Preparation of an efficient magnetic nano-sorbent based on modified cellulose and carboxylated carbon nano-tubes for extraction of pesticides from food and agricultural water samples before GC-FID analysis.

This paper reports the direct synthesis approach of carboxamide functionalized magnetic nano-composite named Fe3O4@SiO2-NH2@dialdehyde cellulose (DAC)@CNT-COOH as an effectual sorbent for the co-extraction of seven agricultural insecticides and herbicides from vegetable, fruit, and water samples using the magnetic dispersive micro-solid-phase extraction procedure. Under the optimized extraction conditions (sorbent amount: 18.1 mg; desorption time: 6.5 min; desorption solvent volume: 185 µL; desorption solvent: acetonitrile; extraction time: 9.5 min; pH of sample solution: 7.0, and salt content: 5.0 % w/v sodium chloride), good linearity within the range 0.5-1200 ng/mL (R2 ≥ 0.998) was achieved. Extraction efficiencies were in the range 63.4-84.1 %, the limits of detection were 0.08-1.0 ng/mL, and acceptable relative recoveries (87.6-103.8 %), and precisions were also achieved (RSDs < 6.8 %, n = 3). Ultimately, the obtained results showed that the developed method could be applied to determine trace amounts of desired analytes in various agricultural water and food samples.

Carboxymethyl cellulose/tetracycline@UiO-66 nanocomposite hydrogel films as a potential antibacterial wound dressing.

Designing an antibacterial agent with a suitable water vapor permeability, good mechanical properties, and controlled antibiotic release is a promising method for stopping bacterial infection in wound tissue. In this respect, this work aims to prepare novel flexible polymeric hydrogel films via integrating UiO-66 into the polymeric carboxymethyl cellulose (CMC) hydrogel for improving the mechanical and antibiotic release performances. First, we performed a green hydrothermal synthetic method to synthesis UiO-66 and followed by encapsulating Tetracycline (TC) through immersion in its aqueous solution. Also, the casting technique was utilized to integrate different concentrations of the TC-encapsulated UiO-66 (TC@UiO-66, 5% to 15%) in the polymeric CMC matrix (CMC/TC@UiO-66) cross-linked by citric acid and plasticized by glycerol. The release performance showed a low initial burst release with a controlled release over 72 h in the artificial sweat and simulated wound exudate (PBS, pH 7.4) media. The in vitro cytotoxicity and antibacterial activity results revealed a good cytocompatibility toward Human skin fibroblast (HFF-1) cells and a significant activity against both E. coli and S. aureus with 1.3 and 1.7 cm inhibition zone, respectively. The obtained results recommend CMC/TC@UiO-66 films as a potential antibacterial wound dressing.

Cu-decorated cellulose through a three-component Betti reaction: An efficient catalytic system for the synthesis of 1,3,4-oxadiazoles via imine CH functionalization of N-acylhydrazones.

Materials functionalization through multicomponent reactions (MCRs) has recently attracted great attention due to the generation of outstanding features in materials. Herein, an efficient novel heterogeneous catalytic system was designed and synthesized via the MCRs functionalization of the most abundant biopolymer in nature, cellulose. In this regard, cellulose was oxidized using periodate as an oxidant agent, and then the resulted carbonyl functional groups participated in the three-component Betti reaction. The ICP-OES analysis was revealed that the functionalization of cellulose via this three-component reaction effectively improved the complexing ability of functionalized cellulose with Cu(II). The synthesized biocatalyst was characterized by FT-IR, 1H NMR, XRD, SEM, EDS, ICP, and TGA techniques. The efficiency of the designed biocatalyst was investigated in the CH functionalization reaction of N-acylhydrazones to synthesize 1,3,4-oxadiazoles. This biocatalyst's outstanding advantages are high yields, non-hazardous catalyst, mild reaction conditions, operational simplicity, and reusability.