Multiclawed SiO2 Nano-Antibacterial Agent Based on Charge Inversed Ce6 Ionic Liquid Polymers for Combating Oral Biofilm Infection

Photodynamic antimicrobial chemotherapy (PACT) is a promising therapy against biofilm infection. However, due to the saliva clearance and obstacle of biofilm, the photosensitizer is difficult to concentrate in the infection site; then, the PACT is less effective on oral biofilm infection. In this article, we report a special nano-antibacterial agent (SiO2-PCe6-IL) to solve the bottleneck problem of PACT in treatment of oral biofilm infections. The SiO2-PCe6-IL was composed of SiO2 and poly ionic liquid photosensitizer (PCe6-IL) and had tri-fold features of eliminate biofilm infection: high binding ability, breaking biofilm barriers, and enrichment photosensitizer in infection site. In oral biofilm, the SiO2-PCe6-IL changed to SiO2-PIL+ like claws of octopus that could hold tightly with biofilm. Then, the poly-dodecyl on the SiO2-PIL+ broke down the barrier of biofilm. The results of HR-MS and zeta potential indicated that SiO2-PCe6-IL could change to positive (SiO2-PIL+) in acidic environment. The interaction forces and morphology results proved that the SiO2-PIL+ had a higher affinity to biofilm and could destroy the biofilm structure. Then, the photosensitizer was enriched in biofilm at sites of infection. The in vitro and in vivo experiments showed that SiO2-PCe6-IL could effectively eradicate oral biofilm infections and control of dental caries.

Production Technology and Damping Properties of Aerated Polymer Coatings

The process of obtaining aerated (filled with air bubbles) polymer coatings has been developed and investigated by the method of flame spraying with an assessment of their ability to damp vibrations. A technology for the controlled formation of aerated polymer coatings has been developed while using the capabilities of the ОИМ (OIM) 050 polymer thermal atomizer design which consists in providing a concurrent air flow between the flame torch and the jet of powder material. The experiments have been carried out with such thermoplastic polymers as polyethylene terephthalate, high pressure polyethylene, ultra high molecular weight polyethylene, polyamide. It has been found that the aeration coefficient grows almost in direct proportion with an increase in the amount of air in the concurrent flow for all investigated polymer coatings. It is noted that the aeration process is influenced by the rheological properties of liquid polymers, or rather, the value of the polymer melt flow rate. The limiting values of air in the concurrent flow have been determined, which make it possible not to reduce the adhesion of polymer coatings to steel substrates by less than 6 MPa and not to decrease their hardness by more than 25–30 %. Studies of the damping properties of samples with polymer coatings have been carried out on a stand, the kinematic diagram of which is based on loading the free end of a cantilever sample, abrupt removal of the load and registration of free damped oscillations by an induction-type contactless sensor connected to a computer. It is shown that the use of aeration when forming noise-absorbing coatings on steel samples can increase their logarithmic damping decrement by 18–26 %.

Thermodynamic Analysis of Brownian Motion-Induced Particle Agglomeration Using the Taylor-Series Expansion Method of Moments

On the basis of binary perfectly inelastic collision theory, the time evolutions of kinetic energy and surface area for a particle agglomerate system, due to Brownian motion, are investigated by using the Taylor series expansion technology. The asymptotic behaviors over a long time period show a significantly negative power function of time. The thermodynamic constraints of this system are then obtained according to the principle of maximum entropy, which establishes a relationship of inequality between the first three particle moments and some physical parameters (i.e., surface tension and temperature). In the thermodynamic equilibrium state, this function provides a new approach for estimating the effect of molecular structure on surface tension of liquid polymers.