Fine-Tuning the Endcap Chemistry of Acrylated Poly(Ethylene Glycol)-Based Hydrogels for Efficient Burn Wound Exudate Management

Most commercial dressings with moderate to high exudate uptake capacities are mechanically weaker and/or require a secondary dressing. The current research article focuses on the development of hydrogel-based wound dressings combining mechanical strength with high exudate absorption capacities using acrylate-endcapped urethane-based precursors (AUPs). AUPs with varying poly(ethylene glycol) backbone molar masses (10 and 20 kg mol⁻¹) and endcap chemistries are successfully synthesized in toluene, subsequently processed into UV-cured hydrogel sheets and are benchmarked against several commercial wound dressings (Hydrosorb, Kaltostat, and Mepilex Ag). The AUP materials show high gel fractions (>90%) together with strong swelling degrees in water, phosphate buffered saline and simulated wound fluid (12.7–19.6 g g⁻¹), as well as tunable mechanical properties (e.g., Young's modulus: 0.026–0.061 MPa). The AUPs have significantly (p < 0.05) higher swelling degrees than the tested commercial dressings, while also being mechanically resistant. The elasticity of the synthesized materials leads to an increased resistance against fatigue. The di- and hexa-acrylated AUPs show excellent in vitro biocompatibility against human foreskin fibroblasts, as evidenced by indirect MTS assays and live/dead cell assays. In conclusion, the processed AUP materials demonstrate high potential for wound healing application and can even compete with commercially available dressings.     

The Algebra of {{\mathbf{SL}}_3}\left( \mathbb{C} \right) Conformal Blocks

We construct and study a family of toric degenerations of the Cox ring of the moduli of quasi-parabolic principal SL₃( $ \mathbb{C} $ ) bundles on a smooth, marked curve (C, $ \vec{p} $ ): Elements of this algebra have a well known interpretation as conformal blocks, from the Wess-Zumino-Witten model of conformal field theory. For the genus 0; 1 cases we find the level of conformal blocks necessary to generate the algebra. In the genus 0 case we also find bounds on the degrees of relations required to present the algebra. As a consequence we obtain a toric degeneration for the projective coordinate ring of an effective divisor on the moduli $ {{\mathcal{M}}_{{C,\vec{p}}}}\left( {\mathrm{S}{{\mathrm{L}}_3}\left( \mathbb{C} \right)} \right) $ of quasi-parabolic principal SL₃( $ \mathbb{C} $ ) bundles on (C, $ \vec{p} $ ). Along the way we recover positive polyhedral rules for counting conformal blocks.     

Interactions in confined polariton condensates

We investigate the effect of interactions in zero-dimensional polariton condensates. The shape of the condensate wave function is shown to be modified by repulsive interactions with the reservoir of uncondensed excitons. In large micropillar cavities, when uncondensed excitons are located at the center, the condensate is ejected toward the pillar edges. The same effect results in the generation of optical traps in wire cavities. Once polariton condensates are spatially separated from the excitonic reservoir, spectral signatures of polariton-polariton interactions within the condensate are evidenced.     

Partial Characterization of Xylanase Produced by Caldicoprobacter algeriensis,a New Thermophilic Anaerobic Bacterium Isolated from an Algerian Hot Spring

To date, xylanases have expanded their use in many processing industries, such as pulp, paper, food, and textile. This study aimed the production and partial characterization of a thermostable xylanase from a novel thermophilic anaerobic bacterium Caldicoprobacter algeriensis strain TH7C1^T isolated from a northeast hot spring in Algeria. The obtained results showed that C. algeriensis xylanase seems not to be correlated with the biomass growth profile whereas the maximum enzyme production (140.0 U/ml) was recorded in stationary phase (18 h). The temperature and pH for optimal activities were 70 °C and 11.0, respectively. The enzyme was found to be stable at 50, 60, 70, and 80 °C, with a half-life of 10, 9, 8, and 4 h, respectively. Influence of metal ions on enzyme activity revealed that Ca⁺² enhances greatly the relative activity to 151.3 %; whereas Hg²⁺ inhibited significantly the enzyme. At the best of our knowledge, this is the first report on the production of xylanase by the thermophilic bacterium C. algeriensis. This thermo- and alkaline-tolerant xylanase could be used in pulp bleaching process.     

Synthesis of benzocyclobutenes by palladium-catalyzed C-H activation of methyl groups: method and mechanistic study

An efficient catalytic system has been developed for the synthesis of benzocyclobutenes by C-H activation of methyl groups. The optimal conditions employed a combination of Pd(OAc) 2 and P ( t )Bu 3 as catalyst, K 2CO 3 as the base, and DMF as solvent. A variety of substituted BCB were obtained under these conditions with yields in the 44-92% range, including molecules that are hardly accessible by other methods. The reaction was found limited to substrates bearing a quaternary benzylic carbon, but benzocyclobutenes bearing a tertiary benzylic carbon could be obtained indirectly from diesters by decarboxylation. Reaction substrates bearing a small substituent para to bromine gave an unexpected regioisomer that likely arose from a 1,4-palladium migration process. The formation of this "abnormal" regioisomer could be suppressed by introducing a larger subsituent para to bromine. DFT(B3PW91) calculations on the reaction of 2-bromo-tert-butylbenzene with Pd(P ( t )Bu 3) with different bases (acetate, bicarbonate, carbonate) showed the critical influence of the coordination mode of the base to induce both an easy C-H activation and to allow for a pathway for 1,4-palladium migration. Carbonate is shown to be more efficient than the two other bases because it can abstract the proton easily and at the same time maintain kappa (1)-coordination without extensive electronic reorganization.     

A New Route for the Modification of Halogen End Groups to Amino End‐Functionalized Poly(tert‐butyl acrylate)s

The synthesis of primary amine end‐functional poly(tert‐butyl acrylate)s has been achieved by using the Gabriel reaction. Polymerization of tert‐butyl acrylate was first achieved by atom transfer radical polymerization using ethyl‐2‐bromoisobutyrate or paramethoxyphenyl‐2‐bromoisobutyrate as initiator. Both resulting polymers, with a bromide‐end atom, were converted into phthalimido intermediates which then were successfully hydrolyzed using potassium hydroxide in tert‐butyl alcohol to result in poly(tert‐butyl acrylate)s terminated by a primary amine function. End group interconversions were followed by ¹H NMR, FT‐IR, and MALDI‐TOF MS measurements. All the results proved that quantitative transformations were achieved at each step. Moreover, the method developed is very easy to carry out.