The quartz crystal microbalance (QCM) is used as a non-destructive and efficient characterization tool for thin thermoplastic starch (TPS) films. Thin TPS films (1-2 μm) were prepared with 30% (w/w starch) plasticizers using either glycerol or an ionic liquid, 1-ethyl-3-methylimidiazolium acetate ([emim+][Ac-]), as the plasticizer. The differences in the mechanical properties and environmental effects on the plasticized TPS films were explored. The modulus of starch-glycerol films was higher than starch-[emim+][Ac-], consistent with literature data and bulk AFM measurements, likely due to superior plasticization by the ionic liquid. The starch-[emim+][Ac-] films were shown to have relative stable properties at low humidity that may be due to some antiplasticization effects at low water content despite absorbing more water than starch-glycerol films at higher humidity.The inherently unpredictable complexity of tumors impedes the widespread practice of the molecular biomarkers in outcome prediction. Alternatively, from the biophysical perspective, this study sought to investigate the applicability of the cell detachment ratio (CDR) derived from pH-responsive chitosan as a biometrical identifier for the disease state in cancer prognostic judgment and drug efficacy assessment. In the targeted therapy model, the repression of tumor dissemination in cells harboring aberrant ErbB signals (human non-small cell lung cancer cell line PC9 and breast cancer cell line BT474) were first demonstrated both in vitro and in vivo. Consequently, the corresponding CDR profile goes synchronously with the extent of cancer regression in response to the medication. Definitive integrins that drive the cell detachment were also verified through CDR examination following the integrin functional blockade. Conclusively, CDR is a promising clinical index for evaluation of the metastatic cell behaviors in terms of the cell detachment.In this study, copper oxide nanoparticles, prepared using pistacia vera hull extract, were immobilized onto chitosan. FT-IR spectrum of copper oxide-chitosan exhibited chemical shifting of the main peaks of the biopolymer indicating that hydroxyl and amino groups were reacted with copper oxide nanoparticles. SEM features showed spherical surface and physical stability of the composite. The shifting of the burning temperature in DTA from 278.5 °C to 212.6 °C in the composite proved the interaction between chitosan and copper oxide nanoparticles. The composite was applied for the oxidative degradation of naphthol blue black in the presence of H2O2. The change of copper oxide nanoparticles loading, time, dye concentration, temperature, and oxidant dose were studied. The degradation yield reached 86 % (C0 = 30 mg/L, T=20 °C, H2O2 = 8 mL/L). The activation energy (Ea), entropy (ΔS*) and enthalpy (ΔH*) were equal to 45.558 KJ. mol-1, -116.203 J mol-1 K-1 and 42.986 kJ mol-1, respectively.Development of hybrid materials with molecular structure of organic-inorganic co-network is a promising method to enhance the stability and mechanical properties of biopolymers. Chitosan-silica hybrid nanocomposite scaffolds loaded with mangiferin, a plant-derived active compound possessing several bioactivities, were fabricated using the sol-gel synthesis and the freeze-drying processes. Investigation on the physicochemical and mechanical properties of the fabricated scaffolds showed that their properties can be improved and tailored by the formation of 3-dimensional crosslinked network and the addition of ZnO nanoparticles. The scaffolds possessed porosity, fluid uptake, morphology, thermal properties and mechanical strength suitable for bone tissue engineering application. Investigation on the biomineralization and cell viability indicated that the inclusion of bioactive mangiferin further promote potential use of the hybrid nanocomposite scaffolds in guided bone regeneration application.Chitosan, a low-cost and multipurpose polymer with numerous desired physicochemical and biological properties has been tested for various applications in agriculture, pharmacy, and biomedicine industries. The availability of functional groups along the backbone makes chitosan readily available for other polymers and metal ions to form bio-nanocomposites. Different types of chitosan-based nanocomposites have been designed and tested for the enhancement of chitosan efficiency and ultimately widening the application areas of chitosan in plants. These nanocomposites serve different purposes such as eliciting plant's defence systems against different threats (pathogen attack), antimicrobial agent against bacteria, fungi and viruses, enhancement of nutrient uptake by plants, control release of micro/macronutrients, fungicides and herbicides. In this review, an extensive outlook has been provided (mainly in the last five years) to recent trends and advances in the fabrication and application of chitosan-based composites. Finally, current challenges and future development opportunities of chitosan-based nanocomposites for plants are discussed.A facile and effective "grafting from" method by ROP of N-sulfonyl aziridines toward cellulose-g-polysulfonamides has been developed for efficient oil/water separation. The cellulose paper was initially succinylated to transform the hydroxyl to carboxyl acid groups, which act as the initiating sites for the ring-opening copolymerization of fluorescent 2-methyl-1-dansylaziridine and 2-methyl-1-tosylaziridine (TsMAz) towards the grafted cellulose. Both steps are catalyzed by the same compound, 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (MTBD). The grafted polysulfonamide ratio was up to 136 wt%, and the surface contact angle up to 147°. A one-pot tandem strategy was applied to produce the grafted cellulose paper with a grafting ratio ranging from 96 to 150 % and a contact angle over 127°. The modified cellulose paper material showed promising properties for efficient oil/water separations.Effective hydrolysis of cellulose to glucose is a crucial step to produce fuels and chemicals from lignocellulosic biomass.  https://www.selleckchem.com/products/borussertib.html  Solid acids are promising alternatives of cellulases and homogenous acids for hydrolyzing cellulose. In this study, porous polymeric solid acids bearing hydroxyl and sulfonic acid groups were fabricated for cellulose hydrolysis in water through the low-cost Friedel-Crafts "knitting" polymerization of hydroxyl-containing aromatic monomers followed by sulfonation. The synthesized bifunctional solid acids could effectively hydrolyze microcrystalline cellulose (Avicel) to glucose by as high as 93 % at 120 °C within 48 h and ball-milled Avicel by 98 % at 120 °C in 24 h. The evidence from this study indicated that the outstanding catalytic performance of the solid acids was attributed to the porous structure (large surface area) and the presence of the hydroxyl (cellulose-binding group) in the solid acids.