Polymerization Of Dopamine Research Articles

Swarming Magnetic Fe3O4@Polydopamine-Tannic Acid Nanorobots: Integrating Antibiotic-Free Superficial Photothermal and Deep Chemical Strategies for Targeted Bacterial Elimination.

Micro/nanorobots (MNRs) are envisioned to provide revolutionary changes to therapies for infectious diseases as they can deliver various antibacterial agents or energies to many hard-to-reach infection sites. However, existing MNRs face substantial challenges in addressing complex infections that progress from superficial to deep tissues. Here, we develop swarming magnetic Fe3O4@polydopamine-tannic acid nanorobots (Fe3O4@PDA-TA NRs) capable of performing targeted bacteria elimination in complicated bacterial infections by integrating superficial photothermal and deep chemical strategies. The Fe3O4@PDA-TA nanoparticles (NPs), serving as building blocks of the nanorobots, are fabricated by insitu polymerization of dopamine followed by TA adhesion. When driven by alternating magnetic fields, Fe3O4@PDA-TA NPs can assemble into large energetic microswarms continuously flowing forward with tunable velocity. Thus, the swarming Fe3O4@PDA-TA NRs can be navigated to achieve rapid broad coverage of a targeted superficial area from a distance and rapidly eradicate bacteria residing there upon exposure to near-infrared (NIR) light due to their efficient photothermal conversion. Additionally, they can concentrate at deep infection sites by traversing through confined, narrow, and tortuous passages, exerting sustained antibacterial action through their surface TA-induced easy cell adhesion and subsequent membrane destruction. Therefore, the swarming Fe3O4@PDA-TA NRs show great potential for addressing complex superficial-to-deep infections. This study may inspire the development of future therapeutic microsystems for various diseases with multifunction synergies, task flexibility, and high efficiency.

The dual nature of biomimetic melanin.

Melanin-inspired nanomaterials offer unique photophysical, electronic and radical scavenging properties that are widely explored for health and environmental preservation, or energy conversion and storage. The incorporation of functional melanin building blocks in more complex nanostructures or surfaces is typically achieved via a bottom-up approach starting from a molecular precursor, in most cases dopamine. Here we demonstrate that indeed, the oxidative polymerization of dopamine, for the synthesis of melanin-like polydopamine (PDA), leads to the simultaneous formation of more than one nanosized species with different compositions, morphologies and properties. In particular, a low-density polymeric structure and dense nanoparticles (NP) are simultaneously formed. The two populations could be separated and analyzed in real time using a chromatographic technique free of any stationary phase (flow field fractionation, FFF). The results following the synthesis of melanin-like PDA showed that the NP are formed only during the first 6 hours as a result of a supramolecular self-assembly-driven polymerization, while the formation of the polymer continues for about 36 hours. The two populations were also separated and characterized using TEM, UV-vis absorption spectroscopy, fluorescence and light scattering spectroscopy, DLS, FTIR, ζ-potential measurements, gel electrophoresis and pH titrations. Interestingly, very different properties between the two populations were observed: in particular the polymer contains a higher number of catechol units (8 mmol g-1 -OH) with respect to the NP (1 mmol g-1 -OH) and presents a much higher antioxidant activity. The attenuation of light by NP is more efficient than that by the polymer especially in the Vis-NIR region. Moreover, while the NP scatter light with an efficiency up to 27% they are not fluorescent, and the polymer does not scatter light but shows an excitation wavelength-dependent fluorescence typical of multi-fluorophoric uncoupled systems.

Activated carbon fibers functionalized with superhydrophilic coated pDA/TiO2/SiO2 with photoluminescent self-cleaning properties for efficient oil-water separation

The adhesion of high-viscosity oil contamination poses limitations on three-dimensional (3D) materials' practical use in treating oilfield-produced water (OPW). In this study, we developed a hybrid pDA/TiO2/SiO2 coating (PTS) on the surface of hydrophilic activated carbon (ACF1) through a combination of dopamine (DA) polymerization, ethyl orthosilicate (TEOS) hydrolysis, and the condensation of TiO2 nanoparticles (NPs) with SiO2 NPs. This coating was designed for gravity-based oil-water separation. The inherent porosity and generous pore size of ACF1-PTS conferred it an ultra-high permeation flux (pure water flux of 3.72 × 105 L∙m−2∙h−1), allowing it to effectively separate simulated oil-water mixtures and oil-water emulsions while maintaining exceptional permeation flux and oil rejection efficiency. When compared to cleaning methods involving ethanol aqueous solutions and NaClO, ultraviolet (UV) illumination cleaning proved superior, enabling oil-contaminated ACF1-PTS to exhibit remarkable flux recovery efficiency and oil-removal capabilities during cyclic separation of actual OPW. Furthermore, the ACF1-PTS material demonstrated impressive stability and durability when exposed to acidic environments (acid, alkali, and salt), robust hydraulic washout conditions, and 25-cycle tests. This study offers valuable insights and research avenues for the development of highly efficient and environmentally friendly 3D oil-water separation materials for the actual treatment of OPW.

Polydopamine‐Enabled Biomimetic Surface Engineering of Materials: New Insights and Promising Applications

AbstractSurface modification is an important approach to modify the properties of materials. Numerous approaches have been adopted to tailor the properties of such materials, which have been proven successful at many scales and parameters. However, most of these techniques are often tedious, poorly adhesive, costly, sometimes hazardous, and surface‐specific, hence cannot be extended on a large scale and all kinds of surfaces. These shortcomings have led to the emergence of new dopamine (DA) based green surface modification technique where a thin polydopamine (PDA) layer is deposited on surfaces through a facile polymerization of DA under alkaline conditions to enable the surface for various applications. This surface modification strategy has several advantages over other techniques in deposition processing under mild conditions, cost‐effective and straightforward ingredients, and applicability to all kinds of surfaces regardless of their sizes, shapes, and types. Moreover, the PDA layer enhances the surface functionality. Therefore, it can serve as a versatile platform for various secondary reactions for a wide range of applications. Herein, the chemistry of DA is summarized and its polymerized form PDA for the modification of different families of materials’ surfaces with an emphasis on energy, environmental and biological applications.

Ozone-Induced Rapid and Green Synthesis of Polydopamine Coatings with High Uniformity and Enhanced Stability.

The development of green, controllable, and simplified pathways for rapid dopamine polymerization holds significant importance in the field of polydopamine (PDA) surface chemistry. In this study, a green strategy is successfully devised to accelerate and control the polymerization of dopamine through the introduction of ozone (O3 ). The findings reveal that ozone serves as an eco-friendly trigger, significantly accelerating the dopamine polymerization process across a broad pH range, spanning from 4.0 to 10.0. Notably, the deposition rate of PDA coatings on a silicon wafer reaches an impressive value of ≈64.8nmh-1 (pH 8.5), which is 30 times higher than that of traditional air-assisted PDA and comparable to the fastest reported method. Furthermore, ozone exhibits the ability to accelerate dopamine polymerization even under low temperatures. It also enables control over the inhibition-initiation of the polymerization process by regulating the "ON/OFF" mode of the ozone gas. Moreover, the ozone-induced PDA coatings demonstrate exceptional characteristics, including high homogeneity, good hydrophilicity, and remarkable chemical and mechanical stability. Additionally, the ozone-induced PDA coatings can be rapidly and effectively deposited onto a wide range of substrates, particularly those that are adhesion-resistant, such as polytetrafluoroethylene (PTFE).

Flax fiber treatment by an alkali solution and poly(dopamine) coating: Effects on the fiber physico-chemistry and flax/Elium® composite interfacial properties

The use of natural fibers to reinforce polymer-based composites is gaining interest to replace conventional synthetic fibers due to their sustainability. In this frame, optimizing the adhesion between natural fibers and the polymer matrix is crucial to ensure high mechanical properties. To improve the adhesion between flax fiber and an acrylic-based thermoplastic resin, the combining of alkalization and poly(dopamine) (PDA) coating as fiber treatments has been investigated in this paper. It is found that applying an alkalization with sodium hydroxide (3 wt%, 2 h, 21 ± 2 °C), followed by dopamine polymerization (2 g/L, pH of 8.5, 24 h, 21 ± 2 °C) in the presence poly(ethylene imine) (600 g/mol, 1 g/L) as a polyelectrolyte, provides the highest increase in composite interfacial shear strength (+22.0 %) and interlaminar shear strength (+63.2 %) compared to the composite with untreated fibers. The results are discussed based on the fiber physico-chemical properties and composite interfacial aspects.

Lubricating Micro‐Interface Assisted General Strategy for Preparing dECM‐Microparticle–Based Heterogeneous Granular Inks toward 3D Printing

AbstractDecellularized extracellular matrix (dECM) retains the bioactive components to mimic tissue‐specific microenvironment. Designing dECM‐based inks for 3D printing to prepare scaffolds can enhance the regeneration of corresponding tissues. However, due to the strict requirements for inks, how to efficiently prepare dECM‐based inks is a challenge. Inspired by granular lubrication, the present study proposes an effective and general method for preparing granular ink from dECM microparticles (MP) with high content. Through dopamine polymerization, dECM‐MPs are coated with polydopamine (PDA). Meanwhile, gelatin methacryloyl (GelMA)‐based microspheres (GelMA‐MSs) are prepared with available double bonds. dECM‐MPs (30–40 wt%) and GelMA‐MSs assemble to form a granular ink, exhibiting well‐performed extrudability, plasticity, and fidelity. Further inspired by joint lubrication, hyaluronic acid (HA) is introduced into PDA coating and GelMA‐MSs to reduce the micro‐interface friction, further promoting the printability and broadening the printable window of dECM‐MPs content to 30–60 wt%. Osteochondral scaffold and skin wound dressing are fabricated through 3D printing from the corresponding dECM‐MPs, enhancing the regeneration of the corresponding tissues in vivo. Especially, the realization of printability of highly rigid dECM‐MPs confirms the universality, reliability and efficiency of the present strategy.

Intestine-Targeted Explosive Hydrogel Microsphere Promotes Uric Acid Excretion for Gout Therapy.

Uric acid metabolism disorder triggers metabolic diseases, especially gout. However, increasing uric acid excretion remains a challenge. Here, an accelerative uric acid excretion pathway via an oral intestine-explosive hydrogel microsphere merely containing uricase and dopamine is reported. After oral administration, uricase is exposed and immobilized on intestinal mucosa along with an in situ dopamine polymerization via a cascade reaction triggered by the intestinal specific environment. By this means, trace amount of uricase is required to in situ up-regulate uric acid transporter proteins of intestinal epithelial cells, causing accelerated intestinal uric acid excretion. From in vitro data, the uric acid in fecal samples from gout patients could be significantly reduced by up to 37% by the mimic mucosa-immobilized uricase on the isolated porcine tissues. Both hyperuricemia and acute gouty arthritis in vivo mouse models confirm the uric acid excretion efficacy of intestine-explosive hydrogel microspheres. Fecal uric acid excretion is increased around 30% and blood uric acid is reduced more than 70%. In addition, 16S ribosomal RNA sequencing showed that the microspheres optimized intestinal flora composition as well. In conclusion, a unique pathway via the intestine in situ regulation to realize an efficient uric acid intestinal excretion for gout therapy is developed.

Polydopamine-functionalized natural cellulosic Juncus effusus fiber for efficient and eco-friendly Cr (VI) removal from wastewater

Biomass adsorbents have received extensive attention for the removal of heavy metals, but most of them had very limited adsorption capacity or needed to be modified with environmentally unfriendly chemicals to achieve acceptable performance. In this study, a green biomass adsorbent was fabricated using an abundant natural cellulosic Juncus effusus (JE) fiber and natural melanin polydopamine (PDA) through a simple mussel-inspired polymerization strategy. JE's unique hollow three-dimensional network structure provided an ideal scaffold substrate with abundant sites for dopamine polymerization deposition. This enabled the modified PDA@JE fibers to be rich in amino, hydroxyl, and other active adsorption sites, thereby endowing the PDA@JE fiber adsorbent with a promising Cr (VI) adsorption capacity of up to 145.8 mg / g. This capacity was significantly higher than that of most previously reported biomass-based adsorbents. Furthermore, 10–20 times the concentration of common interfering ions such as Ca2+, Cd2+, Cu2+, NO3-, Cl-, SO42- and PO43- had little effect on the adsorption efficiency. This study provided a green and general mussel-inspired strategy for preparing effective biomass adsorbent, offering a promising approach for utilizing natural cellulosic fibers in eco-friendly applications.

Self-Assembled and Multilayer-Overlapped ESM-PDA@rGO Nanofilm-Based Flexible Wearable Sensor for Real-Time Body Temperature Monitoring.

There is an urgent need for wearable sensors that continuously monitor human physiological conditions in real time. Herein, an ESM-PDA@rGO-based flexible wearable temperature sensor was successfully constructed by integrating an eggshell membrane (ESM) with reduced graphene oxide (rGO) through dopamine (DA) polymerization. Depending on the "bridge effect" of diversified polydopamine (PDA) chains, on the one hand, a staggered arrangement of PDA-rGO frameworks and a lot of conductive pathways were produced and acted as an active layer. On the other hand, PDA-rGO frameworks were linked with ESM by PDA chains as a flexible sensing nanofilm. As a result, these mechanical merits of the ESM-PDA@rGO exhibited a 1.8-fold increase in Young' s modulus and 1.4-fold increase in tensile strength. Thereby, the conformability and performance of the temperature sensor were greatly enhanced, showing excellent sensitivity (-2.23%/°C), good linearity (R2 = 0.979), as well as stability. Especially, the flexible sensing nanofilm is evolved from the staggered arrangement of PDA-rGO frameworks, which endows it with rapid response (only 4-8 s), high resolution (0.1 °C), as well as excellent long-term durability (10 weeks). More importantly, the temperature sensor demonstrates insensitivity to bending deformation, ensuring reliable wearing stability. The sensor allows for online, real-time monitoring of human body temperature, encompassing both core (forehead, temple, cochlea, and exhale gas) and shell (palm and back of the hand, fingertip, and instep) temperatures. Particularly, it can accurately assess minor changes in peripheral body temperature before and after exercise, and it is capable of mapping daily patterns of body temperatures. The developed temperature sensor will provide us new materials design concepts and holds considerable promise in the fields of e-skin, disease surveillance, prediction, and diagnose.

Multifunctional coatings hinging on the catechol/amine interplay

AbstractDesign and implementation of functional coatings is a topic of active research in a variety of health‐related applications, most of which require wet adhesion. The powerful wet adhesion of mussel byssus proteins rich in DOPA and lysine residues provided a clue to realize that the combination of a catechol and an amine component has a specific role in the interfacial adhesion. From this natural model, polydopamine (PDA)‐based coatings have been developed that result from the oxidative polymerization of dopamine combining the catechol and amine functionalities in the same molecule. Covalent interactions resulting from Michael‐type addition or Schiff‐base formation of the polymeric products from dopamine oxidation as well as non‐covalent π‐stacking and cation‐π interactions exemplify the diverse mode of catechol/amine interplay that have been identified as responsible of the adhesion and cohesion properties of PDA. In the last decade coatings inspired to the same chemistry but using different starting materials have been explored particularly catechols of natural origin and different amine components, while mechanistic studies with model compounds have allowed to rationalize the structural requirements for adhesion and to expand the potential of these functional coatings.

Preparation of Superhydrophobic Fabric Based on Dopamine and Michael Addition under Ultraviolet Light.

This work reports a simple, stable, and environmentally friendly method to prepare durable superhydrophobic surfaces. First, a polydopamine coating is formed by oxidative polymerization of dopamine to form a secondary reaction platform to provide reaction sites for subsequent experiments. We applied a polydopamine layer onto a fiber surface using the Michael addition-reaction-grafted tetrakis (3-mercaptopropionic acid) pentaerythritol ester, followed by the introduction of tetraallyl silane and (mercapto) methyl siloxane-dimethyl siloxane copolymer on the polydopamine by a thiol-ene click-reaction under ultraviolet light. The resulting superhydrophobic Nylon 56 fabric exhibited a 166° static contact angle as well as excellent stability. The surface morphology of all samples was observed by field emission scanning electron microscope, X-ray photoelectron spectroscopy and energy dispersion spectroscopy, and the elemental composition and surface chemical state of the samples were analyzed. It also had the ability of oil-water separation. Fabric with such benefits broadens the applicability and innovation of superhydrophobic textiles for environmental and industrial applications.

Ultrafine nano-copper derived from dopamine polymerization & synchronous adsorption achieve electrochemical purification of nitrate to ammonia in complex water environments

Electrochemical-nitrate-reduction-reaction (eNitRR) synthesis of ammonia is an effective way to treat nitrate wastewater and alleviate the pressure of the Haber-Bosch ammonia production industry. How to develop effective catalysts to electrochemically reduce nitrate to ammonia and purify sewage under complex environmental conditions is the focus of current research. Herein, the dopamine polymerization process and the [(C₁₂H₈N₂)2Cu]2+ complex embedding process were run simultaneously in time and space, and ultrafine Cu nanoparticles (Cu/CN) were effectively loaded on nitrogen-doped carbon after heat treatment. Using Cu/CN as the catalyst, the ammonia yield rate and Faradaic efficiency of the electrochemical conversion of NO3− to NH3 are highly 8984.0 µg h−1 mgcat.−1 and 95.6%, respectively. Even in the face of complex water environments, such as neutral media, acidic media, coexisting ions, and actual nitrate wastewater, nitrate wastewater can be effectively purified to form high value-added ammonia. The strategy of simultaneous embedding increases the exposure rate of Cu sites, and the support of CN is also beneficial to reduce the energy barrier of *NO3 activation. This study rationally designed catalysts that are beneficial to eNitRR, and considered the situation faced by practical applications during the research stage, reducing the performance gap between laboratory exploration and industrial applications.

Pathologically catalyzed physical coating restores the intestinal barrier for inflammatory bowel disease therapy

Intestinal epithelia impairment of inflammatory bowel disease (IBD) leads to the leakage of bacteria and antigens and the consequent persistent immune imbalance. Restoring the epithelial barrier is a promising therapeutic target but lacks effective and safe clinical interventions. By identifying the catalase (CAT) presence in the IBD pathological environment, we herein develop a CAT-catalyzed pathologically coating on the damaged epithelial barrier to inhibit intestinal leakage for IBD therapy. With the codelivery of CaO2 (a CAT substrate) and dopamine, the nanosystem can enable CAT-catalyzed oxygen (O2) production and in-situ polymerization of dopamine and then yield a thin and integrative polydopamine (PDA) coating on the intestinal barrier due to the highly adhesive property of PDA. In vivo study demonstrates that PDA coating provides not only a protective barrier by restricting intestinal leakage but also a favorable anti-inflammation effect. Beyond drug management, this work provides a physical repair strategy via catalyzed coating for IBD therapy.

Pyrrole-Doped Polydopamine-Pyrrole (PDA-nPY) Nanoparticles with Tunable Size and Improved NIR Absorption for Photothermal Therapy.

Polydopamine (PDA) as a melanin-like biomimetic material with excellent biocompatibility, full spectrum light absorption capacity and antioxidation property has been extensively applied in the biomedical field. Based on the high reactivity of dopamine (DA), exploiting new strategies to fabricate novel PDA-based nano-biomaterials with controllable size and improved performance is valuable and desirable. Herein, we reported a facile way to synthesize pyrrole-doped polydopamine-pyrrole nanoparticles (PDA-nPY NPs) with tunable size and enhanced near-infrared (NIR) absorption capacity through self-oxidative polymerization of DA with PY in an alkaline ethanol/H2O/NH4OH solution. The PDA-nPY NPs maintain excellent biocompatibility and surface reactivity as PDA. By regulating the volume of added PY, PDA-150PY NPs with a smaller size (<100 nm) and four-fold higher absorption intensity at 808 nm than that of PDA can be successfully fabricated. In vitro and in vivo experiments effectively further demonstrate that PDA-150PY NPs can effectively inhibit tumor growth and completely thermally ablate a tumor. It is believed that these PY doped PDA-nPY NPs can be a potential photothermal (PT) agent in biomedical application.

Sn3O4 nanosheets with N-doped carbon coating for high performance lithium storage

Tin-based oxides are promising anode materials for lithium ion batteries (LIBs) in virtue of their many advantages including high capacity, abundant reserves and environmental friendliness. Yet, previous studies mainly focus on the SnO2-based anodes for lithium storage. Considering that the mixed valence and layered crystal structure of Sn3O4 may lead to better lithium storage properties, Sn3O4-based anode material is designed and synthesized through a facile hydrothermal method in this work. The as-prepared Sn3O4 nanosheets are coated with N-doped carbon layers (∼15 nm) on both sides through dopamine polymerization and subsequent polydopamine carbonization to solve the issues of poor intrinsic electronic conductivity and drastic volume change during LiSn alloying/dealloying, which have hindered their application in LIBs. With the structural and composition advantages brought by the thick N-doped carbon layers, the Sn3O4@NC nanosheets delivered a remarkable reversible capacity (1222 mAh g−1 after 50 cycles at 200 mA g−1) and excellent rate performance when applied in LIB as anode material, owing to the improved electrical conductivity and strengthened structure stabilities. Importantly, we demonstrate a convenient strategy to realize carbon coating in the fabrication of Sn3O4-based anode materials, which could inspire the development of other Sn3O4-based anode materials with excellent lithium storage properties.

Polydopamine-modified magnetic foam composites synergistically activate peroxymonosulfate with visible light for sulfadiazine degradation and oil–water separation

This study used a CuSO4/H2O2 catalyst to accelerate the oxidation and polymerization of dopamine in solution to facilitate the rapid deposition of polydopamine (PDA) onto a melamine foam. Dopamine provided the Fe3O4 adhesive layer and additional photocatalytic electron transfer channels for the foam. Stearic acid (SA) was used as the final incorporation on the surface of melamine foam(MF) to further superhydrophobically modify the magnetic foam (MF@PDA/Fe3O4) to obtain superhydrophobic magnetic MF@PDA/Fe3O4@SA foam. The foam has excellent capacity, acid resistance, alkali resistance, flame retardant, and salt resistance and can be conveniently separated, recycled, and recovered using magnetism. At the same time, peroxymonosulfate (PMS) can be activated to generate super-active radicals. Within 16 min, the degradation rate of sulfadiazine (SDZ) reached 99.8 %. Trapping experiments and EPR analysis confirmed the critical roles of ·OH, ·SO4− and 1O2 in SDZ removal. The wide pH working range (1.0 ∼ 13.0) and the slight toxicity of photocatalytic intermediates indicate that the as-prepared MF@PDA/Fe3O4@SA/PMS system has good application potential. The foam has potential practical applications in emergency oil spill rescue and oil/organic solvent wastewater treatment. Furthermore, this study provides a promising strategy for designing and fabricating a novel magnetic foam and photoactivated PMS synergistic system to eliminate pharmaceutical antibiotics effectively.

Paper-based biomimetic test-strip for CA15-3 with coloured readout

The combination of molecularly-imprinted polymers (MIPs) on paper substrates for capturing a cancer antigen 15–3 (CA15-3) with the traditional coloured transduction scheme of enzyme-linked immunosorbent assay (ELISA) using 3,3′,5,5′-tetramethylbenzidine (TMB), horseradish peroxidase (HRP) and H2O2 is presented here for the first time.Here, the paper surface was modified with a silane derivative containing an amine function that allows subsequent binding of 3-aminophenylboronic acid (3-APBA). The target protein, CA15-3, was then bound via the boronic groups of APBA. The empty space around CA15-3 was filled by polymerization of dopamine. Finally, the CA15-3 template was removed by breaking the imine function to create vacant sites for which CA15-3 has a high affinity. Binding of CA15-3 was detected by oxidation of TMB substrate by HRP in the presence of H2O2.The results showed that the MIP was able to selectively recognize CA15-3 within 3–500 U mL−1, even in complex samples. Quantitative data were extracted by analysing the colour coordinates of images captured with a smartphone using ImageJ. This selective behaviour was confirmed by comparison with a control material (non– polymer, NIP).Overall, the described approach has advantages over conventional ELISA, namely low cost and high stability, which is due to the use of MIP as a trapping element acting as a selective pre-concentration point of CA15-3. To our knowledge, this is the first biomimetic ELISA (B-ELISA) on paper substrate used for macromolecules such as proteins. We believe that this approach has the potential to be applied to other protein disease biomarkers, making it a suitable tool for screening glycoproteins at the point-of-care.

Dopamine as a polymerizable reagent for enzyme-linked immunosorbent assay using horseradish peroxidase

We demonstrate that dopamine can be used as a reagent for colorimetric enzyme-linked immunosorbent assay (ELISA) using horseradish peroxidase (HRP). Dopamine was able to be polymerized in the presence of HRP and H2O2, and black polydopamine was obtained after the enzymatic reaction. Because of the black color, the absorbance was significantly changed in the whole range of the visible light region. Here, an indirect competitive ELISA based on the polymerization of dopamine was performed to detect a fluoroquinolone antibiotic, enrofloxacin. The antibiotic is commonly used in livestock farming. The anti-antibiotics antibody was produced from egg yolk from chicken hens. In the visible range, sufficient absorbance changes of ∼0.4∼0.5 and a low background level for the ELISA response were obtained, and the 50 % inhibitory concentration value at 450 nm was determined to be 26 ppb. The performance of the indirect competitive ELISA based on the polymerization of dopamine was compared to that based on the oxidation of catechol because dopamine has a catechol skeleton. By the complex of HRP and H2O2, catechol can be oxidized to o-benzoquinone having a maximum absorption wavelength of 420 nm. It was shown that the absorbance change in the case of polydopamine was about 2.5 times higher than that of catechol, where the background levels were similar. This confirms that the polymerization of dopamine significantly enhanced the photosignal.

Insight into polydopamine coating on microfiltration membrane with controlled surface pore size for enhanced membrane rejection

Membrane modification with polydopamine (PDA) is a common practice to enhance membrane selectivity and improve membrane compatibility with nanoparticles or thin films. Depending on the membrane surface properties, dopamine can deposit or penetrate into microporous membranes, leading to alteration in the membrane's physicochemical properties and consequently its performance. In this study, microfiltration (MF) polyethersulfone membranes with varying surface pore sizes were fabricated by manipulating the precasting time (solvent evaporation time of 3s, 15s, 30s and 60s) prior to non-solvent induced phase separation (NIPS) process. Notably, the coating of PDA slightly reduced the membrane's surface pore size and membrane's porosity. M60 membrane which possessed the smallest mean surface pores (∼300 nm), exhibited PDA clusters predominantly formed on top of the membrane surface. With an increase in surface pore size, dopamine can penetrate the porous structure of the MF membrane, leading to the polymerization of dopamine into PDA aggregates on both the membrane surface and inner pores. The M30 membrane had the largest surface pore size (∼500 nm), showing the formation of large PDA globules in the finger-like pores. The membrane (M30P) experienced significant narrowing of the inner pores, resulting in reduced water permeability. Overall, all PDA-coated membranes exhibited improved sucrose rejection (85–95%) compared to the uncoated ones (64–83%). These finding provides insight into the polymerization mechanism of dopamine on porous membranes prior to the incorporation of nanomaterials or thin film coating.