Activity

The advent of electric skins (E-skin) with tactile sensation, flexibility, and human affinity characteristics have attracted considerable attention in extensive research fields, including intelligent robots and health monitoring, etc. To improve the intrinsic brittleness of hydrogels, a multifunctional E-skin was fabricated involving a TEMPO-NFC and a covalently cross-linked polyacrylamide (PAM) network. In this work, silver nanoparticles (AgNPs) as long-term antibacterial agent and conductive fillers were coated onto NFC nanofibers. Subsequently, this nanocomposite hydrogel was synthesized by free radical copolymerization of AM monomers with PNAg fibers as interpenetrating fibers network. Importantly with NFC present, the nanocomposite hydrogel exhibited superior mechanical performance and excellent self-recovery ability. The obtained sensor with excellent mechanical stability and sensing performance could detect mechanotransduction signal of human movements. This work provides a practicable method to prepare high antibacterial efficiency, excellent mechanical performance, and dual-modal nanocellulose-based hydrogel sensor for the broad-range application in human-motion detection and intelligence skins.Glycosylated pH-sensitive mesoporous silica nanoparticles (MSNs) of capecitabine (CAP) were developed for targeting colorectal cancer. The MSNs possessed an average pore diameter of 8.12 ± 0.43 nm, pore volume of 0.73 ± 0.21 cm3/g, and particle size of 245.24 ± 5.75 nm. A high loading of 180.51 ± 5.23 mg/g attributed to the larger pore volume was observed. The surface of the drug-loaded MSNs were capped with chitosan-glucuronic acid (CHS-GCA) conjugate to combine two strategies viz. pH-sensitive, and lectin receptor mediated uptake. In vitro studies demonstrated a pH-sensitive and controlled release of CAP which was further enhanced in the presence of rat caecal content. Higher uptake of the (CAP-MSN)CHS-GCA was observed in HCT 116 cell lines. The glycosylated nanoparticles revealed reduction in the tumors, aberrant crypt foci, dysplasia and inflammation, and alleviation in the toxic features. This illustrated that the nanoparticles showed promising antitumor efficacy with reduced toxicity and may be used as a effective carrier against cancer.In recent decades, magnetic bead material has attracted considerable attention in water and wastewater purification. In this study, the potential of magnetic kaolinite immobilized in chitosan beads (MKa@CB) to remove Pb(II) and Cd(II) ions from an aqueous environment has been successfully investigated. The addition of magnetic kaolinite generates more active sites, whereas that of chitosan enhances the stability of synthesized bead materials, which enable them to effectively interact with the targeted contaminants. Various factors including agitation time, solution pH, and competitive ions were examined to optimize the removal efficiency of the MKa@CB. The adsorption kinetics and isotherm studies indicated that the adsorption fitted well to the pseudo-second-order kinetic model as well as to the Langmuir isotherm. The prepared adsorbent could be reused up to four cycles without any significant adsorption capacity loss. Thus, the synthesized MKa@4%CB can be a promising adsorbent in effectively removing Pb(II) and Cd(II) from water.In this study, three magnetic flocculants, namely, MC, MC-g-PAM, and MC-g-PAA, were prepared. The structure characteristics, flocculation performance, and floc characteristics of the three magnetic flocculants were systematically studied and compared. SEM, FT-IR, XPS, XRD, TG-DSC, and VSM characterization results show that MC, MC-g-PAM, and MC-g-PAA are successfully prepared and exhibit good magnetic induction. The removal rates of copper ions by MC, MC-g-PAM, and MC-g-PAA under the optimal coagulation conditions are 93.39 %, 88.64 %, and 61.41 %, respectively. Kinetic fitting shows that the flocculation reaction process of MC and MC-g-PAM conforms to pseudo first-order kinetics, while the flocculation reaction process of MC-g-PAA conforms to pseudo second-order kinetics. The flocs produced by MC-g-PAA have larger particle size and fractal dimension than those by MC and MC-g-PAM. At 80 mg/L dosage and pH 6, the floc size and floc fractal dimension obtained by MC-g-PAA reach the maximum values of 48.28 um and 1.468, respectively. Zeta potential studies show that the flocculation functions of the three flocculants are mainly adsorption bridging, adsorption electric neutralization, and chelating precipitation. selleck inhibitor Recycling experiments show that MC-g-PAA has good recyclability, and the recovery rate after the fifth use is 77.24 % with the Cu(II) removal rate of 67.53 %.This work was aimed to synthesize novel crosslinked carboxymethyl chitosan nanoparticles (CMCS NPs) containing metformin hydrochloride (MET) using microfluidics (MF) and evaluate their performance for diabetes therapy. The field emission-scanning electron microscopy (FE-SEM) images and dynamic light scattering (DLS) results showed that the NPs average size was 77 ± 19 nm with a narrow size distribution. They exhibited a high encapsulation efficiency (∼90 %) and the controlled drug release while crosslinking using CaCl2. Eventually, the in vivo assessments dedicated an increased body weight up to 7.94 % and a decreased blood glucose level amount of 43.58 % for MF MET-loaded CMCS NPs with respect to the free drug in diabetic rats. Also, the results of histopathological studies revealed the size of the pancreatic islets to be 2.32 μm2 and β cells intensity to be 64 cells per islet for the diabetic rats after treating with the MF-based sample. These data were close to those obtained for the healthy rats.Liver glycogen is a branched glucose polymer that functions as a blood-sugar buffer in animals. Previous studies have shown that glycogen’s molecular structure affects its properties. This makes it important to develop a technique that extracts and purifies a representative sample of glycogen. Here we aim to optimize the sucrose density gradient centrifugation method for preserving glycogen’s molecular structure by varying the density of the sucrose solution. The preservation of glycogen’s structure involves 1) minimizing molecular damage and 2) obtaining a structurally representative sample of glycogen. The addition of a 10-minute boiling step was also tested as a means for denaturing any glycogen degrading enzymes. Lower sucrose concentrations and the introduction of the boiling step were shown to be beneficial in obtaining a more structurally representative sample, with the preservation of smaller glycogen particles and decreased glycogen chain degradation.