Iron-driven self-assembly of dopamine into dumbbell-shaped nanozyme for visual and rapid detection of norfloxacin on a smartphone-assisted platform.

Antibiotics in aquatic environments raise health concerns. Therefore, the rapid, on-site, and accurate detection of antibiotic residues is crucial for protecting the environment and human health. Herein, a dumbbell-shaped iron (Fe3+)-dopamine coordination nanozyme (Fe-DCzyme) was developed via an iron-driven self-assembly strategy. It exhibited excellent peroxidase-like activity, which can be quenched by adding l-cysteine to prevent Fe3+/Fe2+ electron transfer but restored by adding norfloxacin. Given the 'On-Off-On' effect of peroxidase-like activity, Fe-DCzyme was used as a colourimetric sensor for norfloxacin detection, and showed a wide linear range from 0.05 to 6.00 µM (R2 = 0.9950) and LOD of 27.0 nM. A portable smartphone-assisted detection platform using Fe-DCzyme was also designed to convert norfloxacin-induced color changes into RGB values as well as to realise the rapid, on-site and quantitative detection of norfloxacin. A good linear relation (0.10-6.00 µM) and high sensitivity (LOD = 79.3 nM) were achieved for the smartphone-assisted Fe-DCzyme detection platform. Its application was verified using norfloxacin spiking methods with satisfactory recoveries (92.66%-119.65%). Therefore, the portable smartphone-assisted Fe-DCzyme detection platform with low cost and easy operation can be used for the rapid, on-site and visual quantitative detection of antibiotic residues in water samples.

High strength chitin/chitosan-based aerogel with 3D hierarchically macro-meso-microporous structure for high-efficiency adsorption of Cu(II) ions and Congo red.

A high-strength aerogel with a 3D hierarchically macro-meso-microporous structure (HPS-aerogel) was designed based on biological macromolecules of chitin and chitosan. The macropores can be created within HPS-aerogel after CaCO3 removal, and meso-micropores resulting from water sublimation during freeze-drying. The macro-meso-microporous structure endowed HPS-aerogel with high porosity, good mechanical properties, and excellent compression strength (1472 kPa at strain of 80 %). The HPS-aerogel exposed many adsorption sites and was used as an adsorbent to simultaneously remove Cu(II) and Congo red (CR) from water for the first time. The adsorption capability for Cu(II) and CR was 59.21 mg/g and 2074 mg/g at 303 K, respectively, and the adsorption processes matched Pseudo-second-order and Langmuir models with spontaneous and endothermic nature. Additionally, HPS-aerogel showed good anti-interference ability for coexisting pollutant. Importantly, HPS-aerogel exhibited an effective fixed-bed column adsorption performance for dynamic Cu(II) and CR with superior reusability and stability. Furthermore, HPS-aerogel showed outstanding adsorption efficiencies for Cu(II) and CR in real samples. The main adsorption mechanism for Cu(II) was attributed to the electrostatic attraction and chelation, and which was electrostatic attraction, Schiff base, and hydrogen bonding for CR. Therefore, HPS-aerogel should to be a promising adsorbent for removing both heavy-metal ions and dyes from wastewater.

3D Hierarchical Porous and N-Doped Carbonized Microspheres Derived from Chitin for Remarkable Adsorption of Congo Red in Aqueous Solution.

A novel adsorbent of N-doped carbonized microspheres were developed from chitin (N-doped CM-chitin) for adsorption of Congo red (CR). The N-doped CM-chitin showed spherical shape and consisted of carbon nanofibers with 3D hierarchical architecture. There were many micro/nano-pores existing in N-doped CM-chitin with high surface area (455.703 m2 g-1). The N element was uniformly distributed on the carbon nanofibers and formed with oxidize-N graphitic-N, pyrrolic-N, and pyridinic-N. The N-doped CM-chitin showed excellent adsorption capability for CR and the maximum adsorption amount was approximate 954.47 mg g-1. The π-π/n-π interaction, hydrogen-bond interactions, and pore filling adsorption might be the adsorption mechanisms. The adsorption of N-doped CM-chitin was considered as a spontaneous endothermic adsorption process, and which well conformed to the pseudo-second-order kinetic and Langmuir isotherm model. The N-doped CM-chitin exhibited an effective adsorption performance for dynamic CR water with good reusability. Therefore, this work provides new insights into the fabrication of a novel N-doped adsorbent from low-cost and waste biomasses.

A novel pectin from Akebia trifoliata var. australis fruit peel and its use as a wall-material to coat curcumin-loaded zein nanoparticle.

In this study, a pectin was extracted from Akebia trifoliata var. australis fruit peel waste using water solution, and its physicochemical properties were evaluated. The pectin was rich in galacturonic acid (GalA) content (76.68%). The degree of esterification (DE) and molecular weight (Mw) were 37.60% and 29,890 Da, respectively. The pectin structure was determined using Fourier transform-infrared (FT-IR) and Hydrogen nuclear magnetic resonance (H-NMR). The pectin exhibited an amorphous nature, negative charge, and good solubility. The pectin was then used as a wall-material to coat curcumin-loaded zein nanoparticles for the first time. The obtained nanoparticles (curcumin-loaded core-shell nanoparticle, CLCSNs) exhibited a core (zein)-shell (pectin) structure and a spherical shape with an average diameter of 230 nm. The electrostatic attraction, hydrogen bonding, and intermolecular interaction were involved in the CLCSNs formation. A high encapsulation efficiency (EE, 89.65%) and loading capacity (LC, 10.35%) of the CLCSNs were obtained for the curcumin. The solubility, stability, antioxidant activity, and in vitro bioavailability of the curcumin were significantly increased after loading into the CLCSNs. Therefore, this sustainable pectin from Akebia trifoliata var. australis fruit peel waste represents a promising natural macromolecule for use in the pharmaceutical and food industries.

New pectin-induced green fabrication of Ag@AgCl/ZnO nanocomposites for visible-light triggered antibacterial activity.

The pectin (CEP) was used as matrix material to prepare Ag@AgCl/ZnO nanocomposites with a green method for photocatalytic antibacterial activity in visible-light. Briefly, Ag@AgCl plasmonic hybrids were prepared in the CEP macromolecule matrix with size control, which was attributed to the stability of carboxyl and hydroxyl groups on the CEP. Subsequently, an effective and green two-steps approach was explored for the fabrication of CEP-Ag@AgCl/ZnO nanocomposites with resource saving and environment friendly. Interestingly, more Ag+ was converted into metallic Ag in the CEP-Ag@AgCl/ZnO than that in the CEP-Ag@AgCl. This phenomenon was attributed that the reducibility of free hemiacetal hydroxyl groups on CEP was realized with the help of NaOH in the preparation of CEP-ZnO. In addition, the CEP chains were not obviously destroyed except for the change in the crystallinity after the preparation of the CEP-Ag@AgCl/ZnO nanocomposites, indicating that the method was non-destructive. Moreover, the pH triggered release of Zn2+ and low release of Ag+ in CEP-Ag@AgCl/ZnO nanocomposites with excellent photocatalytic antibacterial activity were confirmed in this work. The proposed green process provides a new idea for the large-scale production of antibacterial pectin-based nanocomposites in industry with a low-cost.

A novel antibacterial agent based on AgNPs and Fe3O4 loaded chitin microspheres with peroxidase-like activity for synergistic antibacterial activity and wound-healing.

In this study, a novel antibacterial agent was developed based on chitin nanofibrous microspheres loaded with AgNPs and Fe3O4 nanoparticles (Ag-Fe3O4-NMs) for synergistic antibacterial activity and wound healing. Ag-Fe3O4-NMs was prepared via an in situ synthetic method which showed an excellent porosity and wettability. Moreover, Ag-Fe3O4-NMs were capable of sustained release of Ag+ and catalysed the decomposition of low H2O2 concentrations to generate hydroxyl radical (OH). The OH and Ag+ showed higher antibacterial activity and inhibited the toxicity with high dose of AgNPs and H2O2. In vitro biocompatibility results suggested that Ag-Fe3O4-NMs have low toxicity and low hemolysis. Thus, a novel antibacterial agent with enhanced synergistic antibacterial activity was obtained by combination of Ag-Fe3O4-NMs and H2O2 at a low and biologlically safe dosage, which could facilitate fibroblast growth, accelerate epithelialization, and promote the healing rate of infected wounds.