Fourier Transform Infrared Spectroscopy Studies Research Articles

Revolutionizing Drug Delivery: Nicardipine Nanosuspension Formulation and In-Vitro Evaluation

Nicardipine hydrochloride, is a potent calcium channel blocker, is commonly used in the management of hypertension and angina. It is a BCS class II drug which has low aqueous solubility and high permeability. In the present study, an attempt was made to formulate and evaluate nanosuspension of Nicardipine hydrochloride using different stabilizers, namely Tween 80, PVP K30, Poloxamer 188 by using Nanoprecipitation method with the objective to improve solubility and enhance dissolution of Nicardipine hydrochloride. Prepared nanosuspensions were evaluated for drug-excipient compatibility, particle size, PDI (Polydispersity Index), Zeta potential, Drug content, Saturation solubility, In-vitro release study, Scanning electron microscopy (SEM). FTIR (Fourier Transform Infrared Spectroscopy) studies revealed the compatibility of the drug with excipients. Nanosuspension (F3), which had the lowest particle size and the highest % Drug Release, was selected as the optimum formulation. It showed the droplet size, PDI, ZP,% Drug content and %Drug release of 150.4 nm,0.243, -30.6 mV,95.52%,91.24%. Kinetic release profiles of the NS F3 revealed that it followed First order kinetics. This study showed the ability of nanosuspension system in improving the solubility and drug release of Nicardipine.
 Keywords: Nicardipine, Nanosuspension, Solubility, % Drug Release, % Drug content, Scanning electron microscopy.

Simultaneously Inhibiting P-gp Efflux and Drug Recrystallization Enhanced the Oral Bioavailability of Nintedanib.

Nintedanib (NDNB) is a novel triple-angiokinase inhibitor for the treatment of lung cancer. However, the oral bioavailability of NDNB is only 4.7% owing to the poor solubility and the efflux of P-glycoprotein (P-gp). The aim was to explore the potential applications of a hydrogel of NDNB/hydroxypropyl-β- cyclodextrin (HP-β-CD) complex combined with a strong P-gp inhibitor Itraconazole (ITZ) for augmenting the oral delivery of NDNB. The NDNB/HP-β-CD complex was prepared and characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and molecular simulation and was subjected to in vitro and in situ studies. Then the NDNB/HP-β-CD complex was dispersed in carbopol 934 hydrogel and the gel was evaluated for pharmacokinetic and pharmacodynamics studies. The HP-β-CD and NDNB formed complex by van der Waals and hydrogen bonding interaction forces by XRD, FT-IR, and molecular simulation studies. When the molar ratio of NDNB/HP-β-CD was 1:20, the complex exhibited high drug inclusion efficiency and excellent stability. The in situ perfusion results revealed that the permeability of the combination of complex and ITZ enhanced about 3.0-fold compared with the NDNB solution. The oral bioavailability of the sequential administration of ITZ and NDNB/HP-β-CD complex gels was increased 3.5-fold by preventing recrystallization, extending the residence time in the gastrointestinal tract, and inhibiting P-gp in comparison with NDNB soft capsules. The co-therapy with NDNB/HP-β-CD complex gels and ITZ exerted a strong anti-tumor effect. In conclusion, NDNB/HP-β-CD complex gels combined with P-gp inhibitor were a potential strategy for enhancing the oral bioavailability and anti-tumor effect of NDNB.

Structural study and physical properties of tellurite glasses containing lead bromide

In this work, a suggested approach based on ion exchange process (IXP) between Br− ions from PbBr2 and O ions from Ag2O was applied to obtain crystalline glass ceramic directly from glasses. Silver-borate glasses in the system: xPbBr2-(45-x) Ag2O55TeO2, with (x = 0, 10, 15, 20, 22.5, and 25 mol.% PbBr2) were synthesized by melt quenching technique. X-ray diffraction (XRD), Raman spectroscopy, and Fourier transform infrared spectroscopy (FTIR) were used to investigate the structure and properties of the as prepared glasses. According to both Raman and FTIR studies, as PbBr2 content increases, some of the TeO4 and TeO3+1 units are converted to TeO3, which contains more NBO. Increasing the latter with increasing PbBr2 content was discussed on the basis of the ion exchange process. According to X-ray results, the addition of lead bromide causes a noticeable change in the nature of the glass. The lead-bromide-free glass implies two crystalline extremes that can be attributed to the formation of the silver tellurite crystalline phase (Ag2TeO3). Upon the addition of lead bromide, even with small concentrations up to 20 mol.%, the most prominent structure is amorphous. On the other hand, increasing the concentration of lead bromide forms lead tellurite crystalline phase (Pb3TeO6). Data based on density, packing density, molar volume, free molar volume, and oxygen molar volume were discussed and correlated with the structural changes caused by addition of PbBr2. In view of a potential application on ion exchange process, formation of crystalline dispersed phases in host tellurite matrices will be object of a further investigation.

Facile Extraction of Natural Hydroxyapatite (HA) from Biowaste and Its Characterizations

Natural Hydroxyapatite (HA) with chemical formula Ca10(PO4)6(OH)2 is a major mineral storage form of calcium and phosphorous in bone and it has been applied in many fields. In the present study, HA was extracted from biowaste; namely the buffalo bone by alkaline hydrolysis process followed by calcination at 900°C with holding time 6 hrs. in muffle furnace. The isolated material was analyzed by X-ray Diffraction (XRD), Fourier Transform Infra-Red Spectroscopy (FTIR) and Field Emission Scanning Electron Microscopy (FESEM) etc. The SEM image suggested the isolated material had rod shaped and agglomerated. FTIR study indicated the phosphate and hydroxide were the major functional groups along with carbonate present in it. Further, XRD analysis inferred that the isolated material was only HA phased. The specific surface area of the isolated HA was determined by methylene blue adsorption method and it was found to be 141.12 m2 /g and pH point of zero charge (pHPZC) of the extracted biomaterial was determined to be 6.8 by pH the drift method. Thus the pure HA powder was synthesized by an environmentally friendly, cost effective method and may be applicable in many fields including waste water treatment and biomedicine etc.

Preparation and characterization of corn cob cellulose acetate for potential industrial applications

Background: Locally generated biopolymers are amenable to further processing to widen their industrial applications. The study was aimed at generating low-cost cellulose acetate from corn cob residue and its characterizations for potential applications in biopolymer industries. Methods: Cellulose was extracted from the corn cob residue using the sodium hydroxide method. Acetylation of the cellulose to obtain corn cob cellulose acetate was carried out by adding appropriate quantities of a glacial acetic and acetylating mixture of acetic anhydride and sulphuric acid. The corn cob native cellulose and corn cob cellulose acetate were characterized using scanning electron microscopy (SEM) to examine their morphology, Fourier-transform infrared spectroscopy (FTIR) and powder X-ray diffraction (XRD) for structural elucidation while differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) were employed to investigate their thermal properties. Results: - Two corn cellulose acetate samples with degree of substitutions 1.87 and 2.65 for samples CDA and CA respectively were obtained. They had improved solubilities in some organic solvents compared to the corn cob cellulose. The SEM examination showed the surface of the corn cob native cellulose (NC) was smooth and had a regular bundle-like structure while acetylation destroyed the original cellulose structure. Cellulose acetate samples showed a cluster-like structure with different sizes and a rough flake-like surface. FTIR and XRD studies showed that acetyl groups substituted cellulose hydroxyl groups. While FTIR study showed that the cellulose acetates had sharp bands between 1728 cm-1 to 1733 cm-1 and around 1368 cm-1 wavenumber unlike the corn cob cellulose sample, the data generated from XRD study indicated that acetylation of the corn cob cellulose led to 47% and 77% decrease in the crystallinity of CDA and CA samples respectively. The thermal analysis data from DSC and TGA studies confirmed that the acetylation improved the corn cob cellulose's thermal stability as indicated by the degradation of cellulose acetate samples at higher temperatures. Conclusion: The study concluded that low-cost cellulose acetate generated from corn cob residue could be potentially employed as a renewable, biodegradable, biocompatible polymer for industrial applications.

Efficient photocatalytic degradation of water pollutant Brufen using lutetium doped cerium oxide nanoparticles synthesized by chemical precipitation method

BackgroundPlants act the foremost source of molecules for the advancement of new drugs regarding anti-inflammatory action. In recent years, pharmaceutical compounds have been categorized as the emerging pollutants and have grabbed the attention of the researchers due to their existence in wastewater. They have been detected in drinking water which shows that the wastewater treatment plants are always not efficacious. These contaminants are pernicious if present in higher dosage and cause several risk factors to humans, animals, and aquatic systems. Ibuprofen, one of the most prescribed analgesics found to cause severe damage to stomach and intestine has been subjected to photocatalytic degradation using Lutetium doped Cerium oxide nanoparticles. The nanoparticles were synthesized using chemical precipitation method which is cost effective, simple, and ecofriendly. MethodsThe synthesized nanomaterial was characterized and confirmed using several analytical techniques like X-Ray Diffraction studies (XRD), Fourier Transform-Infrared Spectroscopy (FT-IR), UV-Diffuse Reflectance Spectroscopy (UV-DRS), High Resolution Scanning Electron Microscopy (HRSEM), X-Ray energy dispersive spectroscopy (EDAX), High Resolution Transmission Electron Microscopy (HRTEM), and X-ray Photoelectron Spectroscopy (XPS). Significant findingsXRD data revealed the cubic shape of the nanoparticles with approximate size of 6–12 nm. FT-IR study confirmed the presence of metal oxide peak at 550 cm−1 along with the peaks of other functional groups. HRSEM and HRTEM images confirmed cubic structure validating the XRD results. The band gap of the synthesized nanoparticles decreased from 3.25 eV to 2.90 eV in comparison with the pristine CeO2 with LuCeO2. XPS results revealed the oxidation state of lutetium as +3. The photocatalytic conditions were optimized and the optimization study confirms that the catalyst effectively degrades the drug. The degradation efficiency was calculated and was observed to be 92%. Real sample analysis was also performed using Brufen 200 tablet which confirms the practical application of the photocatalyst.

(Invited) Electrochemical and in Situ FTIR Spectroscopic Studies of CO2 Reduction at 3D Nanostructured Catalysts

There is a growing interest in developing high-performance catalysts for the electrochemical reduction of carbon dioxide (CO2) to address the increasingly serious impacts of global climate change. In this talk, we report on the design of advanced three-dimensional (3D) nanomaterials (e.g., nanoporous gold, Cu nanodendrites and Co nanodendrites) for the efficient electrochemical reduction of CO2. The morphology, composition and structure of the synthesized 3D nanomaterials were characterized with various imaging and spectroscopic techniques, including FE-SEM, XRD, EDX and XPS. The effects of an applied potential on the electrochemical reduction of CO2 were investigated using various electrochemical methods. The products generated from the CO2 electrochemical reduction were identified by gas chromatography and nuclear magnetic resonance (NMR) spectroscopy. The kinetics of the CO2 reduction reaction at the 3D nanomaterials was further studied using in situ electrochemical Fourier transform infrared (FTIR) spectroscopy. The critical roles of nanostructured surfaces in the electrochemical reduction of CO2 are discussed.

FTIR study of H2O in silicate minerals and mineral inclusions in chromite from the peridotite zone of the Stillwater complex (Montana, USA): Evidence for chromitite formation in an H2O-rich environment

Although the involvement of hydrous fluids has been frequently invoked in the formation of stratiform chromitites in layered intrusions, there is a lack of natural evidence to signify their presence and mechanism. Here, Fourier-transform infrared spectroscopy (FTIR) of H2O in silicate minerals in the lowermost layer and G chromitite layer of the Stillwater complex, Montana, USA, shows that olivine grains have 20−55 ppm H2O, orthopyroxene has 30−45 ppm H2O, and clinopyroxene has 144−489 ppm H2O. The jointly increasing H2O contents of olivine and orthopyroxene in silicate cumulates along with magma differentiation record a negative correlation in chromitites. On the basis of poikilitic clinopyroxene, we calculated that the interstitial melts had averages of 1.3 wt% and 2.3 wt% H2O in dunite and chromitite, respectively, showing significant differences between chromitites and silicate cumulates. More than 10% of the chromite grains contained polymineralic inclusions up to 100 μm in size that were composed mainly of orthopyroxene, hornblende, plagioclase, and phlogopite. Most of these minerals were characterized by higher MgO and fluid-mobile element contents, such as Na and K, than minerals in associated silicates. Based on the mineral modes of the hydrous phases and their compositions, the trapped fluids contained ∼2.6 wt% H2O, consistent with the FTIR estimates, indicating the inclusion compositions represent interstitial melts instead of parental magmas. These observations indicate that the chromite microlites collected fluids during early crystallization, leading to a heterogeneous fluid redistribution in the melt. The fluids were collected on the surface of chromite grains during crystallization and then dissolved into poikilitic pyroxene. Chromite grains could also be efficiently floated by these fluids, causing them to migrate away from the silicate minerals in the magma channel and leading to the formation of nearly monomineralic chromitite seams. This process serves as a kinetic model indicating that chromite could be completely separated from silicates during mechanical sorting in layered intrusions.

Gold Nanoparticles AuNP Decorated on Fused Graphene-like Materials for Application in a Hydrogen Generation.

The search for a sustainable, alternative fuel source to replace fossil fuels has led to an increased interest in hydrogen fuel. This combustible gas is not only clean-burning but can readily be produced via the hydrolysis of sodium borohydride. The main drawback of this reaction is that the reaction occurs relatively slowly and requires a catalyst to improve efficiency. This study explored a novel composite material made by combining gold nanoparticles and fused graphene-like materials (AuFGLM) as a catalyst for generating hydrogen via sodium borohydride. The novel fused graphene-like material (FGLM) was made with a sustainable dextrose solution and by using a pressure-processing method. Imaging techniques showed that FGLM appears to be an effective support template for nanoparticles. Transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and Raman spectroscopy were used to characterize and determine the size, shape, and structure of nanoparticles and composites. The TEM study characterized the fused carbon backbone as it began to take on a rounder shape. The TEM images also revealed that the average diameter of the gold nanoparticle was roughly 23 nm. The FTIR study confirmed O-H, C-C, and C=O as functional groups in the materials. The EDS analysis showed that the composite contained approximately 6.3% gold by weight. The crystal structures of FGLM and AuFGLM were identified via P-XRD analysis. Various reaction conditions were used to test the catalytic ability of AuFGLM, including various solution pHs, temperatures, and doses of NaBH4. It was observed that optimal reaction conditions included high temperature, an acidic solution pH, and a higher dose of NaBH4. The activation energy of the reaction was determined to be 45.5 kJ mol-1, and it was found that the catalyst could be used multiple times in a row with an increased volume of hydrogen produced in ensuing trials. The activation energy of this novel catalyst is competitive compared to similar catalysts and its ability to produce hydrogen over multiple uses makes the material an exciting choice for catalyzing the hydrolysis of NaBH4 for use as a hydrogen fuel source.

Methyl esters synthesis from Luffa cylindrica seeds oil using green copper oxide nanoparticle catalyst in membrane reactor

This study investigates the potential role of Juglans sp. root extract-mediated copper oxide nanoparticles of Luffa cylindrica seed oil (LCSO) into methyl esters. The synthesized green nanoparticle was characterized by Energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FT-IR), and Scanning electron microscopy (SEM) spectroscopies to find out the crystalline size (40 nm), surface morphology (rod shape), particle size (80–85 nm), and chemical composition (Cu = 80.25% & O = 19.75%), accordingly. The optimized protocol for the transesterification reaction was adjusted as oil to methanol molar ratio (1:7), copper oxide nano-catalyst concentration (0.2 wt %), and temperature (90 °C) corresponding to the maximum methyl esters yield of 95%. The synthesized methyl esters were characterized by GC-MS, 1H NMR, 13C NMR, and FT-IR studies to know and identify the chemical composition of newly synthesized Lufa biodiesel. The fuel properties of Luffa cylindrica seed oil biofuel were checked and compared with the American Biodiesel standards (ASTM) (D6751-10). Finally, it is commendable to use biodiesel made from wild, uncultivated, and non-edible Lufa cylindrica to promote and adopt a cleaner and sustainable energy method. The acceptance and implementation of the green energy method may result in favourable environmental effects, which in turn may lead to better societal and economic development.

A FTIR and DFT Combination Study to Reveal the Mechanism of Eliminating the Azeotropy in Ethyl Propionate-n-Propanol System with Ionic Liquid Entrainer.

Ionic liquids (ILs) have presented excellent behaviors in the separation of azeotropes in extractive distillation. However, the intrinsic molecular nature of ILs in the separation of azeotropic systems is not clear. In this paper, Fourier-transform infrared spectroscopy (FTIR) and theoretical calculations were applied to screen the microstructures of ethyl propionate-n-propanol-1-ethyl-3-methylimidzolium acetate ([EMIM][OAC]) systems before and after azeotropy breaking. A detailed vibrational analysis was carried out on the v(C=O) region of ethyl propionate and v(O-D) region of n-propanol-d1. Different species, including multiple sizes of propanol and ethyl propionate self-aggregators, ethyl propionate-n-propanol interaction complexes, and different IL-n-propanol interaction complexes, were identified using excess spectroscopy and confirmed with theoretical calculations. Their changes in relative amounts were also observed. The hydrogen bond between n-propanol and ethyl propionate/[EMIM][OAC] was detected, and the interaction properties were also revealed. Overall, the intrinsic molecular nature of the azeotropy breaking was clear. First, the interactions between [EMIM][OAC] and n-propanol were stronger than those between [EMIM][OAC] and ethyl propionate, which influenced the relative volatilities of the two components in the system. Second, the interactions between n-propanol and [EMIM][OAC] were stronger than those between n-propanol and ethyl propionate. Hence, adding [EMIM][OAC] could break apart the ethyl propionate-n-propanol complex (causing the azeotropy in the studied system). When x([EMIM][OAC]) was lower than 0.04, the azeotropy still existed mainly because the low IL could not destroy the whole ethyl propionate-n-propanol interaction complex. At x(IL) > 0.04, the whole ethyl propionate-n-propanol complex was destroyed, and the azeotropy disappeared.

Controlled Synthesis of Polyaniline/Iron Oxide Nanocomposites for Thermoelectric Applications

Polyaniline (PANI) / iron oxide (Fe3O4) nanocomposites were synthesized via the sol-gel method by tuning the weight ratios of Fe3O4 (2wt %, 4wt % and 6wt %). The functional groups, crystal structure and surface morphologies of the PANI/Fe3O4 nanocomposites were analyzed using Fourier transform infrared spectroscopy (FTIR), X–ray powder diffraction and Scanning electron microscopy (SEM) respectively. The thermoelectrical properties were also analyzed. Based on the FTIR studies, the presence of functional groups of PANI/Fe3O4 nanocomposites was revealed. From SEM observations, spherical nanoparticles were found. As the temperature increases from 30°C to 90°C, the electrical conductivity of the nanocomposites increases from 34.01 to 39.54 mS/cm and the thermal conductivity decreases from 1.401 to 0.765 Wm-1K-1. Among the three different PANI/Fe3O4 nanocomposites characterized, the PANI/Fe3O4 nanocomposite with 6wt % gives better results by showing an excess figure of merit of 0.016. Henceforth, as the weight percentage of iron oxide with polyaniline increases, the thermoelectric properties of the nanocomposites drastically improve.

EFFECT OF PREPARATION TEMPERATURE ON ETHYLCELLULOSE MICROSPHERE PROPERTIES PREPARED BY OIL-IN-OIL EMULSION SOLVENT EVAPORATION PROCESS

The present study aims to formulate ethylcellulose microspheres using the oil-in-oil emulsion solvent evaporation method and judge the outcome of processing temperature on their features. The effects of the evaporation rate of the solvent on the particle properties and drug release characteristics of the microspheres were studied. Here, microspheres were prepared at different processing temperatues, viz., 10 0 C, 25 0 C, and 40 0 C, and their impact on the various characteristics of microspheres like surface topography, micrometrics, yield percent, encapsulation efficiency, in vitro dissolution, Fourier-transform infrared spectroscopy (FTIR) and release kinetics were elaborately studied. The FTIR study revealed that processing temperature did not affect drug-polymer compatibility. The study observed that the processing temperature had a great influence on the various characteristics of the prepared microsphere. It was observed from sieve analysis that the mean particle size of the microsphere increased with an increase in processing temperature, and the SEM study also corroborated the same result. SEM photographs showed processing at a higher temperature resulted in particles with a smooth surface, in contrast to a lower processing temperature that forms a bumpy surface. Furthermore, a higher temperature favoured formulation with a higher entrapment efficiency (94.42 ± 0.9 %) as compared to a lower temperature (85.2 ± 0.72 %). For a noteworthy timeframe, indinavir sulfate frames a solid solution in the ethylcellulose matrix and proceeds with the amorphous state. The results of an in vitro drug dissolution study showed that microspheres formulated at a higher temperature had a more sustaining effect as compared to those formulated at a lower temperature, which may have resulted due to their higher mean particle size. Using the Korsemeyer Peppas power law, it was found that the way drugs are released is controlled by diffusion.

SILK FIBROIN-BASED ANASTROZOLE NANOPARTICLE LOADED IN SITU INJECTABLE: DEVELOPMENT AND CHARACTERIZATION

Objective: The study aims to find a suitable method of developing silk fibroin-based anastrozole nanoparticles and formulate in situ injectables by loading the optimized nanoparticle formulation for the sustained release treatment of breast cancer. Methods: The nanoparticles were formulated utilizing two different methods, solvent change and precipitation approach using silk fibroin. Prepared nanoparticles characterized in terms of size, zeta potential, polydispersity, and entrapment efficiency. The chosen optimized formulation (SF-ANS-NPs-1) was subsequently analyzed for compatibility investigations by Fourier-transform infrared spectroscopy (FT-IR), thermal analysis, surface morphology, x-ray diffraction, transmission electron spectroscopy, cumulative drug release, and stability studies as per ICH guidelines. Followed by formulating and evaluating in situ injectable gel using pluronic F-127. Results: A particle size of 181.70±1.3 nm was reported by the optimized SF-ANS-NPs-1 formulation. FT-IR and thermal studies confirmed the compatibility of the drug with the polymers, and x-ray diffraction studies indicated crystalline nature. Surface morphology analysis indicated nano-size particle formation. A cumulative drug release (%CDR) of 94.15% was noted at the 168th hour. The results of the stability studies were indicated to be consistent over 90 d. In situ gel formulation showed desired spreadability, sol-gel transition temperature (37±0.5 ℃), viscosity (9.37±1.2 mPa·s), desired acidic pH, and a sustained release for 21 d (98.11%) with three months accelerated stability. Conclusion: The results suggested that the combination of anastrozole with silk fibroin in the form of nanoparticles and in situ gelling systems could be an undoubtedly effective delivery method for prolonging breast cancer therapy.

Biodegradable Green Composites: Effects of Potassium Permanganate (KMnO4) Treatment on Thermal, Mechanical, and Morphological Behavior of Butea Parviflora (BP) Fibers.

This study emphasizes the importance of utilizing biodegradable material Butea parviflora (BP) fiber for sustainable solutions. BP fiber offers numerous ecological benefits, such as being lightweight, biodegradable, and affordable to recycle. The study examines the effects of potassium permanganate (KMnO4) treatment on BP fiber and analyzes its physical and chemical behavior using various methods, including X-ray Diffraction (XRD) analysis, tensile testing, thermogravimetric analysis, thermal conductivity, Scanning Electron Microscopy (SEM), and Fourier Transform Infrared spectroscopic (FTIR) analysis. The results demonstrate that BP fiber possesses low density (1.40 g/cc) and high cellulose content (59.4%), which fosters compatibility between the matrix and resin. XRD analysis indicates a high crystallinity index (83.47%) and crystallite size (6.4 nm), showcasing exceptional crystalline behavior. Treated fibers exhibit improved tensile strength (198 MPa) and Young's modulus (4.40 GPa) compared to untreated fibers (tensile strength-92 MPa, tensile modulus-2.16 GPa). The Tg-DTA thermograms reveal the fiber's thermal resistance up to 240 °C with a kinetic activation energy between 62.80-63.46 KJ/mol. Additionally, the lowered thermal conductivity (K) from Lee's disc experiment suggests that BP fiber could be used in insulation applications. SEM photographic results display effective surface roughness for composite making, and FTIR studies reveal vibrational variations of cellulosic functional groups, which correlates with increased cellulosic behavior. Overall, the study affirms the potential of BP fiber as a reinforcing material for composite-making while emphasizing the importance of utilizing biodegradable materials for sustainability.

Analysis of changes on substrates filling constructed wetland systems after landfill leachate treatment - FTIR study

A rapid and inexpensive method, Fourier transform infrared spectroscopy (FTIR), can be used to identify impurities and determine the functional groups responsible for the sorption of specific ions. The FTIR method has already been used in research. However, there is a lack of research on constructed wetland (CW) infill materials used to treat landfill leachate (LL). Therefore, the aim of this study was to verify the changes occurring in selected substrates (zeolite, expanded clay and bark) constituting vertical flow CW infill (VFCW) supplied with municipal LL. The principal component analysis carried out mainly showed differences in the results between the variants of the experiment with an infill of expanded clay and the others (for the values obtained at wave numbers in the range 1600-400 cm−1, in which most changes occurred). All peaks of the FTIR spectra of the pine bark filling the CW differ in location and intensity between the samples. In most cases, the stripes were elongated at exposure to 25% and 100% LL (compared to tap water). In all CW variants infill made of zeolite, peaks occurred at wave numbers within 1049-1012 cm−1, which were most likely caused by the presence of inorganic substances corresponding to clay minerals, and to silica. The FTIR spectra for zeolites, do not show large differences between the different infill samples used for LL treatment (100% LL and 25% LL). In all CW variants with expanded clay infill, peaks in the 1250-900 cm−1 wave number region, possibly indicating the presence of polysaccharides and phosphodiesters. FTIR spectroscopy has proven to be a very useful tool for rapid grade assessment determination of changes occurring on selected substrates and the identification of contaminants that remained after treatment in VFCWs fed with LL.

Preparation and characterization of naproxen solid dispersion using different hydrophilic carriers and in-vivo evaluation of its analgesic activity in mice

BackgroundSolid dispersion (SD) has been used conventionally as a successful technique for improving the dissolution profile and bioavailability of poorly water-soluble drugs. The aim of this study was to progress the dissolution rate and bioavailability of naproxen (BCS class II) by SD technique. Materials & methodsIn this study, hydrophilic carriers are used for preparing solid dispersion of naproxen by evaporation method. The prepared optimized SDNs were evaluated by in-vitro drug dissolution test, differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), powder X-ray diffraction (PXRD), and scanning electron microscopy (SEM). The in-vivo analgesic effects tests of the optimized SDNs (SDN-2 and SDN-5) were performed by tail immersion method and writhing method. ResultsAll the prepared SDNs exhibited a significant increase in the dissolution of naproxen compared to that of the pure drug. Among them, SDN-2 (the dispersion with sodium starch glycolate at 1:2 ratio of naproxen and sodium starch glycolate) and SDN-5 (using the combination of PEG-8000 and sodium starch glycolate with naproxen at 1:1:1 ratio) showed faster dissolution rate as compared to other solid dispersions (SDNs) and pure naproxen. SDN-2 showed 5.4 times better dissolution rate and SDN-5 depicted 6.5-fold increment of dissolution rate compared to pure naproxen drug. DSC, PXRD and SEM microscopy showed that the drugs crystallinity was decreased during the preparation process. FTIR study revealed that naproxen was stable in polymeric dispersions and there was no interaction among the drug and polymers. In writhing method, the percentage inhibition of the number of writhes showed significantly greater (p < 0.01), (p < 0.0001) analgesic activity for the higher dose treatment groups SDN-2(H), and SDN-5(H), respectively, when contrasted to the pure drug naproxen. For tail immersion test, there is increase in latency time at 90 min which is significantly greater (P < 0.01), (P < 0.05), (P < 0.01) for treatment groups SDN-2(H), SDN-5(L), and SDN-5(H), respectively that ultimately authenticates that the optimized SDNs (SDN-2, SDN-5) showed better analgesic activity in mice in comparison with the pure drug. ConclusionIt can be concluded that dissolution of the naproxen could be improved by the making solid dispersion using sodium starch glycolate and/or combination of sodium starch glycolate and PEG 8000 due to the complete transformation of drug into amorphous form with the entire loss of crystallinity, as evidenced by DSC, PXRD, and SEM and also consequences the enhanced analgesic activity in mice.

Flame-retardant hybrid composite manufacturing through reinforcing lignocellulosic and carbon fibers reinforced with epoxy resin (F@LC)

Novel flame retardant hybrid composites were developed from lignocellulosic and carbon fibers reinforced with epoxy resin using hot pressing technology. The size of the lignocellulosic fibers was within 0.045 to 0.8 mm, and the carbon fibers ranged from 5 to 8 mm. The nominal thickness of the composites was 10 mm, whereas the nominal density was 730 kg/m3. The composite dimensions were 400 × 400 mm2. The developed panels were tested for internal bonding strength and flexural properties to investigate their mechanical performance. Furthermore, SEM (Scanning electron microscopy) test was conducted to examine the morphologies of the products before and after fracture and found substantial quantities of both types of fiber in the composite system. The EDX (Energy disruptive X-ray) analysis also displayed the chemical elements present in the developed products. Moreover, an FTIR (Fourier transform infrared spectroscopy) study showed strong chemical interactions among the lignocellulosic and carbon fibers with the thermosetting epoxy polymers. The flame retardancy tests of the composite materials also showed significant thermal stability, especially after loading carbon fibers in the composite system. Moreover, dimensional stability showed an improving trend with the increase of carbon fibers as the reinforcement. Overall, the composite materials developed using lignocellulosic and carbon fibers with epoxy resin are showing a novel route to develop composites with high mechanical performance and considerable flame retardancy.Graphical abstract

Application of 3&lt;sup&gt;2&lt;/sup&gt; Factorial Design in Formulation and Evaluation of Olmesartan Medoxomil Floating Microsponges

The goal of the research was to formulate floating microsponges of Olmesartan medoxomil by 3² factorial design to enhance bioavailability in the gastric region. The quasi-emulsion solvent diffusion method was used to prepare gastroretentive floating microsponges. In this study, the concentration of Eudragit L-100 (X₁) and the concentration of polyvinyl alcohol (PVA) (X₂) were chosen as independent factors at three distinct levels using Design-Expert® software (trial version 13.1.0, Stat-Ease). The dependent variables chosen were the % Buoyancy (Y₁) and % cumulative drug release (Y₂). The percent yield, particle size, bulk density, % buoyancy, % entrapment efficiency, in vitro drug release, the kinetics of drug release, variation of the model, Fourier Transform Infrared Spectroscopy (FTIR) studies, and stability studies for the optimized formulation were conducted. From the design expert, the optimized formula was found to be OLM-MSG7. The magnitude of the coefficient of both X₁ and X₂ showed a positive effect on the buoyancy of the floating microsponges. As the concentration of eudragit L-100, the buoyancy of the microsponges increased. The reason for the buoyancy due to the high concentration of eudragit L-100 may be attributed to the low density of the polymer. However, an antagonistic linear effect of PVA was observed. X₁ and X₂ i.e., polymer concentration and PVA had a positive effect on % CDR of microsponges which indicates that the higher amount of eudragit L-100 contributes to an increase in % CDR. FTIR studies show there is no chemical interaction between the drug and the polymer in the formulation.

Competent antioxidant and antiglycation properties of zinc oxide nanoparticles (ZnO-NPs) phyto-fabricated from aqueous leaf extract of Boerhaavia erecta L.

During the present century, plant-based zinc oxide nanoparticles (ZnO-NPs) are exploited extensively for their vast biological properties due to their unique characteristic features and eco-friendly nature. Diabetes is one of the fast-growing human diseases/abnormalities worldwide, and the need for new/ novel antiglycation products is the need of the hour. The study deals with the phyto-fabrication of ZnO-NPs from Boerhaavia erecta, a medicinally important plant, and to evaluate their antioxidant and antiglycation ability in vitro. UV-visible spectroscopy (UV-Vis), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS) were used to characterize the phyto-fabricated ZnO-NPs. The characterization of nanoparticles revealed that the particles showed an absorption peak at 362nm and band gap energy of 3.2eV, approximately 20.55nm in size, with a ZnO elemental purity of 96.61%. The synthesized particles were found agglomerated when observed under SEM, and the FT-IR studies proved that the phyto-constituents of the extract involved during the different stages (reduction, capping, and stabilization) of nanoparticles synthesis. The antioxidant and metal chelating activities confirmed that ZnO-NPs could inhibit the free radicals generated, which was dose-dependent with an IC50 value between 1.81 and 1.94mgmL-1, respectively. In addition, the phyto-fabricated nanoparticles blocked the formation of advanced glycation end products (AGEs) as noticed through inhibition of Amadori products, trapping of reactive dicarbonyl intermediate and breaking the cross-link of glycated protein. It was also noted that the phyto-fabricated ZnO-NPs significantly prevented the damage of red blood corpuscles (RBCs) induced by MGO. The present study's findings will provide an experimental basis for exploring ZnO-NPs in diabetes-related complications.