Biocompatible and biodegradable poly-l-lactic acid (PLLA) processed into piezoelectric structures has good potential for use in medical applications, particularly for promoting cellular growth during electrostimulation. Significant advantages like closer contacts between cells and films are predicted when their surfaces are modified to make them more hydrophilic. However, there is an open question about whether the surface modification will affect the degradation process and how the films will be changed as a result. For the first time, we demonstrate that improving the polymer surface’s wettability affects the position of enzyme-driven degradation. Although it is generally considered that proteinase K degrades only the polymer surface, we observed the enzyme’s ability to induce both surface and bulk degradation. In hydrophilic films, degradation occurs at the surface, inducing surface erosion, while for hydrophobic films, it is located inside the films, inducing bulk erosion. Accordingly, changes in the structural, morphological, mechanical, thermal and wetting properties of the film resulting from degradation vary, depending on the film’s wettability. Most importantly, the degradation is gradual, so the mechanical and piezoelectric properties are retained during the degradation.

The cell stimulation using piezoelectric polymers, known as piezostimulation, is innovative approach in designing antimicrobial protection. As antibiotic-free and inorganic nanoparticle-free approach, it uses physical stimuli to target bacterial cells...

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Designing useful functionalities in clinically validated, old antibiotics holds promise to provide the most economical solution for the global lack of effective antibiotics, as undoubtedly a serious health threat. Here we show that using the surface chemistry of the cyclodextrin (βCD) cycle and arginine (arg) as a linker, provides more stable ternary antibiotic complex (βCD-arg-cpx). In contrast to classical less stable inclusion complexes, which only modify antibiotic solubility, here-presented ternary complex is more stable and controls drug release. The components of the complex intensify interactions with bacterial membranes and increase the drug’s availability inside bacterial cells, thereby improving its antimicrobial efficacy and safety profile. Multifunctional antibiotics, formulated as drug delivery systems per se, that take the drug to the site of action, maximize its efficacy, and provide optical detectability are envisaged as the future in fighting against infections. Their role as a tool against multiresistant strains remains as interesting challenge open for further research.

Poly‐L‐lactide (PLLA) offers a unique possibility for processing into biocompatible, biodegradable, and implantable piezoelectric structures. With such properties, PLLA has potential to be used as an advanced tool for mimicking biophysical processes that naturally occur during the self‐repair of wounds and damaged tissues, including electrostimulated regeneration. The piezoelectricity of PLLA strongly depends on the possibility of controlling its crystallinity and molecular orientation. Here, it is shown that modifying PLLA with a small amount (1 wt%) of crystalline filler particles with a high aspect ratio, which act as nucleating agents during drawing‐induced crystallization, promotes the formation of highly crystalline and oriented PLLA structures. This increases their piezoelectricity, and the filler‐modified PLLA films provide a 20‐fold larger voltage output than nonmodified PLLA during ultrasound (US)‐assisted activation. With 99% PLLA content, the ability of the films to produce reactive oxygen species (ROS) and increase the local temperature during interactions with US is shown to be very low. US‐assisted piezostimulation of adherent cells directly attach to their surface (such as skin keratinocytes), stimulate cytoskeleton formation, and as a result cells elongate and orient themselves in a specific direction that align with the direction of PLLA film drawing and PLLA dipole orientation.

The combination of plasmonic material and magnetic metal oxide nanoparticles is widely used in multifunctional nanosystems. Here we propose a method for the fabrication of a gold/cobalt ferrite nanocomposite for biomedical applications. The composite includes gold cores of ~10 nm in diameter coated with arginine, which are surrounded by small cobalt ferrite nanoparticles with diameters of ~5 nm covered with dihydrocaffeic acid. The structure and elemental composition, morphology and dimensions, magnetic and optical properties, and biocompatibility of new nanocomposite were studied. The magnetic properties of the composite are mostly determined by the superparamagnetic state of cobalt ferrite nanoparticles, and optical properties are influenced by the localized plasmon resonance in gold nanoparticles. The cytotoxicity of gold/cobalt ferrite nanocomposite was tested using T-lymphoblastic leukemia and peripheral blood mononuclear cells. Studied composite has selective citotoxic effect on cancerous cells while it has no cytotoxic effect on healtly cells. The results suggest that this material can be explored in the future for combined photothermal treatment and magnetic theranostic.