delivery. DXS polyanion can bind with metal oxide nanomaterials, biological receptors and therapeutic drug molecules. By taking advantage of these intriguing properties, DXS is used to functionalize or construct nanocarriers for specific applications. In particular, the diagnostic or therapeutic active agent-loaded DXS nanoparticles are prepared by simple coating, formation of polyelectrolyte complexes with other positively charged polymers or through self-assembly of amphiphilic DXS derivatives. These nanoparticles show a potential to localize the active agents at the pathological site and minimize undesired side effects. As DXS can recognize and be taken up by macrophage surface receptors, it is also used as a targeting ligand for drug delivery. Besides as a nanocarrier scaffold material, DXS has intrinsic therapeutic potential. DXS binds to thrombin, acts as an anticoagulant and exhibits an inhibitory effect against coagulation, retrovirus, scrapie virus and human immunodeficiency virus (HIV). Herein, biomedical applications involving the use of DXS as nanocarriers for drugs, biomolecules, and imaging agents have been reviewed. A special focus has been made on strategies used for loading and delivering of drugs and biomolecules meant for treating several diseases, including cancer, inflammatory diseases and ocular disease.

Grape Seed Extract Assisted Synthesis of Dual-Functional Anatase TiO2 Decorated Reduced Graphene Oxide Composite for Supercapacitor Electrode Material and Visible Light Photocatalytic Degradation of Bromophenol Blue Dye.

The grape extract is a potential natural reducing agent because of its high phenolic content. The extracts of seeds, skin, and pulp of grape were prepared by digestion, grinding, and soxhlet methods and used for reducing graphene oxide (GO). The reduced GO made using the soxhlet extract of grape seed (GRGO) was hydrothermally treated with titanium dioxide (TiO2) for the synthesis of GRGO-TiO2 nanocomposite. The X-ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier transform infrared (FT-IR), UV-vis, photoluminescence, and Raman spectra studies further confirmed the formation of GRGO and the GRGO-TiO2 hybrid. Scanning electron microscope and transmission electron microscope studies showed the decoration of spherical TiO2 particles (<100 nm) on the few-layered GRGO sheets. The GRGO-TiO2 hybrid was explored as a working electrode for supercapacitors and visible light photocatalyst for water decontamination. GRGO-TiO2 showed higher specific capacitance (175 F g-1) than GRGO (150 F g-1) and TiO2 (125 F g-1) in an aqueous electrolyte. GRGO-TiO2 exhibited 83.6% capacitance retention even after 2000 cycles, indicating the good stability of the material. Further, under visible light irradiation (λ > 400 nm), GRGO-TiO2 showed ∼30% higher photo-oxidation of the bromophenol blue (BPB) dye than TiO2. Also, GRGO-TiO2 decreased the total organic carbon content of BPB from 92 to 18 ppm. Overall, the soxhlet extract of grape seed was found to be a cost-effective reducing agent for the preparation of GRGO, which is a suitable material to be used in supercapacitors and photocatalysis.

Proving the robustness of a PEDOT:PSS-based thermistor via functionalized graphene oxide-poly(vinylidene fluoride) composite encapsulation for food logistics.

The instability of poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) under a humid condition is the major limitation in the practical development of a flexible thermistor. Here, we introduced a functionalized graphene oxide-polyvinylidene fluoride (FGO-PVDF) composite as an encapsulation layer to prove the reliability of PEDOT:PSS thermistors under high-humidity conditions. The FGO-PVDF-encapsulated thermistor exhibited good linearity, a resolution of 1272.57 Ω per °C, a temperature coefficient of resistance equal to -3.95 × 10-3 per °C, stable performance, and an acceptable response time (∼40 s per °C) calibrated in the temperature range between -10 °C and 30 °C, resembling the temperature of a cold chain system. For applications in a food cold chain system, this thermistor was integrated into a roll-to-roll (R2R) gravure-printed NFC antenna, a microcontroller-embedded Si-chip transponder, and a printed battery to work as a smart label to wirelessly monitor the time-temperature history (TTH) of a food package. A proof-of-concept study was demonstrated by attaching an NFC-enabled hybrid TTH logger, a smart label, in a chicken package.

RF magnetron sputtering mediated NiTi/Ag coating on Ti-alloy substrate with enhanced biocompatibility and durability.

Mechanically robust, biocompatible and corrosion resistant Ag doped NiTi (NiTi/Ag) coatings were formed on implant grade commercially pure titanium substrates by R.F. magnetron sputtering. Five samples with varying silver content (0, 1, 3, 7, and 10 at.%) were prepared by controlling the power applied to Ag and NiTi targets. The intensity of X-ray photoelectron spectra peaks corresponding to Ni2p, Ti2p, Ag3d components were found proportional to respective coating compositions. The soft Ag crystallites were decreased the roughness and crystallinity of NiTi/Ag. Among all compositions, NiTi/Ag coating with 3 at.% Ag exhibited lowest friction coefficient (0.1) and wear rate (0.69 × 10-07 mm3/N ∗ mm). Electrochemical corrosion measurements indicated that Ag incorporation increased the corrosion resistance of NiTi. Increase in Ag content shifted Ecorr values in the anodic direction, and reduced the current density by one-order-of-magnitude. When cultured on NiTi/Ag coating with 3 at.% Ag, human dermal fibroblast neonatal cells demonstrated highest cell viability. The fluorescence micrographic image of the immunostained cells showed a well grown actin filament network. Overall, NiTi/Ag coated titanium substrates were found to be a promising orthopedic implant material.