Sensitive polydopamine bi-functionalized SERS immunoassay for microalbuminuria detection
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One aspect of the invention is a polymer material comprising a capsule coated with PDA. In certain embodiments, the capsule encapsulates a functional agent. The encapsulated functional agent may be an indicating agent, healing agent, protecting agent, pharmaceutical drug, food additive, or a combination thereof.
The separation of lithium from magnesium ions in salt brines is an important step in producing raw lithium for prospective use in electrochemical storage systems. Liquid–liquid extraction of Mg 2+ ions from Li + ions is challenging because of comparable thermodynamic behavior in aqueous solutions. Removing Mg 2+ ions from brines using consumable ion-exchange membranes is also a challenging prospect due to poor chemical selectivity and compromised sustainability. In this work, we propose the use of redox-active catechols in the form of melanin pigments for selective removal of Mg 2+ ions from aqueous solutions. Synthetic melanin films are oxidatively polymerized on stainless steel meshes from aqueous solutions of dopamine precursors to create electrochemically functionalized polydopamine membranes. The binding selectivity of redox-active catechol-bearing polydopamine melanin for Mg 2+ ions in aqueous solutions was measured as a function of electrochemical cycling. The binding kinetics of Mg 2+ ions to polydopamine pigments was measured. Mg 2+ ions binding selectivity to polydopamine in mixed aqueous solutions containing both Li + and Mg 2+ ions were also measured. Additionally, the equilibrium binding concentrations of Mg 2+ ions to polydopamine were achieved very rapidly (<1 min). Finallym, redox-active polydopamine membranes therefore show promise as functional materials for the separation of Mg 2+ and Li + ions in aqueous solutions.
We present the synthesis and multifunctional utilization of core-satellite carbon-Fe{sub 3}O{sub 4} nanoparticles to serve as the enabling platform for a range of applications including oxygen reduction reaction (ORR) and magnetic adsorbent. Starting from polydopamine (PDA) nanoparticles and Fe(NO{sub 3}){sub 3}, carbon-Fe{sub 3}O{sub 4} core–satellite nanospheres are synthesized through successive steps of impregnation, ammoniation and carbonization. The synergistic combination of Fe{sub 3}O{sub 4} and N-doped carbon endows the nanocomposite with high electrochemical activity in ORR and mainly four electrons transferred in reaction process. Furthermore, carbon-Fe{sub 3}O{sub 4} nanoparticles used as magnetic adsorbent exhibit the efficient removal of Rhodamine B from an aqueous solution. The recovery and reuse of the adsorbent is demonstrated 5 times without any detectible loss in activity. - Graphical abstract: Starting from polydopamine (PDA) nanoparticles and Fe(NO{sub 3}){sub 3}, carbon-Fe{sub 3}O{sub 4} core–satellite nanospheres are synthesized through successive steps of impregnation, ammoniation and carbonization. The nanocomposites serve as the enabling platform for a range of applications including oxygen reduction reaction (ORR) and magnetic adsorbent. - Highlights: • Carbon-Fe{sub 3}O{sub 4} core–satellite nanospheres are synthesized through successive steps of impregnation, ammoniation and carbonization. • Polydopamine and Fe(NO{sub 3}){sub 3} are precursors for N-doped carbon source and Fe{sub 3}O{sub 4} nanoparticles, respectively. • The nanocomposites exhibit high electrochemical activity in ORR. • The nanocomposites effectively adsorb organic dyes with magnetic recovery and good recycle property.
Pure metal–organic framework (MOF) layers deposited on porous supports are important candidates for molecular sieving membranes, but their performance usually deviates from theoretical estimations. Here, we combine stepwise scanning electron microscopy imaging, time-resolved synchrotron X-ray scattering, terahertz infrared spectroscopy, and density functional theory calculation to investigate the ZIF-8 membrane formation on two types (polydopamine and TiO2) of functionalized porous supports. Though molecular sieving of ZIF-8 membranes for smaller gases (He, H 2 , and CO 2 ) can be achieved with both types of functionalized supports, we unravel that the strong interaction between MOF and polydopamine can disrupt the formation of “perfect” MOF crystals at the interface, leading to a “contracted” MOF structure with partially uncoordinated imidazolate ligands. This further affects the low-frequency dynamical parameters of the framework and inhibits the effective seeded growth. Eventually, it leads to an unexpected loss of selectivity for the bulkier gases (N 2 and CH 4 ) for ZIF-8 on polydopamine-functionalized supports. This work links the dynamical aspects of MOFs with their gas transport behavior and highlights the importance of regulating the interfacial weak forces to preserve the ideal molecular sieving efficiency of MOF membranes, which a
Membrane fouling is one of the most severe problems restricting membrane separation technology for wastewater treatment. This work reports a photocatalytic nanofiltration membrane (NFM) with self‐cleaning property fabricated using a facile biomimetic mineralization process. In this strategy, a polydopamine (PDA)/polyethyleneimine (PEI) intermediate layer is fabricated on an ultrafiltration membrane via a co‐deposition method followed by mineralization of a photocatalytic layer consisting of β‐FeOOH nanorods. The PDA–PEI layer acts both as a nanofiltration selective layer and an intermediate layer for anchoring the β‐FeOOH nanorods via strong coordination complexes between Fe 3+ and catechol groups. In visible light, the β‐FeOOH layer exhibits efficient photocatalytic activity for degrading dyes through the photo‐Fenton reaction in the presence of hydrogen peroxide, endowing the NFM concurrently with effective nanofiltration performance and self‐cleaning capability. Moreover, the mineralized NFMs exhibit satisfactory stability under simultaneous filtration and photocatalysis processing, showing great potential in advanced wastewater treatment.
In this work the tribological properties of 45 ± 2 μm-thick polytetrafluoroethylene (PTFE) and polydopamine (PDA) + PTFE coatings in oil-lubricated conditions were investigated under a normal load of 10 N and a linear reciprocating speed of 0.1 m/s. Both the PTFE and the PDA + PTFE coatings were deposited using an in-house spray-coating method. The PDA + PTFE coating was five times more durable compared to the PTFE coating in oil-lubricated conditions. Both PTFE and PDA + PTFE coatings showed lower COF in oil-lubricated conditions than in dry conditions. The nanomechanical properties measured by PeakForce Quantitative Nanomechanical (PFQNM) characterization method showed an increase in Young’s modulus and adhesion force for the PDA + PTFE coatings compared to the PTFE coatings. Chemical analysis showed that the cross-linking between PDA and PTFE polymer chains occurred during the high-temperature sintering procedure. Finally, the higher adhesion of PDA + PTFE coating to the cast iron substrate and the stronger cohesion due to the cross-linking between PDA and PTFE contributed to the higher durability of the PDA + PTFE composite coatings.
This study presents a novel metal-organic-framework-engaged synthesis route based on porous tellurium nanotubes as a sacrificial template for hierarchically porous 1D carbon nanotubes. Furthermore, an ultrathin Fe-ion-containing polydopamine layer has been introduced to generate highly effective FeN x C active sites into the carbon framework and to induce a high degree of graphitization. The synergistic effects between the hierarchically porous 1D carbon structure and the embedded FeN x C active sites in the carbon framework manifest in superior catalytic activity toward oxygen reduction reaction (ORR) compared to Pt/C catalyst in both alkaline and acidic media. A rechargeable zinc-air battery assembled in a decoupled configuration with the nonprecious pCNT@Fe@GL/CNF ORR electrode and Ni-Fe LDH/NiF oxygen evolution reaction (OER) electrode exhibits charge–discharge overpotentials similar to the counterparts of Pt/C ORR electrode and IrO 2 OER electrode.
Microbial bioelectronic devices integrate naturally occurring or synthetically engineered electroactive microbes with microelectronics. These devices have a broad range of potential applications, but engineering the biotic–abiotic interface for biocompatibility, adhesion, electron transfer, and maximum surface area remains a challenge. Prior approaches to interface modification lack simple processability, the ability to pattern the materials, and/or a significant enhancement in currents. We report a novel conductive polymer coating that significantly enhances current densities relative to unmodified electrodes in microbial bioelectronics is reported. The coating is based on a blend of poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) crosslinked with poly(2-hydroxyethylacrylate) (PHEA) along with a thin polydopamine (PDA) layer for adhesion to an underlying indium tin oxide (ITO) electrode. When used as an interface layer with the current-producing bacterium Shewanella oneidensis MR-1, this material produces a 178-fold increase in the current density compared to unmodified electrodes, a current gain that is higher than previously reported thin-film 2D coatings and 3D conductive polymer coatings. The chemistry, morphology, and electronic properties of the coatings are characterized and the implementation of these coated electrodes for use in microbial fuel cells, multiplexed bioelectronic devices, and organic electrochemical transistor based microbial sensors are demonstrated. It is envisioned that this simple coating will advance the development of microbial bioelectronic devices.
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Janus particles are widely sought for applications related to colloidal assembly, stabilization of emulsions, and development of active colloids, among others. Here we report a versatile route to the fabrication of well-controlled Janus particles by simply breaking the symmetry of spherical particles with swelling. When a polystyrene (PS) sphere covered by a rigid shell made of silica or polydopamine is exposed to a good solvent for PS, a gradually increased pressure will be created inside the shell. If the pressure becomes high enough to poke a hole in the shell, the spherical symmetry will break while pushing out the swollen PS through the opening to generate a Janus particle comprised of two distinct components. One of the components is made of PS and its size is controlled by the extent of swelling. The other component is comprised of the rigid shell and remaining PS, with its overall diameter determined by the original PS sphere and the rigid shell. This solution-based route holds promises for the scalable production of complex Janus particles with a variety of compositions and in large quantities.
ABSTRACT In this work, silver nanoparticle functionalized polyamide 6 (PA6) fibers were prepared using the electroless plating method. The surface of PA6 fibers was modified by exploiting dopamine/CuSO 4 /H 2 O 2 system prior to electroless plating to enhance the bonding force between the fiber and the silver nanoparticles. It was found that both the formation rate and the chemical stability of polydopamine (PDA) coatings on the PA6 fiber surface were improved by the introduction of CuSO 4 /H 2 O 2 . The results confirmed the successful deposition of silver nanoparticles on PA6 fiber surface and the average particle diameter of 223 nm. Compared with uncoated fibers, the silver plated PA6 fibers exhibited excellent antimicrobial activity to both Escherichia coli and Staphylococcus aureus (with an antimicrobial efficiency of 99.9% and 100%, respectively). The electrical resistance of the silver coated PA6 fibers reached 0.98 Ω over a length of 1 cm, indicating a good electrical conductivity. In particular, coating durability of the formed silver layer was investigated by subjecting the fibers to various mechanical deformations, and the results showed that the formed silver layer was maintained well after 50 times of cyclic stretching at a constant displacement of 10 mm. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136 , 47584.