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Introduction: Acinetobacter spp. has emerged as an important hospital-acquired and opportunistic agent due to its survival capability in adverse conditions, saprophytic presence, and increasing resistance to antimicrobials. The irrational use of antibiotics, along with biofilm formation, plays an important role in producing Extensively Drug-resistant (XDR) and MultidrugResistant (MDR) Acinetobacter species, especially Acinetobacter calcoaceticus-baumannii complex (Acb complex), in the hospital environment, contributing to morbidity and mortality. Aim: To detect biofilm production among Acinetobacter species isolated from various clinical samples received from Intensive Care Units (ICUs) as well as their antibiotic sensitivity pattern. Materials and Methods: A cross-sectional study was conducted in the Microbiology Department at Teerthanker Mahaveer Medical College and Research Centre, Moradabad, Uttar Pradesh, India from January 2022 to April 2023. Patients of all age groups and both genders were included in the study after obtaining informed consent. Clinical specimens, including endotracheal secretions, endotracheal tips, pus, urine, sputum, tissue, and other body fluids, were collected from ICUs where Acinetobacter spp. was detected. A total of 223 cases were included. The specimens were collected using clean, leak-proof, sterile containers with proper aseptic precautions. Antimicrobial susceptibility testing was performed according to the guidelines set by the Clinical and Laboratory Standards Institute (CLSI) in 2022 and identifies MDR and XDR strains. The biofilm production of isolates was determined using a quantitative adherence assay. The data generated was entered into Microsoft excel, and statistical analysis was conducted using International Business Machines (IBM) Statistical Package for Social Sciences (SPSS) statistical software version 28.0. The results were then presented as descriptive statistics. Results: Among the 223 Acinetobacter spp. isolates, 159 (71.3%) were identified as Acb complex (Acinetobacter calcoaceticusbaumannii complex), followed by A.lwofi with 39 (17.5%) isolates and A. haemolyticus with 16 (7.2%) isolates. Acinetobacter showed resistance, in descending order of frequency, to amoxicillin+clavulanic acid (211 isolates, 94.6%), ciprofloxacin (211 isolates, 94.6%), trimethoprim-sulfamethoxazole (208 isolates, 93.3%), cefotaxime (198 isolates, 88.8%), cefepime (187 isolates, 83.8%), gentamycin (178 isolates, 79.8%), amikacin (152 isolates, 68.2%), piperacillin-tazobactam (68 isolates, 30.5%), imipenem (72 isolates, 32.3%), meropenem (71 isolates, 31.8%), polymyxin B (12 isolates, 5.4%), and colistin (2 isolates, 0.9%). The maximum antibiotic resistance was observed in Acb complex, with 208 (93.3%) strains being MDR producers and 32 (14.3%) strains being XDR producers. Biofilm production was observed in 214 isolates (95.9%), with 127 (56.9%) exhibiting strong biofilm production 63 (28.2%) showing moderate biofilm production, and 24 (10.8%) showing weak biofilm production. All MDR strains were found to produce biofilm, and out of those, 127 (61.1%) exhibited strong biofilm production. Among the XDR strains, all 32 (100%) were found to produce strong biofilm. Conclusion: In conclusion, Acinetobacter spp. has a high propensity for developing MDR, and the formation of biofilms further aids the organism in surviving under strenuous conditions, making it difficult to treat. Therefore, regular surveillance of Hospital-acquired Infections (HAI), the prevention of misuse and overuse of antibiotics, prescribing antibiotics based on antibiogram patterns, formulating antibiotic policies, and implementing bundle care approaches for the prevention of HAI are crucial in preventing antibiotic resistance.

In a solid-state dye-sensitized solar cell, a fast-ion conducting (σ25°C > 10−4 S cm−1) solid redox mediator (SRM; electrolyte) helps in fast dye regeneration and back-electron transfer inhibition. In this work, we synthesized solid Co2+/3+ redox mediators using a [(1 − x)succinonitrile: x poly(ethylene oxide)] matrix, LiX, Co(tris-2,2′-bipyridine)3(bis(trifluoromethyl) sulfonylimide)2, and Co(tris-2,2′-bipyridine)3(bis(trifluoromethyl) sulfonylimide)3 via the solution-cast method, and the results were compared with those of their acetonitrile-based liquid counterparts. The notation x is a weight fraction (=0, 0.5, and 1), and X represents an anion. The anion was either bis(trifluoromethyl) sulfonylimide [TFSI−; ionic size, 0.79 nm] or trifluoromethanesulfonate [Triflate−; ionic size, 0.44 nm]. The delocalized electrons and a low value of lattice energy for the anions made the lithium salts highly dissociable in the matrix. The electrolytes exhibited σ25°C ≈ 2.1 × 10−3 (1.5 × 10−3), 7.2 × 10−4 (3.1 × 10−4), and 9.7 × 10−7 (6.3 × 10−7) S cm−1 for x = 0, 0.5, and 1, respectively, with X = TFSI− (Triflate−) ions. The log σ–T−1 plot portrayed a linear curve for x = 0 and 1, and a downward curve for x = 0.5. The electrical transport study showed σ(TFSI−) > σ(Triflate−), with lower activation energy for TFSI− ions. The anionic effect increased from x = 0 to 1. This effect was explained using conventional techniques, such as Fourier transform infrared spectroscopy (FT-IR), X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), UV–visible spectroscopy (UV-vis), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). [ABSTRACT FROM AUTHOR]

In the process of solar photovoltaic, ferroelectric semiconductors such as BiFeO3 are found to be new class of materials as an alternative to traditional semiconductors for more energy generations. The efficient chare transformation as well as the enhanced optical absorbance are the key factors for better performance of these ferroelectric semiconductors, which can be facilitated by depositing plasmonic Au nanoparticles on the surface of BiFeO3. As a result, the photoelectrochemical (PEC) and photovoltaic (PV) performance of BFO could be enhanced. We developed the BiFeO3 nanostructures via a facile approach and then we have deposited Au nanoparticles on the surfaces of the BiFeO3 nanoparticles. Electron microscopic images revealed the aggregation of 20–40 nm sized BiFeO3 nanoparticles and the spherical shaped Au nanoparticles of ~ 30 nm. In addition to a noticeable enhancement in the optical spectrum, the plasmonic effect could be seen in the absorbance spectra after the decoration of Au nanoparticles. In order to assess the enhanced photovoltaic and photoelectrochemical performance of the Au-decorated BFO nanostructures, a comparative examination of pristine BFO was performed. Studies on the time-dependent photocurrent density also confirmed the stability of treated photoelectrode materials using Au nanoparticles. This really raised the charge transfer efficiency by delivering better conductivity, which was investigated using Nyquist plot. The incident photon-to-current conversion efficiency [IPCE(%)] also confirmed the enhancement of photovoltaic by Au nanoparticles. The DSSC efficiency of produced Au-decorated BiFeO3 nanostructures is ~ 20% higher than the pristine BiFeO3-based cells. [ABSTRACT FROM AUTHOR]

We report Na-Alginate-based hydrogels with high ionic conductivity and water content fabrication using poly (3,4-ethylene dioxythiophene) (PEDOT): poly (4-styrene sulfonic acid) (PSS) and a hydrogel matrix based on dimethyl sulfoxide (DMSO). DMSO was incorporated within the PEDOT:PSS hydrogel. A hydrogel with higher conductivity was created through the in-situ synthesis of intra-Na-Alginate, which was then improved upon by H2SO4 treatment. Field emission scanning electron microscopy (FESEM) was used to examine the surface morphology of the pure and synthetic hydrogel. Structural analysis was performed using Fourier-transform infrared spectroscopy (FTIR). Thermogravimetric analysis (TGA), which examines thermal properties, was also used. A specific capacitance of 312 F/g at 80 mV/s (energy density of 40.58 W/kg at a power density of 402.20 W/kg) at 100 DC mA/g was achieved by the symmetric Na-Alginate/PEDOT:PSS based flexible supercapacitor. The electrolyte achieved a higher ionic conductivity of 9.82 × 10−2 and 7.6 × 10−2 Scm−1 of Na-Alginate and a composite of Na-Alginate/PEDOT:PSS at 25 °C. Furthermore, the supercapacitor Na-Alginate/PEDOT:PSS//AC had excellent electrochemical stability by showing a capacity retention of 92.5% after 3000 continuous charge–discharge cycles at 10 mA current density. The Na- Alginate/PEDOT:PSS hydrogel displayed excellent flexibility and self-healing after re-contacting the two cut hydrogel samples of electrolyte for 90 min because of the dynamic cross-linking network efficiently dissipated energy. The illumination of a light-emitting diode (LED) verified the hydrogel's capacity for self-healing. [ABSTRACT FROM AUTHOR]

A conductive cotton hydrogel with graphene and ions can come into contact with electrodes in solid electrolytes at the molecular level, leading to a more efficient electrochemical process in supercapacitors. The inherently soft nature of cotton mixed with hydrogel provides superior flexibility of the electrolyte, which benefits the devices in gaining high flexibility. Herein, we report on the current progress in solid-state hydrogel electrolytes based on 3D pure cotton/graphene and present an overview of the future direction of research. The ionic conductivity of a complex hydrogel significantly increased by up to 13.9 × 10−3 S/cm at 25 °C, due to the presence of graphene, which increases ionic conductivity by providing a smooth pathway for the transport of charge carriers and the polymer. Furthermore, the highest specific capacitance of 327 F/g at 3 mV/s was achieved with cyclic voltammetry measurement and a galvanostatic charge–discharge measurement showed a peak value of 385.4 F/g at 100 mA/g current density. Furthermore, an electrochemical analysis demonstrated that a composite cotton/graphene-based hydrogel electrolyte is electrically stable and could be used for the design of next-generation supercapacitors. [ABSTRACT FROM AUTHOR]

Herein, we report single-wall carbon nanotubes (SWCNT)/poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT: PSS) loading on the transparency and conductivity of pure cotton and systematically studied using a four-probe stack made of copper (Cu) which showed a surface resistance of 0.08 Ω/cm. Moreover, the treated cotton cloth retained its maximum resistance even after three months. Surface morphology was investigated by scanning electron microscopy (SEM) and elemental structure analysis was performed by energy-dispersive X-ray (EDX), while the structural analysis was performed using Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) techniques, confirming that there is a good dispersion of SWCNTs/PEDOT: PSS in the cotton sample. The composite cotton/hydrogel polymer/composite cotton achieved a specific capacitance of 212.16 F/g at 50 mV/s. Thermal properties were also investigated using thermogravimetric analysis (TGA) and differential scale calorimetry (DSC). The low surface resistance and thermal stability show that cotton fabric can be a promising candidate for smart wearable textiles and modern circuitry applications. [ABSTRACT FROM AUTHOR]

An all-solid–state dye-sensitized solar cell is one of the non-fossil fuel-based electrochemical devices for electricity generation in a high-temperature region. This device utilizes a redox mediator, which is a fast ion-conducting solid polymer electrolyte (SPE). The SPE makes the device economical, thinner, and safer in high-temperature regions. The SPE generally has a form of matrix−plasticizer−redox salts. Succinonitrile (SN) is generally employed as a plasticizer for reducing the crystallinity of poly(ethylene oxide), abbreviated as PEO, a common polymeric matrix. In the present paper, the structural and thermal properties of tetramethyl succinonitrile (TMSN) were compared with SN for its application as a solid plasticizer. TMSN and SN both are plastic crystals. TMSN has four methyl groups by replacing the hydrogen of the SN, resulting in higher molecular weight, solid–solid phase transition temperature, and melting temperature. We thoroughly studied the structural, thermal, and electrical properties of the [(1−x)PEO: xTMSN] blend for utilizing it as a matrix, where x = 0–0.25 in mole fraction. The FT-IR spectra and XRD patterns of the blends exhibited PEO-alike up to x = 0.15 mole and TMSN-alike for x > 0.15 mole. Differential scanning calorimetry revealed formation of a eutectic phase from x = 0.1 mole and phase separation from x = 0.15 mole. The blends with x = 0.1–0.15 mole had a low value of PEO crystallinity. Thermogravimetric analysis showed thermal stability of the blends up to 75 °C. The blends exhibited electrical conductivity, σ25°C more than 10−9 S cm−1, and Arrhenius behavior (activation energy, ~0.8 eV) in a temperature region, 25–50 °C. [ABSTRACT FROM AUTHOR]

The solar cell has been considered one of the safest modes for electricity generation. In a dye-sensitized solar cell, a commonly used iodide/triiodide redox mediator inhibits back-electron transfer reactions, regenerates dyes, and reduces triiodide into iodide. The use of iodide/triiodide redox, however, imposes several problems and hence needs to be replaced by alternative redox. This paper reports the first Co2+/Co3+ solid redox mediators, prepared using [(1−x)succinonitrile: xPEO] as a matrix and LiTFSI, Co(bpy)3(TFSI)2, and Co(bpy)3(TFSI)3 as sources of ions. The electrolytes are referred to as SN_E (x = 0), Blend 1_E (x = 0.5 with the ethereal oxygen of the PEO-to-lithium ion molar ratio (EO/Li+) of 113), Blend 2_E (x = 0.5; EO/Li+ = 226), and PEO_E (x = 1; EO/Li+ = 226), which achieved electrical conductivity of 2.1 × 10−3, 4.3 × 10−4, 7.2 × 10−4, and 9.7 × 10−7 S cm−1, respectively at 25 °C. Only the blend-based polymer electrolytes exhibited the Vogel-Tamman-Fulcher-type behavior (vitreous nature) with a required low pseudo-activation energy (0.05 eV), thermal stability up to 125 °C, and transparency in UV-A, visible, and near-infrared regions. FT-IR spectroscopy demonstrated the interaction between salt and matrix in the following order: SN_E < Blend 2_E < Blend 1_E << PEO_E. The results were compared with those of acetonitrile-based liquid electrolyte, ACN_E. [ABSTRACT FROM AUTHOR]

Dye‐sensitized solar cell (DSSC) is a promising alternative to the commercially available amorphous silicon‐based solar cell because of several advantageous properties. A DSSC with a fast ion conducting solid polymer electrolyte is required for the arid atmosphere of Gulf countries. In this work, a new matrix, poly(ethylene oxide)‐tetramethyl succinonitrile blend to synthesize a blend‐LiI‐I2 solid polymer electrolyte for the DSSC application has been proposed. The tetramethyl succinonitrile is a member of plastic crystal with a solid–solid phase transition temperature (Tpc) of ≈71 °C and melting temperature (Tm) of ≈170.5 °C. Its molar fraction, 0.1–0.15 is sufficient enough for synthesizing a polymer electrolyte with electrical conductivity of >10–4 S cm–1 at room temperature. This electrolyte shows Vogel–Tamman–Fulcher type behavior with a low value (≈0.083 eV) of pseudo‐activation energy for easy ion transport. The results of Fourier‐transform infrared spectroscopy, X‐ray diffractometry, and differential scanning calorimetry studies reveal the plasticizing effect of tetramethyl succinonitrile to form an amorphous phase. This electrolyte results in a ≈661% gain in short‐circuit current density and thereby a ≈552% gain in the cell efficiency (≈3.5%) with respect to the DSSC prepared with the tetramethyl succinonitrile‐free electrolyte. [ABSTRACT FROM AUTHOR]

The finely controlled nanostructured cubic spinel ferrites pave the way to synthesize nanomaterials with specific properties for particular applications. In this paper, we report sol-gel synthesis of Zn doped spinel Co1-xZnxFe2O4 (where x= 0.0, 0.1, 0.2, and 0.3) ferrite nanoparticles. X-ray diffraction confirms the single phase cubic structure of nano ferrites with average particle size estimated between 55.38 to 32.87 nm and validated by Transmission electron microscopy (TEM) results (±1). The lattice parameter was found to increase with increasing Zn doping concentration. The samples exhibit normal dielectric behaviour of Maxwell-Wagner type of interfacial polarization that decreases with increasing frequency of the applied field. Temperature-dependent magnetic properties were investigated with the aid of physical property system. The hysteresis measurements of the samples show clearly enhancement in magnetic parameters as the temperature goes down to 20 K. Tuning of magnetic properties has been witnessed as a function of doping and temperature under the influence of externally applied magnetic field, has been discussed in this paper. [ABSTRACT FROM AUTHOR]

Hosts and microbes have co-evolved over millions of years. Inflammatory bowel diseases (IBDs), including Crohn's disease (CD) and ulcerative colitis (UC), are chronic immune-mediated diseases. Although the etiology of IBD remains an enigma, various studies have proposed the involvement of mucosa-associated Escherichia coli (E. coli) strains in the pathogenesis of IBD. E. coli, a usual inhabitant of the intestine, causes disease after acquiring virulence factors; however, the mechanisms underlying this phenomenon are not well understood. In the present review, we will discuss recent findings on how gut E. coli regulates and controls gut homeostasis and the pathogenesis of IBD. We will also summarize current knowledge regarding the cause, mechanism, genetics, and environmental factors involved in the regulation of IBD. Furthermore, we will discuss the possibility of alterations in innate and acquired immunity during the course of disease as well as possible treatment. [ABSTRACT FROM AUTHOR]

The search of eco-friendly technologies for nano-synthesis is significant to expand their applications in human welfare. Nowadays, various inorganic nanoparticles with beneficial features have been synthesized via physical, chemical, and biological means. Significant biological applications of silver nanoparticles include on-infectious microbes, target drug delivery, cancer and vector-borne disease control. Their syntheses have been tested from plant fungi, bacteria, and viruses. The bacterial mediated synthesis of silver, gold, zinc and other metal leads to a milestone in nano-medicines. Thus, in this review, we focus on the contribution of Bacilli in the synthesis of silver nanoparticles, the mechanism of action and their potential application in the welfare of human beings. [ABSTRACT FROM AUTHOR]

Accumulating evidence has recently supported the association of bacterial infection with the growth and development of cancers, particularly in organs that are constantly exposed to bacteria such as the lungs, colon, cervical cancer etc. Our in silico study on the proteome of Chlamydia pneumoniae suggests an unprecedented idea of the etiology of lung cancer and have revealed that the infection of C. pneumoniae is associated with lung cancer development and growth. It is reasonable to assume that C. pneumoniae transports its proteins within host-intracellular organelles during infection, where they may work with host-cell proteome. The current study was performed for the prediction of nuclear targeting protein of C. pneumoniae in the host cell using bioinformatics predictors including ExPASy pI/Mw tool, nuclear localization signal (NLS) mapper, balanced sub cellular localization predictor (BaCeILo), and Hum-mPLoc 2.0. We predicted 47/1112 nuclear-targeting proteins of C. pneumoniae connected with several possible alterations in host replication and transcription during intracellular infection. These nuclear-targeting proteins may direct to competitive interactions of host and C. pneumoniae proteins with the availability of same substrate and may be involved as etiological agents in the growth and development of lung cancer. These novel findings are expected to access in better understanding of lung cancer etiology and identifying molecular targets for therapy. [ABSTRACT FROM AUTHOR]

3-Nitro- N-(phenylsulphonyloxy)phthalimide ( IIIa) and N-(phenylsulphonyloxy)phthalimide ( IIIb) were synthesised as key intermediates in good yield. Their structures were confirmed by H NMR and FTIR spectral data. The reaction of the key intermediates with allylamine produced 3-allyl-5-nitroquinazoline-2,4-(1 H,3 H)-dione ( IVa) and 3-allylquinazoline-2,4-(1 H,3 H)-dione ( IVb), respectively. Luminescence emission and excitation spectra of IVa and IVb are also presented. [ABSTRACT FROM AUTHOR]

A series of amide derivatives of stilbene was synthesized and investigated for osteogenic activity. Out of sixteen, seven compounds viz 19c , 19g , 19i , 24b , 25a , 25c and 26a showed significant osteoblast differentiation within 1 pM–1 µM concentrations. Amongst all, 26a was identified as most active molecule which presented effective mineralization of osteoblasts and expression of mRNA of osteogenic marker gene such as BMP-2, ALP, and Runx-2 at 1 pM. In estrogen-deficient balb/c mice, 26a showed significant osteogenic activity at 5 mg-kg−1 body weight dose. The protein expression study for estrogen receptors α and β (ER-α & ER-β) using mouse calvarial osteoblasts (MCOs) and molecular docking analyses showed preferential expression of ER-β by 26a indicating the possibility of ER-β mediated osteogenic activity of 26a. [ABSTRACT FROM AUTHOR]

• For the first time, waste polyethylene was recycled into Kish graphite using an indigenous set-up. • The tafel studies show the anticorrosive nature with the corrosion potential of −1.6 V. • Mg-O 2 battery with Kish graphite air cathode, shows long cell life and discharge capacity of 1226.51 mAh g−1. • Based on the ORR assessment, incorporation of Mn 2 O 3 in KG was optimized for preferable four electron pathway. Polyethylene plastic is a threat to the environment because of its enormous usage and limited recycling options. Herewith, the study reports the synthesis of Kish graphite from polyethylene waste. These wastes was mixed with molten iron and cooled into a rod-shaped mold. The molded iron ingots contain precipitated carbon material in 2D graphitic nature, which was obtained as Kish graphite after several acid treatments. The tafel studies show the anticorrosive nature of the sample with the corrosion potential of −1.6 V. Kish graphite and manganese oxide in the ratio 40:9 exhibited higher catalytic activity towards oxygen reduction reaction. Discharge studies of Mg-air battery with graphite (80%) air cathode recorded the highest capacity of 1226.51 mAh g−1, discharge life of 73.6 h and enhanced performance characteristics. Thus, waste polyethylene was effectively used as an supportive electrocatalyst in the Mg-air battery system. [ABSTRACT FROM AUTHOR]