Enhanced electron transfer mediated detection of hydrogen peroxide using a silver nanoparticle–reduced graphene oxide–polyaniline fabricated electrochemical sensor

The current study aims at the development of an electrochemical sensor based on a silver nanoparticle–reduced graphene oxide–polyaniline (AgNPs–rGO–PANI) nanocomposite for the sensitive and selective detection of hydrogen peroxide (H₂O₂). The nanocomposite was fabricated by simple in situ synthesis of PANI at the surface of rGO sheet which was followed by stirring with AEC biosynthesized AgNPs to form a nanocomposite. The AgNPs, GO, rGO, PANI, rGO–PANI, and AgNPs–rGO–PANI nanocomposite and their interaction were studied by UV-vis, FTIR, XRD, SEM, EDX and XPS analysis. AgNPs–rGO–PANI nanocomposite was loaded (0.5 mg cm⁻²) on a glassy carbon electrode (GCE) where the active surface area was maintained at 0.2 cm² for investigation of the electrochemical properties. It was found that AgNPs–rGO–PANI–GCE had high sensitivity towards the reduction of H₂O₂ than AgNPs–rGO which occurred at −0.4 V vs. SCE due to the presence of PANI (AgNPs have direct electronic interaction with N atom of the PANI backbone) which enhanced the rate of transfer of electron during the electrochemical reduction of H₂O₂. The calibration plots of H₂O₂ electrochemical detection was established in the range of 0.01 μM to 1000 μM (R² = 0.99) with a detection limit of 50 nM, the response time of about 5 s at a signal-to-noise ratio (S/N = 3). The sensitivity was calculated as 14.7 μA mM⁻¹ cm⁻² which indicated a significant potential as a non-enzymatic H₂O₂ sensor.

The current study aims at the development of an electrochemical sensor based on a silver nanoparticle–reduced graphene oxide–polyaniline (AgNPs–rGO–PANI) nanocomposite for the sensitive and selective detection of hydrogen peroxide (H₂O₂).     

Ternary composites of Ni–polyaniline–graphene as counter electrodes for dye-sensitized solar cells

Dye-sensitized solar cells (DSSCs), different in principle from the conventional solar cells based on p–n junctions, are competitively cost-effective. For development of this kind of emerging solar cell, it is very significant to reduce their cost and improve their energy conversion efficiency to the maximum extent. In this article, ternary composites (Ni–PANI–G composites) consisting of nickel nanoparticles, polyaniline (PANI), and graphene (G) were prepared for the first time and used as counter electrodes to replace the noble metal Pt in DSSCs. In the case of PANI, the introduction of Ni nanoparticles can improve the electrocatalytic ability for the reduction of triiodide ions in the counter electrode, while in the meantime, the addition of graphene in the Ni–PANI–G composites can increase the electrical conductivity of the counter electrode. The optimized DSSCs fabricated by using the Ni–PANI–G composites as the counter electrode exhibit an overall power conversion efficiency of 5.80% compared to 5.30% for reference platinum (Pt) counter-electrodes. Electrochemical impedance spectra (EIS) show that the charge-transfer resistance at the interface between electrolyte and counter-electrode in the case of the ternary composite is obviously decreased. These results are significant to develop low-cost counter electrode materials for DSSCs.

In this article, ternary composites (Ni–PANI–G composites) consisting of nickel nanoparticles, polyaniline (PANI), and graphene (G) were prepared for the first time and used as counter electrodes to replace the noble metal Pt in DSSCs.     

Humidity sensor based on poly(lactic acid)/PANI–ZnO composite electrospun fibers

The electrospinning technique has been successfully used to prepared micro-fibers of the poly(lactic acid)/polyaniline–zinc oxide (PLA/PANI–ZnO) composite. The polyaniline–zinc oxide (PANI–ZnO) nanocomposites are synthesized by hydrothermal and in situ polymerization methods. X-ray diffraction techniques are used to study the structural properties of the PLA/PANI–ZnO composite fibers and the PANI–ZnO nanocomposite. The average crystallite size of the PANI–ZnO nanocomposite is found to be 36 nm. The morphology and diameter of the composite fibers are analyzed by scanning electron microscopy (SEM). The average fiber diameter of the pure poly(lactic acid) (PLA) fiber is around 2.5 μm and that of the PLA/PANI–ZnO composite fiber is around 1.4 μm. Differential scanning calorimetry (DSC) provides the thermal properties of the PLA/PANI–ZnO composite fibers. The melting temperature (T_m) for the pure PLA is observed at 149.3 °C, and it is shifted to 153.0 °C for the PLA/PANI–ZnO composite fibers. The enhanced thermal properties of the composite fibers are due to the interaction between the polymer and the nanoparticles. The water contact angle measurements probe the surface hydrophilicity of the PLA/PANI–ZnO composite fibers. The role of the PANI–ZnO nanocomposite on the sensing behavior of PLA fibers has also been investigated. The humidity sensing properties of the composite fiber based sensor are studied in the relative humidity (RH) range of 20–90% RH. The experimental results show that the composite fiber exhibited good response (85 s) and recovery (120 s) times. These results indicate that the one-dimensional (1D) fiber structure enhances the humidity sensing properties.

The electrospinning technique has been successfully used to prepared micro-fibers of the poly(lactic acid)/polyaniline–zinc oxide (PLA/PANI–ZnO) composite for humidity sensor application.     

Flexible PANI/SWCNT thermoelectric films with ultrahigh electrical conductivity

The effects of polyaniline (PANI) with different polymerization times on the film-forming and thermoelectric properties as well as on the performance of SWCNTs/PANI composites were systematically investigated in this study. It was found that the film-forming and flexibility of PANI films improved with the increase in polymerization time. We showed that a super high conductivity of ∼4000 S cm⁻¹ can be achieved for the SWCNTs/PANI composite film, which is the highest value for the SWCNTs/PANI system at present. Both the electrical conductivity and power factor increase by an order of magnitude than that of pure PANI films and far exceed the theoretical value of the mixture model. These results suggest that the sufficiently continuous and ordered regions on the interlayer between the filler and matrix are key to improve the electrical conductivity of composites. Finally, the maximum PF reaches 100 μW m⁻¹ K⁻² at 410 K for the 0.6CNT/PANI5h. Furthermore, it is found that the composite films have excellent environmental and structural stability. Our results can deepen the understanding of organic–inorganic thermoelectric composite systems and facilitate the practical application of flexible and wearable thermoelectric materials.

Flexible PANI/SWCNT thermoelectric films with ultrahigh electrical conductivity of ~4000 S cm⁻¹. The maximum PF reaches 100 μW m⁻¹ K⁻² at 410 K for the 0.6CNT/PANI.     

Fabrication of photo-Fenton self-cleaning PVDF composite membrane for highly efficient oil-in-water emulsion separation

The anti-fouling performance of membranes is an important performance in the separation of oil/water. However, the membrane with anti-fouling performance will also have surface scaling phenomenon when it runs for a long time. Therefore, there is still a great demand for stain-resistant membranes with good self-cleaning ability and high flux recovery rate. Based on this, this paper firstly prepared a hydrophilic membrane with carboxyl group and carboxyl ion by blending poly(ethylene-alt-maleic anhydride) (PEMA) and polyvinylidene fluoride (PVDF), and then prepared a self-cleaning composite membrane by in situ mineralization of β-FeOOH particles on the surface of the membrane for efficient oil-in-water emulsion separation. A large number of –COOH/COO⁻ and β-FeOOH particles on the membrane surface make the composite membrane have strong hydrophilic properties (WCA = 20.34°) and underwater superoleophobicity (UOCA = 155.10°). These composite membranes have high separation efficiency (98.8%) and high flux (694.56 L m⁻² h⁻¹ bar⁻¹) for soybean oil-in-water emulsion. Importantly, the as-prepared membrane shows excellent flux recovery rate (over 99.93%) attributed to the robust photo-Fenton catalytic activity of β-FeOOH, and the β-FeOOH is chemically bonded to the as-prepared membrane, which makes the as-prepared membrane have good reusability. This work provides hope for the application of self-cleaning membranes in the construction of anti-fouling membranes for wastewater remediation.

The anti-fouling performance of membranes is an important performance in the separation of oil/water.     

Deposition of an ultra-thin polyaniline coating on a TiO2 surface by vapor phase polymerization for electrochemical glucose sensing and photocatalytic degradation

Here, we have synthesized an ultra-thin coating of polyaniline on a TiO₂ nanoparticle surface (PANI–TiO₂) using a simple vapor phase polymerization method. By this method, an ultra-thin layer of PANI is obtained selectively on the TiO₂ surface. This ultra-thin coating exhibits the properties of both the parent materials due to the composite surface causing an effective synergistic effect. SEM, TEM, and EDX studies and elemental mapping confirmed the formation of ultra-thin films on the TiO₂ surface. TGA, UV/Vis and XRD studies were also done for further characterization. The composite has been used as a biosensor for glucose detection by immobilization of the enzyme glucose oxidase (GOx). Cyclic voltammetry, electrochemical impedance spectroscopy and amperometry studies were performed for glucose sensing. The linear range was observed from 20 to 140 μM glucose concentration from the amperometric analysis. The LOD of the biosensor was found to be 5.33 μM. The composite has also been used for photocatalytic degradation of the cationic dye Rhodamine B (RB). The order of degradation efficiency of RB is found to be PANI < TiO₂ < PANI–TiO₂. The synergetic effect of PANI and TiO₂ is the reason for the enhanced degradation efficiency of the composite PANI–TiO₂.

Here, we have synthesized an ultra-thin coating of polyaniline on a TiO₂ nanoparticle surface (PANI–TiO₂) using a simple vapor phase polymerization method.     

A novel composite of CdS nanorods growing on a polyaniline-Cd2+ particles surface with excellent formaldehyde gas sensing properties at low temperature

A novel composite, CdS nanorods growing on a polyaniline-Cd²⁺ particles surface (CdS/PANI) with a hexagonal wurtzite structure phase, was prepared using a hydrothermal synthesis method. Methods of XRD, SEM, and FTIR were used to analyze the structure and morphology of the compounds. SEM shows that CdS/PANI consists of sea urchin-like nanorods of about 200–500 nm in length and about 50 nm in diameter. Furthermore, the FTIR spectra show that some characteristic peaks of CdS/PANI are much weaker than those of PANI and the corresponding peaks shift to a higher wavenumber. In addition, the IR stretching frequency of the Cd–S bond for CdS/PANI moved from 630 cm⁻¹ to 674 cm⁻¹. In the gas sensing experiments, the CdS/PANI-based sensor showed an excellent response to low concentration formaldehyde gas in a wide temperature range of 80–140 °C. The highest response of CdS/PANI could reach about 4.8 to 5 ppm formaldehyde gas at 120 °C. The response and recovery times of the sensor based on CdS/PANI were about 25 s and 30 s to 10 ppm formaldehyde gas, respectively.

A novel composite, CdS nanorods growing on a polyaniline-Cd²⁺ particles surface (CdS/PANI) with a hexagonal wurtzite structure phase, was prepared using a hydrothermal synthesis method.     

Enhanced photoelectrochemical biosensing performance for Au nanoparticle–polyaniline–TiO2 heterojunction composites

A new photoelectrochemical (PEC) sensing platform comprising TiO₂ nanotube arrays (TiONTAs), polyaniline (PANI), and gold nanoparticles (AuNPs) was successfully fabricated. After loading the enzyme, this Au–PANI–TiONTA electrode showed excellent response to glucose at a linear range of 2–36 mM with a 0.02 mM detection limit. Good PEC performance was obtained due to the following advantages of the material: high visible-light harvesting ability for excellent light trapping capacity of PANI and AuNPs, good separation of the photo-induced charges related to the specific Au–PANI–TiONTA heterostructure, efficient electrode surface reaction kinetics derived from the large specific surface area of TiONTAs and improved electrode catalytic activity. This work proposed a new and general PEC enzymatic format and can be extended to prepare different PEC biosensors for biomolecules such as DNA, proteins and substrates of oxidases.

A novel photoelectrode for glucose PEC biosensing composed of TiONTAs, PANI, and AuNPs was successfully obtained. The GOx@Au–PANI–TiONTA electrode exhibited a wide response range (2–36 mM) with a low detection limit (0.02 mM) and good stability.     

In situ polymerization of graphene-polyaniline@polyimide composite films with high EMI shielding and electrical properties

With the increasing demands of the electronics industry, electromagnetic interference (EMI) shielding has become a critical issue that severely restricts the application of devices. In this work, we have proposed a “non-covalent welding” method to fabricate graphene-polyaniline (Gr-PANI) composite fillers. The Gr sheets are welded with PANI via π–π non-covalent interactions. Furthermore, a flexible polyimide (PI) composite film with superior EMI shielding effectiveness is prepared by in situ polymerization. The 40% content of Gr-PANI_10:1 (the mass ratio of Gr to PANI is 10 : 1) shows a superior electrical conductivity (σ) as high as 2.1 ± 0.1 S cm⁻¹, 1.45 times higher than that of Gr@PI film at the same loading. Moreover, the total shielding effectiveness (SE_T) of EMI of the Gr-PANI_10:1@PI reaches ∼21.3 dB and an extremely high specific shielding effectiveness value (SSE) of 4096.2 dB cm² g⁻¹ is achieved. Such a “non-covalent welding” approach provides a facile strategy to prepare high-performance PI-based materials for efficient EMI shielding.

With the increasing demands of the electronics industry, electromagnetic interference (EMI) shielding has become a critical issue that severely restricts the application of devices.     

An effective utilization of MXene and its effect on electromagnetic interference shielding: flexible,free-standing and thermally conductive composite from MXene–PAT–poly(p-aminophenol)–polyaniline co-polymer

MXene and conductive polymers are attractive candidates for electromagnetic interference shielding (EMI) applications. The MXene–PAT-conductive polymer (CP) composites were fabricated by a cost-effective spray coating technique and characterized using X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), X-ray diffraction (XRD) and Raman spectroscopy. A new approach has been developed for the synthesis of exfoliated MXene. The MXene–PAT–poly(p-aminophenol)–polyaniline co-polymer composite exhibited good electric conductivity (EC) of 7.813 S cm⁻¹. The composites revealed an excellent thermal properties, which were 0.687 W (m K)⁻¹ thermal conductivity, 2.247 J (g K)⁻¹ heat capacity, 0.282 mm² s⁻¹ thermal diffusivity and 1.330 W s^1/2 m⁻² K⁻¹ thermal effusivity. The composites showed 99.99% shielding efficiency and the MXene–PAT–PANI–PpAP composite (MXPATPA) had EMI shielding effectiveness of 45.18 dB at 8.2 GHz. The reduced form of MXene (r-Ti₃C₂T_x) increased the shielding effectiveness (SE) by 7.26% and the absorption (SE_A) was greatly enhanced by the ant farm like structure. The composites possess excellent thermal and EMI SE characteristics, thus can be applied in areas, such as mobile phones, military utensils, heat-emitting electronic devices, automobiles and radars.

MXene and conductive polymers are attractive candidates for electromagnetic interference shielding (EMI) applications.     

Pseudo in situ construction of high-performance thermoelectric composites with a dioxothiopyrone-based D–A polymer coating on SWCNTs

Organic polymer/inorganic particle composites with thermoelectric (TE) properties have witnessed rapid progress in recent years. Nevertheless, both development of novel polymers and optimization of compositing methods remain highly desirable. In this study, we first demonstrated a simulated in situ coagulation strategy for construction of high-performance thermoelectric materials by utilizing single-walled carbon nanotubes (SWCNTs) and a new D–A polymer TPO-TTP12 that was synthesized via incorporating dioxothiopyrone subunit into a polymeric chain. It was proven that the preparation methods have a significant influence on thermoelectric properties of the TPO-TTP12/SWCNT composites. The in situ prepared composite films tend to achieve much better thermoelectric performances than those prepared by simply mixing the corresponding polymer with SWCNTs. As a result, the in situ compositing obtains the highest Seebeck coefficient of 66.10 ± 0.05 μV K⁻¹ at the TPO-TTP12-to-SWCNT mass ratio of 1/2, and the best electrical conductivity of up to 500.5 ± 53.3 S cm⁻¹ at the polymer/SWCNT mass ratio of 1/20, respectively; moreover, the power factor for the in situ prepared composites reaches a maximum value of 141.94 ± 1.47 μW m⁻¹ K⁻², far higher than that of 104.68 ± 0.86 μW m⁻¹ K⁻² for the by-mixing produced composites. This indicates that the dioxothiopyrone moiety is a promising building block for constructing thermoelectric polymers, and the simulated in situ compositing strategy is a promising way to improve TE properties of composite materials.

High-performance thermoelectric composites with a dioxothiopyrone unit have been constructed utilizing SWCNTs and polymer TPO-TTP12via a simulated in situ compositing strategy based on the coagulation method.     

Synthesis and characterization of polyaniline–hydrotalcite–graphene oxide composite and application in polyurethane coating

In this paper, a composite from polyaniline and graphene oxide-hydrotalcite hybrid (PAN–HG) was fabricated by direct polymerization of aniline using ammonium persulphate as an oxidant in the presence of a HG hybrid. The structure and morphological properties of synthesized PAN–HG composites were characterized by Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), Raman spectra, and scanning electron microscopy (SEM) techniques. The electrochemical properties of the composite particles were also analyzed by potentiodynamic polarization curves to evaluate the corrosion inhabitation. The results were calculated by Tafel fitting and showed that the effective corrosion protection values were 73.11%, 88.46%, and 95.49%, corresponding to HG, 1PAN–HG, and 2PAN–HG. The influence of PAN–HG on the corrosion protection of the polyurethane coating applied on the CT3 steel was investigated. As a result, the PU containing 0.5% of 2PAN–HG showed the most effective protection of the CT3 steel substrate. The R_C of the coating was about 1.61 × 10⁷ Ω cm², and after immersion for 30 days, the R_C value was 0.17 × 10⁶ Ω cm². From all the analyzed results, PAN–HG has enhanced the corrosion protection and a complicated protection mechanism was also concluded and explained.

Corrosion protection: PAN–HG performed effect of 95.49% protection of CT3-steel in NaCl 3.5%. PU(PAN–HG) coating provides good corrosion protection with complex mechanism of high barrier, ion-exchange and e⁻ trapping to HG structure.     

Synergistically assembled graphene/ZnO composite to enhance anticorrosion performance of waterborne epoxy coatings

In this work, waterborne epoxy resin and graphene/ZnO (Gr/ZnO) were employed as the matrix and nanofiller to construct composite coatings with enhanced anticorrosive performance. The corrosion protection properties of the coatings were significantly improved by the dispersed Gr sheets, as well as the parallelly assembled ZnO nanoparticles. The most remarkable improvement was achieved by adding 0.04 wt% of Gr and 0.4 wt% of ZnO in the Waterborne Epoxy (WEP) coatings, where the highest impedance was 200 530 Ω cm² on Gr_0.04–ZnO_0.4, far more than pure epoxy with 6186 Ω cm² after 7 days of immersion in electrolytes. Furthermore, the Gr_0.04–ZnO_0.4 coatings and corresponding corrosion products immersed in a 3.5% NaCl solution for 30 days were also characterized, which could further reveal anticorrosion mechanisms of the graphene modified WEP coatings and the passivated effect of ZnO. Through the mechanism analysis, we also found that ZnO could be employed as the barrier reinforcement to improve the dispersibility of graphene in WEP coatings, and the parallel assembly of graphene occurs spontaneously, leading to remarkable improvement of anticorrosion properties.

This is the first example of synergistically assembled Gr/ZnO sheets to improve the corrosion protection properties of WEP coatings, and Gr_0.04–ZnO_0.4 exhibited the highest impedance of 200 530 Ω cm² compared to pure WEP of 6186 Ω cm².     

Formation and dissociation of synthetic hetero-double-helix complex in aqueous solutions: significant effect of water content on dynamics of structural change

A 1 : 1 mixture of the ethynylhelicene pseudoenantiomers (M)-tetramer and (P)-pentamer, which possess hydrophilic terminal tri(ethyleneglycol) (TEG) groups, changes their structures in the water–THF (10 μM) solvent system between dissociated random-coils and an associated hetero-double-helix upon heating and cooling. A small change in water content between 30 and 33% significantly affects the dynamics of structural changes. At 30% water content, heating to 60 °C causes rapid formation of random-coil and cooling to 10 °C causes the rapid formation of hetero-double-helix, accompanied by repeated changes in Δε at 369 nm between 0 and −2000 cm⁻¹ M⁻¹. Heating and cooling experiments at constant rates between 60 and 10 °C resulted in sigmoidal curves in Δε/temperature profiles, which indicate rapid structural changes. Different phenomena occurred at 33% water content. Heating to 60 °C and cooling to 0 °C initially induced changes in Δε between 0 and −2000 cm⁻¹ M⁻¹, and repeated cycles gradually reduced the range between 0 and −500 cm⁻¹ M⁻¹. Heating and cooling experiments at constant rates between 60 and 10 °C caused small changes in Δε, and repeated cycles at 10 °C gradually increased Δε to −500 cm⁻¹ M⁻¹. These phenomena involved rapid changes in molecular structure and slow structural changes in the water–THF solvent system. The sharp switching of the dynamics of structural changes at water content between 30 and 33% indicated discontinuous structural changes in the hydration of TEG and/or in water clusters in the vicinity of oligomer molecules.

Significant structural changes by small change in water content from 30 to 33%.     

Enhanced electrical and thermal properties of semi-conductive PANI-CNCs with surface modified CNCs

Cellulose nanocrystals (CNCs) are the most commonly used natural polymers for biomaterial synthesis. However, their low dispersibility, conductivity, and poor compatibility with the hydrophobic matrix hinder their potential applications. Therefore, we grafted sulfate half-ester and carboxylic functional groups onto CNC surfaces (S-CNC and C-CNC) to overcome these shortcomings. The effect of the dopants, surfactant ratios, and properties of CNCs on the thermal stability, conductivity, and surface morphology of polyaniline (PANI)-doped CNC nanocomposites were investigated through emulsion and in situ polymerization. The higher electrical conductivity and well-dispersed morphology of SCNC–PANI₃₀ (1.1 × 10⁻² S cm⁻¹) but lower thermal stability than that of CCNC–PANI₃₀ (T₀: 189 °C) nanocomposites are highly related to dispersibility of S-CNCs. However, after 4-dodecylbenzenesulfonic acid (DBSA) was added, the conductivity and thermal stability of SCNC/PANI increased up to 2.5 × 10⁻¹ S cm⁻¹ and 192 °C with almost no particle aggregation because of the increase in charge dispersion. The proposed biodegradable, renewable, and surface-modified S-CNC and C-CNC can be used in high-thermal-stability applications such as food packaging, optical films, reinforcement fillers, flexible semiconductors, and electromagnetic materials.

Biodegradable surface-modified CNCs were synthesized found high dispersibility and flexibility. Polyaniline-doped CNCs nanocomposites were exhibited high conductivity and thermal stability that may be promising for flexible semiconductors.     

Efficient nickel or copper oxides decorated graphene–polyaniline interface for application in selective methanol sensing

Graphene sheets decorated with nickel or copper oxides that were anchored on polyaniline (denoted as PANI-graphene/NiO and PANI-graphene/CuO) were prepared by a simple, easy to-control electrochemical method and applied as novel materials for sensitive and selective methanol sensing. The fabricated sensors exhibited good electrocatalytic activity, appropriate dynamic linear range (20–1300 mM), sensitivity (0.2–1.5 μA mM⁻¹ cm⁻²) and excellent selectivity towards methanol. It should be highlighted from the selectivity tests that no significant interference was observed from ethanol and other alcohols. To our best knowledge, using inexpensive but efficient transition metals like Ni, Cu instead of Pt, Pd and their composites with PANI, graphene would be scientifically novel and practically feasible approach for sensor fabrication that could be potentially used to identify methanol adulteration in counterfeit alcoholic beverages.

PANI/graphene/NiO or PANI/graphene/CuO were prepared by a simple, easy to-control electrochemical method and applied as novel materials for sensitive and selective methanol sensing.     

Coatings of hydroxyapatite–bioactive glass microparticles for adhesion to biological tissues

Adsorption of particles across interfaces has been proposed as a way to create adhesion between hydrogels and biological tissues. Here, we explore how this particle bridging approach can be applied to attach a soft polymer substrate to biological tissues, using bioresorbable and nanostructured hydroxyapatite–bioactive glass microparticles. For this, microparticles of aggregated flower-like hydroxyapatite and bioactive glass (HA–BG) were synthesized via a bioinspired route. A deposition technique using suspension spreading was developed to tune the coverage of HA–BG coatings at the surface of weakly cross-linked poly(beta-thioester) films. By varying the concentration of the deposited suspensions, we produced coatings having surface coverages ranging from 4% to 100% and coating densities ranging from 0.02 to 1.0 mg cm⁻². The progressive dissolution of these coatings within 21 days in phosphate-buffered saline was followed by SEM. Ex vivo peeling experiments on pig liver capsules demonstrated that HA–BG coatings produce an up-to-two-fold increase in adhesion energy (9.8 ± 1.5 J m⁻²) as compared to the uncoated film (4.6 ± 0.8 J m⁻²). Adhesion energy was found to increase with increasing coating density until a maximum at 0.2 mg cm⁻², well below full surface coverage, and then it decreased for larger coating densities. Using microscopy observations during and after peeling, we show that this maximum in adhesion corresponds to the appearance of particle stacks, which are easily separated and transferred onto the tissue. Such bioresorbable HA–BG coatings give the possibility of combining particle bridging with the storage and release of active compounds, therefore offering opportunities to design functional bioadhesive surfaces.

Coatings of hydroxyapatite–bioactive glass microparticles are proposed as a way to create adhesion between hydrogels and biological tissues using adsorption of the microparticles across the interface.     

Nisin/polyanion layer-by-layer films exhibiting different mechanisms in antimicrobial efficacy

Nisin/polyanion Layer-by-Layer (LbL) films are reported to exhibit different mechanisms in antimicrobial efficacy depending on the type of polyanion. LbL films consisting of nisin as the polycationic component were prepared using two different polyanionic constituents: poly acrylic acid (PAA) and dextran sulfate (DX). Due to the weaker interaction strength of carboxylate groups with nisin compared to sulfate/nisin, a larger molecular weight of PAA was needed to achieve LbL assembly. PAA-100K/nisin and DX-15K/nisin multilayer films exhibited significantly different properties. PAA–nisin films grew faster compared to DX–nisin films and showed, for 60 bilayer films, an average bilayer thickness of 21.6 nm compared to that of 6.1 nm in DX–nisin films. The total amount of nisin was found to be 17.1 ± 2.2 μg cm⁻² in (PAA–nisin)₆₀ and 6.8 ± 0.4 μg cm⁻² in (DX–nisin)₆₀ films. The stability of the films was investigated at three different pH values of 6.0, 7.4 and 9.5. (PAA–nisin)₆₀ films exhibited the release of nisin into the solution which resulted in the disintegration of the film over several hours. A burst release was observed in the first hour followed by a slower release and disintegration over 24 hours with a complete release at pH 9.5. The bacterial growth inhibition test against Staphylococcus epidermidis confirmed the antimicrobial activity of nisin released from PAA–nisin films. PAA was found to stabilize nisin and the film-released nisin retained its antimicrobial activity in the neutral and alkaline pH values. Unlike PAA–nisin films, (DX–nisin)₆₀ films were stable at the physiological conditions up to 14 days with no release of nisin. DX–nisin films were found to inhibit the attachment of Staphylococcus epidermidis and prevent biofilm formation. These results clearly demonstrate the effect of different polyanions on nisin LbL films to achieve different mechanisms in antimicrobial efficacy and show the potential of PAA–nisin multilayer films as promising local delivery systems for treatment of burns and wounds, while DX–nisin multilayer films can be employed as stable coatings against bacterial attachment and biofilm formation.

Polyanion–nisin multilayer films exhibit antimicrobial activity by controlled release of nisin or as stable biofilm inhibiting coatings depending on polyanion.     

A cellulose/β-cyclodextrin nanofiber patch as a wearable epidermal glucose sensor

In this study, we aimed to develop a cellulose/β-cyclodextrin (β-CD) electrospun immobilized GOx enzyme patch with reverse iontophoresis for noninvasive monitoring of interstitial fluid (ISF) glucose levels (0.1–0.6 mM dm⁻³). In vitro analysis, performed using a sensor attached to flexible substrates, revealed that the high diffusion coefficient (9.0 × 10⁻⁵ cm² s⁻¹), the linear correlation coefficient (R² = 0.998), the detection limit (9.35 × 10⁻⁵ M), and the linear range sensitivity (0–1 mM) of the sensor (5.08 μA mM⁻¹) remained unaffected by the presence of interfering substances (e.g., fructose, sucrose, uric acid, and acetaminophen) at physiological levels. The present results indicate that the new epidermal sensing strategy using nanofibers for continuous glucose monitoring has potential to be applied in diagnosis of diabetes.

In this study, we aimed to develop a cellulose/β-cyclodextrin (β-CD) electrospun immobilized GOx enzyme patch with reverse iontophoresis for noninvasive monitoring of interstitial fluid (ISF) glucose levels (0.1–0.6 mM dm⁻³).     

A novel MnO–CrN nanocomposite based non-enzymatic hydrogen peroxide sensor

A MnO–CrN composite was obtained via the ammonolysis of the low-cost nitride precursors Cr(NO₃)₃·9H₂O and Mn(NO₃)₂·4H₂O at 800 °C for 8 h using a sol–gel method. The specific surface area of the synthesized powder was measured via BET analysis and it was found to be 262 m² g⁻¹. Regarding its application, the electrochemical sensing performance toward hydrogen peroxide (H₂O₂) was studied via applying cyclic voltammetry (CV) and amperometry (i–t) analysis. The linear response range was 0.33–15 000 μM with a correlation coefficient (R²) value of 0.995. Excellent performance toward H₂O₂ was observed with a limit of detection of 0.059 μM, a limit of quantification of 0.199 μM, and sensitivity of 2156.25 μA mM⁻¹ cm⁻². A short response time of within 2 s was achieved. Hence, we develop and offer an efficient approach for synthesizing a new cost-efficient material for H₂O₂ sensing.

A MnO–CrN composite was obtained via the ammonolysis of the low-cost nitride precursors Cr(NO₃)₃·9H₂O and Mn(NO₃)₂·4H₂O at 800 °C for 8 h using a sol–gel method.