Fourier Transform Infrared Analysis Research Articles

Effect of wood and peanut shell hydrochars on the desiccation cracking characteristics of clayey soils

Soil cracking can significantly alter the water and nutrient migration pathways in the soil, influencing plant growth and development. While biochar usage has effectively addressed soil cracking, the feasibility of using less energy-intensive hydrochars in desiccating soils remains unexplored. This study investigates the impact of wood and peanut shell hydrochars on the desiccation cracking characteristics of clayey soil. A series of controlled environmental laboratory incubations with regular imaging was conducted to determine crack development's dynamic in unamended and hydrochar-amended soils. The results reveal that the addition of wood hydrochar at 2% and 4% dosage reduced the crack intensity factor (CIF) by 22% and 43%, respectively, compared to the unamended control soil. Similarly, the inclusion of peanut shell hydrochar at 2% and 4% lowered the CIF by 22% and 51%, respectively. The presence of hydrophilic groups on the surface of hydrochars, such as O–H, CH, and C–O–C, enhanced the water retention capacity, as confirmed by Fourier-transform infrared analysis. The CIF decrease is attributed to mitigated water evaporation rates, enabled by enhanced water retention within the hydrochar pore spaces. These findings are supported by scanning electron microscopy analyses of the hydrochar morphology. Despite CIF reduction with hydrochar incorporation, the crack length density (CLD) increased across all hydrochar-amended series. In contrast to unamended soil which exhibited pronounced widening of large cracks and extensive inter-pore voids, the incorporation of hydrochar resulted in higher CLD due to the formation of finer interconnecting crack meshes. Consequently, the unamended control soil suffered greater water loss due to heightened evaporation rates. This study sheds new light on the potential of hydrochars in addressing desiccation-induced soil cracking and its implications for water conservation.

Biosynthesis, characterization, and anticoagulant properties of copper nanoparticles from red seaweed of Acanthophora sp.

In the last few decades, nanoparticles have found extensive use in a variety of biological applications. Traditional medicine widely uses Acanthophora sp., a marine macroalgae, to cure and prevent diabetes, skin disorders, and blood clotting. The present study aims to investigate whether green-synthesized copper nanoparticles (CuNPs) might work as an anticoagulant. The CuNPs were made using an environmentally friendly method that uses Acanthophora extract. We used UV-vis spectroscopy to assess the surface plasmon resonance of the material, scanning electron microscopy (SEM) to analyze its form, and energy dispersive X-ray (EDX) spectroscopy to identify the material's constituent elements. Furthermore, Fourier-transform infrared (FT-IR) determined the functional groups of the CuNPs. The biosynthesis of CuNPs was confirmed by UV-vis spectroscopy, which showed a surface plasmon resonance peak at 570 nm. The FT-IR analysis showed that certain functional groups are involved in the formation of CuNPs. These groups include OH stretching, C=O stretching, C-H bonding, C-N bonding, and Cu vibration. SEM analysis demonstrated the morphology of CuNPs synthesized, with a size of 0.5μm, while EDS analysis confirmed their purity. The anticoagulant activity of prothrombin time (PT) and activated partial thromboplastin time (aPTT) assays showed that the clotting time got longer depending on the concentration. The CuNPs synthesized from Acanthophora had strong anticoagulant effects at 100 μg/mL, further suggesting that they might be useful as a natural blood thinner. The interesting thing we observed is that the green-synthesized CuNPs made from Acanthophora extract could be used in anticoagulation therapy.

Conductive polypyrrole: synthesis, characterization, thermal, and electrical properties for different applications

Pyrrole monomer (mPPy) in an aqueous solution was used to create the conductive polymer polypyrrole (a homo-PPy) using a chemical oxidative polymerization process over a period of several hours at room temperature. Ferric chloride (FeCl3) oxidant was used, and sodium dodecyl sulphate (C12H25NaO4S), a surfactant. The produced PPy samples were characterized using a variety of methods, including X-ray diffraction (XRD), the Fourier transform infrared (FTIR), differential scanning calorimetry (DSC), Differential Thermal analysis (DTA), Thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). SEM images revealed that nanoparticles of a homo-PPy with radii of 60–90 nm were well evenly distributed in the structure. The thermal stability and electrical conductivity of homo-PPy nanoparticles were observed to rise with a solvent ethylene glycol. As temperature rises, the conductivity of homo-PPy samples is significantly raised, and electrical conductivities ranging from.0.44 to 2.2 (Ω.m)−1. Results from FTIR and XRD analysis confirmed the structural formation of a homo-polypyrrole during synthesis from pyrrole monomer. Because of their improved electrical conductivity and thermal stability, homo-PPy nanoparticles have potential applications in energy storage, adsorption and contamination elimination, electromagnetic protection, and resistance to corrosion.

Green and sustainable synthesis of the ZnONPs using leaf extract of Guazuma ulmifolia for antioxidant and antimicrobial activities

AbstractThe main objectives of the current study were synthesis and characterization of zinc oxide nanoparticles (ZnONPs) using the aqueous leaf extract of Guazuma ulmifolia (G. ulmifolia) plant and assessing its antimicrobial and antioxidant potential. The nanoparticles were characterized using Ultraviolet Visible (UV–Vis), Fourier Transform Infrared (FTIR) Spectroscopy, X-ray diffraction (XRD), Energy-dispersive X-ray (EDS) and Scanning electron microscopy (SEM). ZnONPs exhibited a maximum peak at 342 nm in the UV–Vis spectrum, indicating their absorption properties. FTIR analysis confirmed the presence of functional groups, such as OH and COOH which likely contributed to the stability of the nanoparticles. The XRD analysis confirmed the spherical structure of the nanoparticles as indicated by distinct diffraction peaks corresponding to the lattice planes of the ZnO standard. The EDS analysis confirmed the presence of Zn, C and O in the ZnONPs. SEM analysis provided insights into the nanoparticles size, shape and surface morphology, showing an average size between 19 and 41 nm. Furthermore, the synthesized ZnONPs demonstrated excellent antioxidant and antibacterial activities against various bacteria and Candida species. This study highlights the promising potential of ZnONPs in diverse fields, including biomedicine, due to their low toxicity, economic viability and beneficial properties. It is crucial to conduct further in vivo investigations in order to determine the safety, effectiveness and compatibility of G. ulmifolia ZnONPs.

Characterization and Cytotoxicity Assessment of Synthesized Palladium (II) Complex-Encapsulated Zinc Oxide Nanoparticles for Cancer Treatment.

The treatment of cancer often leads to a range of adverse effects. Encapsulating drugs can mitigate these effects and enhance drug efficacy by enabling a controlled release at the site of interest. This study details the successful synthesis of zinc oxide nanoparticles (ZnONPs) through the precipitation of Zn(NO3)2·6H2O with KOH. A Pd(II) complex drug was synthesized from a Schiff base ligand derived from 2-hydroxybenzohydrazide and (E)-1-(2-(p-tolyl)hydrazono)propan-2-one using potassium tetrachloropalladate(II). This complex was subsequently incorporated into ZnONPs. Characterization of the resulting compounds was performed using Transmission Electron Microscopy (TEM), Dynamic Light Scattering (DLS), Zeta Potential, Fourier Transform Infrared (FTIR) Spectroscopy, and UV-visible spectroscopy. TEM imaging revealed particle sizes of 160.69 ± 4.74 nm for ZnONPs and 185.28 ± 2.3 nm for the Pd(II) complex-encapsulated ZnONPs. The Zeta potential values were 6.53 mV for ZnONPs and 7.36 mV for Pd(II) complex-encapsulated ZnONPs. UV-visible spectroscopy showed an absorption peak at 360 nm for ZnONPs, while the Pd(II) complex-encapsulated ZnONPs exhibited a peak at 410 nm. FTIR analysis indicated the presence of the Pd(II) complex within the ZnONPs, as evidenced by a consistent Zn-O vibrational band at 832 cm-1 and a shift in another peak from 460 to 413 cm-1. Additionally, the detection of a C = N stretching vibration at 1548 cm-1 and a carbonyl stretch at 1626 cm-1 was observed. The Encapsulation Efficiency (E.E.) of the Pd(II) complex was 97.2%. A drug release experiment conducted at pH 7 showed a steady-state release pattern after 16 h, with a cumulative release of 44.3%. The cytotoxic effects of the Pd(II) complex and its encapsulated form in ZnONPs on the MCF-7 cell line were assessed via MTT test. The Pd(II) complex encapsulated within ZnONPs exhibited decreased toxicity relative to the unencapsulated drug, as evidenced by a higher IC50 value of 418.5 μg/ml. This suggests that the encapsulation facilitates a sustained release, which allows for targeted accumulation within cells. The elevated IC50 value indicates that the drug delivery system may be engineered to modulate the release of the drug in a more controlled manner, potentially resulting in a prolonged release profile rather than an immediate therapeutic impact.

Evaluation of Viscoelastic Performance and Molecular Structures of Natural Rubber/NBR Blends Reinforced by Carbon Black and Nano-Silica

This study focuses on the evaluation of the dynamic mechanical properties, molecular structure, density, hardness, swelling behavior of natural rubber blends (NR) and nitrile rubber (NBR) reinforced with carbon black and/or nano-silica. An experimental work has been conducted to study of the effects of increasing NR content and incorporating nano-silica on the mechanical properties and molecular structure were studied using dynamic mechanical analysis (DMA) and Fourier transform infrared (FTIR) spectroscopy. The results show that increasing the NR content and/or incorporating nano-silica into the elastomer leads to a higher storage modulus with no significant change in the glass transition temperature. FTIR analysis indicates the compatibility of the polyblends and the presence of oxidation of the main polymer chain generated during the grinding of the rubber. Additionally, the results of the swelling study demonstrate that stronger molecular interactions occur on the surface of the nano-silica between the nitrile radicals in the NBR and the silanol (Si-OH) radicals. These findings suggest that blending NR and NBR with carbon black and/or nano-silica can improve the mechanical properties and compatibility of the resulting polyblends, with potential applications in the development of advanced elastomeric materials.

Impact of Cobalt-Doping on the Optical, Magnetic, and Electronic Features of Hexagonal Cadmium Sulfide

CdS and Cd0.9Co0.1S samples were prepared under an N2 atmosphere. The structural analysis was conducted using X-ray diffraction. The structural and microstructure parameters were determined using Rietveld refinement method. The incorporation of cobalt ions into CdS matrix was confirmed by energy-dispersive spectroscopy and Fourier-transform infrared analysis. CdS sample has a non-magnetic feature while the Co-doped sample exhibited a magnetic behavior. The origin of magnetic property transformation has been investigated, revealing the emergence of ferromagnetic ordering and the conversion to a diluted magnetic semiconductor (DMS) with a calculated magnetic moment of 2.56 μ B upon Co doping. We also investigated how this Cobalt-doping-driven transformation affected optical, photoluminescence, and electronic properties. These effects correlated with the emergence of hyper-deep defect states. Electronic properties were calculated using density functional theory (DFT) with the HSE06 hybrid functional approximation. The calculated energy bandgaps for both Co-doped and pure CdS were 2.13 and 2.12 eV, respectively, while experimental measurements from our UV analysis yielded values of 2.26 and 2.15 eV. DFT calculations were employed to explore the magnetic properties, absorption coefficients, refractive indices, real and imaginary dielectric components, and energy loss spectra in both samples.

Optical properties, FTIR, and electron spin resonance analysis on the impact of gamma irradiation on fluorophosphate glasses doped with Iron(III) oxide

In the present investigation, conventional melting techniques were employed to fabricate the fluorophosphate glass composites with a composition of 20NaF–60P2O5–20Na2O–3Fe2O3 (mol.%). An investigation was conducted to analyze the impact of various doses of gamma-ray irradiation on certain optical properties. The alteration in the localized defects caused by gamma irradiation can explain the reduction in the refractive index (n) as the doses of gamma-ray irradiation increase, up to 10 kGy. The results of the solar skin protection factor (SSPF) and solar material protection factor (SMPF) tests demonstrate that the un-irradiated composite offers the highest level of protection against the harmful effects of solar energy on both human skin and materials. Some optical parameters, such as the concentrations of the charge carrier (Nopt), the relaxation time (τ), the optical electronegativity (ηopt), and the optical mobility (μopt) showed gamma dose-dependent. The effects of gamma-ray irradiation on the composites were analyzed using Electron Spin Resonance (ESR) and Fourier Transform Infrared (FTIR) spectroscopic studies, both before and after exposure to 10 and 20 kGy.

Modulation of micro-structural, opto-electronic and photo-induced fluorescence properties in sol-gel derived Pb1-xZnxO nanoparticles through the analytical study of vacancy-type defects

In the present work, the doping effect of Zn2+ ion (varying doping concentrations in the range of 0% to 30%) on PbO nanoparticles (NPs) has been investigated proficiently. This study aims at in-depth analysis of the structure-property relationships of the sol-gel derived Zn doped PbO (Pb1-xZnxO) NPs, especially the vacancy evolved properties and the luminescence properties. The X-ray powder diffraction (XRD), high resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), field emission scanning electron microscopy (FESEM) and Fourier-transform infrared (FT-IR) spectroscopic characterization analyses justified the nanocrystallinity of the Pb1-xZnxO powdered NPs while the mean crystallite sizes were located in between 12–36 nm range. Williamson – Hall (W – H) method revealed a monotonous increase of the lattice strain which is compatible with the decrease of NPs’ crystallite size by increase in the Zn2+ doping level. The replacement of Pb2+ ions with the Zn2+ ions caused the reduction of crystallite size by the higher Zn2+ doping level. Prominent peaks of Zn, Pb and O elements are noticed in energy dispersive X-ray spectroscopic (EDS) characterization. The elemental distributions of the chemicals present in the NPs were explored by the elemental mapping analysis. The optical absorption (OA) analysis indicated that the energy band gap (Eg) can be estimated to be 2.21, 2.36, 2.55 and 2.70 eV for 0, 10, 20 & 30% Zn doped PbO NPs, respectively. The positron annihilation lifetime (PAL) spectroscopic studies evidenced the presence of vacancy type defects within the NPs and an increase in defect concentrations has been observed by the increase in Zn concentrations. The photo-induced fluorescence (FL) emission spectra exhibited three luminescence peaks around the wavelengths 430 nm, 490 nm and 522 nm for all the NPs. The observations suggested the possibility of tailoring the characteristics of the synthesized NPs for practical applications in the field of optoelectronics.

Biogenic synthesis of Psidium guajava‐mediated silver nanoparticles: A comprehensive antibiofilm and antivirulence study

AbstractIn this study, at sub‐MIC, the efficacy of green synthesized Psidium guajava‐mediated silver nanoparticles (Pg@AgNPs) in inhibiting quorum sensing facilitated virulence factors and suppressing biofilm formation was evaluated against clinical multidrug resistant (MDR) isolates, specifically Chromobacterium violaceum MCC‐2290 and Pseudomonas aeruginosa PAO1. The AgNPs were synthesized by adding the leaf extract to a solution of silver nitrate, and the reduction of Ag+ ions to Ag0 was confirmed by the appearance of brown color. The Pg@AgNPs were characterized using Fourier transform infrared (FTIR), UV/Vis spectroscopy, TEM, and XRD. The UV/Vis spectrum showed the characteristic absorption peak of Pg@AgNPs in the range of 350–480 nm. FTIR analysis substantiated the existence of functional groups implicated in the synthesis and stabilization of AgNPs. The XRD analysis elucidated the crystalline characteristics of the nanoparticles. The TEM images further confirmed the spherical shape and size of the nanoparticles, which ranged between 5 and 25 nm. The AgNPs demonstrated notable antibacterial efficacy against C. violaceum and P. aeruginosa. Moreover, the Pg@AgNPs effectively suppressed both biofilm formation and the production of quorum sensing‐mediated virulence factors such as pyoverdin (77.2%), pyocyanin (78.12%), and violacein (83.4%). Additionally, the Pg@AgNPs demonstrated broad‐spectrum activity against biofilm formation, showing the biofilm inhibition in C. violaceum and P. aeruginosa by 81.86% and 87.89%, respectively. Under light microscopy, it is also observed that Pg@AgNPs reduce the formation of biofilm in both tested bacteria. The present finding highlights the potential of green‐synthesized AgNPs using P. guajava leaf extract as antimicrobial agents with potential applications in combating bacterial infections and biofilm‐related diseases.

Phytochemical screening, FTIR and GCMS analysis of Cucurbita pepo seeds cultivated in Kiambu county, Kenya

Bioactive compounds and other constituents of plants have been shown to vary by cultivation region, species, environmental conditions and method of extraction among others. Phytochemical analysis of Cucurbita pepos farmed in Kiambu County, Kenya, or their seeds has not been documented. The present research aimed to bridge this knowledge gap by screening phytochemicals and characterizing the seed extracts of Cucurbita pepo cultivated in Kiambu County, Kenya. Cucurbita pepo seeds extracted using organic solvent extraction method employing methanol and preconcentrated in a vacuum rotatory evaporator. The extracts were characterized by GCMS and Fourier transform infrared (FTIR) techniques. Phytochemical analysis of the seeds revealed the presence of flavonoids, alkaloids, saponins, cardiac glycosides, and steroids. FT-IR analysis showed significant peaks for C–N, N–H, C–O, C–H, and CH3 functional groups. The GCMS studies revealed a significant number of fatty acids and their derivatives with 12-cis-octadecadienoate being the most abundant in the oil (53.93 %). A significant amount of the macrocyclic lactone 7,9-ditert-butyl-1-oxaspiro [4.5] deca-6,9-diene-2,8-dione (0.58 %) in the seeds was reported. Macrocyclic lactones are generally a class of anthelminthic drugs. These reported biologically active compounds have a wide range of medicinal and nutritional value. One interesting compound from the GCMS analysis of the seed extracts analyzed was the macrocyclic lactone providing a basis for further research on the anthelminthic actions of the seeds.

An Assessment of the In Vitro Antioxidant Activity of Cobalt Nanoparticles Synthesized From Millettia pinnata, Butea monosperma, and Madhuca indica Extracts: A Comparative Study.

Objective This study aimed to synthesize cobalt nanoparticles (CoNPs) via the green synthesis method using Millettia pinnata(M. pinnata), leaf (MPL), Butea monosperma(B. monosperma)flower (BMF), and Madhuca indica(M. indica)flower (MIF) as eco-friendly reducing agents. It further aimed to compare the effectiveness of these plant extracts in CoNPs production and evaluate the antioxidant activities of the synthesized nanoparticles (NPs), establishing a link between the phytochemical constituents of the extracts and the antioxidant capacity of CoNPs for potential applications in drug development and environmental sustainability. Materials and methods CoNPs were synthesized using aqueous extracts of MPL, BMF, and MIF. These extracts act as stabilizing and self-reducing agents. Initially, the presence of CoNPs was detected visually by observing a color change. To confirm this observation, UV-visible spectroscopy and Fourier transform infrared (FTIR) spectroscopy were employed. UV-visible spectroscopy helps in analyzing the absorption of light by the CoNPs, while FTIR spectroscopy is used to identify the functional groups present in the NPs. Subsequently, the antioxidant activity of the synthesized CoNPs was assessed using the 1,1-diphenyl-2-picryl hydroxyl (DPPH) radical-scavenging assay. This assay measures the ability of antioxidants to neutralize free radicals by determining the reduction in the DPPH radical's absorption. To ensure the reliability of the results, the experiments were conducted in triplicate. Statistical analysis was then performedto compare the antioxidant effectiveness of the different plant extracts used in synthesizing the CoNPs. This analysis helps in determining any significant differences in antioxidant activity among the extracts. Results UV-visible spectral analysis confirmed the successful synthesis of CoNPs, revealing characteristic absorption peaks. For M. pinnata leaf extract (MPLE), the maximum peak was observed at ~272 nm, while B. monosperma flower extract (BMFE) exhibited a peak at ~276 nm, and M. indica flower extract (MIFE) revealed a maximum peak at ~320 nm. FTIR analysis further validated the presence of organic molecules from plant components on the outer layer of CoNPs, indicating successful capping and stabilization by phytochemicals from the extracts. The spectra displayed various peaks at different wavenumbers: MPLE showed prominent peaks at 3335 cm-1, BMFE showed distinct peaks at 3314 cm-1, and MIFE exhibited significant peaks at 3261 cm-1. Among the three types of CoNPs tested, those synthesized using MIFEexhibited the highest inhibition of 87.67% at a concentration of 60 µL. This higher inhibition was compared to those synthesized using BMFEand MPLE. This study suggests that the CoNPs synthesized on MIFEcan serve as an antioxidant agent because of their remarkable free radical-scavenging activity. Conclusions The study highlights the potential of CoNPs synthesized using MIFE as they exhibited superior antioxidant activity compared to those synthesized with BMFE and MPLE. Therefore, the study underscoresthe promise of MIFE as a valuable natural resource for producing CoNPs abundant in antioxidants. Furthermore, it emphasizes the importance of implementing environmentallyfriendly synthesis techniques to produce nanomaterials that are both safe for the environment and biologically effective.

Preparation and Characterization of SPEEK–PVA Blend Membrane Additives with Colloidal Silica for Proton Exchange Membrane Fuel Cell

AbstractAn inexpensive membrane with high proton conductivity and high fuel cell performance, which can be an alternative to Nafion for PEMFC (Proton exchange membrane fuel cell), will overcome the obstacle to widespread commercialization of fuel cells due to high cost. For this purpose, SPEEK (sulfonated polyether ether ketone)-PVA (polyvinyl alcohol) blend membranes with colloidal silica additives were synthesized in this study. Ludox AS-40 was used as the colloidal silica source and the blend membrane was prepared by solution casting method. Water uptake capacity, swelling property, size change, dynamic mechanical analysis, ion exchange capacity, AC impedance analysis, hydrolytic and oxidative stability experiments of the synthesized Ludox additives blend membranes for fuel cell application were carried out, and the membranes were also characterized by FTIR (Fourier transform infrared) analysis. While the water uptake capacities of SPEEK/PVA membranes containing 1% Ludox, 5% Ludox, and 10% Ludox at room temperature were found to be 14.08%, 14.84%, and 16.6%, respectively, the water uptake capacities at 80oC increased to 14.73%, 15.17%, and 17.11%. The proton conductivities of 1% Ludox, 5% Ludox and 10% Ludox doped SPEEK/PVA membranes at 80oC were 0.25 S/cm, 0.56 S/cm, and 0.65 S/cm, respectively. Similarly, ion exchange capacities were determined to be 1.41 meq/g, 1.63 meq/g, and 1.71 meq/g, respectively. All Ludox-added membranes exhibited excellent hydrolytic stability, retaining approximately 88% of their mass after 650 h. In addition, in oxidative stability experiments carried out in 4 ppm Fe+ 2 at 80oC, the 10% Ludox-added membrane exhibited the highest weight loss of 88.8% at the end of 24 h, while the 5% Ludox-additive membrane retained 91.6% of its total weight. Considering the proton conductivity and longevity tests of the synthesized membranes, they are thought to be promising structures. Graphical Abstract

Polyvinyl alcohol as solid proton donor to modify g-C3N4via hydrogen bonding enabling efficient photocatalytic H2O2 production from H2O and O2.

Polyvinyl alcohol (PVA) was used as a solid proton donor to improve the photocatalytic performance of graphitic carbon nitride (CN) for hydrogen peroxide (H2O2) production. The modified CN (CN/PVA) was prepared by mixing CN and PVA at room temperature. The H2O2 production efficiency of CN/PVA was 5.65 times higher than that of CN in pure water. Photocurrent measurement, electrochemical impedance spectroscopy (EIS), and photoluminescence (PL) analysis proved that PVA increased charge separation of CN. X-ray photoelectron spectroscopy (XPS), and Fourier-transform infrared (FTIR) analyses further suggested that PVA acted as the proton donor during H2O2 production by interacting with CN via hydrogen bonds. The combination of the charge separation enhancer and proton donor from PVA promoted the sequential two-step single-electron reduction of O2 for H2O2 production. This study paves the way for the modification of g-C3N4 with hydroxyl-containing materials as solid proton donors for photocatalytic H2O2 production.

Formulation of a Novel Polymeric Hydrogel Membrane for Periodontal Tissue Regeneration Using Tricalcium Phosphate-Alginate Reinforcement.

The primary goal of periodontal therapy is to facilitate the regeneration of tissues damaged by periodontal disease. In recent years, there has been a growing utilization of guided tissue regeneration (GTR) membranes with bioabsorbable properties as these membranes are increasingly employed to guide the growth of gingival tissue away from the root surface. Both resorbable and non-resorbable membranes currently employed act as physical barriers, preventing the ingrowth of connective and epithelial tissues into the defect and thereby facilitating periodontal tissue regeneration. This study aimed to develop a polymeric hydrogel membrane reinforced with tricalcium phosphate (TCP)-alginate and assess its potential for periodontal regeneration. TCPnanoparticles were incorporated into the alginate mixture to form TCP alginate. Subsequently, the mixture was cross-linked with calcium chloride to produce a TCP-alginate polymeric hydrogel membrane. The membrane underwent hemocompatibility analysis, and also scanning electron microscopyand Fourier-transform infrared (FTIR) spectroscopy analyses were done. The SEM analysis revealed granulations and a bonded thread-like structure in the membrane, indicative of favorable conditions for cell attachment necessary for periodontal regeneration. FTIR analysis showed characteristic peaks in the spectrum, including those attributed to phosphate ion (PO4-3) at 1000.85 cm-1 and 600 cm-1, indicating the presence of β-TCP phases. Hemocompatibility assessment demonstrated a hemolysis rate of less than 5% for the TCP-alginate membrane, which is found to be within the limits. The developed TCP-reinforced alginate membrane exhibited hemocompatibility and safety, suggesting its suitability for utilization in periodontal therapy as an effective regenerative material.

Sorafenib and Piperine co-loaded PLGA nanoparticles: Development, characterization, and anti-cancer activity against hepatocellular carcinoma cell line

Hepatocellular carcinoma (HCC) exhibits high mortality rates in the advanced stage (>90 %). Sorafenib (SORA) is a targeted therapy approved for the treatment of advanced HCC; however, the reported response rate to such a therapeutic is suboptimal (<3%). Piperine (PIP) is an alkaloid demonstrated to exert a direct tumoricidal activity in HCC and improve the pharmacokinetic profiles of anticancer drugs including SORA. In this study, we developed a strategy to improve efficacy outcomes in HCC using PIP as an add-on treatment to support the first-line therapy SORA using biodegradable Poly (D, L-Lactide-co-glycolide, PLGA) nanoparticles (NPs). SORA and PIP (both exhibit low aqueous solubility) were co-loaded into PLGA NPs (PNPs) and stabilized with various concentrations of polyvinyl alcohol (PVA). The SORA and PIP-loaded PNPs (SP-PNPs) were characterized using Fourier Transform Infrared (FTIR) Spectroscopy, X-ray Powder Diffraction (XRD), Dynamic Light Scattering (DLS), and Scanning Electron Microscopy (SEM), Release of these drugs from SP-PNPs was investigated in vitro at both physiological and acidic pH, and kinetic models were employed to assess the mechanism of drug release. The in vitro efficacy of SP-PNPs against HCC cells (HepG2) was also evaluated. FTIR and XRD analyses revealed that the drugs encapsulated in PNPs were in an amorphous state, with no observed chemical interactions among the drugs or excipients. Assessment of drug release in vitro at pH 5 and 7.4 showed that SORA and PIP loaded in PNPs with 0.5 % PVA were released in a sustained manner, unlike pure drugs, which exhibited relatively fast release. SP-PNPs with 0.5 % PVA were spherical, had an average size of 224 nm, and had a high encapsulation efficiency (SORA ∼ 82 %, PIP ∼ 79 %), as well as superior cytotoxicity compared to SORA monotherapy in vitro. These results suggest that combining PIP with SORA using PNPs may be an effective strategy for the treatment of HCC and may set the stage for a comprehensive in vivo study to evaluate the efficacy and safety of this novel formulation using a murine HCC model.

Extraction and characterization of natural dye from leaves of Lannea coromandelica and application on cotton fabric

Purpose The purpose of this study is to extract and characterize a novel natural dye from the leaves of Lannea coromandelica and the extraction with finding ways of dyeing cotton fabric using three mordants. Design/methodology/approach The colouring agents were extracted from the leaves of Lannea coromandelica using an aqueous extraction method. The extract was characterized using analysis methods of pH, gas chromatography-mass spectrometry (GC-MS), Fourier transform infrared (FTIR), ultraviolet-visible (UV-vis) and cyclic voltammetry measurement. The extract was applied to cotton fabric samples using a non-mordant and three mordants under the two mordanting methods. The dyeing performance of the extracted colouring agent was evaluated using colour fastness properties, colour strength (K/S) and colour space (CIE Lab). Findings The aqueous dye extract showed reddish-brown colour, and its pH was 5.94. The GC-MS analysis revealed that the dye extract from the leaves of Lannea coromandelica contained active chemical compounds. The UV-vis and FTIR analyses found that groups influenced the reddish-brown colour of the dye extraction. The cyclic voltammetry measurements discovered the electrochemical properties of the dye extraction. The mordanted fabric samples showed better colour fastness properties than the non-mordanted fabric sample. The K/S and CIE Lab results indicate that the cotton fabric samples dyed with mordants showed more significant dye affinities than non-mordanted fabric samples. Originality/value Researchers have never discovered that the Lannea coromandelica leaf extract is a natural dye for cotton fabric dyeing. The findings of this study showed that natural dyes extracted from Lannea coromandelica leaf could be an efficient colouring agent for use in cotton fabric.

Optimized extraction and nanoencapsulation of artemisia essential oils: A comprehensive analysis of bioactives and structural characterization

This study pertains to essential oil extraction from Artemisia absinthium L and a comparison of multiple extraction techniques. Ultrasound-assisted extraction emerged as the superior method, demonstrating remarkable extract recovery in contrast to microwave and hydrodistillation approaches. Bioactive compounds within the extracted Artemisia essential oils were meticulously identified through Gas Chromatography-Mass Spectrometry (GCMS), shedding light on the chemical composition. Furthermore, we employed maltodextrin nanoparticles as a sophisticated nanocarrier for encapsulating the extracted oil. Our investigation encompassed various maltodextrin-to-artemisia extract ratios (1:10, 1:20, and 1:30), revealing encapsulation efficiencies of 75.21%, 78.23%, and 85.24%, respectively. Characterization of the nanoencapsulated powders through scanning electron microscopy unveiled their distinctive irregular morphology. X-ray diffraction (XRD), full width at half maximum for artemisia extract powder and nanoencapsulated powder were 0.12, 8.2, 8.70, and 8.89 and Fourier-transform infrared (FTIR), typical bands were 1348, 1625, 1596, 1614, 2920 cm−1. XRD and FTIR analyses furnished compelling evidence of successful encapsulation, presenting the artemisia extract in an amorphous state. Notably, the XRD patterns indicated a low degree of crystallinity, affirming the innovative nature of our approach. Significantly, the encapsulated powders retained the characteristic absorption bands of the artemisia extract, underscoring the preservation of its essential chemical properties throughout the encapsulation process.

Optimization of Coagulation to Remove Turbidity from Surface Water Using Novel Nature-Based Plant Coagulant and Response Surface Methodology

Plant-based natural coagulants are considered potential alternatives to chemical coagulants. These are eco-friendly, non-toxic, and produce less sludge compared to chemical coagulants. This study aims to evaluate the coagulation potential of a novel plant-based coagulant Sorghum for canal water treatment. In addition, a coagulant aid, i.e., Aloe Vera, was also tested to examine any further increase in turbidity removal through a jar test apparatus. Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM) were used to characterize the coagulants. The experiment was designed using response surface methodology (RSM). When used alone, Sorghum resulted in a maximum turbidity removal of 87.73% at pH 2 and a dose of 40 mg/L, while the combination of Sorghum and Aloe Vera resulted in a turbidity removal of 84.2% at pH 2.7, and the doses of Sorghum and Aloe Vera were 17.1 mg/L and 0.9% (v/v), respectively. Thus, the Sorghum dose was significantly reduced when Aloe Vera was used in combination. At a pH of 7, Sorghum achieved 54% turbidity removal at a dose of 55.7 mg/L. Analyses of variance revealed that pH plays a more vital role in the removal of turbidity than the coagulant dose. FTIR and SEM analyses revealed that adsorption is the dominant coagulation mechanism for plant-based coagulants. The Sorghum powder exhibited carboxylic, amine, and carbonyl groups that functioned as active adsorption sites for suspended solids. In a similar vein, the coagulant aid Aloe Vera gel facilitated the adsorption process by fostering intermolecular hydrogen bonding between suspended particles and amine groups present within the gel.

Comparative Antioxidant Efficacy of Green-Synthesised Selenium Nanoparticles From Pongamia pinnata, Citrus sinensis, and Acacia auriculiformis: An In Vitro Analysis.

Aim This study aims to synthesise selenium nanoparticles (SeNPs) using extracts from Citrus sinensis peel (CSP), Millettia pinnata Leaf (MPL), and Acacia auriculiformis bark (AAB) as eco-friendly reducing agents. It seeks to compare the effectiveness of these plant extracts in the production of SeNPsand evaluate the antioxidant activities of the synthesised nanoparticles, establishing a link between the phytochemical constituents of the extracts and the antioxidant capacity of SeNPs for their potential applications in drug development and environmental sustainability. Introduction Nanotechnology offers innovative solutions in various fields, including medicine, environmental science, and materials engineering. SeNPs are of particular interest due to their unique properties and potential applications. The methods for synthesizing nanoparticles often involve hazardous chemicals, posing risks to the environment and human health. In response, green synthesis methods utilizing plant extracts have emerged as a sustainable alternative. This study focuses on utilizing CSP, MPL, and AAB extracts, rich in natural reducing agents such as flavonoids and phenolic acids, for the eco-friendly synthesis of SeNPs. These plant sources are chosen based on their known phytochemical profiles and potential antioxidant activities, and we aim to explore the correlation between the extracts' phytochemical composition and the antioxidant capabilities of the synthesised SeNPs. Methods SeNPs were synthesised using aqueous extracts of CSP, MPL, and AAB through a reduction process, in which selenium ions (Se4+) are reduced to elemental selenium. The presence of SeNPs was first visually monitored by colour change and then confirmed through UV-Vis spectroscopy and Fourier transform infrared (FTIR) spectroscopy analyses. The antioxidant activity of the synthesised SeNPs was assessed using the 1,1-diphenyl-2-picryl hydroxyl (DPPH) radical scavenging assay and the efficacy of SeNPs synthesised from different plant extracts was compared. Results The UV-Vis spectral analysis indicated a successful synthesis of SeNPs, as evidenced by the characteristic absorption peaks. The FTIR analysis confirmed the presence of organic molecules derived from the plant components on the outer layer of SeNPs, suggesting successful capping and stabilization of nanoparticles by phytochemicals in the extracts. Among the three types of SeNPs, those synthesised using Citrus sinensis peel extract (CSPE) exhibited the highest DPPH radical scavenging activity, indicating superior antioxidant properties compared to SeNPs synthesised from Millettia pinnata leaf extract (MPLE) and Acacia auriculiformis bark extract (AABE). This suggests that the antioxidant capacity of SeNPs is significantly influenced by the phytochemical composition of the plant extract used for synthesis. Conclusion The study highlights the potential of CSPE as an effective natural source for synthesising antioxidant-rich SeNPs and underscores the importance of green synthesis approaches in producing environmentally friendly and biologically active nanomaterials.