Search

In the quest to advance wearable electronics, this study presents a novel method using nitrogen-doped lutetium-carbon microspheres (N, Lu-CMS) for high-performance piezoelectric energy harvesting. The synthesis of N, Lu-CMS begins with the polymerization of sucrose, followed by the preparation of N, Lu-CMS metal complexes through the incorporation of lutetium (III) nitrate hydrate and thiourea, yielding a black powder product. The wearable electronic device is designed with a silicon rubber (SR) matrix, reinforced with 0D fillers such as N, Lu-CMS, or molybdenum disulfide (MoS₂). Mechanical testing revealed a significant improvement in compressive modulus, reaching 3.7 MPa (N, Lu-CMS) at a concentration of 3 parts per hundred rubber (phr). Electromechanical assessments demonstrated efficient energy conversion, while biomechanical analysis, including thumb pressing tests, showed a notable increase in output voltage, peaking at ≈285 mV (N, Lu-CMS) at 3 phr. This research provides a foundation for future engineering applications, particularly in electronic packaging for wearable electronics and smart devices, underscoring the significant impact of N, Lu-CMS in this emerging field. The surface power density achieved is 0.026 nW cm - 2 (N, Lu-CMS) and 0.0056 nW cm - 2 (Hybrid). Lastly, the conversion efficiency is 6.26% for N, Lu-CMS, and 1.05% for the hybrid system., (© 2024 Wiley‐VCH GmbH.)

Mesoporous bioactive glass, with its versatile characteristics and morphology, holds significant potential as an ideal hemostatic material. However, limited data is available regarding its toxicity levels. Consequently, this research intends to assess the acute and repeated dose dermal toxicity of Mesoporous antibacterial bioactive glass microsphere impregnated nonwoven surgical cotton gauze (MABGmscg) dressing in albino Wistar rats, following the standards set by the Organization for Economic Cooperation and Development. In the acute dermal toxicity study, the impact of MABG (@2000mg/kg BW) mscg dressing was assessed following a single dermal application in both male and female Wistar rats (n = 10). Mortality, clinical signs, body weight fluctuations and gross observations were consistently monitored over a14 day period following the single dose. The results indicated that, MABG (@2000mg/kg BW) mscg dressing upon dermal exposure did not cause any adverse effect in acute dermal toxicity study in Wistar rats compared to control group. Given that 2000 mg/kg BW of MABG was deemed a nontoxic dose, a repeated dose dermal toxicity study of MABGmscg dressing was subsequently conducted at three dose levels (@200, 500, 1000 mg/kg BW) over 28 consecutive days in Wistar rats. During the study period, no unscheduled deaths occurred, and there were no clinical signs associated with treatment, body weight variations or abnormal gross findings at necropsy in any groups. The analysis concluded that, MABGmscg dressing is safe to be considered as a hemostatic dressing at the various tested dose levels in Wistar rats.

We assessed the oxidative potential (OP) of PM 2.5 ( n = 230) using dithiothreitol (DTT) assay to identify the major emission sources in Bhubaneswar (20.20°N, 85.80°E), one of the non-attainment cities under the National Clean Air Program, situated on the eastern coast of India. Continuous day and night PM 2.5 samples were collected during periods influenced by marine airmass (MAM; April-May 2019) as well as continental airmass (CAM; October 2019-December 2019). Volume normalized DTT (DDTv) activities were approximately two times higher during CAM compared to MAM periods. In contrast, mass normalized DTT activity (DDTm) showed insignificant variations between CAM and MAM periods. This might be due to particulate organic matter, which accounted for more than one-fifth of the PM 2.5 mass loading and remained surprisingly invariant during the study periods. Positive matrix factorization (PMF) identified secondary aerosols (MAM: 26% and CAM: 33%) as dominant contributors to PM 2.5 mass in both periods. OP, is, however, dominated by vehicular emissions (21%) as identified through multiple linear regression. Conditional Bivariate Probability Function (CBPF) analysis indicated that local sources were the primary drivers for the catalytic activity of PM 2.5 in the study region. Additionally, stagnant meteorological conditions, combined with the chemical aging of species during regional transport of pollutants, likely enhanced redox activity of PM 2.5 during the CAM period. The study highlights that increasing traffic congestion is primarily responsible for adverse health outcomes in the region. Therefore, it is important to regulate mobility and vehicular movement to mitigate the hazardous impact of PM 2.5 in Bhubaneswar.

High- T C ferro-/ferrimagnetic quadruple perovskites constitute an important class of oxides that has garnered a lot of research attention in recent times, but their synthesis is commonly achieved under high-pressure conditions. Thus, the development of high- T C quadruple perovskites that can be synthesized under ambient pressure can be a key to the above problem. Herein, we report ambient pressure synthesis of a series of new A-site ordered quadruple perovskites, LnCu 3 Mn 1+ x Ti 3- x O 12 (Ln = La, Nd; x = 0, 0.3), by coupled aliovalent-cation manipulation in CaCu 3 Ti 4 O 12 . The effect of smaller lanthanide Nd incorporation in place of La has been investigated. Furthermore, 30% mixed valency of Mn per Mn 3+ has been introduced in place of Ti 4+ following similar strategies adopted to achieve giant magnetoresistive manganites La 0.7 A 0.3 MnO 3 (A = Ca, Sr, Ba) from LaMnO 3 . Mn is present in the 3+ state for x = 0 and in a mixed valent state (3+ and 4+) for x = 0.3, whereas Cu exists in the 2+ state in all the compounds. While LaCu 3 MnTi 3 O 12 and LaCu 3 Mn 1.3 Ti 2.7 O 12 show the onset of ferrimagnetic order at ∼60 and 110 K, respectively, the corresponding Nd analogs, NdCu 3 MnTi 3 O 12 and NdCu 3 Mn 1.3 Ti 2.7 O 12 , exhibit enhanced T C 's of ∼80 and 140 K, respectively. This work reveals an effective strategy of mixed-valent Mn incorporation in the B-sublattice and smaller rare-earth cation incorporation to achieve higher ferrimagnetic ordering temperatures in quadruple perovskites.

Hydrogels, known for their unique ability to retain large amounts of water, have emerged as pivotal materials in both tissue engineering and biosensing applications. This review provides an updated and comprehensive examination of cutting-edge hydrogel technologies and their multifaceted roles in these fields. Initially, the chemical composition and intrinsic properties of both natural and synthetic hydrogels are discussed, highlighting their biocompatibility and biodegradability. The manuscript then probes into innovative scaffold designs and fabrication techniques such as 3D printing, electrospinning, and self-assembly methods, emphasizing their applications in regenerating bone, cartilage, skin, and neural tissues. In the realm of biosensing, hydrogels' responsive nature is explored through their integration into optical, electrochemical, and piezoelectric sensors. These sensors are instrumental in medical diagnostics for glucose monitoring, pathogen detection, and biomarker identification, as well as in environmental and industrial applications like pollution and food quality monitoring. Furthermore, the review explores cross-disciplinary innovations, including the use of hydrogels in wearable devices, and hybrid systems, and their potential in personalized medicine. By addressing current challenges and future directions, this review aims to underscore the transformative impact of hydrogel technologies in advancing healthcare and industrial practices, thereby providing a vital resource for researchers and practitioners in the field.

The development of vaccines has entered a new era with the advent of nanotechnology, particularly through the utilization of nanoparticles. This review focuses on the role of nanoparticles in enhancing the efficacy and stability of mRNA vaccines. Nanoparticles, owing to their unique properties such as high surface area, tunable size, and their ability to be functionalized, have emerged as powerful tools in vaccine development. Specifically, lipid nanoparticles (LNPs) have revolutionized the delivery of mRNA vaccines by protecting the fragile mRNA molecules and facilitating their efficient uptake by cells. This review discusses the various types of nanoparticles employed in mRNA vaccine formulations, including lipid-based, polymer-based, and inorganic nanoparticles, highlighting their advantages and limitations. Moreover, it explores the mechanisms by which nanoparticles improve immune responses, such as enhanced antigen presentation and the prolonged release of mRNA. This review also addresses the challenges and future directions in nanoparticle-based vaccine development, emphasizing the need for further research to optimize formulations for broader applications. By providing an in-depth analysis of the current advancements in and potential of nanoparticles in mRNA vaccines, this review aims to shed light on their critical role in combating infectious diseases and improving public health outcomes.

This review explores the latest advancements in nanoporous materials and their applications in biomedical imaging and diagnostics. Nanoporous materials possess unique structural features, including high surface area, tunable pore size, and versatile surface chemistry, making them highly promising platforms for a range of biomedical applications. This review begins by providing an overview of the various types of nanoporous materials, including mesoporous silica nanoparticles, metal-organic frameworks, carbon-based materials, and nanoporous gold. The synthesis method for each material, their current research trends, and prospects are discussed in detail. Furthermore, this review delves into the functionalization and surface modification techniques employed to tailor nanoporous materials for specific biomedical imaging applications. This section covers chemical functionalization, bioconjugation strategies, and surface coating and encapsulation methods. Additionally, this review examines the diverse biomedical imaging techniques enabled by nanoporous materials, such as fluorescence imaging, magnetic resonance imaging (MRI), computed tomography (CT) imaging, ultrasound imaging, and multimodal imaging. The mechanisms underlying these imaging techniques, their diagnostic applications, and their efficacy in clinical settings are thoroughly explored. Through an extensive analysis of recent research findings and emerging trends, this review underscores the transformative potential of nanoporous materials in advancing biomedical imaging and diagnostics. The integration of interdisciplinary approaches, innovative synthesis techniques, and functionalization strategies offers promising avenues for the development of next-generation imaging agents and diagnostic tools with enhanced sensitivity, specificity, and biocompatibility.

Quadruple perovskites with high magnetic transition temperatures are an interesting class of compounds but are synthesized typically under high pressure. Ambient pressure synthesis of new multinary quadruple perovskites having a high global instability index (GII) and transition temperature can be interesting for future exploration of high- T C oxides. A new A- and B-site ordered multinary quadruple perovskite, LaCu 3 Fe 2 RuSbO 12 , is synthesized by conventional solid-state reactions at ambient pressure. Rietveld structure refinement revealed that the compound crystallizes in the Pn 3̄ space group with a lattice parameter of 7.4556(4) Å. The compound showed complete 1 : 3 ordering of La and Cu at the A-site and 1 : 1 rock-salt ordering of Fe with Ru/Sb at the B-site. The compound is also probed with scanning and transmission electron microscopy and XPS to investigate the chemical composition, microstructure, lattice and oxidation states of the elements. Magnetic studies revealed antiferromagnetic (AFM) correlations with magnetic ordering transitions at ∼170 and 40 K. Furthermore, the M-H hysteretic behavior at 100 and 5 K indicated ferrimagnetism due to short-range AFM interactions among Fe 3+ (3d 5 ) and Ru 4+ (4d 4 ) spins involving Cu 2+ (↑)-Fe 3+ (↓)-Ru 4+ (↑) triads. The specific heat data reaffirmed the magnetic signatures while electrical transport showed semiconducting behavior with variable range hopping. The details of synthesis and structural and compositional studies along with the magnetic and electrical transport properties of LaCu 3 Fe 2 RuSbO 12 are reported in this paper.

Clonidine Hydrochloride is a centrally acting alpha-agonist hypotensive agent available as tablets for oral administration in three dosage strengths: 0.1 mg, 0.2 mg and 0.3 mg. A review of the therapeutic uses of clonidine hydrochloride reveals the need for flexibility in dosing. This flexibility is readily achieved using an oral liquid dosage form. However, no commercial liquid dosage form of clonidine hydrochloride currently exists. An extemporaneously compounded suspension from pure drug powder would provide a flexible, customizable option to meet unique patient needs with convenient and accurate dosing options. The purpose of this study was to determine the physicochemical and microbiological stability of extemporaneously compounded clonidine hydrochloride suspensions in the PCCA Base, SuspendIt. This base is a sugar-free, paraben-free, dye-free, and gluten-free thixotropic vehicle containing a natural sweetener obtained from the monk fruit. The study design included two clonidine hydrochloride concentrations to provide stability documentation over a bracketed concentration range for eventual use by compounding pharmacists. A robust stability-indicating high-performance liquid chromatographic assay for the determination of the chemical stability of clonidine hydrochloride in PCCA SuspendIt was developed and validated. Suspensions of clonidine hydrochloride were prepared in PCCA SuspendIt at 20-mcg/mL and 100-mcg/mL concentrations, selected to represent a range within which the drug is commonly dosed. Given the potent nature of the drug, a 2% triturate of clonidine hydrochloride in microcrystalline cellulose was used to prepare the samples. Samples were stored in amber plastic prescription bottles at two temperature conditions (5°C and 25°C). Samples were assayed initially, and on the following time points (days): 7, 14, 28, 42, 63, 91, 119 and 182. Physical data such as pH, viscosity and appearance were also noted. Microbiological stability was tested. All measurements were obtained in triplicate. A stable extemporaneous product is defined as one that retains at least 90% of the initial drug concentration throughout the sampling period and is protected against microbial growth. Using this criterion, no significant degradation of the clonidine hydrochloride was observed over the 182-day test period for either concentration under refrigerated conditions. Drug concentrations were at, or above 94.6% of initial values. However, at room temperature the concentration of the 20-mcg/mL samples dropped below 90% after 119 days. No microbial growth was observed. pH values remained fairly constant. The viscosity of the suspensions allowed easy re-dispersal of the drug particles upon shaking. This study demonstrates that clonidine hydrochloride is physically, chemically, and microbiologically stable in PCCA SuspendIt for 182 days in the refrigerator and for 119 days at room temperature at both concentrations studied, thus providing a viable, compounded alternative for clonidine hydrochloride in a liquid dosage form, with an extended BUD to meet patient needs., (Copyright© by International Journal of Pharmaceutical Compounding, Inc.)

Carbon-based nanomaterials, such as carbon quantum dots (CQDs) and carbon 2D nanosheets (graphene, graphene oxide, and graphdiyne), have shown remarkable potential in various biological applications. CQDs offer tunable photoluminescence and excellent biocompatibility, making them suitable for bioimaging, drug delivery, biosensing, and photodynamic therapy. Additionally, CQDs' unique properties enable bioimaging-guided therapy and targeted imaging of biomolecules. On the other hand, carbon 2D nanosheets exhibit exceptional physicochemical attributes, with graphene excelling in biosensing and bioimaging, also in drug delivery and antimicrobial applications, and graphdiyne in tissue engineering. Their properties, such as tunable porosity and high surface area, contribute to controlled drug release and enhanced tissue regeneration. However, challenges, including long-term biocompatibility and large-scale synthesis, necessitate further research. Potential future directions encompass theranostics, immunomodulation, neural interfaces, bioelectronic medicine, and expanding bioimaging capabilities. In summary, both CQDs and carbon 2D nanosheets hold promise to revolutionize biomedical sciences, offering innovative solutions and improved therapies in diverse biological contexts. Addressing current challenges will unlock their full potential and can shape the future of medicine and biotechnology.

Intensive crop residue burning (CRB) in northern India triggers severe air pollution episodes over the Indo-Gangetic Plain (IGP) each year during October and November. We have quantified the contribution of hotspot districts (HSDs) and total CRB to poor air quality over the IGP. Initially, we investigated the spatiotemporal distribution of CRB fire within the domain and pinpointed five HSD in each Punjab and Haryana. Furthermore, we have simulated air quality and quantified the impact of CRB using the Weather Research and Forecasting model coupled with Chemistry (WRF-Chem), incorporating recent anthropogenic emissions (EDGAR v5) and biomass burning emissions (FINN v2.4) inventories, along with MOZART-MOSAIC chemistry. The key finding is that HSDs contributed ∼80% and ∼50% of the total fire counts in Haryana and Punjab, respectively. The model effectively captured observed PM₂.₅ concentrations, with a normalized mean bias (NMB) below 0.2 and R-squared (R 2 ) exceeding 0.65 at the majority of validation sites. However, some discrepancies were observed at a few sites in Delhi, Punjab, Haryana, and West Bengal. The National Capital Region experienced the highest PM₂.₅ concentrations, followed by Punjab, Haryana, Uttar Pradesh, Bihar, and West Bengal. Moreover, HSDs were responsible for about 70% of the total increase in CRB-induced PM₂.₅ in the western, central, and eastern cities, and around 50% in the northern cities. By eliminating CRB emissions across the domain, we could potentially save approximately 18,000 lives annually. Policymakers, scientists, and institutions can leverage the framework to address air pollution at national and global scales by targeting source-specific hotspots. This approach, coupled with appropriate technological and financial solutions, can contribute to achieving climate change and sustainable development goals., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Introduction: The Sunderban area of West Bengal is home to tribal and religious minorities inhabiting various islands. There is a high prevalence of thalassemia among poverty-stricken residents of this region living with meagre health care facilities. This work was planned to determine the proportion of four viral transfusion-transmitted infections (TTIs): HIV-1, HIV-2, hepatitis B virus (HBV) and hepatitis C virus (HCV) among thalassemia patients attending the sole rural medical college in the region., Materials and Methods: Thalassemia patients ( n = 359, age ranging from 1 year to 60 years) attending the thalassemia clinic or being admitted to the indoor facilities for better management were included in the study. Only patients diagnosed with high-performance liquid chromatography (HPLC) and with classical clinical features were included in the study. Blood samples of these patients were tested for HIV as per NACO protocol. For HBV and HCV, samples were first tested serologically; reactive samples were collected and sent in the cold chain to a higher centre for nucleic acid amplification testing (NAAT) for qualitative and quantitative estimation. Clinical and laboratory data was collected, patients were followed up for complications and hospitalisation during the study period, and statistical analysis was performed., Results: Majority of our patients had E-beta-thalassemia (245, 59.81%), followed by beta-thalassemia major (102, 28.30%). NAAT-confirmed HCV infection (14.21%) infection was the most common, followed by HBV (2.51%), and lastly by HIV-1 (0.58%) infection. Among infected thalassemia patients, the mean HCV RNA was 741063 ± 438514.67 IU/ml while the mean HBV DNA level was 4082863 ± 7298514 IU/ml. Co-infections of HIV-1 and HCV and that of HBV and HCV were noted in one patient each (0.28%). HCV-related liver disease (14.21%) and growth retardation (10.31%) were the most typical complication noted, and death occurred in five patients (1.39%) during the study period., Conclusion: Primary care physicians should know HCV infection is the most common TTI among thalassemia patients in rural eastern India., Competing Interests: There are no conflicts of interest., (Copyright: © 2024 Journal of Family Medicine and Primary Care.)

Topotactic ion exchange is ubiquitous in the preparation of many metastable solids with layered structures. In recent times, the scope of chimie-douce ion exchange has been extended to quasi-2D and -3D structures including nanocrystals. The low-temperature solid-state exchange is yet another unique synthetic tool to access preconceived structures for the rational design of solids. Although rational synthesis using inorganic synthons is rare, few examples exist among inorganic solids with layered structures. Herein, we extend the scope further by transforming a simple perovskite (ABO 3 ) into a high-pressure quadruple (AA' 3 B 4 O 12 ) perovskite. The transformation is achieved at moderate temperatures and ambient pressure via a solid-state metathesis reaction, wherein the transition metal adopts a new A-cation coordination upon exchange. Such coordination switching upon ion exchange will open up possibilities for functionality-driven structural transformations and the rational design of new solids.

Electrochemical water splitting, which is a highly promising and environmentally friendly technology for H 2 fuel production, faces significant hurdles due to the sluggish kinetics of the oxygen evolution reaction. Co -based oxides have garnered significant attention as alternative catalysts for the oxygen evolution reaction owing to the Co 2+ /Co 3+ redox couple. Enhancing the challenging Co 2+ → Co 3+ oxidation process can further improve the catalytic oxygen evolution reaction. The aim of our work was to design a Co 3 O 4 -based catalyst to enhance reactivity by increasing the number of Co 3+ active sites, serving as an excellent platform for facilitating the oxygen evolution reaction. To drive the effectiveness of the catalyst, in this study, we synthesized Co 3 O 4 anchored on CeO 2 (Co 3 O 4 /CeO 2 ). The kinetics and efficacy of the oxygen evolution reaction catalysed by Co 3 O 4 /CeO 2 was significantly improved by aliovalent doping of Sr into Ce sites and Cu into Co sites. The reducible nature of Ce stimulates the formation of Co 3+ ions, resulting in an increased production of intermediate -OOH species, thus expediting the reaction. The transformation of Co 2+ to Co 3+ consequently leads to an increase in anion vacancies, which, in turn, promotes the adsorption of more intermediate species at the active site. The Sr- and Cu-doped Co 3 O 4 /CeO 2 catalyst exhibited a high current density of 200 mA cm -2 at 580 mV and a low overpotential of 297 mV at 10 mA cm -2 . The study functions as a key indicator to establish a connection between oxygen vacancies and metal oxidation states in order to investigate the mechanistic aspects of the oxygen evolution reaction on mixed metal oxides. Moreover, this study is expected to pave the way for the development of innovative oxygen evolution reaction catalysts with reducible supports, thus offering a new pathway for their design.

This study reports size-resolved dithiothreitol (DTT)-based oxidative potential (OP: total and water-soluble) in rural kitchens using liquefied petroleum gas (LPG), firewood (FW), and mixed biomass (MB) fuels in northeastern (NE) India. In comparison to LPG, volume-normalized total OP (OP total(v) DTT ) was enhanced by a factor of ∼5 in biomass-using kitchens (74 ± 35 to 78 ± 42 nmol min -1 m -3 ); however, mass-normalized total OP (OP total(m) DTT ) was similar between LPG and FW users and higher by a factor of 2 in MB-using kitchens. The water-insoluble OP (OP wi(v, m) DTT ) fraction in OP total(v, m) DTT was greater than 50% across kitchens. Size distributions across kitchens and OP DTT categories ranged from unimodal to trimodal. OP ws(v) DTT was driven by metals as well as organics across size fractions while OP wi(v) DTT was majorly constrained by metals with an increasing importance of organics in fine particles of biomass-using kitchens. Multiple linear regression analysis revealed that Cu and Ba explained 71% of the OP total(v) DTT variability in LPG-using kitchens, while water-soluble organic carbon (WSOC) and Ba were responsible for 44% variability in FW-using kitchens. Finally, the high internal dose of OP total(v) DTT (28-31 nmol min -1 m -3 ) in biomass-using kitchens established the severity of oxidative stress on the exposed population., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Water is crucial for life. Being the world's third-largest industry, the textile industry pollutes 93 billion cubic meters of water each year. Only 28% of textile wastewater is treated by lower- to middle-income countries due to the costly treatment methods. The present work demonstrates the utilization of surface oxygen defects and nanopores in Mg 0.8 Li 0.2 Fe 2 O 4 (Li-MgF) to treat textile effluents by a highly economical, scalable, and eco-friendly process. Nanoporous, oxygen-deficient Li-MgF splits water by a nonphotocatalytic process at room temperature to produce green electricity as hydroelectric cell. The adsorbent Li-MgF can be easily regenerated by heat treatment. A 70-90% reduction in the UV absorption intensity of adsorbent-treated textile effluents was observed by UV-visible spectroscopy. The oxygen defects on Li-MgF surface and nanopores were confirmed by X-ray photoelectron spectroscopy and Brunauer-Emmett-Teller (BET) measurements, respectively. To analyze the adsorption mechanism, three known organic water-soluble dyes, brilliant green, crystal violet, and congo red, were treated with nanoporous Li-MgF. The dye decolorization efficiency of Li-MgF was recorded to be 99.84, 99.27, and 99.31% at 250 μM concentrations of brilliant green, congo red, and crystal violet, respectively. The results of Fourier transform infrared (FTIR) spectroscopy confirmed the presence of dyes on the material surface attached through hydroxyl groups generated by water splitting on the surface of the material. Total organic carbon analysis confirmed the removal of organic carbon from the dye solutions by 82.8, 77.0, and 46.5% for brilliant green, Congo red, and crystal violet, respectively. Based on the kinetic and isotherm models, the presence of a large number of surface hydroxyl groups on the surface of the material and OH - ions in solutions generated by water splitting was found to be responsible for the complete decolorization of all of the dyes. Adsorption of chemically diverse dyes by the nanoporous, eco-friendly, ferromagnetic, economic, and reusable Li-MgF provides a sustainable and easy way to treat textile industry effluents in large amounts., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Published by American Chemical Society.)

The present study frames the physico-chemical characteristics and the source apportionment of PM 10 over National Capital Region (NCR) of India using the receptor model's Positive Matrix Factorization (PMF) and Principal Momponent Mnalysis/Absolute Principal Component Score-Multilinear Regression (PCA/APCS-MLR). The annual average mass concentration of PM 10 over the urban site of Faridabad, IGDTUW-Delhi and CSIR-NPL of NCR-Delhi were observed to be 195 ± 121, 275 ± 141 and 209 ± 81 µg m -3 , respectively. Carbonaceous species (organic carbon (OC), elemental carbon (EC) and water-soluble organic carbon (WSOC)), elemental constituents (Al, Ti, Na, Mg, Cr, Mn, Fe, Cu, Zn, Br, Ba, Mo Pb) and water-soluble ionic components (F - , Cl - , SO 4 2- , NO 3 - , NH 4 + , Na + , K + , Mg 2+ , Ca 2+ ) of PM 10  were entrenched to the receptor models to comprehend the possible sources of PM 10 . The PMF assorted sources over Faridabad were soil dust (SD 15%), industrial emission (IE 14%), vehicular emission (VE 19%), secondary aerosol (SA 23%) and sodium magnesium salt (SMS 17%). For IGDTUW-Delhi, the sources were SD (16%), VE (19%), SMS (18%), IE (11%), SA (27%) and VE + IE (9%). Emission sources like SD (24%), IE (8%), SMS (20%), VE + IE (12%), VE (15%) and SA + BB (21%) were extracted over CSIR-NPL, New Delhi, which are quite obvious towards the sites. PCA/APCS-MLR quantified the similar sources with varied percentage contribution. Additionally, catalogue the Conditional Bivariate Probability Function (CBPF) for directionality of the local source regions and morphology as spherical, flocculent and irregular were imaged using a Field Emission-Scanning Electron Microscope (FE-SEM)., (© 2024. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)

In developing nations, solid residential fuels are the major sources of primary energy for various domestic activities. To date, the emission inventory of inorganic trace gases over National Capital Territory (NCT) was prepared using either default or country-specific emission factors. In this paper, we report (for the first time) the spatial variation of emission factors (EFs) of inorganic trace gases (SO 2 , NO, NO 2 , CO, CO 2 , and CH 4 ) from the residential fuels used in slums and rural areas of NCT determined using dilution chamber in the laboratory. 147 residential fuel samples, including fuelwood, dung cake, crop residues, coal, etc., were collected at 149 NCT locations out of 675 slum clusters and 146 rural villages. The range of EF(s) of SO 2 (0.02 ± 0.01 to 0.04 ± 0.01 g kg -1 ), CH 4 (0.10 to 0.34 g kg -1 ), NO 2 (0.01 to 0.02 g kg -1 ) is lower than the CO (3.55 ± 1.72 to 6.07 ± 1.53 g kg -1 ) and CO 2 (0 to 129.45 ± 46.94 g kg -1 ). The north and north west districts of NCT are emission hotspots for CH 4 , NO, and NO 2 emissions, whereas, the southern and northern areas of NCT are for CO 2 . These citywide emission inventories (0.05° × 0.05°) of inorganic trace gases are prepared using laboratory-determined EFs and available consumption data determined by recent survey information. Among solid residential fuels, fuel wood, and dung cake are two major contributors to inorganic trace gases in NCT., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Background Dental diseases like caries, periodontal diseases, and oral mucosal lesions (OML) are common findings in rural adult populations that greatly impact their quality of life. Aim To assess OML, periodontal health conditions, and unmet dental treatment needs in the rural adult population in Jharkhand. Methodology A total of 700 permanent residents of Bero Block, Jharkhand, North India, in the age group of 35-44 years, participated in this cross-sectional study. Both men and women were equally represented. Their socio-demographic characteristics and previous dental visits were collected using standardized proforma. An assessment of periodontal health conditions, OML, and unmet dental treatment needs was done using the World Health Organization (WHO) Oral Health Assessment Proforma of 1997. Results It was found that over half (54.3%) of the study population had the adverse habit of smoking and chewing  paan . Males were more likely to experience leukoplakia (18.87%), whereas females were more likely to experience abscesses (9.43%). The majority of males and females had a community periodontal index (CPI) score and loss of attachment (LOA) score greater than two, which indicated poor periodontal health as assessed by the periodontal index. Both males and females needed extraction of the diseased teeth as their primary treatment. Conclusion The rural adult population residing in the Bero block of Jharkhand showed poor periodontal health and high unmet dental treatment needs. These people need effective oral health promotion policies and dental health education to improve their oral health., Competing Interests: The authors have declared that no competing interests exist., (Copyright © 2023, Kumar et al.)

This study reports day-night and seasonal variations of aqueous brown carbon (BrC aq ) and constituent humic-like substances (HULIS) (neutral and acidic HULIS: HULIS-n and HULIS-a) from the eastern Indo-Gangetic Plain (IGP) of India during 2019-2020. This is followed by the application of the receptor model positive matrix factorization (PMF) for optical source apportionment of BrC aq and the use of stable isotopic ratios (δ 13 C and δ 15 N) to understand atmospheric processing. Nighttime BrC aq absorption and mass absorption efficiencies (MAE) were enhanced by 40-150 % and 50-190 %, respectively, compared to the daytime across seasons, possibly as a combined effect from daytime photobleaching, dark-phase secondary formation, and increased nighttime emissions. MAE 250 nm /MAE 365 nm (i.e., E 2 /E 3 ) ratios and Angstrom Exponents revealed that BrC aq and HULIS-n were relatively more aromatic and conjugated during the biomass burning-dominated periods while BrC aq and HULIS-a were comprised mostly of non-conjugated aliphatic structures from secondary processes during the photochemistry-dominated summer. The relative radiative forcing of BrC aq with respect to elemental carbon (EC) was 10-12 % in the post-monsoon and winter in the 300-400 nm range. Optical source apportionment using PMF revealed that BrC aq absorption at 300, 365 and 420 nm wavelengths in the eastern IGP is mostly from biomass burning (60-75 %), followed by combined marine and fossil fuel-derived sources (24-31 %), and secondary processes (up to 10 %). Source-specific MAEs at 365 nm were estimated to be the highest for the combined marine and fossil fuel source (1.34 m 2  g -1 ) followed by biomass burning (0.78 m 2  g -1 ) and secondary processing (0.13 m 2  g -1 ). Finally, δ 13 C and δ 15 N isotopic analysis confirmed the importance of summertime photochemistry and wintertime NO 3 - -dominated chemistry in constraining BrC characteristics. Overall, the quantitative apportionment of BrC aq sources and processing reported here can be expected to lead to targeted source-specific measurements and a better understanding of BrC climate forcing in the future., Competing Interests: Declaration of competing interest The authors declare no conflicts of interest., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Second-generation bioenergy, a carbon neutral or negative renewable resource, is crucial to achieving India's net-zero emission targets. Crop residues are being targeted as a bioenergy resource as they are otherwise burned on-field, leading to significant pollutant emissions. But estimating their bioenergy potential is problematic because of broad assumptions about their surplus fractions. Here, we use comprehensive surveys and multivariate regression models to estimate the bioenergy potential of surplus crop residues in India. These are with high sub-national and crop disaggregation that can facilitate the development of efficient supply chain mechanisms for its widespread usage. The estimated potential for 2019 of 1313 PJ can increase the present bioenergy installed capacity by 82% but is likely insufficient alone to meet India's bioenergy targets. The shortage of crop residue for bioenergy, combined with the sustainability concerns raised by previous studies, imply a need to reassess the strategy for the use of this resource., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Urinary tract infection (UTI), which can be caused by various pathogens, if not detected at an early stage can be fatal. It is essential to identify the specific pathogen responsible for UTI for appropriate treatment. This study describes a generic approach to the fabrication of a prototype for the noninvasive detection of a specific pathogen using a tailor-made plasmonic aptamer-gold nanoparticle (AuNP) assay. The assay is advantageous because the adsorbed specific aptamers passivate the nanoparticle surfaces and reduce and/or eliminate false-positive responses to nontarget analytes. Based on the localized surface plasmon resonance (LSPR) phenomena of AuNP, a point-of-care aptasensor was designed that shows specific changes in the absorbance in the visible spectra in the presence of a target pathogen for robust and fast screening of UTI samples. In this study, we demonstrate the specific detection of Klebsiella pneumoniae bacteria with LoD as low as 3.4 × 10 3 CFU/mL.

Oxidative potential (OP) of fine marine aerosols (PM 2.5 ) over the northern Indian Ocean (N_IO) and equatorial Indian Ocean (E_IO) were studied using shipborne measurements conducted as part of the Integrated Campaign for Aerosols, gases and Radiation Budget (ICARB-2018). During the study, an enhanced concentration of PM 2.5 was found over N_IO (27.22 ± 14.29 μg.m -3 ) compared with E_IO (15.91 ± 2.58 μg.m -3 ), as N_IO experiences continental outflow from anthropogenically dominated South Asian region. However, E_IO received pristine air masses from the middle of the Arabian Sea, implying a reduced concentration. The OP of PM 2.5 was evaluated using a dithiothreitol (DTT) assay. The mass (DTTm or intrinsic OP) and volume (DTTv or extrinsic OP) normalized DTT exhibited a significant spatial variation over the Indian Ocean (IO). Intrinsic OP showed ∼2 times higher values over N_IO than E_IO, indicating aging of aerosols during long-range transport impacts OP of marine aerosol. Similarly, increased concentrations of anthropogenic species such as non-sea sulfate (nssSO 4 2- ), nitrate (NO 3 - ), ammonium (NH 4 + ), non-sea potassium ion (nssK + ), water-soluble transition metals (Fe, Ti, Zn, Cu, Mn, Cr), elemental carbon (EC), organic carbon (OC), water-soluble organic carbon (WSOC), were also observed over N_IO compared with E_IO. Pearson correlation and multiple linear regression (MLR) analysis revealed that combustion sources, chemical processing and co-transportation of anthropogenic species during long-range transport are the main drivers of intrinsic OP in the outflow region., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

The use of polymer gels for the removal of toxic chemicals from wastewater is an important area in terms of both academic and industrial research. This work presents a simple approach to the fabrication of chemically cross-linked cationic hydrogel adsorbents using designed ionic liquid-based cross-linkers and their successful use in the removal of organic dyes. Two different ionic liquid cross-linkers, [VIm-4VBC][Cl] (ILA)/[DMAEMA-4VBC][Cl] (ILB), are synthesized by the simple nucleophilic substitution reaction of 4-vinylbenzyl chloride (4VBC) separately with 1-vinylimidazole (VIm) and 2-(dimethylamino)ethyl methacrylate (DMAEMA). Cross-linked poly(acrylamide) (CPAam) and poly(2-hydroxyethyl methacrylate) (CPHEMA) hydrogels are then prepared from the corresponding monomers and as-synthesized cross-linkers (ILA and ILB) by free radical polymerization in the presence of a redox initiator combining ammonium persulfate (APS) and N , N , N ', N '-tetramethylethylenediamine (TEMED). The dried CPAam and CPHEMA xerogels exhibit macroporous morphology and high thermal stability. The hydrogel samples exhibit high swelling behavior, and the diffusion of water molecules into the hydrogels follows pseudo-Fickian kinetics. The cationic cross-linking sites in the hydrogel networks allow preferable binding with anionic dyes, and these dye uptake capacities are determined using different model anionic dyes via UV-vis spectroscopy. The dye adsorption onto these hydrogels follows a pseudo-second-order kinetic model. The adsorption mechanism is also analyzed by employing intraparticle diffusion and Boyd kinetic models. The relationship between the maximum equilibrium adsorption capacity ( q m ) of the hydrogels for eosin B (EB) dye and the equilibrium EB concentration can be better described by Langmuir and Freundlich isotherm models, and the estimated q m using the Langmuir isotherm can reach more than 100 mg g -1 . The cross-linked hydrogels can be easily regenerated and have a recycling efficiency of >80% for up to three consecutive dye adsorption-desorption cycles, which is promising for their use in wastewater treatment.

Azathioprine is used to treat the symptoms of rheumatoid arthritis and for the prevention of transplant rejection. A review of the therapeutic uses of Azathioprine reveals the need for flexibility in dosing. This flexibility is readily achieved using an oral liquid dosage form. However, no commercial liquid dosage form of Azathioprine currently exists. Azathioprine is commercially available only as a 50-mg tablet. An extemporaneously compounded suspension from pure drug powder would provide a flexible, customizable option to meet unique patient needs with convenient and accurate dosing options. The purpose of this study was to determine the physicochemical and microbiological stability of extemporaneously compounded Azathioprine suspensions in the PCCA Base, SuspendIt. This base is a sugar-free, paraben free, dye-free, and gluten-free thixotropic vehicle containing a natural sweetener obtained from the monk fruit. The study design included two Azathioprine concentrations to provide stability documentation over a bracketed concentration range for eventual use by compounding pharmacists. A robust stability-indicating high-performance liquid chromatographic assay for the determination of the chemical stability of Azathioprine in PCCA SuspendIt was developed and validated. Suspensions of Azathioprine were prepared in PCCA SuspendIt at 10-mg/mL and 50-mg/mL concentrations, selected to represent a range within which the drug is commonly dosed. Samples were stored in amber plastic prescription bottles at two temperature conditions (5°C and 25°C). Samples were assayed initially, and on the following time points (days): 7, 14, 28, 49, 63, 90, 119, and 182. Physical data such as pH, viscosity, and appearance were also noted. Microbiological stability was tested. All measurements were obtained in triplicate. A stable extemporaneous product is defined as one that retains at least 90% of the initial drug concentration throughout the sampling period and is protected against microbial growth. The study showed that Azathioprine concentrations did not go below 96.8% of the label claim (initial drug concentration) at both temperatures studied. No microbial growth was observed. The pH values remained constant. The viscosity of the suspensions allowed easy re-dispersal of the drug particles upon shaking. This study demonstrates that Azathioprine is physically, chemically, and microbiologically stable in PCCA SuspendIt for 182 days in the refrigerator and at room temperature, thus providing a viable, compounded alternative for Azathioprine in a liquid dosage form, with an extended beyond-use date to meet patient needs., (Copyright© by International Journal of Pharmaceutical Compounding, Inc.)

We report co-electrolysis of seawater and carbon dioxide (CO 2 ) gas in a solar cell-integrated membraneless microfluidic reactor for continuous synthesis of organic products. The microfluidic reactor was fabricated using polydimethylsiloxane substrate comprising of a central microchannel with a pair of inlets for injection of CO 2 gas and seawater and an outlet for removal of organic products. A pair of copper electrodes were inserted into microchannel to ensure its direct interaction with incoming CO 2 gas and seawater as they pass into the microchannel. The coupling of solar cell panels with electrodes generated a high-intensity electrical field across the electrodes at low voltage, which facilitated the co-electrolysis of CO 2 and seawater. The paired electrolysis of CO 2 gas and seawater produced a range of industrially important organics under influence of solar cell-mediated external electric field. The, as synthesized, organic compounds were collected downstream and identified using characterization techniques. Furthermore, the probable underlying electrochemical reaction mechanisms near the electrodes were proposed for synthesis of organic products. The inclusion of greenhouse CO 2 gas as reactant, seawater as electrolyte, and solar energy as an inexpensive electric source for co-electrolysis initiation makes the microreactor a low-cost and sustainable alternative for CO 2 sequestration and synthesis of organic compounds., (© 2023. The Author(s).)

Here, we report an effect driven by repetitive heating and cooling; as a result, 2D and 1D nanomaterials are parallelly produced locally in a single reactor from the same precursors. Afterward, more repetitive heating and cooling induced the self-folding approach of a 2D nanomaterial with a 1D nanomaterial, giving them a self-assembled biconcave disk-shaped 3D nanostructure. The microscopy and spectroscopy studies reveal that the nanostructure has a diameter of nearly 200 nm and is composed of Fe, C, O and incorporated N and P. This 3D nanostructure composite shows red-shifted dual emission (430 nm and 500 nm) at two different excitations (350 nm and 450 nm), accompanied by a rare large Stokes shift (LSS), and it was employed in the detection of targeted short single-stranded DNA sequences (ssDNA). Upon the addition of target DNA, the specific binding of 3D nanostructure probes with the target triggers variations (off/on) of two signals, and by considering the decreased emission (fluorescence quenching) at 500 nm, we can detect the target ssDNA at the single-molecule level. The change of fluorescence intensity and the concentration of complementary target ssDNA sequences show a better linear relationship than a single emission-based probe, and the limit of detection (LOD) was as low as 0.47 nM.

The development-oriented anthropogenic activities have led to intensive increase in emission of various organic pollutants, which contribute considerably to human health risk. In the present study, chemical, physical and spectral characterisation of fine particulate matter (PM 2.5 ), collected at Faridabad city, in northern India, were examined. Seasonal variation of organic compounds [n-alkanes, polyaromatic hydrocarbons (PAHs) and phthalic acid esters (PAEs)], and potential health risk of Polyaromatic hydrocarbons (PAHs) exposure using toxic equivalency potential (TEQ) approach had been assessed. These showed seasonal average values ranging from 156.4 ± 57.0 ng/m 3 to 217.6 ± 72.9 ng/m 3 , 98.0 ± 21.4 ng/m 3 to 177.8 ± 72.8 ng/m 3 , and 30.9 ± 11.9 ng/m 3 to 82.5 ± 29.2 ng/m 3 , respectively, with the highest value for winter. It is noteworthy that unlike, n-alkanes and PAEs, PAHs were least during spring. The high molecular weight PAHs (BaP, BkF, DahA and IcdP) were found to exhibit higher TEQ values (ranging from 0.7 to 9.7) despite of their lower concentrations. The PAH diagnostic ratio, carbon preference index and total index revealed the enhanced impact of biogenic sources of emissions in comparison to diesel emission sources during winter., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

This work has aimed to synthesize less cytotoxic but antibacterial effective materials. Here we synthesized zinc, titanium nanoparticles based multishell hollow spheres (ZnO@TiO2 MSHS) via sequential template approach (STA) and studied their comparative antimicrobial activity with pure zinc and titanium nanoparticles (NPs). Various techniques have been used to explore the physico-chemical properties of the hybrid shells (ZnO@TiO2 MSHS). FTIR, XRD measurements approved the enhanced crystallinity of synthesized hybrid MSHS via STA technique constructed by ZnO, TiO2 NPs. The optical transmittance was enhanced 67.08% for ZnO@TiO2 MSHS where 50.59 %, and 53.32 % of pure ZnO, TiO2 NPs respectively. TEM images showed MSHS made up of zinc and titanium nanoparticles distributed evenly in the structure. The antibacterial activity has been studied and measured via MIZ confirmed that the ZnO@TiO2 multishell hollow spheres exhibit the antibacterial performance. On the other hand the cytotoxicity studies show the cell toxicity was decreased for ZnO@TiO2 MSHS than pure ZnO and TiO2 NPs. So it is recommended that ZnO@TiO2 multishell hollow spheres may be used as a safe and potential antibacterial agent in the field of food packaging, painting, drug delivery and other antibacterial applications.

The over-dependence of human society on fossil fuels for energy is exhausting the level of such non-renewable energy sources. Alternative energy storage systems have gained more popularity recently to counter this issue. In this context, we report the fabrication of N-doped carbon dot (N-CD)-decorated ZnO-based electrodes for supercapacitor applications. Due to the light-responsive nature of the N-CDs and ZnO, the electrode was also responsive under the influence of UV light. After the experimental tests, it was found that the areal capacitance value of the supercapacitor increased upto ∼58.9% when illuminated compared to that under the dark conditions. Moreover, the device showed a maximum areal capacitance of 2.6 mF/cm 2 after photocharging and galvanostatically discharging at a current density value of 1.6 μA/cm 2 , which is quite comparable with the previously reported data. The doping of N-CDs with ZnO showed a significant improvement in the areal capacitance value under both illuminated (∼58.64%) and dark conditions (∼22.08%) compared to the case of pristine ZnO, which justifies the purpose of attaching N-CDs with ZnO. Therefore, in brief, we have fabricated a photoresponsive electrode material for supercapacitor application by combining N-CDs and ZnO. An explicit electrochemical characterization of the electrode was also done to identify the contribution from diffusion-controlled capacitance and double layer capacitance, and it was observed that the diffusion-controlled capacitance gets reduced from 59.1 to 33.6% when the scan rate is increased from 2 to 75 mV/s. Moreover, a detailed study has also been done to understand the reaction mechanism. It was confirmed that the defects in the electrode material played a vital role in the intercalation of K + ions.

In this study we have analysed the elemental composition of fine particulate matter (PM 2.5 ) to examine the seasonal changes and sources of the elements in Delhi, India from January, 2017 to December, 2021. During the entire sampling period, 19 elements (Al, Fe, Ti, Cu, Zn, Cr, Ni, As, Mo, Cl, P, S, K, Pb, Na, Mg, Ca, Mn, and Br) of PM 2.5 were identified by Wavelength Dispersive X-ray Fluorescence Spectrometer. The higher annual mean concentrations of S (2.29 µg m -3 ), Cl (2.26 µg m -3 ), K (2.05 µg m -3 ), Ca (0.96 µg m -3 ) and Fe (0.93 µg m -3 ) were recorded during post-monsoon season followed by Zn > Pb > Al > Na > Cu > Ti > As > Cr > Mo > Br > Mg > Ni > Mn > and P. The annual mean concentrations of elemental composition of PM 2.5 accounted for 10% of PM 2.5 (pooled estimate of 5 year). Principal Component Analysis (PCA) identified the five main sources [crustal/soil/road dust, combustion (BB + FFC), vehicular emissions (VE), industrial emissions (IE) and mixed source (Ti, Cr and Mo rich-source)] of PM 2.5 in Delhi, India., (© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)

Pyrimethamine is an antiparasitic compound available only in tablet form for oral administration. A review of the therapeutic uses of pyrimethamine reveals the need for flexibility in dosing. This flexibility is readily achieved using an oral liquid dosage form. However, no commercial liquid dosage form of pyrimethamine currently exists. Pyrimethamine is available commercially only as 25-mg tablets. An extemporaneously compounded suspension from pure drug powder would provide a flexible, customizable option to meet unique patient needs with convenient and accurate dosing options. The purpose of this study was to determine the physicochemical and microbiological stability of extemporaneously compounded pyrimethamine suspension in PCCA Base, SuspendIt. This base is a sugar-free, paraben-free, dye-free, and gluten-free thixotropic vehicle containing a natural sweetener obtained from the monk fruit. A robust stability-indicating high-performance liquid chromatographic assay for the determination of the chemical stability of pyrimethamine in PCCA SuspendIt was developed and validated. Suspensions of pyrimethamine were prepared in PCCA SuspendIt at a 2-mg/mL concentration, selected to provide flexibility in customizing individual doses. Samples were stored in amber plastic prescription bottles at two temperature conditions (5°C and 25°C). Samples were assayed initially, and on the following time points (days): 7, 14, 28, and 42. Physical data such as pH, viscosity, and appearance were also noted. Microbiological stability was tested. All measurements were obtained in triplicate. A stable extemporaneous product is defined as one that retains at least 90% of the initial drug concentration throughout the sampling period and is protected against microbial growth. The study showed that pyrimethamine concentrations did not go below 96% of the label claim (initial drug concentration) at both temperatures studied. No microbial growth was observed. pH values remained constant. The viscosity of the suspensions allowed easy re-dispersal of the drug particles upon shaking. This study demonstrates that pyrimethamine is physically, chemically, and microbiologically stable in PCCA SuspendIt for 42 days stored in the refrigerator and at room temperature, thus providing a viable, compounded alternative for pyrimethamine in a liquid dosage form., (Copyright© by International Journal of Pharmaceutical Compounding, Inc.)

The impact of an oil droplet on a water surface has been explored with the aid of computational fluid dynamics simulations. The study reveals the details of the spatiotemporal evolution of such a ternary system with a triplet of interfaces, e.g., air-water, oil-water, and oil-air, when the impact velocity of the oil droplet with the water surface is high. The oil droplet is found to flatten, spread, stretch, and eventually dewet on the water surface of the deep crater to show a host of interesting post-impact flow morphologies. Furthermore, at higher impact velocities, the formation of a biphasic oil-water crown is observed followed by the ejection of secondary water droplets from the crown tip due to capillary instability. The rapidly spreading oil film on the "crater" of the water surface is found to undergo Kelvin-Helmholtz instability before dewetting the same due to cohesion failure. Subsequently, the formation of an array of secondary oil droplets is observed during the process of dewetting. The dominant wavelength evaluated from the linear stability analysis of a representative flow system could faithfully predict the simulated spacing of dewetted oil droplets floating on the crater. Importantly, the variations in Laplace pressure around the curvatures of the undulatory interfaces along with sharp viscosity gradients across the three-phase contact line is found to engender interesting recirculation patterns, which eventually shed to form a coherent wake region in air near the crater. We also uncover the conditions under which the counter-rotating vortices shed along the oil-water interface resembling a von Kármán vortex street.

Stimuli-responsive copolymers are of great interest for targeted drug delivery. This study reports on a controllable post-polymerization quaternization with 2-bromomethyl-4-fluorophenylboronic acid of the poly(4-vinyl pyridine) (P4VP) block of a common poly(styrene)- b -poly(4-vinyl pyridine)- b -poly(ethylene oxide) (SVE) triblock terpolymer in order to achieve a selective responsivity to various diols. For this purpose, a reproducible method was established for P4VP block quaternization at a defined ratio, confirming the reaction yield by 11 B, 1 H NMR. Then, a reproducible self-assembly protocol is designed for preparing stable micelles from functionalized stimuli-responsive triblock terpolymers, which are characterized by light scattering and by cryogenic transmission electron microscopy. In addition, UV-Vis spectroscopy is used to monitor the boron-ester bonding and hydrolysis with alizarin as a model drug and to study encapsulation and release of this drug, induced by sensing with three geminal diols: fructose, galactose and ascorbic acid. The obtained results show that only the latter, with the vicinal diol group on sp 2 -hybridized carbons, was efficient for alizarin release. Therefore, the post-polymerization method for triblock terpolymer functionalization presented in this study allows for preparation of specific stimuli-responsive systems with a high potential for targeted drug delivery, especially for cancer treatment.

The megacities experience poor air quality frequently due to stronger anthropogenic emissions. India had one of the longest lockdowns in 2020 to curb the spread of COVID-19, leading to reductions in the emissions from anthropogenic activities. In this article, the frequency distributions of different pollutants have been analysed over two densely populated megacities: Delhi (28.70° N; 77.10° E) and Kolkata (22.57° N; 88.36° E). In Delhi, the percentage of days with PM 2.5 levels exceeding the National Ambient Air Quality Standards (NAAQS) between 25 March and 17 June dropped from 98% in 2019 to 61% in 2020. The lockdown phase 1 brought down the PM 10 (particulate matter having an aerodynamic diameter ≤ 10 μm) levels below the daily NAAQS limit over Delhi and Kolkata. However, PM 10 exceeded the limit of 100 μgm -3 during phases 2-5 of lockdown over Delhi due to lower temperature, weaker winds, increased relative humidity and commencement of limited traffic movement. The PM 2.5 levels exhibit a regressive trend in the highest range from the year 2019 to 2020 in Delhi. The daily mean value for PM 2.5 concentrations dropped from 85-90 μgm -3 to 40-45 μgm -3 bin, whereas the PM 10 levels witnessed a reduction from 160-180 μgm -3 to 100-120 μgm -3 bin due to the lockdown. Kolkata also experienced a shift in the peak of PM 10 distribution from 80-100 μgm -3 in 2019 to 20-40 μgm -3 during the lockdown. The PM 2.5 levels in peak frequency distribution were recorded in the 35-40 μgm -3 bin in 2019 which dropped to 15-20 μgm -3 in 2020. In line with particulate matter, other primary gaseous pollutants (NO x , CO, SO 2 , NH 3 ) also showed decline. However, changes in O 3 showed mixed trends with enhancements in some of the phases and reductions in other phases. In contrast to daily mean O 3 , 8-h maximum O 3 showed a reduction over Delhi during lockdown phases except for phase 3. Interestingly, the time of daily maximum was observed to be delayed by ~ 2 h over Delhi (from 1300 to 1500 h) and ~ 1 h over Kolkata (from 1300 to 1400 h) almost coinciding with the time of maximum temperature, highlighting the role of meteorology versus precursors. Emission reductions weakened the chemical sink of O 3 leading to enhancement (120%; 11 ppbv) in night-time O 3 over Delhi during phases 1-3., (© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Background: Endodontic flareups are always very difficult to treat because of reasons like drug resistance previously sodium hypochlorite and chlorhexidine have been used in the literature but with advancements newer materials like herbal products have been tried for this purpose. Thus, present vitro study was conducted to comparatively evaluate the efficacy of herbal formulations on commensals of oral cavity and root canal., Materials and Methods: In this in vitro study antimicrobial efficacy of chlorhexidine 2%, Septilin and Triphala wer evaluated with the help of Kirby Bauer test. The microorganisms used were Staphylococcus aureus and Escherichia coli . The samples were placed in standardized wells and were subjected to incubation. Subsequently zones of inhibition were measured with the help of a caliper. One-factor analysis of variance, Tukey's least significant difference post hoc test and Student's independent t -test were performed to find a significant difference ( P < 0.05) in the two groups., Results: For chlorhexidine in S. aureus mean antibacterial efficacy was 11.10 ± 1.25 and in E. coli 10.0 ± 1.33. The value for S. aureus was lesser in Triphala with a value of 10.35 ± 1.63 and in E. coli mean value was 9.05 ± 1.27. For Septilin the mean for S. aureus was 10.40 ± 1.04, and the mean antibacterial efficacy in E. coli was 9.65 ± 1.38., Conclusion: Septilin and Triphala showed remarkable efficacy concerning zones of inhibition. These herbal formulations have tremendous potential to be used as adjuncts to traditional disinfection modalities though it has scope of further research., Competing Interests: There are no conflicts of interest., (Copyright: © 2022 Contemporary Clinical Dentistry.)

The potent anti-cancer activity of naturally occurring organopolysulfides has attracted wide research attention over the last two decades. Sustained donation of hydrogen sulfide (H 2 S) from organopolysulfides is found to be beneficial for the treatment of several organ-specific cancers. In the present study, for the first time, the mechanism of action for the potent anti-cancer activity of bis(3,5-dimethoxybenzyl) trisulfide 4 against highly aggressive triple-negative breast cancer cells (MDA-MB-231) is described. Preliminary in vitro studies revealed potent anti-proliferative activity of the trisulfide 4 against triple-negative breast cancer cells with an IC 50 value of 1.0 μM. Mechanistic studies reveal that the compound exhibited anti-cancer activity, primarily by targeting and suppressing the Wnt/β-catenin signaling pathway. The inactivation of the β-catenin level was associated with the cell cycle arrest in the G2/M phase and the significant down-regulation of downstream signaling genes such as Cyclin D1 and c-Myc expression. Several control experiments with analogous organosulfur compounds and the key enzyme inhibitors reveal that the presence of a trisulfide unit in the compound is crucial for the desired inactivation of β-catenin expression, which is promoted by GSK-3β-induced phosphorylation of β-catenin and its proteasomal degradation. Moreover, the trisulfide unit or the released H 2 S induced down-regulation of the p53 expression with the possible S-sulfhydration process led to p53-independent up-regulation of p21 expression. Therefore, the key results of this study highlighting the potency of synthetic benzylic organotrisulfide and the released H 2 S towards the growth inhibition of triple-negative breast cancer via Wnt/β-catenin signaling pathway would certainly be helpful for further studies and developing small-molecule anti-cancer therapeutics in future., Competing Interests: Declaration of competing interest No conflict of interest., (Copyright © 2022 Elsevier Inc. All rights reserved.)