Buffer Solution pH Research Articles

Development of pivalic acid conjugated Nafion modified glassy carbon electrode for sensitive detection of Cu(II) by electrochemical approach

In this work, pivalic acid (pivH) molecule is employed for an electrochemical sensing of copper cations in an aqueous medium. For sensitive as well as selective potential sensor application, pivH was fabricated onto a glassy carbon electrode (GCE) facilitated by adhesive conducting binder, nafion, so as make it selective and effective electrochemical probe (pivH/Nafion/GCE) towards specific heavy metal cations. This newly fabricated pivH/Nafion/GCE reveals enhance electrochemical activity toward copper ions in the presence of other interfering heavy metal cations in phosphate buffer solution (PBS) of pH=7. The calibration plot was linear (r2 = 0.9879) across broad linear dynamic range (LDR) spanning Cu2+ concentration from 0.1 nM to 0.01 M. The sensitivity and detection limit was found to be 0.0212 × 10−2 µAµM−1cm−2 and 0.014 nM, respectively. So, this newly fabricated GCE as selective electrochemical probe offers a sensitive as well as selective detection of Cu2+ cations in real environmental samples using a novel electrochemical, current–potential (I-V), approach, for the first time. Further, we explored pivalic acid for the preparation of new di-nuclear copper complex, [Cu2(piv)4(pivH)2] (where piv = pivalate; pivH=pivalic acid) and characterized by Fourier transform infrared spectroscopy (FTIR) spectroscopy, elemental analysis and single crystal X-ray diffractometry. Density functional theory (DFT) calculations were carried out to confirm the interactions and these calculations well-support to experimental data. In case of deprotonated form of pivH, Molecular Electrostatic Potential (MEP) analysis exhibits electrostatic potential equals to −148.4 kcal/mol which suggest about the strong interaction of –COOH with copper centers. Similarly, interaction energies, the quantum theory of atoms in molecules (QTAIM) study and Natural Bond Orbital (NBO) analysis also favor to experimental work. Thus, this novel study demonstrates an excellent approach for highly selective and sensitive detection of Cu2+ cations in short response time with low detection limit and good reproducibility by using I-V method based on newly designed pivH/Nafion/GCE as selective Cu2+ cationic electrochemical sensor. The experimental data was compactable with theoretical calculations.

Starch-Based Functional Films Enhanced with Bacterial Nanocellulose for Smart Packaging: Physicochemical Properties, pH Sensitivity and Colorimetric Response.

Starch-based pH-sensing films with bacterial nanocellulose (BNC) and red cabbage anthocyanins (RCA) as active components were investigated in this research. Their structural, physical, surface and colorimetric properties were analyzed, mainly as a function of BNC concentration. The aim of the research was to relate the changes in the intermolecular interactions between the components of the films (starch, anthocyanins and BNC) to the physical, surface and colorimetric properties that are important for the primary intended application of the produced films as pH indicators in smart packaging. The results showed that maize starch (MS) was more suitable as a matrix for the stabilization of anthocyanins compared to potato starch (PS). PS-based films showed a lower value of water contact angle than MS-based films, indicating stronger hydrophilicity. The swelling behavior results indicate that the concentrations of BNC in MS-based films (cca 10%) and the concentration of about 50% BNC in PS-based films are required if satisfactory properties of the indicator in terms of stability in a wet environment are to be achieved. The surface free energy results of PS-based films with BNC were between 62 and 68 mJ/m2 and with BNC and RCA between 64 and 68 mJ/m2; for MS-based films, the value was about 65 mJ/m2 for all samples with BNC and about 68 mJ/m2 for all samples with BNC and RCA. The visual color changes after immersion in different buffer solutions (pH 2.0-10.5) showed a gradual transition from red/pink to purple, blue and green for the observed samples. Films immersed in different buffers showed lower values of 2 to 10 lightness points (CIE L*) for PS-based films and 10 to 30 lightness points for MS-based films after the addition of BNC. The results of this research can make an important contribution to defining the influence of intermolecular interactions and structural changes on the physical, surface and colorimetric properties of bio-based pH indicators used in smart packaging applications.

Enantioselective Detection of (D)- and (L)-Limonene from Essential Oil Samples Using a Molecularly Imprinted Polypyrrole Electrochemical Sensor

Limonene is a monoterpene compound that has two enantiomers, (D)- and (L)-limonene, in different quantities and proportions in several essential oils, and it is used in the chemical, pharmaceutical, and food industries. While the (D)-limonene is widely found in citrus, the (L)-limonene is found mainly in oils of Pinus and Mentha. The enantioselective detection holds the fact that the two isomers are found together in different quantities, in which each has its properties. The preferential use of one depends on the purpose, (D)-limonene is used in the pharmaceutical and chemical industry, while (L)-limonene has organoleptic properties and is used in the food industry, cosmetic, and personal hygiene industries. The methods existing in the literature involve the detection of the enantiomers by gas chromatography-mass spectrometry and high-performance liquid chromatography. Since the two enantiomers can be found together in different samples, is very important to have a simple and faster method to determine both. This work aims to develop an electrochemical sensor using a “dual template” technique, with both limonene enantiomers and a monomer (pyrrole), forming a molecularly imprinted polymer (MIP) film and determining the analyte “one-by-one”, by saturating the cavities of one specific enantiomer to determine the other one, using differential pulse voltammetry (DPV). This is the first electrochemical sensor for the enantioselective determination of (D) and (L)-limonene. Initially, a suspension of 0.4 mg mL-1 of graphene oxide in 0.1 mol L-1 of Na2SO4 solution was directly reduced on a glassy carbon electrode surface through chronoamperometry, applying a potential of -1.4 V for 500s. Then, AuNPs were electrodeposited from a 5.0×10-4 mol L-1 HAuCL solution in 0.5 mol L-1 H2SO4 onto the GCE/rGO electrode, also through chronoamperometry, in which a potential of 0.4 V was applied until the charge of 1.0x10-3 C was reached. Next, for the electropolymerization process, a solution containing 3.0x10-2 mol L-1 pyrrole and both (D)- and (L)-limonene enantiomers in a phosphate buffer solution (pH 7.0), was used in 5 consecutive voltammetric cycles on the GCE/rGO/AuNPS electrode, applying a potential range from 0.0 to 1.0 V in a scan rate of 0.02 V s-1, forming the MIP film. The extraction of the template molecules involved the application of 5 consecutive voltammetric cycles in NaOH 0.1 mol L-1 in a potential range from 0.0 to 1.5 V (0.05 V s-1). For the rebinding process, the electrode was placed for five minutes in different concentrations of one specific enantiomer after saturation of the other one, in PB solution pH 7.0. All the experimental parameters that influence the analytical performance of the device were optimized, such as pyrrole concentration, electropolymerization and extraction cycles, rebinding times, electropolymerization and rebinding pH, and nanoparticle charge. The electrode was characterized by scanning electron microscopy, electrochemical impedance spectroscopy, and cyclic voltammetry. The analytical methodology was developed, with a limit of detection (LOD) for (D)-limonene of 1.8x10-12 mol L-1, a limit of quantification (LOQ) of 5.5x10-12 mol L-1, and an amperometric sensibility (AS) of 5.8x105 A L mol-1. For the (L)- enantiomer, the LOD, LOQ, and AS are 1.4x10-12 mol L-1, 4.3x10-12 mol L-1, and 6.2 A L mol-1, respectively. The linear range is from 2.0x10-12 to 1.0x10-11 mol L-1 for both enantiomers. It was analyzed the stability and repeatability inter and intra-day of the sensor. The selectivity study of both analytes was evaluated with the imprinted factor (α) and the selectivity factor (β) with different molecules present in the sample, showing that the sensor is capable of selectively recognizing limonene. Furthermore, this method was applied to real samples of the essential oil of orange (Citrus aurantium), the essential oil of peppermint (Mentha piperita), and the essential oil of Siberian pine (Abies sibirica). The quantification of (D)- and (L)-limonene was successfully performed using the standard addition method and the results obtained were validated by recovery assays. All relative standard deviations were below 5%. These results indicate that the proposed sensor exhibits good analytical performance, being suitable for the determination of both limonene enantiomers in essential oils.Acknowledgements:São Paulo Research Foundation (FAPESP) (Grants: 2023/00817-9 and 2017/22401-8)

Targeted and Therapeutic Efficacy of 5-Fluorouracil-Loaded Polylactic Acid Nanocomplexes in Gastric Cancer

Gastric cancer (GC), arising from gastric mucosal cells, necessitates innovative treatment strategies beyond conventional surgical approaches. While 5-fluorouracil (5-FU) has demonstrated efficacy in various cancers, its lack of selectivity for cancer cells and limited half-life pose challenges. This study focuses on assessing the therapeutic potential of 5-FU-loaded L-polylactic acid (PLLA) nanofibers (NFs) for targeted GC treatment. The preparation of 5-FU/PLLA NFs involved refining the drug delivery approach to enhance drug impact on GC cell proliferation and apoptosis. Utilizing an organic phase separation methodology, 5-FU was incorporated into PLLA NFs, and the NF morphology was examined using scanning electron microscopy, with optical microscopy used for diameter measurement. Fourier-transform infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC) explored binding state and PLLA crystallinity. Drug loading (DL) capacity and in vitro release characteristics were evaluated by UV-visible spectrophotometry, while NF degradation and stability were assessed. The human gastric adenocarcinoma (AGS) cell line was employed in cell experiments, with three groups: normal culture (Normal group), single drug treatment with 5-FU (5 μmol/L, 5-FU group), and 5-FU-loaded PLLA group (5-FU/PLLA group) containing 5 μmol/L 5-FU. Cell Counting Kit-8 gauged cell proliferation and viability, and Annexin V-FITC/PI assay determined cell apoptosis. Results revealed a (1,230.8±18.9) nm diameter for 5-FU/PLLA NFs with 18.3% crystallinity. FTIR and DSC analyses indicated a simple physical mixture of 5-FU and PLLA in 5-FU/PLLA. DL capacity was (18.1±2.3)%, with a DL efficiency of (92.5±9.4)%. in vitro release performance of 5-FU/PLLA surpassed that of raw 5-FU. The mass loss rate of 5-FU/PLLA was consistent across different pH buffer solutions, with a stable drug release (DR) rate over various storage times. In cell experiments, both 5-FU and 5-FU/PLLA groups exhibited reduced proliferation and viability compared to the Normal group, with higher apoptosis rates (P < 0.05). Furthermore, the 5-FU/PLLA group showed decreased proliferation and viability compared to the 5-FU group, accompanied by higher apoptosis rates (P < 0.05). In conclusion, 5-FU-loaded PLLA NFs, with excellent DR properties, demonstrated significant inhibitory and cytotoxic effects on GC cells.

Studies on pharmacokinetic properties and intestinal absorption mechanism of sanguinarine chloride: in vivo and in situ

Sanguinarine (SAN) is an alkaloid with multiple biological activities, mainly extracted from Sanguinaria canadensis or Macleaya cordata. The low bioavailability of SAN limits its utilization. At present, the nature and mechanism of SAN intestinal absorption are still unclear. The pharmacokinetics, single-pass intestinal perfusion test (SPIP), and equilibrium solubility test of SAN in rats were studied. The absorption of SAN at 20, 40, and 80 mg/L in different intestinal segments was investigated, and verapamil hydrochloride (P-gp inhibitor), celecoxib (MPR2 inhibitor), and ko143 (BCRP inhibitor) were further used to determine the effect of efflux transporter proteins on SAN absorption. The equilibrium solubility of SAN in three buffer solutions (pH 1.2, 4.5 and 6.8) was investigated. The oral pharmacokinetic results in rats showed that SAN was rapidly absorbed (Tmax=0.5 h), widely distributed (Vz/F = 134 L/kg), rapidly metabolized (CL = 30 L/h/kg), and had bimodal phenomena. SPIP experiments showed that P-gp protein could significantly affect the effective permeability coefficient (Peff) and apparent absorption rate constant (Ka) of SAN. Equilibrium solubility test results show that SAN has the best solubility at pH 4.5. In conclusion, SAN is a substrate of P-gp, and its transport modes include efflux protein transport, passive transport and active transport.

Enhanced modified poly-tyrosine voltammetric sensor for the quantification detection of salivary pepsin

Pepsin as an aspartic acid protease member and one of the three foremost proteolytic enzymes in the digestive system is essential to be detected. An electrochemically polymerized tyrosine film on carbon paste electrode (pTyr/CPE) has been synthesized by electro-polymerization donating an affordable electrochemical sensor to sense salivary pepsin as a diagnostic technique for gastroesophageal reflux disease (GRD) due to saliva collection is non-invasive and relatively comfortable. The pTyr/CPE was applied for Voltammetric sensing of pepsin and its quantification in phosphate buffer solution of pH 2.0 (PBS). Scanning electron microscopy (SEM) was conducted to learn the surface morphology. Cyclic voltammetry (CV), differential pulse voltammetry (DPVs), chronoamperometry (CA), and electrochemical impedance spectroscopy (EIS) were developed to realize the electrocatalytic activity of the sensor. The pTyr/CPE proceeded as a sensitive detector to pepsin with two linear ranges from 1 to 20 & 20 to 100 ng/mL donating two limits of detection as 0.5 & 0.09 ng/mL, respectively, and high selectivity toward pepsin, as well as stability and fast response of 1.5 s. Consequently, it is guessed that the pTyr/CPE sensor could be supportive for the initial diagnosis of GRD through the detection of pepsin in saliva. Finally, we quantified the pepsin levels in saliva samples of LPR patients (n = 2), showing that the results were agreeable with those from the electrochemical sensor.

Mycotoxins in vegetating corn plants from experimental mono-sowing

The aim of present study was to reveal the mycotoxin contamination of vegetative maize (Zea mays L.) plants during the periods of leaf formation and panicle emergence. Early maturing hybrids of the varieties Krasnodarsky 194 MV, Ladozhsky 175 MV and Competence®, resistant to fungal diseases, were grown in the spring-summer period of 2023 on the experimental field of the Russian State Agrarian University – Moscow Agricultural Academy (Moscow) with sod-podzolic soil and the application of NPK fertilizers 16:16:16. For mycotoxicological analysis, aerial parts of plants were collected weekly from the phase of formation of the 3rd leaf (18 days after sowing. Samples of seedlings, leaves and stems (total number – 172), after drying, were ground in a laboratory mill and extracted with a mixture of acetonitrile and water in a volumetric ratio of 84:16 with a consumption of 10 ml per 1 g of sample. Mycotoxin content was determined in extracts after 10-fold dilution with phosphate-salt buffer solution pH 7.5 by indirect competitive enzyme immunoassay. T-2 toxin, deoxynivalenol, diacetoxiscirpenol, roridin A, sterigmatocystin and PR toxin were absent in the samples. Corn seedlings and leaves contained cyclopiazonic acid (CPA), emodin (EMO), mycophenolic acid (MPA), alternariol (AOL), ergot alkaloids (EA), aflatoxin B1 (AB1) and single samples – zearalenone (ZEN), ochratoxin A (OA) and citrinin (CIT) in concentrations from 16 up to 35 μg/kg. Fumonisins of group B are found only in early seedlings. The permanent contaminant of the stems was MPA, whereas EA and CIT were absent. In the seedlings and leaves of all hybrids, the detection of AOL and EA remained stable during the change of development phases, as did the average concentrations of CPA (about 100 μg/kg), AOL (from 17 to 27 μg/kg), EMO (35–58 μg/kg), MPA (28–41 μg/kg), EA (6–18 μg/kg) and AB1 (2 μg/kg). In the stems of plants in phases 7–9 of leaf and sweeping, variation in cases of detection of CPA, EMO, AOL, AB1 and OA was noted by varieties.

Covalent versus noncovalent attachments of [FeFe]‑hydrogenase models onto carbon nanotubes for aqueous hydrogen evolution reaction

In an effort to develop the biomimetic chemistry of [FeFe]‑hydrogenases for catalytic hydrogen evolution reaction (HER) in aqueous environment, we herein report the integrations of diiron dithiolate complexes into carbon nanotubes (CNTs) through three different strategies and compare the electrochemical HER performances of the as-resulted 2Fe2S/CNT hybrids in neutral aqueous medium. That is, three new diiron dithiolate complexes [{(μ-SCH2)2N(C6H4CH2C(O)R)}Fe2(CO)6] (R = N-oxylphthalimide (1), NHCH2pyrene (2), and NHCH2Ph (3)) were prepared and could be further grafted covalently to CNTs via an amide bond (this 2Fe2S/CNT hybrid is labeled as H1) as well as immobilized noncovalently to CNTs via π-π stacking interaction (H2) or via simple physisorption (H3). Meanwhile, the molecular structures of 1–3 are determined by elemental analysis and spectroscopic as well as crystallographic techniques, whereas the structures and morphologies of H1-H3 are characterized by various spectroscopies and scanning electronic microscopy. Further, the electrocatalytic HER activity trend of H1 > H2 ≈ H3 is observed in 0.1 M phosphate buffer solution (pH = 7) through different electrochemical measurements, whereas the degradation processes of H1-H3 lead to their electrocatalytic deactivation in the long-term electrolysis as proposed by post operando analysis. Thus, this work is significant to extend the potential application of carbon electrode materials engineered with diiron molecular complexes as heterogeneous HER electrocatalysts for water splitting to hydrogen.

Structures and dynamics of 8-oxo-7,8-dihydro-2'-deoxyguanosine in neutral and basic aqueous solutions by spectroscopy.

8-oxo-7,8-dihydro-2'-dexyoguanine (8-oxo-dG) can be tautomerized to a 6-enolate,8-keto tautomer through nearby-NH deprotonation at elevated pH. In this work, the N3-protonated 8-oxo-dG tautomers in deuterated pH-buffer solutions were studied using steady-state UV/Vis, FTIR, and ultrafast two-dimensional IR spectroscopies. The presence of 6,8-diketo and C6-anionic tautomers at neutral to basic conditions (pD = 7.4-12.0) was revealed by UV/Vis and FTIR results and was further confirmed by 2D IR signals in both diagonal and off-diagonal regions. However, the C6-enol tautomer, which may be an intermediate during the transition from 6,8-diketo to C6-enolate,C8-keto, was not observed appreciably due to its extreme low population. Furthermore, the neutral-to-anionic tautomeric transition of N3H-8-oxo-dG studied in this work occurs under more basic conditions than the N1H-8-oxo-dG reported previously, showing a higher pKa value for N3H than N1H. Finally, vibrational relaxation of the carbonyl stretching mode was found to be both molecular site dependent and pD dependent for 8oxo-dG. Taken together, this work shows that the ultrafast infrared spectroscopic method is effective for examining tautomers and their dynamics in nucleic acids.

Highly Compressible, Superabsorbent, and Biocompatible Hybrid Cryogel Constructs Comprising Functionalized Chitosan and St. John's Wort Extract.

Biobased porous hydrogels enriched with phytocompounds-rich herbal extracts have aroused great interest in recent years, especially in healthcare. In this study, new macroporous hybrid cryogel constructs comprising thiourea-containing chitosan (CSTU) derivative and a Hypericum perforatum L. extract (HYPE), commonly known as St John's wort, were prepared by a facile one-pot ice-templating strategy. Benefiting from the strong interactions between the functional groups of the CSTU matrix and those of polyphenols in HYPE, the hybrid cryogels possess excellent liquid absorption capacity, mechanical resilience, antioxidant performance, and a broad spectrum of antibacterial activity simultaneously. Thus, owing to their design, the hybrid constructs exhibit an interconnected porous architecture with the ability to absorb over 33 and 136 times their dry weight, respectively, when contacted with a phosphate buffer solution (pH 7.4) and an acidic aqueous solution (pH 2). These cryogel constructs have extremely high compressive strengths ranging from 839 to 1045 kPa and withstand elevated strains of over 70% without developing fractures. Moreover, the water-swollen hybrid cryogels with the highest HYPE content revealed a complete and instant shape recovery after uniaxial compression. The incorporation of HYPE into CSTU cryogels enabled substantial improvement in scavenging reactive oxygen species and an expanded antibacterial spectrum toward multiple pathogens, including Gram-positive bacteria (Staphylococcus aureus and Staphylococcus epidermidis), Gram-negative bacteria (Escherichia coli and Pseudomonas aeruginosa), and fungi (Candida albicans). Cell viability experiments demonstrated the cytocompatibility of the 3D cryogel constructs, which did not induce changes in the fibroblast morphology. This work showcases a simple and effective strategy to immobilize HYPE extracts on CSTU 3D networks, allowing the development of novel multifunctional platforms with promising potential in hemostasis, wound dressing, and dermal regeneration scaffolds.

Moment analysis method for determination of rate constants of solute permeation across interface of spherical molecular aggregates by means of high-performance liquid chromatography

A moment analysis method was developed for the study of solute permeation at the interface of spherical molecular aggregates. At first, new moment equations were developed for determining the partition equilibrium constant (Kp) and permeation rate constants (kin and kout) of solutes from the first absolute (μ1A) and second central (μ2C) moments of elution peaks measured by using high-performance liquid chromatography (HPLC). Then, the method was applied to the analysis of mass transfer phenomena of three solutes, i.e., hydroquinone, resorcinol, and catechol, at the interface of sodium dodecylsulfate (SDS) micelles. HPLC data were measured by using an ODS column and an aqueous phosphate buffer solution (pH = 7.0) as the mobile phase solvent. Pulse response experiments were conducted while changing SDS concentration (5 - 20 mmol dm−3) in the mobile phase under the conditions that the surface of ODS stationary phase was dynamically coated by SDS monomers. In order to demonstrate the effectiveness of the moment analysis method using HPLC, the values of Kp, kin, and kout were determined for the three solutes as 35 - 69, 2.4 × 10−8 - 1.4 × 10−6 m s−1, and 7.0 × 10−10 - 2.1 × 10−8 m s−1, respectively. Their values increase with an increase in the hydrophobicity of the solutes. The method has some advantages for the study of interfacial solute permeation of molecular aggregates. For example, neither immobilization nor chemical modification of both solute molecules and molecular aggregates is required when elution peaks are measured by using HPLC. Interfacial solute permeation takes place in the mobile phase without any chemical reaction or physical action on molecular aggregates. The values of Kp, kin, and kout were analytically determined from those of μ1A and μ2C by using the moment equations. The results of this study must contribute to the dissemination of an opportunity for studying the interfacial solute permeation of molecular aggregates to many researchers because of extremely high versatility of HPLC.

Ultrasensitive tadalafil detection with eco-friendly CeO2/Al-pillared clay incorporated pencil graphite paste electrode

In this study, we have constructed a novel voltammetric sensor based on montmorillonite clay (MMT) incorporated with CeO2 nanoparticles using a composite graphite paste electrode as a cross linker (MMT-CeO2NPs/GPG-PE) for the trace determination of tadalafil (TAD) drug. The characterization of CeO2 nanoparticles has been conducted using various analytical techniques, including X-ray diffraction, transmission electron microscopy, and high-resolution transmission electron microscopy. The morphology of the composite of CPG and MMT-CeO2NPs/CPG was elucidated through scanning electron microscopy (SEM). The newly developed sensor (MMT-CeO2NPs/CPG-PE) exhibited remarkable efficiency towards TAD oxidation using adsorptive stripping square-wave voltammetry (AdS-SWV) in Mcllvaine buffer solution (pH 8.0). A highly selective and sensitive method for TAD detection has been successfully applied based on MMT-CeO2NPs/CPG-PE, showing two different linear concentration ranges of 0.005−0.1 and 0.1–9.9 µM. The LOD and LOQ were determined to be 1.97 × 10−10 and 6.57 × 10−10 M, respectively, with a sensitivity of 3916 µA µM−1 cm−2. Interestingly, the sensing electrode exhibited excellent reproducibility, reusability, and stability even after 30 days. Moreover, the newly developed nano-sensor (MMT-CeO2NPs/CPG-PE) has been effectively utilized for the accurate detection of TAD in pharmaceutical formulations and spiked human blood serum and urine samples, demonstrating no interference from other substances.

Eco-Friendly Straws: A Fusion of Soy Protein Isolate and Cassava Starch Coated with Beeswax and Shellac Wax.

This research aimed to produce eco-friendly straws using soy protein isolate (SPI) and cassava starch (CS) at different ratios by the extrusion technique and by coating with beeswax and shellac wax. Three straw formulations (F) (F1: 24.39% SPI-24.39% CS; F2: 19.51% SPI-29.37% CS; and F3: 14.63% SPI-34.15% CS) were prepared, incorporating glycerol (14.6% w/w) and water (36.6% w/w). After extrusion and drying at 80 °C for 20 h, visual assessment favored F2 straws due to smoother surfaces, the absence of particles, and enhanced straightness. For the physical property test, the straws were softened in pH buffer solutions for 5 min. To simulate practical application, mechanical bending strength was studied under different relative humidity (RH) settings. Water absorption reduced the strength as RH increased. F2 straws outperformed other formulations in bending strength at 54% RH. For hydrophobic coatings, F2 was chosen. Beeswax- and shellac wax-coated straws displayed negligible water absorption and sustained their integrity for over 6 h compared to uncoated straws. This study shows that extrusion and natural coatings may make sustainable straws from SPI and CS. These efforts help meet the growing demand for eco-friendly plastic alternatives, opening up new options for single-use straws.

Porous-anodic-alumina-templated Ta-Nb-alloy/oxide coatings via the magnetron-sputtering/anodizing as novel 3D nanostructured electrodes for energy-storage applications

The Ta-52 at.%Nb thin alloy films were magnetron sputter-deposited over a low-aspect-ratio nanoporous anodic-alumina template formed in 0.05 M tartaric acid solution at 250 V and modified by the pore-widening technique to enlarge the pores up to ∼500 nm. The alloy coated the pores evenly, thus forming a 3D continuous conducting nanofilm on the template. Partially anodizing the templated alloy in a borate buffer solution of pH 7.5 generated a compact amorphous mixed-oxide anodic film thickening proportionally to the applied voltage. It was revealed that the oxide on the Ta-52 at.%Nb alloy grows with a slower migration of Ta5+ ions relative to Nb5+ ions, resulting in mixing Ta2O5 and Nb2O5 in the film depth and forming a few-nm-thick Nb2O5 outmost layer. The unique migration of Ta4+, Ta3+, Nb4+, and Nb3+ ions is assumed accountable for forming corresponding suboxides in the 3D anodic film in contrast to a flat Ta-52 at.%Nb alloy film used as a reference. The 3D anodic films behave as an n-type semiconductor with a low donor density Nd = ∼2 × 1018 cm−3, appropriate for dielectric applications. An unusual two-layered structure with a sharp electrical interface revealed in the 3D oxide films anodized to 30–130 V, comprising a low-resistivity layer superimposed on the high-resistivity layer, is explained by an immobile negative space charge in the outer film part. The air-annealing at moderate temperatures releases the space charge and transforms the two layers into a high-resistivity single layer having substantially improved dielectric properties and thermostable (up to 250 °C) capacitance of 1.2 μF cm−2 achieved for the film anodized to practical 50 V. The 3D films having up to 4.5 times enlarged effective surface area can be utilized as novel metal/oxide nanostructured electrodes for electrolytic microcapacitors suitable for classical electronic circuits and energy-storage applications.

Impact of Chemical Corrosion on Mechanical Properties of Boroaluminosilicate Pharmaceutical Glasses.

Boroaluminosilicate (BAS) glasses have excellent chemical durability and mechanical properties and are widely used in the pharmaceutical packaging industry. The corrosion behavior of boroaluminosilicate (BAS) glasses have been investigated for many years; however, the impact of chemical corrosion on mechanical properties of boroaluminosilicate glasses has not been well understood. In this work, the BAS glass samples were corroded in a 20 mM Glycine-NaOH buffer solution (pH = 10) at 80 °C for various durations. Within the corrosion durations, the corrosion of the glass is dominated by congruent dissolution. The results show that the elemental composition and structure of the glass surface are not altered significantly during the congruent dissolution, and the corrosion rate is mainly affected by the Si concentration in the solution. The structural change in the process of micro-crack decay is the main factor affecting the mechanical properties of the glass surface. Corrosion leads to the growth of micro-cracks and tip passivation, which causes the hardness and elastic modulus of the glass to first decrease and then increase. As corrosion proceeds, the microcracks are completely destroyed to form micropores, and the pore size and number increase with the corrosion process, resulting in the decrease in surface mechanical properties again. This work reveals the main influencing factors of congruent dissolution on mechanical properties and provides an important reference for the improvement of pharmaceutical glass strength.

Fast and sustainable production of smart nanofiber mats by solution blow spinning for food quality monitoring: Potential of polycaprolactone and agri-food residue-derived anthocyanins

The shelf life of perishable foods is estimated through expensive and imprecise analyses that do not account for improper storage. Smart packaging, obtained by agile manufacturing of nanofibers functionalized with natural pigments from agri-food residues, presents promising potential for real-time food quality monitoring. This study employed the solution blow spinning (SBS) technique for the rapid production of smart nanofiber mats based on polycaprolactone (PCL), incorporating extracts of agricultural residues rich in anthocyanins from eggplant (EE) or purple cabbage (CE) for monitoring food quality. The addition of EE or CE to the PCL matrix increased the viscosity of the solution and the diameter of the nanofibers from 156 nm to 261–370 nm. The addition of extracts also improved the mechanical and water-related properties of the nanofibers, although it reduced the thermal stability. Attenuated total reflectance Fourier-transform infrared spectroscopy confirmed the incorporation of anthocyanins into PCL nanofibers. Nanofiber mats incorporated with EE or CE exhibited visible color changes (ΔE ≥ 3) in response to buffer solutions (pH between 3 and 10), and ammonia vapor. Smart nanofibers have demonstrated the ability to monitor fish fillet spoilage through visible color changes (ΔE ≥ 3) during storage. Consequently, smart nanofibers produced by the SBS technique, using PCL and anthocyanins from agro-industrial waste, reveal potential as smart packaging materials for food.

Electrochemical and Theoretical Investigations on the Binding of Anticancer Drug Olaparib to Human Serum Albumin

Abstract This article explores the interaction between Olaparib (OLA), an anticancer drug, and human serum albumin (HSA) on a glassy carbon electrode using cyclic voltammetry and differential pulse voltammetry methods. The study investigates the alterations in the electrochemical behavior of [Fe(CN)6]3–/4– redox pairs in a physiological pH buffer solution due to the OLA-HSA interaction. The electrochemical and kinetic parameters of the redox probe were calculated in the presence of both the drug and protein. Notable variations in these parameters were observed, which can be attributed to the formation of an electro-inactive complex between the protein and drug. The study determined the parameters describing the OLA-HSA complex, including the binding constant and complex stoichiometry. The results revealed the formation of a strong singular drug-albumin complex with a binding constant of 1.12 × 105 M–1. Molecular docking studies supported the experimental findings and provided insights into the binding interactions of OLA with HSA. This study provides valuable insights for future research aimed at enhancing drug delivery systems.

Aluminium Interdigitated Electrode with 5.0 μm Gap for Electrolytic Scooting

The goal of the research project is to design, fabricate, and characterize an extremely sensitive biosensor for use in healthcare. Using AutoCAD software, a novel IDE pattern with a 5 μm finger gap was created. Conventional photolithography and regular CMOS technology were used in the fabrication process. A 3D nano profiler, scanning electron microscopy (SEM), high-power microscopy (HPM), and low-power microscopy (LPM) were used to physically characterize the manufactured IDE. Chemical testing was done using several pH buffer solutions, and electrical validation was performed using I-V measurements. The Al IDE was produced, with a tolerance of 0.1 μm between the fabricated IDEs and the design mask. Electrical measurements verified the flawless fabrication of the IDE, and the device's repeatability was validated by the outcomes of comparable IDE samples. For each pH buffer solution, a modest additional volume of 2 μl was used to quantitatively detect slight current fluctuations in the microampere range. Through pH calibration for advanced applications in the realm of chemical sensors using an amperometric method, this research study has verified the chemical behavior of the IDE.

Antibacterial and cytotoxicity studies of pyrrolo-based organic scaffolds and their binding interaction with bovine serum albumin.

Two pyrrolo-based compounds, 1H-pyrrolo[3,2-b]pyridine-3-carboxylic acid (L1) and 1H-pyrrolo[3,2-c]pyridine-4-carboxylic acid (L2), were employed for the detection of bovine serum albumin (BSA) by UV-Vis and fluorescence spectroscopic methods in phosphate buffer solution (pH = 7). In the presence of L1 and L2, the fluorescence emission of BSA at 340 nm was quenched and concomitantly a red-shifted emission band appeared at 420 nm (L1)/450 nm (L2). The fluorescence spectral changes indicate the protein-ligand complex formation between BSA and L1/L2. An isothermal titration calorimetry (ITC) experiment was conducted to determine the binding ability between BSA and L1/L2. The binding constants are found to be 4.45 ± 0.22 × 104 M-1 for L1 and 2.29 ± 0.11 × 104 M-1 for L2, respectively. The thermodynamic parameters were calculated from ITC measurements (i.e. ∆rH = -40 ± 2 kcal/mol, ∆rG = -4.57 ± 0.22 kcal/mol and -T∆rS = 35.4 ± 1.77 kcal/mol), which indicated that the protein-ligand complex formation between L1/L2 with BSA is mainly due to the electrostatic interactions. The protein-ligand interactions were studied by performing molecular docking. Further, the antibacterial assay of L1 and L2 was conducted against gram-positive and gram-negative bacterial strains in an effort to address the difficulties caused by the co-occurrence of antimicrobial and multidrug-resistant bacteria. E. coli and S. aureus were significantly inhibited by L1 and L2. The L1 exhibits 13, 12 and 15 mm, whereas L2 exhibits a 2, 3 and 5 mm zone of inhibition against S. aureus, S. pyogenesand E. coli, respectively. In silico molecular docking of L1 and L2 was performed with bacterial DNA gyrase to establish the intermolecular interactions. Finally, the in vitro cytotoxicity activities of the ligands L1 and L2 have been carried out using drosophila.

Photoelectrochemical immunoassay of cardiac troponin I based on ZnTCPP/CdIn2S4 type-II heterojunction and co-catalyzed precipitation biolabeling.

CdIn2S4 and zinc tetrakis(4-carboxyphenyl)porphyrin (ZnTCPP) were synthesized by hydrothermal method, and an organic dye-sensitized inorganic semiconductor ZnTCPP/CdIn2S4 type II heterojunction was constructed on a fluorine-doped tin oxide (FTO) substrate electrode. Asandwich immunostructure forsignal-attenuation photoelectrochemical (PEC) detection of cardiac troponin I (cTnI) was constructed using the ZnTCPP/CdIn2S4/FTO photoanode and a horseradish peroxidase (HRP)-ZnFe2O4-Ab2-bovine serum albumin (BSA) immunolabeling complex. The bioenzyme HRP and the HRP-like nanozyme ZnFe2O4 can co-catalyze the oxidation of 4-chloro-1-naphthol (4-CN) by H2O2 to produce an insoluble precipitate on the photoanode, thus notably reducing the anodic photocurrent for quantitative determination of cTnI. Under the optimal conditions, the photocurrent at 0V vs. SCE in 0.1M phosphate buffer solution (pH 7.40) containing 0.1M ascorbic acid was linear with the logarithm of cTnI concentration from 500fg mL-1 to 50.0 ng mL-1, and the limit of detection (LOD, S/N = 3) is 0.15 pg mL-1. Spiked recoveries were 95.1% ~ 104% for assay of cTnI in human serum samples.