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Surfaces engineered to identify and enrich glycoproteins are of considerable interest in the diagnostic and detection fields. A boronate affinity (BA) material was proposed as a potential candidate for the isolation of glycoproteins. However, this material has the disadvantages of low efficiency and non-degradability. Herein, a novel dendrimer-amplified BA cellulose foam (PEI-PBA-CF) was fabricated via a mild two-step approach. The as-prepared PEI-PBA-CF exhibited a rapid adsorption equilibrium rate (within 60 min) and outstanding adsorption capacity for horseradish peroxidase (537.4 mg g -1 ) and ovalbumin (495.5 mg g -1 ). Furthermore, competitive adsorption experiments demonstrated that PEI-PBA-CF could achieve selective separation and purification of glycoproteins from complex biological samples due to the synergistic effect of the improved BA capacity by the dendrimer and the well-interconnected porous structure of the biomass matrix. Consequently, these cellulose foams might present new application opportunities in analytical and biomedical fields., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

We report a versatile divergent methodology to construct dendrimers from a tetrafunctional core, utilizing the robust copper(I) catalyzed alkyne-azide cycloaddition (CuAAC, "click") reaction for both dendrimer synthesis and post-synthesis functionalization. Dendrimers of generations 1-3 with 8-32 protected or free OH and acetylene surface groups, were synthesized using building blocks that included acetylene- or azide-terminated molecules with carboxylic acid or diol end groups, respectively. The acetylene surface groups were subsequently used to covalently link cationic amino groups. A preliminary evaluation indicated that the generation one dendrimer with terminal NH₃⁺ groups was the most effective bactericide, and it was more potent than several previously studied dendrimers. Our results suggest that size, functional end groups and hydrophilicity are important parameters to consider in designing efficient antimicrobial dendrimers., Competing Interests: The authors declare no conflict of interest.

With the growing attention on estrogenic effect of Bisphenol A (BPA), the application of BPA derivatives like Bis-GMA in dental materials has also been doubted. In this research, new BPA free dental resin systems were prepared with synthesized dendritic macromer G-IEMA, UDMA, and TEGDMA. Physicochemical properties, such as double bond conversion, polymerization shrinkage, flexural strength and modulus, fracture energy, water sorption and solubility of BPA free resin formulations were investigated. Bis-GMA/TEGDMA resin system was used as a control. Results showed that the prepared BPA free resins could have higher double bond conversion, comparable or lower polymerization shrinkage and water sorption, and lower water solubility, when compared with Bis-GMA/TEGDMA resin. Though flexural strength and modulus of prepared BPA free polymers were lower than those of Bis-GMA/TEGDMA polymer, BPA free polymers had higher fracture energies and showed plastic deformation prior to fracture, all of these two phenomena showed that BPA free polymers in this research might have higher fracture toughness which would be good for the service life of dental materials., (Copyright © 2014 Elsevier Ltd. All rights reserved.)