Attenuated Total Reflectance Fourier Transform Infrared Spectroscopy Research Articles

Electrochemical detection of poly(3-hydroxybutyrate) production from Burkholderia glumae MA13 using a molecularly imprinted polymer-reduced graphene oxide modified electrode.

Thedevelopment and application of an electrochemical sensor is reported fordetection of poly(3-hydroxybutyrate) (P3HB) - a bioplastic derived from agro-industrial residues. To overcome the challenges of molecular imprinting of macromolecules such as P3HB, this study employed methanolysis reaction to break down the P3HB biopolymer chains into methyl 3-hydroxybutyrate (M3HB) monomers. Thereafter, M3HB were employed as the target molecules in the construction of molecularly imprinted sensors. The electrochemical device was then prepared by electropolymerizing a molecularly imprinted poly (indole-3-acetic acid) thin film on a glassy carbon electrode surface modified with reduced graphene oxide (GCE/rGO-MIP) in the presence of M3HB. Electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), scanning electron microscopy with field emission gun (SEM-FEG), Raman spectroscopy, attenuated total reflection Fourier-transform infrared (ATR-FTIR) and X-ray Photoelectron Spectroscopy (XPS) were employed to characterize the electrode surface. Under ideal conditions, the MIP sensor exhibited a wide linear working range of 0.1 - 10nM and a detection limit of 0.3pM (n = 3). The sensor showed good repeatability, selectivity, and stability over time. For the sensor application, the bioproduction of P3HB was carried out in a bioreactor containing the Burkholderia glumae MA13 strain and sugarcane byproducts as a supplementary carbon source. The analyses were validated through recovery assays, yielding recovery values between 102 and 104%. These results indicate that this MIP sensor can present advantages in the monitoring of P3HB during the bioconversion process.

A novel non-aqueous tertiary amine system for low energy CO2 capture developed via molecular dynamics simulation

The current technology for capturing CO2 using alkanolamine aqueous solutions is known for its high energy and capital costs. As a result, developing new absorbents for low-energy CO2 removal remains a challenge. An additional activator can promote CO2 absorption performance. However, it is based on experimental screening. In this study, based on molecular dynamic simulation, we have successfully developed a novel and energy-efficient CO2 absorbent by combining N, N-Dimethylethanolamine (DMEA), and ethylene glycol (EG), with different activators, including ethanolamine (MEA), ethylenediamine (EDA), and piperazine (PZ). The addition of these activators significantly enhances the CO2 absorption performance of DMEA-based absorbents. Among them, DMEA-PZ-EG exhibits the maximum CO2 absorption rate and capacity, achieving 6.35 (g-CO2/(kg-soln.·min.)) and 96.5 (g-CO2/kg-soln.), respectively, representing a 230.1 % and 206.35 % improvement over 2M DMEA-EG absorbent. Moreover, compared to a 30 wt% MEA solution, the energy consumption of DMEA-based absorbents is reduced by 33.93–51.56 %. The reaction products were characterized using various spectroscopic techniques, including Attenuated Total Reflectance Fourier Transform Infrared spectroscopy (ATR-FTIR), and 1D and 2D Nuclear Magnetic Resonance spectroscopy (1H and 13C NMR). The NMR results confirmed that DMEA becomes protonated after CO2 absorption in the DMEA-EG mixture. The deprotonation of EG promote its reaction with CO2, resulting in the forming of EG carbonates. This assumption has been confirmed by the IR spectrum. Furthermore, the effect of activators on CO2 absorption has been analysed at the molecular level through molecular dynamics simulation and a new method is proposed to predict the CO2 absorption performance of non-aqueous solvents. Using non-aqueous DMEA absorbents presents a promising approach for improving CO2 capture efficiency, reducing energy consumption, and facilitating regeneration.

Design, characterizations, and antimicrobial activity of sustainable home furnishing-based waste fabric treated using biobased nanocomposite

Clothing and textile industries are major contributors to environmental pollution including textile manufacturing through garment production, spinning, weaving, and dyeing. In this context, the sustainability textile industry is a big challenge and contributes to serving a large segment of society. Also, textile wastes could be used as a raw material for added-value products. Herein, in this study, recycling of residues fabric was treated with antimicrobial nanocomposite to reach the best use of exhausts and obtain multifunction products of aesthetic via the technical design of the waste raw materials. Besides, solving the unemployment problem by opening fields for small industry projects capable of producing high-value textile artifacts, especially when treated against microbes, can be applied to home furnishings. The waste fabric was treated via green synthesis nanocomposite based on chitosan and in situ prepared ZnONPs and cross-linked with tannic acid. The prepared nanocomposite was characterized using physicochemical analysis including attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) and X-ray diffraction (XRD). Additionally, the nanocomposite and treated fabric topographical behavior were studied using scanning electron microscopy (SEM) attachment with energy dispersive X-ray analysis (EDX), and images were processed to evaluate the roughness structure. Additionally, high-resolution transmission electron microscopy (HR-TEM) and dynamic light scattering (DLS) were performed to ensure the size and stability of the nanocomposite. The obtained results affirmed the green synthesis of nanocomposite with a size around 130 nm, as well as the doped ZnONPs average size of 26 nm and treated waste fabric, performed a promising attraction between nanocomposite and fabric fibers. Moreover, the antimicrobial study observed excellent activity of nanocomposite against bacteria and unicellular fungi as well.

Ga complexes of 8-hydroxyquinoline-2-carboxylic acid: Chemical speciation and biological activity

The binding ability of 8-hydroxyquinoline-2-carboxylic acid (8-HQA) towards Ga3+ has been investigated by ISEH+ (Ion Selective Electrode, glass electrode) potentiometric and UV/Vis spectrophotometric titrations in KCl(aq) at I = 0.2 mol dm−3 and at T = 298.15 K. Further experiments were also performed adopting both the metal (with Fe3+ as competing cation) and ligand-competition approaches (with EDTA as competing ligand). Results gave evidence of the formation of the [Ga(8-HQA)]+, [Ga(8-HQA)(OH)], [Ga(8-HQA)(OH)2]− and [Ga(8-HQA)2]− species, the latter being so far the most stable, as also confirmed by ESI-MS analysis. Experiments were also designed to determine the stability constants of the [Ga(EDTA)]− and [Ga(EDTA)(OH)]2− in the above conditions. Due to the relevance of Ga3+ hydrolysis in aqueous systems, literature data on this topic were collected and critically analyzed, providing equations for the calculation of mononuclear Ga3+ hydrolysis constants at T = 298.15 K, in different ionic media, in the ionic strength range 0 < I / mol dm−3 ≤ 1.0. The synthesis and characterization (by ElectroSpray Ionization – Mass Spectrometry (ESI-MS), Attenuated Total Reflectance - Fourier-Transform Infrared Spectroscopy (ATR-FTIR) and ThermoGravimetric Analysis (TGA)) of Ga3+/8-HQA complexes were also performed, identifying [Ga(8-HQA)2]− as the main isolated species, even in the solid state. Finally, the potential effects of 8-HQA and Ga3+/8-HQA complex towards human microbiota exposed to ionizing radiation were evaluated (namely Actinomyces viscosus, Streptococcus mutans, Streptococcus sobrinus, Pseudomonas putida, Pseudomonas fluorescens and Escherichia coli), as well as their anti-proliferative and anti-inflammatory properties. A radioprotective effect of Ga3+/8-HQA complex was observed on Actinomyces viscosus, while showing a potential radiosensitizing effect against Streptococcus mutans and Streptococcus sobrinus. No cytotoxicity on RAW264.7 murine macrophage cells was observed, neither for the free ligand or Ga3+/8-HQA complex. Nevertheless, Ga3+/8-HQA complex highlighted potential anti-inflammatory properties.

ATR-FTIR spectroscopy imaging of bone repair in mandibular laser-osteotomy.

The aim of this study was to verify the effectiveness of attenuated total reflectance-fourier transform infrared (ATR-FTIR) spectroscopy in the characterization of bone repair in mandibular osteotomy using erbium, chromium-doped yttrium, scandium, gallium and garnet (Er,Cr:YSGG) laser and multilaminate drill on each side. Two mandible bone fragments were removed from 30 rabbits, and the process of bone repair was studied immediately, 3, 7, 15, 21, and 28 days after the surgery. The histological analysis allowed detecting differences in the early stages of tissue repair after bone cutting performed with the Er,Cr:YSGG laser or multilaminate drill. The ATR-FTIR spectroscopy technique was sensitive to changes in the organic content of bone tissue repair process.

Chitosan/Hyaluronate Complex-Coated Electrospun Poly(3-hydroxybutyrate) Materials Containing Extracts from Melissa officinalis and/or Hypericum perforatum with Various Biological Activities: Antioxidant, Antibacterial and In Vitro Anticancer Effects.

The present study aimed to fabricate innovative fibrous materials with various biological activities from poly(3-hydroxybutyrate), sodium hyaluronate (HA), chitosan (Ch), Melissa officinalis (MO), Hypericum perforatum (HP) extract, or a combination of both extracts. Electrospinning or electrospinning followed by dip coating and the subsequent formation of a polyelectrolyte complex were the methods used to prepare these materials. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), and attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR) were applied for investigating the morphology of materials, their thermal characteristics, and their surface chemical composition. The composition and design of the mats had an influence on the in vitro release behavior of the main bioactive compounds present in the MO and HP extracts incorporated in the materials. It was found that as-created materials comprising a combination of both extracts and a Ch/HA complex exerted higher antioxidant activity than that of (non-)coated MO-containing mats and Ch/HA-coated mats containing HP. The novel materials manifested antibacterial efficacy towards the pathogenic bacteria S. aureus and E. coli, as evidenced by the performed microbiological screening. Furthermore, the mats possessed a great growth inhibitory effect on HeLa cancer cells but had a less pronounced effect on the growth of normal mouse BALB/3T3 fibroblasts. The loading of both extracts in the mats and the formation of coating led to the enhancement of the in vitro anticancer and antibacterial activities of the materials. Thus, the novel materials have potential for use in local cancer therapy as well as for use as wound dressings.

Preparation of an anticoagulant polyethersulfone membrane by immobilizing FXa inhibitors with a polydopamine coating

Anticoagulation treatment for patients with high bleeding risk during hemodialysis is challenging. Contact between the dialysis membrane and the blood leads to protein adsorption and activation of the coagulation cascade reaction. Activated coagulation Factor X (FXa) plays a central role in thrombogenesis, but anticoagulant modification of the dialysis membrane is rarely targeted at FXa. In this study, we constructed an anticoagulant membrane using the polydopamine coating method to graft FXa inhibitors (apixaban and rivaroxaban) on the membrane surface. Attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and atomic force microscopy (AFM) were used to characterize the membranes. The apixaban- and rivaroxaban-modified membranes showed lower water contact angles, decreased albumin protein adsorption, and suppressed platelet adhesion and activation compared to the unmodified PES membranes. Moreover, the modified membranes prolonged the blood clotting times in both the intrinsic and extrinsic coagulation pathways and inhibited FXa generation and complement activation, which suggested that the modified membrane enhanced biocompatibility and antithrombotic properties through the inhibition of FXa. Targeting FXa to design antithrombotic HD membranes or other blood contact materials might have great application potential.

Tough Self-Healing Materials via In Situ Growth of Zeolitic Imidazolate Framework-8 Nanocrystals in Polymers.

Construction of self-healing materials with improved mechanical performanceis a great challenge. A strong and tough self-healing composite is fabricated via in situ growth of zeolitic imidazole framework-8 (ZIF-8) nanocrystals in imidazole-containing polymer networks. By adjusting the stoichiometric ratio of the zinc salt to 2-methylimidazole, composites with various mechanical performances are obtained. The existence of ZIF-8 nanocrystals via in situ growth in the polymer networks is confirmed by X-ray diffraction (XRD), transmission electron microscopy (TEM), and atomic force microscopy (AFM). The zinc-imidazole interactions between the ZIF-8 nanocrystals and the polymer are confirmed by attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy. The composites can repair themselves under mild conditions owing to dynamic zinc-imidazole interactions. The self-healing efficiency of composites can reach up to 91% under the condition of 60°C for 48h. In contrast to the pure zinc cation crosslinking system, the composite containing ZIF-8 nanocrystals prepared via in situ growth exhibited enhanced tensile strength and toughness by 43% and 100%, respectively. This study proves that incorporating the metal-organic frameworks(MOFs) materials into a self-healing system via an in situ growth strategy is highly promising for designing self-healing materials with improved mechanical performance.

Effect of wet media milling on starch-quercetin complex: Enhancement of Pickering emulsifying ability and oxidative resistance

This research explored the effect of media milling on complexation of corn starch (CS) and quercetin (QC), interaction mechanism and Pickering emulsifying ability of corn-quercetin (CS-QC) complex. CS-QC with QC/CS ratio of 1:24 had the highest encapsulation efficiency of 76.00 ± 1.30 %. Average volume-mean diameter, average whole molecular size (Rh) and debranchedamylopectinchain length of CS-QC were significantly decreased after milling. Attenuated Total Reflectance-Fourier Transform Infrared spectroscopy (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS) spectra confirmed the complexation between CS and QC. Emulsifying capacity and emulsion stability of Pickering emulsion stabilized by 5 % CS-QC complex particles after 120 min milling reached 100.00 % and 100.00. Pickering emulsions stabilized by these complex particles demonstrated superior oxidative stability. These results demonstrated that media milling could be an efficient physical approach to obtain starch-polyphenol complex by enhancing non-covalent interactions, which could not only be used as food-grade Pickering emulsifiers, but also retard lipid oxidation.

Efficient Phosphate Ions Removal Using Multi-Layered Poly(allylamine hydrochloride)/ Poly(styrene sulfonate) Incorporated Electrospun Cellulose Membrane

Phosphate ion removal in wastewater via nanofiltration is a major challenge in wastewater treatment. In this study, cellulose acetate (CA) incorporated with graphene oxide/ sodium dodecyl sulphate (GO/SDS) and poly(allylamine hydrochloride)/poly(styrene sulfonate) (PAH/PSS) were synthesized using the electrospinning method. The membranes were characterized using attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR), water contact angle, and field emission scanning electron microscope (FESEM). In addition, a multi-layered electrospun cellulose membrane was stacked using a layer-by-layer (LbL) technique to produce a functional ultra-filtration membrane for enhanced phosphate ions removal. The results showed that the modified membranes had better hydrophilicity and lower flux rates as compared to the unmodified membrane. The incorporation of compressed multi-layered for both unmodified and modified membranes also indicated increased phosphate ions removal efficiency up to 18.99 % and 43.08 %, respectively. In addition, post-filtration revealed that phosphate was adsorbed onto the three-layer modified membrane. PAH/PSS-modified CA/GO/SDS membrane is an innovative modification of the cellulose membrane for the phosphate-contaminated water system.

Novel Strategy to Evaluate Platinum Photocatalysts for Hydrosilation-Curable Silicones

UV-activated catalytic hydrosilation is a low-temperature crosslinking process that has attracted attention for its high efficiency and lower energy demand relative to thermal curing. In this study, formulations comprising industrially relevant model silanes and Pt photocatalysts trimethyl(methylcyclopentadienyl)platinum(IV) and trimethyl(pentamethylcyclopentadienyl)platinum(IV) (MeCpPtMe3 and Cp*PtMe3, respectively) were prepared with and without a photosensitizer (PS) and assessed for catalytic performance by a novel strategy. Photopolymerizations were initiated using different wavelengths from LEDs and monitored in real-time using an Attenuated Total Reflectance-Fourier Transform Infrared (ATR-FTIR) “well” strategy to track the degree of cure in ultra-thin films by consumption of hydride via the disappearance of the Si-H bending absorption band at 915 cm−1. Irradiation of formulations with 365 nm excitation showed higher conversions relative to 400 nm light and improvements to calculated initial reaction rates by incorporation of a PS suggested increased sensitization to 365 nm irradiation. To the best of our knowledge, this is the first study to report catalytic performance, electronic absorption spectroscopic data, and the crystal structure of Cp*PtMe3.

Engineering polyvinylidene fluoride membranes using charge tunable dendrimer polyamidoamine to enable microporous membranes for protein separation

Dendrimers are structurally precise molecules, whose peripheral layer provides ample sites for anchoring functional groups of different charges and charge densities. This characteristic renders them capability of providing numerous target functional groups on the surface of filtration membranes when modified by dendrimers. Consequently, there has been a growing interest in dendrimer-modified membranes. In this study, we investigated the engineering of polyvinylidene fluoride (PVDF) membranes using polyamidoamine (PAMAM) dendrimers anchoring different functional groups to tune the charges and charge density of membranes to enable microporous membranes for separation of charged macromolecules. PVDF membranes were functionalized by grafting PAMAM-G3.0 (generation 3) dendrimers with amine groups onto their surfaces and internal surfaces of membrane pores. Subsequently, the peripheral functional groups of dendrimers on the membranes were replaced by carboxyl groups, quaternary ammonium groups, or sulfonic acid groups for charges of different nature and densities. Surface chemical properties, electrical properties, and morphology were characterized using various techniques, including attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and surface zeta potential measurement. The filtration performance of both PVDF and modified membranes was evaluated using polyethylene oxide (PEO), polyacrylic acid (PAA), and whey protein filtration. Among the modified membranes, the G3PA membranes, with carboxyl functional groups, exhibited the most effective whey protein separation performance. The whey protein rejection and permeate flux of the G3PA membranes were 79 % and 30.3 LMH, respectively. As a comparison, the whey protein rejection and permeate flux of the pristine PVDF membranes were 58.9 % and 15.3 LMH, respectively.

PEDOT-Doped Mesoporous Nanocarbon Electrodes for High Capacitive Aqueous Symmetric Supercapacitors.

Poly(3,4-ethylenedioxythiophene) (PEDOT) and PEDOT-functionalized carbon nanoparticles (f-CNPs) were synthesized by in situ chemical oxidative polymerization and pyrolysis methods. f-CNP-PEDOT nanocomposites were prepared by varying the concentration of PEDOT from 1 to 20% by weight (i.e., 1, 2.5, 5, 10, and 20 wt%). Several characterization techniques, such as field-emission scanning electron microscopy (FESEM), attenuated total reflectance-Fourier transform infrared (ATR-FTIR), X-ray diffraction (XRD), N2 Brunauer-Emmett-Teller (BET) and Barrett-Joyner-Halenda (BJH) analyses, as well as cyclic voltammetry (CV), galvanostatic charge discharge (GCD), and electrochemical impedance spectroscopy (EIS), were applied to investigate the morphology, the crystalline structure, the N2 adsorption/desorption capability, as well as the electrochemical properties of these new synthesized nanocomposite materials. FESEM analysis showed that these nanocomposites have defined porous structures, and BET surface area analysis showed that the standalone f-CNP exhibited the largest surface area of 801.6 m2/g, whereas the f-CNP-PEDOT with 20 wt% exhibited the smallest surface area of 116 m2/g. The BJH method showed that the nanocomposites were predominantly mesoporous. CV, GCD, and EIS measurements showed that f-CNP functionalized with 5 wt% PEDOT had a higher capacitive performance compared to the individual f-CNPs and PEDOT constituents, exhibiting an extraordinary specific capacitance of 258.7 F/g, at a current density of 0.25 A/g, due to the combined advantage of enhanced electrochemical activity induced by PEDOT doping, and highly developed porosity of f-CNPs. Symmetric aqueous supercapacitor devices were fabricated using the optimized f-CNP-PEDOT doped with 5 wt% of PEDOT as active material, exhibiting a high capacitance of 96.7 F/g at 1.4 V, holding practically their full charge, after 10,000 charge-discharge cycles at 2 A/g, thus providing the highest electrical electrodes performance. Hereafter, this work paves the way for the potential use of f-CNP-PEDOT nanocomposites in the development of high-energy-density supercapacitors.

Label-Free Electrochemical Dopamine Biosensor Based on Electrospun Nanofibers of Polyaniline/Carbon Nanotube Composites.

The development of conducting polymer incorporated with carbon materials-based electrochemical biosensors has been intensively studied due to their excellent electrical, optical, thermal, physical and chemical properties. In this work, a label-free electrochemical dopamine (DA) biosensor based on polyaniline (PANI) and its aminated derivative, i.e., poly(3-aminobenzylamine) (PABA), composited with functionalized multi-walled carbon nanotubes (f-CNTs), was developed to utilize a conducting polymer as a transducing material. The electrospun nanofibers of the composites were fabricated on the surface of fluorine-doped tin oxide (FTO)-coated glass substrate under the optimized condition. The PANI/f-CNTs and PABA/f-CNTs electrospun nanofibers were characterized by attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM), which confirmed the existence of f-CNTs in the composites. The electroactivity of the electrospun nanofibers was investigated in phosphate buffer saline solution using cyclic voltammetry (CV) before being employed for label-free electrochemical detection of DA using differential pulse voltammetry (DPV). The sensing performances including sensitivity, selectivity, stability, repeatability and reproducibility of the fabricated electrospun nanofiber films were also electrochemically evaluated. The electrochemical DA biosensor based on PANI/f-CNTs and PABA/f-CNTs electrospun nanofibers exhibited a sensitivity of 6.88 µA·cm-2·µM-1 and 7.27 µA·cm-2·µM-1 in the linear range of 50-500 nM (R2 = 0.98) with a limit of detection (LOD) of 0.0974 µM and 0.1554 µM, respectively. The obtained DA biosensor showed great stability, repeatability and reproducibility with precious selectivity under the common interferences, i.e., glucose, ascorbic acid and uric acid. Moreover, the developed electrochemical DA biosensor also showed the good reliability under detection of DA in artificial urine.

Nanocellulose/Nanoporous Silicon Composite Films as a Drug Delivery System.

Nanocellulose (NC) is a promising material for drug delivery due to its high surface area-to-volume ratio, biocompatibility, biodegradability, and versatility in various formats (nanoparticles, hydrogels, microspheres, membranes, and films). In this study, nanocellulose films were derived from "Bolaina blanca" (Guazuma crinita) and combined with nanoporous silicon microparticles (nPSi) in concentrations ranging from 0.1% to 1.0% (w/v), using polyvinyl alcohol (PVA) as a binding agent to create NC/nPSi composite films for drug delivery systems. The physicochemical properties of the samples were characterized using UV-Vis spectroscopy, scanning electron microscopy (SEM), Fourier transform infrared spectroscopy-attenuated total reflectance (FTIR-ATR), X-ray diffraction (XRD), and thermogravimetric analysis (TGA). The mechanical properties and drug release capabilities were also evaluated using methylene blue (MB) as an antibacterial drug model. Antibacterial assays were conducted against S. aureus and E. coli bacteria. The results show that NC/nPSi composites with 1% nPSi increased the T50% by 10 °C and enhanced mechanical properties, such as a 70% increase in the elastic modulus and a 372% increase in elongation, compared to NC films. Additionally, MB released from NC/nPSi composites effectively inhibited the growth of both bacteria. It was also observed that the diffusion coefficients were inversely proportional to the % nPSi. These findings suggest that this novel NC/nPSi-based material can serve as an effective controlled drug release system.

New approach for deacidification and consolidation of bone artifacts

Acidic conditions affect the archaeological bone in the burial and in uncontrolled display and storage environment or due to improper restoration processes. Accordingly, bones become weak and fragile. This study aims to evaluate nano calcium propionate and nano styrene butyl acrylate (used for the first time in the treatment of bones) at different concentrations for deacidification and consolidation of fragile bones. New bone samples were prepared. Artificial accelerated aging (acid and heat) was applied to prepare aged untreated samples. Deacidification and consolidation processes using the materials mentioned above were applied. The analytical techniques used were transmission electron microscope (TEM) and thermal gravimetric analysis (TGA) were used for morphological and thermal stability investigation for the prepared nano styrene butyl acrylate copolymer and its calcium propionate nonocomposites, a digital microscope and scanning electron microscope (SEM) for investigation of the surface morphology, pH value measurement, change of color measurement, attenuated total reflection—Fourier transform infrared spectroscopy (ATR/FTIR), contact angle (wettability), and X-ray diffraction analysis for measurement of bone crystallinity. The results proved that acid-heat aging affected bone properties such as changes in surface morphology and color, decrease in pH value, and contact angle. Bone samples became more crystalline, and the chemical composition of bone was also affected. The treatment of aged untreated bone samples with the materials used in this study improved their properties, such as increasing the pH value and contact angle. The surface morphology, color change, and crystallinity of bone improved and became more stable.

Deciphering the Mortar Composition of Ancient Chinese Pagodas: A Comparative Analysis from the Tang to Ming Dynasties in Shaanxi Province

The mortar materials from the internal and external walls of ancient Chinese pagodas in Shaanxi (Luoshan Temple Pagoda (847–858 AD), Daxiang Pagoda (960–1279 AD), and Qianjin Pagoda (1609 AD)) were investigated. Qualitative and semi-quantitative techniques including scanning electronic microscopy (SEM), energy-dispersive spectroscopy (EDS), X-ray diffraction (XRD), attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) and thermogravimetric analysis with differential scanning calorimetry (TGA-DSC) were employed. The physical and chemical characteristics including microstructural morphology, chemical composition, element distribution, and organic additives of the mortar samples were studied. SEM indicated that the mortar from the external wall exhibits a tightly bonded matrix, with the irregularly shaped particles, and the carbonation of the calcium carbonate in the mortars closely resembles that of aragonite crystals. The results of EDS, XRD, FTIR and TGA-DSC revealed that mortar from external wall of these ancient pagodas were air-hardened lime, and complete carbonization with no traces of calcium hydroxide, while mortars from internal wall primarily comprises local clay and lime. In addition, ATR-FTIR and iodine-starch discoloration tests confirmed that the presence of starch in the external wall of Daxiang Pagoda, whereas no organic additives were detected in the Qianjin and Luoshan Temple Pagoda.

Estimation of Proximate Composition in Rice Using ATR-FTIR Spectroscopy and Chemometrics.

This study presents an innovative approach for estimating the proximate composition of diverse rice varieties using attenuated total reflectance fourier transform infrared (ATR-FTIR) spectroscopy and chemometric techniques. Principal component analysis (PCA) reveals distinct separations among the seven rice varieties based on their FTIR spectra. Robust partial least squares (PLS) regression models, developed with high calibration (R 2) values from 0.778 for protein up to 0.941 for moisture, demonstrate high accuracy in predicting proximate composition. The root mean squared error (RMSE) in percentage values, indicative of prediction accuracy, were low across all proximate components. To ensure the response variable of regression, proximate composition measurements were taken five times, while FTIR spectra were scanned tens of times, employing random numbers around the average with the same standard deviation as the measurement. Notably, the study emphasizes the pivotal role of the amide-III band in protein determination, alongside specific wavenumber regions associated with molecular changes in proximate components. This research underscores the potential of ATR-FTIR spectroscopy and chemometrics for rapid and accurate proximate assessment in food science and agriculture.

Reservoir-type intranasal implants for sustained release of risperidone: A potential alternative for long-term treatment of schizophrenia

To overcome the challenges of the blood-brain barrier for drug delivery to the central nervous system (CNS), intranasal implants were developed to improve the management of CNS conditions, such as schizophrenia. In the present work, we developed and characterised a drug-containing implant consisting of two parts: a core layer made from risperidone (RIS) and water-soluble polymers, including poly(vinylpyrrolidone) (PVP) and poly(ethylene glycol) (PEG), and a coating layer made of poly(caprolactone) (PCL) membrane. The obtained implants, where the core layer contained 75 % w/w risperidone, were characterised using several techniques: scanning electron microscopy (SEM), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and attenuated total reflectance-Fourier transform infrared (ATR-FTIR). Moreover, the in vitro release profile of RIS was studied, showing that the PCL membrane could extend the release of RIS from 2 days up to 100 days. The in vitro release profile of the PCL-coated implant exhibited a linear release over the first 10 days, followed by a slower release rate that reached another linear phase up to 40 days. Subsequently, the drug release rates progressively slowed down. Finally, the results of in vitro biocompatibility studies indicated that the intranasal implants were biocompatible and non-cytotoxic. These findings suggest that the implants prepared in this work have the potential to provide long-acting drug delivery for targeting the brain.

Comparison between acetonitrile-water separation by betaine and betaine hydrochloride

Acetonitrile and water are miscible solvents. This study compares their separation by betaine and betaine hydrochloride. Acetonitrile is a hydrogen (H) bond acceptor and so is betaine, because of its -CO and -CO- groups. Therefore, betaine competes with acetonitrile for interactions with the hydrogens of water molecules, as indicated by attenuated total reflectance - Fourier transform infrared spectroscopy (ATR-FTIR). Therefore, when added to acetonitrile-water mixtures, betaine displaces acetonitrile. Separation into bulk phases occurs with 5–10 wt% betaine (relative to water), for acetonitrile concentrations between 50 and 80 wt% (relative to the aqueous phase). At lower acetonitrile concentrations (e.g., 1 wt%), betaine separates acetonitrile from water to yield emulsified acetonitrile droplets, detected by light scattering. With 1 wt% acetonitrile and betaine, acetonitrile droplets in water are negatively charged due to the -CO- group of betaine, as shown by electrophoretic measurements. In the case of betaine hydrochloride, the negative charge of the -CO- group is shielded by a proton, and interactions with water are weaker. As a result, bulk separation is not observed. Nonetheless, betaine hydrochloride also competes against acetonitrile for interactions with hydrogen atoms of water molecules, albeit not as effectively as betaine. This is shown by ATR-FTIR. Therefore, betaine hydrochloride emulsifies acetonitrile in water into sub-micron droplets. These droplets are positively charged, owing to the positively charged nitrogen atom of betaine hydrochloride. Acidifying mixtures of betaine, acetonitrile and water (with HCl) impedes bulk separation. This result confirms the importance of electrostatic interactions between the hydrogens of water and the unshielded, negative -CO- group of betaine.