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The efficiency of chemotherapy is frequently affected by its multidrug resistance, immune suppression, and severe side effects. Its combination with immunotherapy to reverse immune suppression and enhance immunogenic cell death (ICD) has emerged as a new strategy to overcome the aforementioned issues. Herein, we construct a pH-responsive PAMAM dendritic nanocarrier-incorporated hydrogel for the co-delivery of immunochemotherapeutic drugs. The stepwise conjugation of moieties and drug load was confirmed by various techniques.

Design strategies of smart membranes for switchable gas separation performance.

A novel but simple design is presented of a multi-ion network with polyamic acid that combines high extensibility and toughness with spontaneous healing ability. Taking advantage of the carboxylate structure of polyamic acid, the introduction of a sufficient number of metal ions to neutralize the carboxylated groups can form reversible ionic bonds within the polymeric network. Dry-solid zinc(II)-poly(amic acid-PDMS) is transparent and exhibits good mechanical properties, including good ultimate strength (~0.267 MPa) and high stretchability (~360%). In addition, this dynamic network can self-heal at ambient temperature without requiring stimulation from heat, a plasticizer, or a solvent. The very simple method of our proposed polyamic acid polymers opens up the possibility of increasingly utilizing high-performance, low-cost, and environmentally friendly polyamic acids instead of polyimides. A simplified multi-ion network is presented, which can toughen and modulate the spontaneous self-healing capability of dry-solid Zn(II)-carboxylate polyamic acid under ambient conditions.

In humans, excessive bleeding during civilian accidents, and surgery account for 40% of the mortality worldwide. Hence, the development of biocompatible hemostatic materials useful for rapid hemorrhage control has become a fundamental research problem in the biomedicine community. In this study, we prepared biocompatible gelatin-tannic acid-κ-carrageenan (GTC) microparticles using a facile Tween 80 stabilized water-in-oil (W/O) emulsion method for rapid hemostasis. The formation of GTC microparticles occurs via polyelectrolyte interactions between gelatin and k-carrageenan as well as hydrogen bonding from tannic acid. In addition, the GTC microparticles formulated in our study showed high water adsorption ability with a low volume-swelling ratio for a particle size of 46 μm. In addition, the GTC microparticles displayed80% biocompatibility in NIH 3T3 cells and5% hemocompatibility in hemolysis ratio tests. Notably, the GTC microparticles induced rapid blood clotting in 50 s and blood loss of approximately 46 mg in the femoral artery of BALB/c female mice with a 100% survival rate that was significantly better than the control group (blood clot time:250 s; blood loss: 259 mg). Thus, the findings from our study collectively suggest that GTC microparticles may play a promising clinical role in medical applications to tackle hemorrhage control.

We fabricated a mussel-inspired hemocompatible polycarbonate membrane (PC) modified by the cross-linking of chondroitin sulfate and caffeic acid polymer using CA-CS via a Schiff base and Michael addition reaction and named it CA-CS-PC. The as-fabricated CA-CS-PC membrane shows excellent hydrophilicity with a water contact angle of 0° and a negative surface charge with a zeta potential of -32 mV. The antiadhesion property of the CA-CS-modified PC membrane was investigated by enzyme-linked immunosorbent assay (ELISA), using human plasma protein fibrinogen adsorption studies, and proved to have excellent antiadhesion properties, because of the lower fibrinogen adsorption. In addition, the CA-CS-PC membrane also shows enhanced hemocompatibility. Finally, blood cell attachment tests of the CA-CS-PC membrane were observed by CLSM and SEM, and the obtained results proved that CA-CS-PC effectively resisted cell adhesion, such as platelets and leucocytes. Therefore, this work disclosed a new way to design a simple and versatile modification of the membrane surface by caffeic acid and chondroitin sulfate and apply it for cell adhesion.

This study provides a significant contribution to the development of multiple hydrogen-bonded supramolecular nanocarrier systems by demonstrating that controlling the hydrogen bond strength within supramolecular polymers represents a crucial factor to tailor the drug delivery performance and enhance the effectiveness of cancer therapy. Herein, we successfully developed two kinds of poly(ethylene glycol)-based telechelic polymers Cy-PEG and UrCy-PEG having self-constituted double and quadruple hydrogen-bonding cytosine (Cy) and ureido-cytosine (UrCy) end-capped groups, respectively, which directly assemble into spherical nanogels with a number of interesting physical characteristics in aqueous solutions. The UrCy-PEG nanogels containing quadruple hydrogen-bonded UrCy dimers exhibited excellent long-term structural stability in a serum-containing biological medium, whereas the double hydrogen-bonded Cy moieties could not maintain the structural integrity of the Cy-PEG nanogels. More importantly, after the drug encapsulation process, a series of in vitro experiments clearly confirmed that drug-loaded UrCy-PEG nanogels induced selective apoptotic cell death in cancer cells without causing significant cytotoxicity to healthy cells, while drug-loaded Cy-PEG nanogels exerted nonselective cytotoxicity toward both cancer and normal cells, indicating that increasing the strength of hydrogen bonds in nanogels plays a key role in enhancing the selective cellular uptake and cytotoxicity of drugs and the subsequent induction of apoptosis in cancer cells.

Membrane separation has been an efficient and energy saving technique in dealing with greenhouse gases, but the traditional membrane designs might not be able to handle the concomitant environmental pollution due to their fixed properties. Correspondingly, the use of an active-responsive smart membrane appears to be a new trend for membrane development in the coming future, which shows great potential to deal with the obstacles. In this research, we demonstrate a smart graphene-organic framework membrane to enable reversed electrical-switchable permselectivity in CO2 separation. The addition of polydopamine (PDA) to the polyvinylidene fluoride/Graphene (PVDF/G) membranes was done to (i) induce the β-phase of PVDF, since –NH2-functionalized graphene has specific interactions (dipole induced dipole interaction) between graphene-PDA and PVDF; (ii) modify the organic PVDF-inorganic graphene interface; and (iii) facilitate CO2 selective separation. Permeability and permselectivity was increased after applying voltage that resulted in the increase of gas permselectivity in response to the lowest applied voltage range (0–3 V) to the membrane. Digital image correlation method depicted the response of the membrane to voltage and proved that the membrane has high piezoelectric properties that is switchable. Furthermore, PALS studies confirmed the free volume and interlayers in the membrane. This membrane has unique properties because the pore changes from bimodal to single pore distribution.

Aim: To prepare efficient metal-semiconductor nanoparticles as noninvasive, real-time imaging probes for photothermal therapy (PTT) applications. Materials & methods: A bottom-up approach was used to fabricate core-shell Ag@CuS nanoparticles (NPs). PTT and Raman mapping were done using HeLa cells. Theoretical simulation of electric field enhancement and heat dissipation density of Ag@CuS NPs was performed. Results: PTT-induced hyperthermia was achieved under 940 nm near-infrared light irradiation. Surface-enhanced Raman spectroscopy (SERS) signals of dye molecules were observed when conjugated with Ag@CuS NPs. Conclusion: Ag@CuS NPs are found to be efficient for SERS imaging and localized heating under laser irradiation, making a promising candidate for SERS-guided PTT.

This work reports a study on employing lignin in the formation of a selective layer of thin-film composite (TFC) membranes for pervaporation desalination. The TFC membranes with lignin-based separation layers are fabricated using a solution-casting method. With a reduction of the separation layer thickness to about 0.47 μm, a water permeation flux of 18.5 kg h−1 m−2 and a salt rejection of above 99.95% have been recorded on the lignin based TFC membrane with a feeding solution of 3.5 wt% NaCl(aq) at 45 °C. The membrane also exhibits high stability in long-term operation tests and can be applied for operations on high salinity water (up to 15 wt% NaCl(aq)). While being applied to seawater desalination, the membrane exhibits a water permeation flux of about 20.4 kg h−1 m−2 and a salt rejection of above 99.95% at 45 °C. A membrane separation process, which uses sustainable materials for salty wastewater treatments and water resource generation, has been demonstrated.

Programmed formation of hierarchical graphene nanosheets, based on a combination of first and second exfoliations using the halogenated solvent ortho-dichlorobenzene (ODCB) and an adenine-functionalized supramolecular polymer (A-PPG), respectively, can be used to directly exfoliate graphite into high-quality graphene nanosheets with wide-range tunable layer thickness. In this study, we discover that natural graphite in ODCB can be directly exfoliated into well-dispersed, dozen-layer exfoliated graphite (EG) nanosheets with relatively weak interlayer interactions; this process is called first exfoliation. On subsequent addition of A-PPG into the EG solution (i.e., second exfoliation), the hydrogen-bonded adenine moieties act as indispensable key units that manipulate the self-assembly behavior of the A-PPG polymers to effectively form long-range ordered lamellar nanostructures on the surface of the graphene nanosheets. This process substantially enhances the long-term dispersion stability of EG in ODCB and achieves the production of exfoliated graphene nanosheets with the desired structural characteristics through simply adjusting the content of A-PPG in the composites. These desirable characteristics of non-covalently functionalized graphene with a supramolecular polymer are extremely rare, but highly attractive for the development of physically custom-tailored graphene based on combined first and second exfoliation processes. Thus, this development provides a facile, highly efficient graphene fabrication process for potential applications in various fields.

Water pollution has become a serious problem in aquatic ecology due to the oil spills and the consistent release of industrial pollutants, such as dyes. Herein, we report a simple method to fabricate superwetting caffeic acid (CA)-polyethyleneimine (PEI)-modified melamine sponges (CA-PEI-MS) for oil-in-water emulsion separation and dye adsorption. The as-fabricated CA-PEI-MS exhibited superhydrophilicity with an approximately zero water contact angel (WCA) and underwater superoleophobicity with an underwater oil contact angel (UWOCA) greater than 150°. The compressed CA-PEI-MS showed an excellent oil-in-water emulsion separation performance with a separation efficiency greater than 97% and a water flux of up to 25,480 L h−1 m−2 bar−1. The recyclability test was used to study the stability of the compressed CA-PEI-MS, after washing with acetone; the flux did not show any significant change during the 12-cycle separation test. The separation efficiency in every cycle was greater than 97%. Due to the availability of rich positive charged amino groups, the as fabricated CA-PEI-MS exhibited adsorption ability towards negatively charged dyes such as, rose bengal (RB) and direct red (DR) with 96% adsorption efficiency. Therefore, the as designed low-cost and eco-friendly preparation of CA-PEI-MS has a great potential for practical application as it shows high separation performances and excellent efficiency.

We report a significant breakthrough in the development of complementary hydrogen-bonded drug-carrier systems, namely the construction of self-assembled nanoparticles with desirable functionalities conferred by the presence of stable complementary uracil–adenine (U–A) hydrogen bonding interactions between the drug and carrier complex. Herein, an adenine-functionalized rhodamine derivative (A-R6G) was successfully synthesized, and exhibited a variety of interesting physical properties including unique hydrophobicity, hydrogen bond-modulated green-fluorescence behavior and potent tumor-cell specific cytotoxicity. A-R6G strongly associates with uracil end-capped difunctional poly(propylene glycol) (BU-PPG) to spontaneously form spherical nanoparticles in aqueous solution due to the complementary U–A interactions between the drug and the carrier. These nanoparticles possess several interesting physical properties, such as ultrahigh drug loading content (up to 84.3%), a wide-range tunable drug loading ratio, high A-R6G-encapsulation stability in serum-rich culture media and pH/temperature-sensitive controlled drug release; these properties are very rare in drug-loaded nanoparticles, but are extremely desirable for drug-delivery applications based on polymeric micelles. Surprisingly, A-R6G-loaded nanoparticles exhibited selective cytotoxicity against cancer cells but had no effects on normal cells, whereas control rhodamine 6G-loaded nanoparticles displayed potent non-selective cytotoxicity, suggesting that the U–A interactions within the nanoparticles critically enhance the tumor-selective cytotoxicity of A-R6G towards cancer cells. Importantly, fluorescence imaging and flow cytometric assays confirmed that A-R6G-loaded nanoparticles were selectively delivered into cancer cells via an endocytic pathway and subsequently induced apoptotic cell death, but had minimal cytotoxic effects on normal cells. Thus, this complementary drug-carrier system has the ability to achieve targeted cancer chemotherapy with high therapeutic efficacy and safety.

Graphene possesses a set of unique physicochemical properties including exceptional mechanical, thermal, and electrical properties, making it an excellent candidate for constructing materials for a wide range of applications including the vast field of separation technology using membranes. Separation membranes based on graphene and its derivatives have shown satisfactory results over the years when applied to environmental systems such as wastewater treatment and gas purification, which is a great contribution in sustainable development. However, membrane separation research is generally performed using conventional membranes with fixed driving force and separation properties that suffer from fouling and decline in performance upon long-term use or when a change in the environmental conditions occur. These issues can be solved by employing an emerging technology that makes use of graphene and its derivatives combined with polymeric materials to construct stimuli-responsive or “smart” membranes that respond to the changes in their environment such as chemical cues, temperature, pressure, and external fields, and have a self-regulated separation performance due to reversible physicochemical properties. In this review, we present a report on the recent advancements on graphene-based separation technology including a concise discussion on the basic structure and properties of graphene and its derivatives, various membrane fabrication methods, and their employment on the different areas of membrane separation. More importantly, the main focus of this paper is to evaluate the design and utilization of graphene-based smart separation membranes.

Functionalized amphiphilic polymers consisting of hydrophilic poly(ethylene glycol) pendant groups and a hydrophobic poly(epichlorohydrin) backbone can spontaneously self-organize into single-chain...

Water-soluble conjugated polymers (WCPs) composed of a hydrophobic polythiophene main chain with hydrophilic tertiary amine side-chains can directly self-assemble into sphere-like nano-objects in an aqueous solution due to phase separation between the hydrophilic and hydrophobic segments of the polymeric structure. Due to the presence of gas-responsive tertiary amine moieties in the spherical structure, the resulting polymers rapidly and reversibly tune their structural features, surface charge, and fluorescence performance in response to alternating carbon dioxide (CO2) and nitrogen (N2) bubbling, which leads to significantly enhanced fluorescence and surface charge switching properties and a stable cycle of on and off switching response. In vitro studies confirmed that the CO2-treated polymers exhibited extremely low cytotoxicity and enhanced cellular uptake ability in normal and tumor cells, and thus possess significantly improved fluorescence stability, distribution, and endocytic uptake efficiency within cellular organisms compared to the pristine polymer. More importantly, in vivo assays demonstrated that the CO2-treated polymers displayed excellent biocompatibility and high fluorescence enhancement in living zebrafish, whereas the fluorescence intensity and stability of zebrafish incubated with the pristine polymer decreased linearly over time. Thus, these CO2 and N2-responsive WCPs could potentially be applied as multifunctional fluorescent probes for in vivo biological imaging.

Separation technology by using membranes is an effective choice for water treatment, but fouling is a significant problem for membrane applications. Recently, transition-metal dichalcogenide nanosh...

Effective water use is currently a critical global challenge needed to prevent water shortages and has attracted significant research attention. The realization of solar-driven water evaporation by using effective converters has attracted considerable attention in recent years owing to its potential for seawater desalination and wastewater treatment. Consequently, this paper proposes a simple two-step method to prepare low-cost and self-floating photothermal converters from waste coffee grounds. First, the coffee grounds were carbonized at 1,000 °C to develop broadband absorption, and the carbonized coffee grounds were modified using hydrophobic silane to enhance the water-floatation property of the grounds. The prepared hydrophobic carbonized coffee grounds exhibited good performance for desalination and water purification under sunlight irradiation. The self-floatation ability, low cost, well solar evaporation performance, and easy preparation contribute to the promising potential of using hydrophobic carbonized coffee grounds infuture steps toward eco-friendly desalination procedures.

In this study, we fabricated ultrafiltration mixed-matrix membranes through wet phase-inversion method of cellulose acetate (CA) blended with polydopamine (PDA) particles solution. PDA, as an organic and hydrophilic particle, altered the physicochemical and antifouling property of CA membranes. X-ray photoelectron spectroscopy confirmed the presence of PDA particles on the membrane surface. Adding PDA particles led to the formation of macrovoids onto the cross-sectional morphology of CA membranes. This also improved the membrane porosity, pore size, and hydrophilicity. At an optimum concentration of 0.2 wt% PDA, the membrane presented the highest pure water flux of 771.98 L m−2 h−1 at 1 bar and significant oil rejection (93–99%). Furthermore, the modified membrane exhibited better antifouling property (flux recovery = 87%; irreversible fouling = 12%; Reversible fouling = 80%) contrasted to a pristine CA membrane (flux recovery ratio = 70%; irreversible fouling = 25%; reversible fouling = 45%).

Choosing the property of the supporting membrane is crucial in preparing high performing nanofiltration membranes through interfacial polymerization. In this study, an oxygen rich membrane – cellulose triacetate (CTA) – was used to fabricate the support membrane. Polyamide was deposited onto the CTA support using interfacial polymerization of piperazine (PIP) and trimesoyl chloride (TMC). The concentration of the monomers was optimized. Furthermore, the polyamide layer prepared on CTA support exhibited higher separation efficiency for sodium sulfates and dyes compared to using traditional polysulfone (PSf) support. The oxygen groups of CTA facilitate better adsorption of amines on the surface; thus, using low concentration of PIP could still provide a defect-free polyamide layer. Utilizing the optimum condition, the polyamide/CTA membrane delivered a high pure water flux (operating at 6 bar) of 179.5 L/m2h with the following rejections: Na2SO4 = 98.4%; MgSO4 = 60.3%; MgCl2 = 15.0%; NaCl = 3.7%; Rose Bengal = 95.5%; Brilliant Blue R = 99.9%; Amido Black 10B = 90.6%; Orange G = 67.3%. Moreover, the polyamide/CTA membrane had excellent stability at a wide range operating conditions.

Graphene quantum dots(GQDs) were used to possibly cover the structural defects on the graphitic regions of reduced graphene oxide(rGO). The resulting homostructure nanocomposite fillers(rGO + GQD) were incorporated in an alginate solution creating a dense composite membrane for pervaporation. The membranes were applied to separate alcohol/water mixtures in which the successful covering of structural defects was observed with good separation performance of lower molecular weight alcohols. The Raman spectra and elemental analyses confirmed the successful changes on the physical and chemical structures of the homostructured fillers. The X-ray diffraction pattern showed that the crystallinity of the membrane was greatly affected when incorporated with rGO + GQD. The alginate incorporated with 3 wt% of rGO + GQD(Alg-rGO + GQD) has the best pervaporation performance in separating methanol/water mixture with a permeation flux of 2323 g m−2 h−1 and water concentration in permeate of 92.7% at 70 °C. While the positron annihilation lifetime spectroscopy results supported that the minimization of the structural defects enhanced the water selectivity of the membrane by easy transport of water molecules through the free volume spaces and blocks methanol molecules. The results in this study may provide the possible sealing or curing the defects on rGO with GQDs and improve the interfacial interaction with the polymer matrix.

An easy and novel synthetic concept for building intrinsically stretchable and elastic semiconducting polymers is designed in this study, in which a conjugated rod–coil block copolymer with a rigid...

Water-soluble supramolecular polymers can be created by incorporation of self-complementary multiple hydrogen bonding groups. However, technically simple fabrication of water-soluble supramolecular polymers with highly desirable physical properties—to achieve micelles suitable for effective delivery of drugs for cancer treatment—remains a significant challenge. We developed a new polyethylene glycol-based supramolecular polymer containing self-complementary quadruple hydrogen bonding groups, which spontaneously assembles into nanospherical micelles in an aqueous environment. These supramolecular micelles can be readily controlled to obtain the desired structural stability and possess excellent pH-responsive and drug-loading capabilities, as well as good biocompatibility towards both normal and cancer cells. The resulting drug-loaded micelles exhibit tunable drug loading capacity and excellent long-term drug-entrapment stability due to the strong affinity between the drug and micelle core, which led to highly efficient drug loading. In addition, in vitro release assays indicated the drug-loaded micelles can be triggered to rapidly release the drug under mildly acidic conditions. More importantly, fluorescence microscopy and flow cytometry clearly demonstrated that drug-loaded micelles were effectively endocytosed by cancer cells and induced apoptosis; therefore, this newly developed supramolecular system could serve as versatile drug nanovehicle for safe, effective controlled drug release to achieve superior chemotherapeutic effects.

An ultrasensitive light-responsive block copolymer, a combination of a multiarmed poly(ethylene glycol)

PVDF membranes were prepared with nonsolvent-induced phase separation, using solvents with various dipole moments, including HMPA, NMP, DMAc and TEP. Both the fraction of the polar crystalline phase and the water permeability of the prepared membrane increased monotonously with an increasing solvent dipole moment. FTIR/ATR analyses were conducted at the surfaces of the cast films during membrane formation to provide information on if the solvents were present as the PVDF crystallized. The results reveal that, with HMPA, NMP or DMAc being used to dissolve PVDF, a solvent with a higher dipole moment resulted in a lower solvent removal rate from the cast film, because the viscosity of the casting solution was higher. The lower solvent removal rate allowed a higher solvent concentration on the surface of the cast film, leading to a more porous surface and longer solvent-governed crystallization. Because of its low polarity, TEP induced non-polar crystals and had a low affinity for water, accounting for the low water permeability and the low fraction of polar crystals with TEP as the solvent. The results provide insight into how the membrane structure on a molecular scale (related to the crystalline phase) and nanoscale (related to water permeability) was related to and influenced by solvent polarity and its removal rate during membrane formation.

The separation of oily wastewater, specifically emulsions, is a crucial global issue. Possible strategies for the efficient separation of emulsified oil/water mixtures through sustainable and environmentally friendly materials have recently drawn considerable attention. In our study, we prepared superwetting water caltrop shell biochar (WCSB) via a top-lit-updraft carbonization procedure. The as-prepared WCSB was characterized by superhydrophilicity, underwater superoleophobicity, underoil superhydrophilicity, and underoil water adsorption ability. Because of its superwetting properties, WCSB was used for the separation of both surfactant-stabilized oil-in-water emulsions (SOIWEs) and surfactant-stabilized water-in-oil emulsions (SWIOEs) with very high fluxes (up to 74,700 and 241,000 L m

Description, Cascaded microporosity localized on membrane surfaces markedly improved selective transport of small molecules., In membrane-based separation, molecular size differences relative to membrane pore sizes govern mass flux and separation efficiency. In applications requiring complex molecular differentiation, such as in natural gas processing, cascaded pore size distributions in membranes allow different permeate molecules to be separated without a reduction in throughput. Here, we report the decoration of microporous polymer membrane surfaces with molecular fluorine. Molecular fluorine penetrates through the microporous interface and reacts with rigid polymeric backbones, resulting in membrane micropores with multimodal pore size distributions. The fluorine acts as angstrom-scale apertures that can be controlled for molecular transport. We achieved a highly effective gas separation performance in several industrially relevant hollow-fibrous modular platform with stable responses over 1 year.

Bentazone (BEZ) is one of the utmost selective problematic contact-past herbicide with high toxicity for humans owing to feasible contamination of surface and ground water. In this work, an electrochemical sensor has been developed for the sensitive detection of BEZ, based on hierarchically porous three-dimensional (3D) carbon superstructures (CS)–modified electrodes. The CSs (namely, CSHEX, CSPY, CSACN, and CSNOS) were prepared by the pyrolysis process from organic porous polyacrylonitrile (PAN) superstructure particles (namely, PANHEX, PANPY, PANACN, and PANNOS) obtained by free radical polymerization method using different solvents (hexane, pyridine, acetonitrile, and also no solvent). The assembly with the working electrode of CSs causes the electrocatalytic BEZ oxidation by rapid electron transfer compared to the PAN superstructures and bare electrodes. Intriguingly, compared to all electrodes, CSHEX-modified electrode showed the superior electrochemical detection of BEZ at a working potential of 0.99 V (vs. Ag/AgCl), very low detection limit (0.002 μM), wide dynamic linear range (0.03 to 200 μM), high sensitivity (9.95 μA μM−1 cm−2), and excellent reliability. The advanced sensors displayed an intensification of oxidation peak current of BEZ with high selectivity, remarkable sensitivity, and reproducibility for BEZ detection and received satisfactory outcomes designating the application of sensors for the determination of BEZ in river water samples.

Electrically conductive polymer nanomaterials signify a promising class of sensing platforms in the field of electrochemistry, but their applications as electrocatalysts are commonly limited by their poor colloidal stability in aqueous media and large particle sizes. Inspired by biomineralization approaches for integrating nanoscale materials, herein, a gadolinium (Gd)-integrated polypyrrole (PPy) electrocatalyst (namely, BSA@PPy-Gd) was successfully prepared by choosing bovine serum albumin (BSA) as a stabilizer for biomimetic mineralization and polymerization in a "one-step" manner. BSA@PPy-Gd possesses outstanding water dispersibility, nanoscale morphology, and improved electrical conductivity. The electrocatalytic competency of the electrochemical (EC) sensing platform fabricated for the sensitive detection of nicardipine (NCD) was assessed. The synergy of remarkable conductivity, superior active surface area, and electrostatic interactions stimulated by the combination of BSA with the NH group of PPy on BSA@PPy-Gd and Gd increases the fast electron transfer at the analyte-electrode junction. The fabricated EC sensor, BSA@PPy-Gd/glassy carbon electrode (GCE), exhibits a current intensity greater than that of PPy/GCE, BSA/GCE, and bare GCE in terms of peak height at a pH of 7.0 in phosphate buffer solution. The newly fabricated EC sensing platform shows excellent electrocatalytic activities for the electroreduction of NCD in terms of a low detection limit (2 nM), good sensitivity, linear dynamic detection ranges (0.01-575 μM), operational stability, and repeatability and was also tested on rat and human serum specimens.

In this work, a novel thermoresponsive switching transistor is developed through the rational design of active materials based on the typical field-effect transistor (FET) device configuration, where the active material is composed of a blend of a thermal expansion polymer and a polymeric semiconductor. Herein, polyethylene (PE) is employed as the thermal expansion polymer because of its high volume expansion coefficient near its melting point (90–130 °C), which similarly corresponds to the overheating point that would cause damage or cause fire in the devices. It is revealed that owing to the thermistor property of PE, the FET characteristics of the derived device will be largely decreased at high temperatures (100–120 °C). It is because the high volume expansion of PE at such high temperature (near its Tm) effectively increases the distance of the crystalline domains of poly(3-hexylthiophene-2,5-diyl) to result in a great inhibition of current. Besides, the performance of this device will recover back to its original value after cooling from 120 to 30 °C owing to the volume contraction of PE. The reversible FET characteristics with temperature manifest the good thermal sensitivity of the PE-based device. Our results demonstrate a facile and promising approach for the development of next-generation overheating shutdown switches for electrical circuits.