A growth in the use of antibiotics and the related evolution of patients' drug resistance calls for an urgent response for the development of novel curing approaches without using synthetic antibiotics. Here, the fabrication of a lowcost cryogel for wound dressing applications is demonstrated. The cryogel is composed of only naturally derived components, including chitosan/silk fibroin as the scaffold and tannic acid/ferric ion (TA/Fe 3+ ) as the stimuliresponsive agent for photothermal therapy. Based on the multiple weak hydrogen bonds and metal ligand coordination, the cryogel exhibits good flexibility and recoverability. Its highly porous structure renders the cryogel to be strongly hygroscopic to absorb blood for hemostasis. The cryogel exhibits excellent antibacterial activity to both Gram-negative and positive bacteria, benefiting from the high photothermal transition activity of the TA/Fe 3+ complex. Furthermore, the cryogel can efficiently promote cell proliferation in vitro. Significantly, animal experiments also reveal that the cryogel effectively eradicate microbes at the wound and accelerate the wound healing process. In summary, this novel biorenewable cryogel demonstrates excellent hygroscopic and hemostatic performance, photothermal antimicrobial activity, and accelerates skin regeneration, which has great application potential as a promising wound dressing material in the clinical use.

The impact of the spatial confinement of polystyrene-block-poly(acrylic acid) (PS-b-PAA) block copolymer (BCP) vesicles on the reactivity of encapsulated bovine pancreas trypsin is studied. Enzymes, as well as small molecules, are encapsulated with loading efficiencies up to 30% in BCP vesicles with variable internal volumes between 0.014 aL (internal vesicle diameter, d(in) = 30 nm) and 8 aL (d(in) = 250 nm), obtained by manipulating the vesicle preparation conditions. The kinetics of the trypsin-catalyzed reaction of a fluorogenic substrate inside and outside the vesicles is quantitatively estimated using fluorescence spectroscopic analyses in conjunction with the use of NaNO(2) as selective quencher for non-encapsulated fluorophores. The values of the catalytic turnover number obtained for reactions in differently sized nanoscale reactors show a significant increase (up to approximately 5x) with decreasing BCP vesicle volume, while the values of the Michaelis-Menten constant decrease. The observed increase in enzyme efficiency by two orders of magnitude compared to bulk solution is attributed to an enhanced rate of enzyme-substrate and molecule-wall collisions inside the nanosized reactors, as predicted in the literature on the basis of Monte Carlo simulations.

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Hydrogels with rapid and strong response to external stimuli and possessing high elasticity and strength have been considered as platform materials for numerous applications, e.g., in biomaterials engineering. Thermoresponsive hydrogels based on semi-interpenetrating polymer networks (semi-IPN) featuring N-isopropylacrylamide with copolymers of poly(N-isopropylacrylamide-co-hydroxyethyl methacrylate) p(NIPAM-HEMA) chains are prepared and described. The copolymer was characterized by FTIR, NMR, and GPC. The semi-IPN structured hydrogel and its responsive properties were evaluated by dynamic mechanical measurements, SEM, DSC, equilibrium swelling ratio, and dynamic deswelling tests. The results illustrate that the semi-IPN structured hydrogels possess rapid response and high elasticity compared to conventional pNIPAM hydrogels. By using a microfluidic device with double coaxial laminar flow, we succeeded in fabricating temperature responsive ("smart") hydrogel microfibers with core-shell structures that exhibit typical diameters on the order of 100 μm. The diameter of the fibers can be tuned by changing the flow conditions. Such hydrogel fibers can be used to fabricate "smart" devices, and the core layer can be potentially loaded with cargos to incorporate biological function in the constructs. The platforms obtained by this approach hold promise as artificial "muscles", and also "smart" hydrogel carriers providing a unique biophysical and bioactive environment for regenerative medicine and tissue engineering.

The successful implementation of zwitterionic polymeric brushes as antifouling materials for marine applications is conditioned by the stability of the polymer chain and the brush-anchoring segment in seawater. Here we demonstrate that robust, antifouling, hydrophilic polysulfobetaine-based brushes with diblock architecture can be fabricated by atom-transfer radical polymerization (ATRP) using initiator-modified surfaces. Sequential living-type polymerization of hydrophobic styrene or methyl methacrylate and commercially available hydrophilic sulfobetaine methacrylamide (SBMAm) monomer is employed. Stability enhancement is accomplished by protecting the siloxane anchoring bond of brushes on the substrate, grafted from silicon oxide surfaces. The degradation of unprotected PSBMAm brushes is clearly evident after a 3 month immersion challenge in sterilized artificial seawater. Ellipsometry and atomic force microscopy (AFM) measurements are used to follow changes in coating thickness and surface morphology. Comparative stability results indicate that surface-tethered poly(methyl methacrylate) and polystyrene hydrophobic blocks substantially improve the stability of zwitterionic brushes in an artificial marine environment. In addition, differences between the hydration of zwitterionic brushes in fresh and salt water are discussed to provide a better understanding of hydration and degradation processes with the benefit of improved design of polyzwitterionic coatings.