Fourier Transform Infrared Spectroscopy Analysis Research Articles

The Release of Bound Phenolics to Enhance the Antioxidant Activity of Cornmeal by Liquid Fermentation with Bacillus subtilis

This study investigated the influence of Bacillus subtilis fermentation on the composition of phenolic substances and antioxidant activity in cornmeal. The results indicate that the fermentation process significantly increased both the total phenolic content (TPC) and total flavonoid content (TFC). After 5 days of fermentation, the TPC rose from 31.68 ± 1.72 mg/g to 39.46 ± 2.95 mg/g, representing a 24.56% increase, while the TFC increased from 2.13 ± 0.11 mg/g to 7.56 ± 0.29 mg/g, marking a 254.93% increase. Additionally, the proportion of free phenolic compounds in cornmeal increased from 20.24% to 83.98%, while the proportion of bound phenolic compounds decreased from 79.76% to 16.02%. Furthermore, the hydrolytic enzyme activities of cellulase, β-glucosidase, and xylanase were significantly correlated with the free phenolic content (FPC) (r > 0.85, p < 0.05), indicating their crucial role in releasing free phenolic compounds from cornmeal. Employing scanning electron microscopy, differential scanning calorimetry, X-ray diffraction, and Fourier-transform infrared spectroscopy analyses, we inferred that the carbohydrase enzymes produced by the microorganisms disrupted the cellular structure of cornmeal and weakened the interactions between bound phenolics and the food matrix, thereby facilitating the release of phenolic compounds. This release resulted in an overall increase in the antioxidant activity of the cornmeal. The study provided a novel approach to enhancing the bioavailability of phenolic acids in cornmeal, indicating the potential benefits of fermentation in food processing.

FTIR Spectroscopic Analysis of Plant Proteins and Correlation with Functional Properties.

Development of plant-based products faces challenges like raw material standardization and time-consuming functionality measurements. Fourier Transform Infrared (FTIR) spectroscopy provides a quick, non-destructive way to analyze protein molecular characteristics. This study explored the classification capability of FTIR in analyzing five plant protein isolates-soy, mung bean, pea, fava bean, and lentil-and assessed its predictive ability for functional property measurement such as water absorption capacity (WAC), oil absorption capacity (OAC), Solubility (SOL), foaming, and emulsification. Functional properties were calculated using traditional methods of measurements. Principal Component Analysis (PCA) and Partial Least Square (PLS) Regression Analysis were used to study FTIR spectra and its correlation with functional properties. PCA revealed distinct clusters for each protein source based on their FTIR spectra, indicating molecular differences. WAC and OAC prediction models showed strong correlations, with prediction correlation coefficients (Rp) of more than 0.99 and cross-validation correlation coefficients (Rcv) ranging from 0.85 to 0.92. As sample size increases, SOL, emulsifying, and foaming properties display promising potential. Moreover, WAC and OAC predictions exhibited robust results with protein blends of various ratios. The expanded WAC model predicted with an Rp of 0.99 and an Rcv of 0.95, while the expanded OAC model had an Rp of 0.99 and an Rcv of 0.84. The results underscore FTIR has the potential to identify plant proteins aiding in raw material verification and quality control as well as being an alternative to analyzing functional properties of plant proteins.

Physical and Structural Properties of Chitosan–Squid Gelatin Hydrogels

The development of functional hydrogels is currently receiving great attention. In this study, a squid by-product, gelatin (SG)–acetic acid solution, was added to a commercial chitosan (CH)–acetic acid solution to develop an antioxidant hydrogel. The CH–SG mass ratios evaluated were 1:0, 2:1, and 1:2. Glutaraldehyde was used as cross linker. The effects of the SG addition to the hydrogel on different properties (physical in general, stability in aqueous media at pH 7.2, swelling, textural profile, and antioxidant) were evaluated. The interaction of CH and SG was established by scanning electron microscope microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), and nuclear magnetic resonance spectroscopy (NMR). As a result, the addition of SG decreased the resistance to flow, hardness, chewiness, and stability, but increased the springiness, resilience, and antioxidant properties of CH hydrogels. The SEM analysis revealed that the CH-GS hydrogel showed a relatively more porous structure. FTIR and NMR analyses suggested a good compatibility of the components due mainly to an increased hydrogen bond formation. The present results suggest that CH could establish a valuable interaction with SG, so that a new hydrogel with enhanced textural and antioxidant properties would be produced, which would enable its potential application in biomedical and food industries.

Development of a natural rubber latex-based biodevice with mesenchymal stem cells as a potential treatment for skeletal muscle regeneration in gestational diabetes-induced myopathy.

Women with gestational diabetes mellitus show a high risk of developing Gestational Diabetes Induced Myopathy (GDiM). GDiM is characterized by significant pelvic floor skeletal muscle atrophy and urinary incontinence. This study aimed to develop a natural rubber latex (NRL) based biodevice with mesenchymal/stromal stem cells (MSCs) for skeletal muscle regeneration for women with GDiM. NRL showed porosity, roughness, biocompatibility, and bioactivity. MSCs adhesion on the NRL scaffold surface was assessed by scanning electron microscopy (SEM), confocal microscopy, and zymography. The scaffold's physicochemical and biological properties were carried out by Fourier transform infrared spectroscopy (FTIR), swelling and degradation studies, hemolytic activity, and antioxidant activity (AA), using Electronic Paramagnetic Resonance (EPR). MSCs in culture expressed CD90, adhered to plastic, differentiated, and produced fibroblast colonies. A high rate of cell proliferation was seen in MSCs on the NRL scaffold. FTIR analysis confirmed protein structures and polyisoprene in the scaffold. Swelling and degradation showed low water uptake and weight loss. Furthermore, NRL presented a hemolytic rate of 2.90±0.26% for 24h, and EPR revealed the scaffold's strong AA. The generated biodevice has potential for muscle regeneration and may be useful as a therapeutic option for skeletal muscle disorders in GDiM or urinary incontinence.

Effect on N release by urea coating with chitosan, starch and urease inhibitor.

Food production often relies on nitrogen fertilizers, which can harm the environment when dispersed in agroecosystems. A new urea coating additive, made from chitosan, starch, and N-(n-butyl) thiophosphoric triamide (a urease inhibitor), has been developed to mitigate these effects. The additive was tested for its impact on ammonium (NH4) production and urea release in water, characterized using Fourier transform infrared spectroscopy (FTIR), and subjected to bioassays on lettuce and rocket. The additive decreased the urea release rate in water by 12 %, as predicted by the Korsmeyer and Peppas model, indicating Fickian diffusion controlled by concentration gradients. FTIR analysis revealed that the interaction between chitosan's amine groups and urea's hydroxyl groups slowed the release. In lettuce and rocket, the additive enhanced root development, increasing surface area by 97 %, root volume by 100 %, and thin and thick root growth by 65 % and 131 %, respectively. After 24 h, the fertilizer produced less ammonium when in contact with urease. The production cost of this fertilizer was only 20 % higher than conventional fertilizers, showing that applying NBPT, starch, and chitosan to urea can reduce waste and improve key aspects of sustainable food production.

Green chemistry approach to corrosion control: parthenium hysterophorus extract as an inhibitor for AZ31 alloys

Purpose The purpose of this study is to develop a green corrosion inhibitor (GCI) from the parthenium hysterophorus (PHS) leaf and identifying its efficiency in corrosion inhibition of AZ31 alloy. Design/methodology/approach GCI from PHS leaf is extracted with the aid of Soxhlet apparatus and analysed through Fourier transform infrared spectroscopy (FTIR) and phytochemical tests to identify the functional groups and chemical compounds present. Inhibition efficiency (IE) of PHS extract is identified through polarization analysis and immersion tests in which concentration of PHS extract (0–300 ppm) and temperature (303–353 K) is varied. Findings Maximum IE of 84% is exhibited by the prepared PHS extract at a concentration of 250 ppm at 303 K and further addition diminishes IE. The developed GCI is found effective in room temperature (303 K) as it exhibits lower IE when temperature increased. Both physical and chemical absorption mechanisms were identified for PHS extract over AZ31 surface, whereas FTIR and SEM analysis confirms the development of passivation layer. Originality/value Development of GCI from the leaf of a weed (PHS) that disturbs the ecosystem and identifying its efficiency in preventing corrosion of AZ31 under saline environment.

Phytochemical analysis and antioxidant activities of Indigofera oblongifolia, local plant extract used in traditional medicine: Antimalarial activities

The use of eco-friendly natural products is one of the major areas of research that has anticoccidial properties.This investigation aims to identify and evaluate the bioactive constituents of the Indigofera oblongifolialeaf extract (IOLE), as an antimalarial. Fourier Transform Infrared Spectroscopy (FTIR) was used to determine any significant information about the functional groups, as well as assays for total phenolics, tannins, total flavonoids, DPPH, ABTS tests, XRD, and UV-VIS Spectroscopic analysis. The results of FTIR analysis of the extract showed the presence of 5 phytochemical compounds. Moreover, the quantitative analysis revealed that the concentrations of phenols, tannins, and flavonoids were, 219.106±1.0792, 89.438±0.1599, and 19±0.1500 (mg TAE/g DW), respectively. The results obtained indicate that these extracts have a high level of antioxidant activity and the scavenging activity of DPPH radicals. The UV-VIS showed varying absorbances between 300 and 800 nm. The IOLE proved effective against Plasmodium berghei in mice.

Preparation and Properties of Epoxy Modified Acrylic Polymer

This paper describes the synthesis of a viscosity-reducing agent using butyl acrylate (BA), ethyl methacrylate (EMA), acrylic acid (AA) and N-hydroxymethylacrylamide (N-MAM) monomers through emulsion polymerization. A series of viscosity-reducing agents were developed by incorporating varying amounts of glycidyl methacrylate (GMA) monomers. The reaction mechanism of epoxy acrylate viscosity reducer was analyzed by Fourier transform infrared spectroscopy (FTIR). Additionally, the particle size and Zeta potential were used to analyze the stability of the polymer and the difference in the polymer after adding GMA monomer. Thermogravimetric (TG) analysis indicated a significant improvement in the thermal stability of the resin due to GMA modification. The viscosity reduction test results demonstrated a substantial decrease in the viscosity of heavy oil, along with a notable increase in the viscosity reduction rate. The FTIR analysis results confirmed that GMA successfully introduced polyacrylate molecular chains. Furthermore, particle size and Zeta potential measurements showed that the average particle size of the emulsion increased from 132 nm to 187 nm, while the Zeta potential changed from −43 mV to −40 mV with the addition of 15% GMA. Compared with W0, the final thermal degradation temperature of W15 increased from 450 °C to 517 °C. When the GMA content reached 15 wt%, the maximum weight loss temperature increased by approximately 12 °C compared to the sample without GMA. Specifically, adding 8% W15 epoxy acrylate resulted in an 89% viscosity reduction rate for heavy oil, demonstrating an excellent viscosity reduction effect. This study successfully developed a novel epoxy acrylate viscosity reducer using a simple synthesis method, showcasing excellent stability, cost-effectiveness and remarkable viscosity reduction.

The Effect of Applying Treatment Sludge and Vermicompost to Soil on the Biodegradability of Poly(lactic acid) and Poly(3-Hydroxybutyrate)

In this study, the biodegradability of poly(lactic acid) (PLA), the most widely produced bioplastic, and poly(3-hydroxybutyrate) (PHB), known for its very biodegradability, was investigated in soil and soil amended with nitrogen sources, such as treatment sludge and vermicompost. Biodegradability was evaluated over 180 days by measuring the amount of carbon dioxide (CO2) and analyzing samples with scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). PLA showed a low biodegradation (6%) in soil, but this increased to 40% in soil amended with treatment sludge and 45% in soil amended with vermicompost. PHB completely degraded within 90 days in soil; however, this process extended to 120 days in soil amended with vermicompost and 150 days in soil amended with treatment sludge. The organic and microbial content of the amendments enhanced PLA biodegradation, while PHB degradation slowed after 50 days as microorganisms prioritized other organic matter. SEM and FTIR analyses after 60 days showed more intense degradation of both bioplastics in soil amended with vermicompost. These findings highlight the potential of treatment sludge and vermicompost for improving bioplastic degradation, contributing to sustainable waste management and soil enhancement.

Synthesis and Optimization of Snake Fruit Peel Ash-Derived Silica for Iron (Fe) Removal from Batik Wastewater

The byproduct of the batik industry is a liquid waste containing heavy metals like iron (Fe) which can be harmful to the environment and aquatic ecosystems. The aim of this study is to synthesize and optimize silica derived from snake fruit peel ash as an adsorbent for iron (Fe) in the liquid waste of the batik industry. Snake fruit peel is often overlooked as waste and is identified to have a high silica content. The research method was carried out in the calcination process at a temperature of 650°C for 1 hour to convert and change the snake fruit peel powder into ash, then extracted using a 2M HCl solution. The final stage of silica synthesis is drying and grinding. The Silica characterization was analyzed using the FTIR (Fourier Transform Infrared Spectroscopy) and Surface Area Analyzer (SAA) tests. The metal content in the waste was analyzed with AAS (Atomic Absorption Spectrometer). The results showed that the silica from snake fruit peel ash contains silica constituent groups, namely silanol (Si-OH), as an active site for the adsorption process. The surface area of the silica is around 56.347 m2/g, the total pore volume is about 0.0193 cc/g, and the average pore diameter is approximately 26.6745 mm. The application test on batik liquid waste showed a decrease in Fe concentration from 0.487 mg/L to 0.343 mg/L at contact time of 60 minutes. This research proves that silica from snake fruit peel ash offers an innovative and sustainable solution for the treatment of batik industry liquid waste and in other liquid waste processing.

Anti-Cancer Efficacy of Acacia nilotica Nanoparticles: Apoptosis Induction and Tumor Regression in a DMBA-induced Breast Cancer Rat Model

Background Breast cancer remains a significant global health burden despite advancements in treatment. While conventional therapies often induce adverse effects, there is growing interest in exploring natural alternatives. Acacia nilotica, a traditionally used medicinal plant, has shown promise in cancer management. Purpose This study investigated the therapeutic potential of A. nilotica extract and nanoparticles against 7,12-dimethylbenz[a]anthracene (DMBA)-induced breast cancer in albino rats. Methods The formation of A. nilotica crude solution and nanoparticles was done and characterized via dynamic light scattering (DLS) and Fourier-transform infrared spectroscopy (FTIR). A total of 60 female Wistar albino rats were divided into six groups (10 rats/group) and received care in compliance with the state authorities following the Saudi Arabian rules of animal protection. The animals in the first group were given distilled water, while those in the second group were administered DMBA (50 mg/kg). The third and fourth groups were treated with 10 mg/kg of the A. nilotica crude solution and nanoparticles, respectively. In the fifth and sixth groups, A. nilotica crude solution and nanoparticles were administered with 10 mg/kg after DMBA-induced breast cancer in rats, respectively. After sacrificing the rats, the blood and breast tissues were collected from each rat and processed for histological and apoptotic markers analyses. Results Our findings indicated that the average size of nanoparticles was 162.5 nm in diameter with 0.145 as a polydispersity index (PDI). Functional groups were confirmed via FTIR analysis for A. nilotica crude solution and nanoparticles. Histopathological analysis revealed a marked reduction in tumor size and cellular proliferation in nanoparticle-treated groups. Our data demonstrated that both formulations significantly inhibited tumor growth and induced apoptosis, as evidenced by altered Bcl-2 and BAX expression. Conclusion These findings suggest that A. nilotica nanoparticles warrant further investigation as a potential therapeutic strategy for breast cancer.

Evaluation of Heavy Metal Content in Plastic Bags Used as Improvised Food Cooking Covers: A Case Study from the Mozambican Community

The widespread use of plastic bags as improvised food cooking covers in Mozambican communities has raised public health concerns, increasing interest in studying these plastic bags, which contain heavy metals additives used to improve their physical and chemical properties. This study aims to evaluate the levels of heavy metals commonly used in plastic bags used as improvised food cooking covers, focused on Mozambican communities that have this habit. Using spectroscopic techniques, Fourier Transform Infrared Spectroscopy (FTIR) and Atomic Absorption Spectroscopy (AAS), we analyzed plastic bag samples to identify polymer types, chemical composition, and heavy metal concentrations. FTIR analysis confirmed low- and high-density polyethylene (LDPE and HDPE) as the primary materials, with spectra peaks between 2800 and 3000 cm−1, indicating stretching vibrations characteristic of LDPE and HDPE. The density measurements varied between 0.04 and 0.08 g/cm3 with very low uncertainty values (0.27% and 0.098%). The heavy metal analysis revealed concentrations higher than those stipulated in international standards. The results in terms of the percentage of LDPE samples in relation to the HDPE samples are as follows: Cd: 69.71% (LDPE < HDPE); Cu: 220.44% (LDPE > HDPE); Pb: 24% (LDPE < HDPE); and Zn: 51.53% (LDPE < HDPE). These findings highlight the potential public health risks associated with the use of plastic bags in cooking and underscore the need for regulatory intervention.

The Effect of Silver Diamine Fluoride Combined with Potassium Iodide and Sodium Fluoride on the Remineralisation of Hydroxyapatite.

To compare remineralisation efficacy between silver diamine fluoride (SDF) combined with potassium iodide (KI) and sodium fluoride (NaF) varnish using hydroxyapatite (HAP) artificial white spot lesions (AWSLs) demineralisation model. A total of 25 HAP disks was randomly divided into five groups (n = 5): baseline, AWSLs, deionized water (DW), SDF-KI or F-varnish. After AWSLs were developed, the specimen was treated with either deionized water, SDF-KI or F-varnish. These specimens were then subjected to pH-cycling for 7 days. The remineralisation potential was assessed by measuring changes in Vickers hardness (VHN). Morphological and compositional analyses were conducted using scanning electron microscopy (SEM), energy dispersive x-ray (EDX), x-ray diffraction (XRD), and Fourier-transform infrared spectroscopy (FTIR). Ion-selective electrodes (ISE) were utilised to measure calcium and fluoride release. SDF-KI treatment demonstrated statistically significant remineralisation potential in restoring VHN values vs baseline levels (p 0.001). SEM, EDX, and XRD analyses confirmed the mineral deposits to indicate remineralisation. The uptake of calcium was higher in SDF-KI than in F-varnish (p = 0.011). The fluorapatite (FAP) and fluoride-substituted apatite formation were validated by FTIR and XRD analyses. SDF-KI and F-varnish applications are both effective in promoting remineralisation on HAP disks. The application of SDF-KI affected the physicochemical and mechanical properties of demineralised HAP. The SDF-KI showed more formation of fluoride-substituted apatite and is effective in the hardening of demineralised HAP.

Remote Activation Catalysis: Interparticle Hydrogen Spillover-Assisted Cumene Synthesis from Propane and Benzene.

Hydrogen spillover, particularly when involving "interparticle" hydrogen spillover, offers a unique opportunity to enhance catalytic efficiency by remote activation of surface acidity. Building on this concept, this study aims to investigate physically mixed alumina-supported platinum nanoparticles (Pt/Al2O3) and zirconia-supported tungsten oxide (WO3/ZrO2) in promoting the direct synthesis of cumene from benzene and propane at 300 °C. The reaction with Pt/Al2O3 alone afforded propylene as the only product, indicating the successive reaction route of Pt-catalyzed dehydrogenation of propane, followed by acid-catalyzed alkylation. WO3/ZrO2 with 18 wt.% WO3 loading resulted in high benzene conversion (≈5.0%) and cumene selectivity (≈87.5%), which possesses poly tungstate species on the surface that is active for the acid-catalyzed alkylation. UV-vis-near infrared spectroscopy, X-ray photoelectron spectroscopy, and in situ Fourier-transform infrared spectroscopy analyses revealed that atomic hydrogen abstracted from propane spills over from Pt/Al2O3 particles to WO3/ZrO2 particles to form Brønsted acid sites on the poly tungstate species, whose activity for alkylation between benzene and propylene is double that of the parent WO3/ZrO2.

Characterization of Microcapsules Obtained from Lemon Balm Extract (Melissa officinalis L.) by the Ionic Gelation Process.

The plant specie, lemon balm (Melissa officinalis L.) is one of the most important species of the Lamiaceae family and its use as a plant extract has been highlighted by the population and the scientific community due to its rich chemical composition and the presence of bioactive compounds with potential antioxidant activity, associated with various health benefits. Research and development of innovative technologies are focused on the identification of these substances, their properties and applications. The present study aimed to select a type of lemon balm extract based on its bioactive compounds and antioxidant potential, obtained from lemon balm microcapsules through the ionic gelation process and evaluate the physicochemical changes and the profile of the volatile compounds. The extract obtained from the fresh plant sample infused at 80°C showed a higher content of bioactive compounds. Fourier Transform Infrared Spectroscopy analysis revealed similar spectra between the samples. Terpenes and terpenoids were the predominant class of compounds, with compounds such as (E)-citral and caryophyllene being the major compounds in both the fresh lemon balm sample and the microcapsules. The results were satisfactory in the preservation of aroma and volatile compounds through the microencapsulation process by ionic gelation.

An aqueous, paper, and gel-based method by using eco-friendly synthesised silver nanoparticles towards rapid colorimetric sensing of palladium ion

ABSTRACT In this study, developments were made for silver nanoparticles (AgNPs) synthesis as a colorimetric sensor that is rapid and selective using a bio-reductant of lemongrass extract. The synthesised AgNPs were designed to detect Pd2+ using aqueous, paper, and gel methods. AgNPs were characterised by UV-Vis, FTIR (Fourier Transform Infrared), TEM (Transmission Electron Microscopy), and XRD spectroscopic analysis (X-Ray Diffraction). These AgNPs aqueous colorimetric sensors showed a good selectivity towards Pd metal ions, which was characterised by AgNPs SPR (Surface Plasmon Resonance) tape shifts at 430 nm wavelengths, with the colour change from dark yellow to clear greyish within 5 seconds. The colour changed from yellow to white for AgNPs paper and dark yellow to bright yellow for the gel colorimetric sensor after 5 seconds interaction with Pd2+. The limit of detection for aqueous, paper, and gel were 48.635 ppb, 5 ppm and 5 ppm, respectively. Method validation has been conducted, and these AgNPs sensors were applied for monitoring the Lake Sasak, South Tangerang, water samples and the accuracy and precision of the sensor were tested. This sensor is expected to establish an alternative technique for in situ Pd2+ detection and lake water monitoring.

"Theory of Pore Conflation" and "Shubhjyot's equation" in the treatment of Brilliant green dye-contaminated water using Jamun leaves biochar

This study investigates the adsorption of Brilliant Green (BG) dye onto biochar derived from Syzygium cumini (Jamun) leaves (JLB). Biochar was produced via pyrolysis at 800 °C and examined employing various methods, including Scanning electron microscopy (SEM–EDX), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) analysis, Raman spectroscopy, Zeta potential and X-ray photoelectron spectroscopy (XPS). The optimum parameters for BG dye adsorption, determined by batch adsorption studies, were a temperature of 80 °C, an initial dye concentration of 500 mg L−1, a contact period of 30 min, and an agitation speed of 400 RPM. The maximum adsorption capacity of JLB for BG was 243.90 mg g−1. It was found that the adsorption process adhered to the Freundlich isotherm model and pseudo-second-order kinetics, revealing heterogeneous adsorption with chemisorption. A novel "Theory of Pore Conflation" was proposed to explain enhanced adsorption at higher temperatures, supported by SEM and FTIR analyses. Additionally, a new equation termed "Shubhjyot's equation" was introduced to account for time dependency in adsorption capacity calculations. The thermodynamic analysis demonstrated that the process is endothermic and spontaneous. Isopropanol was the most effective organic solvent for desorption studies, demonstrating biochar regeneration potential for up to five cycles. Phytotoxicity and cyto-genotoxicity assessments demonstrated the environmental safety of JLB compared to BG dye. The use of JLB production offers a way to repurpose agricultural waste, contributing to circular economy principles. This extensive study demonstrates JLB's promise as an effective, economical, and environmentally safe adsorbent for wastewater treatment that eliminates textile dyes.Graphical

Characterization, Bioactive Profiling and Evaluation of the Pharmacological Activities of Ethanol Extract of Lannea welwitschii (Hiern) Engl.

Introduction: Lannea welwitschii is a medicinal plant used in traditional medicine to treat various infectious diseases due to its plethora of bioactive compounds that possess various pharmacological activities. This study aimed to characterize and determine the phytochemical profile and the bioactive compounds responsible for their pharmacological activities. Methods: Phytochemical screening and Gas-Chromatography Mass Spectrometry (GC-MS) analysis were carried out on the ethanolic extract of L. welwitschii to determine the volatile compounds present. Characterization of the crude extract was carried out using Fourier Transform Infrared spectroscopy (FTIR), Scanning Electron Microscopy (SEM), X-ray diffraction (XRD) and Energy Dispersive X-ray spectroscopy (EDX). The antioxidant potential of the extract was evaluated using methods such as 2,2-diphenyl-1-picrylhydrazyl (DPPH) and ferric-reducing antioxidant Potential (FRAP). The antibacterial activities were determined using the macro-broth dilution technique. Results: Secondary metabolites such as saponins, tannins, alkaloids, reducing sugars, and cardiac glycoside were identified. The GC-MS analysis showed the presence of 48 bioactive compounds, out of which 12 had peak area percentages ≥ 1%. Some of the bioactive compounds identified include 2-butoxy-ethanol, Dodecanoic acid, Stigmasterol, Isopropenyl, and n-hexadecanoic acid, which have been reported with different biological activities. FTIR analysis revealed the presence of various functional groups which showed major compounds in the plant extract. The morphological features showed the spherical shape of the plant extract with several aggregates, while the EDX analysis identified elements such as silicon, oxygen, and silver. The extract demonstrated inhibitory potential against some of the bacterial isolates. However, Bacillus pumilus, Klebsiella quasipneumoniae, Klebsiella aerogenes, and Staphylococcus aureus are more susceptible with MIC of 0.313 and 0.625 mg/ml respectively. Conclusion: The presence of secondary metabolites and bioactive compounds revealed by the characterization and phytochemical analysis provided enough evidence for the usage of the plant in the treatment of infectious diseases and thus might be considered a therapeutic agent.

Fourier Transform Infrared Spectroscopy Analysis as a Tool to Address Aβ Impact on Extracellular Vesicles.

Alzheimer's disease is a challenge in modern healthcare due to its complex etiology and increasing prevalence. Despite advances, further understanding of Alzheimer's disease pathophysiology is needed, particularly the role of Aβ neurotoxic peptide. Fourier transform infrared spectroscopy (FTIR) has shown potential as a screening tool for several pathologies, including Alzheimer's disease. Nonetheless, limited research has explored Aβ direct effects on neurons and extracellular vesicles metabolic profiles. Hence, this study aims to investigate Aβ impact on the spectroscopic profiles of neuronal-like cells (N2a) and N2a-derived extracellular vesicles, employing FTIR spectroscopy and focusing on the 1280-900 cm-1 region. A comprehensive analysis of spectral data was carried out, including multivariate partial least squares (PLS) analysis and peak intensities analysis. PLS analysis revealed moderate to strong correlations within this spectral region for both N2a and N2a-derived extracellular vesicles. The peak intensity analysis revealed additional peaks with significant differences in EVs' spectra relative to N2a, following Aβ treatment. Specifically, Aβ seems to cause alterations in protein phosphorylation and in the nucleic acids content of extracellular vesicles. These findings support that Aβ's role in Alzheimer's disease pathology may be mediated by extracellular vesicles and highlight FTIR's potential for advancing Alzheimer's disease research and clinical applications.

Oxaliplatin-Loaded Chitosan Nanoparticles Decorated with Cetuximab Single-Chain Variable Fragment for Human Colorectal Cancer Treatment.

Colorectal cancer (CRC) is the second leading cause of cancer-related deaths worldwide. Engineered biomolecules can be used as a targeted tool to deliver drugs directly to tumors that reduce the adverse effects of conventional treatments. We aimed to prepare non-targeted oxaliplatin-loaded chitosan nanoparticles (OXPT-CS NPs) and targeted OXPT-CS NPs decorated with cetuximab single-chain variable fragment (scFv) to send both NPs to epidermal growth factor receptor (EGFR) overexpressing HCT 116 cells, a human colorectal carcinoma cell line, for comparing their cytotoxicity. In this experimental study, OXPT-CS NPs were synthesized using a fluid system. Encapsulation efficiency percentage (EE%) and oxaliplatin release rate were evaluated. Western blot and cell-based ELISA confirmed scFv production and its binding ability to EGFR, respectively. The Fourier transform infrared spectroscopy (FTIR) determined the conjugation of scFv to OXPT-CS NPs. The NPs were characterized, and their toxicity against the HCT 116 cells was evaluated using 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide (MTT) and flow cytometry assays. The EE% of OXPT-CS NPs was 93%, and the average diameters were 75.85 ± 8.81 nm and 92.48 ± 9.51 before and after scFv conjugation, respectively. The scFv was purified via affinity chromatography. The western blot method and cell-based ELISA revealed successful purification of scFv and its attachment to EGFR on HCT 116 cells. The FTIR analysis determined the interactions between the scFv and OXPT-CS NPs. According to MTT and flow cytometry results, the targeted delivery system significantly reduced HCT 116 cancer cell viability and increased apoptosis induction up to 99.8%. The scFv-OXPT-CS NPs demonstrated an increased cytotoxic function due to the presence of scFv in its formulation. This delivery system offers a promising method for delivering chemotherapy drugs to cancer cells. More research is needed on the best strategies for improving treatment efficacy by targeting cancer cells.