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The present paper is focused on the surface and bulk characterization of poly(lactic acid) (PLA)-based composites that contain hydrolyzed collagen as a biological polymer, silver nanoparticles and vitamin E and epoxidized soybean oil as a plasticizer. The bionanocomposites were obtained by melt processing and evaluated for structural and surface characteristics, biocompatibility, functional properties such as antimicrobial and antioxidant activity and hydrolytic degradation behavior. It has been established that the optimal composition to impart functional properties to the PLA matrix is a formulation containing 15% epoxidized soybean oil, 15% hydrolyzed collagen, 5% Pluronic, 5% vitamin E and 0.3% silver nanoparticles. This bionanocomposite inhibits the growth of both Gram-positive bacteria, Escherichia coli and Salmonella typhimurium, and Gram-negative bacteria, Listeria monocytogenes, and reaches 100% radical-scavenging activity. The PLA-based biomaterials obtained in this study are stable in biological media in the short and medium terms and therefore are recommended as multifunctional biomaterials for the manufacture of medical devices, such as urinary catheters.

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Both cold nitrogen radiofrequency plasma and gamma irradiation have been applied to activate and functionalize the polylactic acid (PLA) surface and the subsequent lactoferrin immobilization. Modified films were comparatively characterized with respect to the procedure of activation and also with unmodified sample by water contact angle measurements, mass loss, X-ray photoelectron spectroscopy (XPS), attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR), atomic force microscopy (AFM), and chemiluminescence measurements. All modified samples exhibit enhanced surface properties mainly those concerning biocompatibility, antimicrobial, and antioxidant properties, and furthermore, they are biodegradable and environmentally friendly. Lactoferrin deposited layer by covalent coupling using carbodiimide chemistry showed a good stability. It was found that the lactoferrin-modified PLA materials present significantly increased oxidative stability. Gamma-irradiated samples and lactoferrin-functionalized samples show higher antioxidant, antimicrobial, and cell proliferation activity than plasma activated and lactoferrin-functionalized ones. The multifunctional materials thus obtained could find application as biomaterials or as bioactive packaging films.

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CO2, N-2, and N-2/H-2 radiofrequency plasma exposure was used for functionalization of poly(vinylidene fluoride) surface aiming the fibrinogen immobilization. Fibrinogen was immobilized onto poly(vinylidene fluoride) surface using both simple plasma activation and covalent coupling. The modified surfaces have been characterized by X-ray photoelectron spectroscopy, attenuated total reflectance-Fourier transform infrared spectroscopy, near infrared-chemical imaging, atomic force microscopy, and wettability measurements, and the obtained materials were tested as supports for fibroblast cell cultures. The plasma type and the immobilization procedure have influenced the fibrinogen attachment onto the poly(vinylidene fluoride) surface, which was achieved mainly through amide bonds when using coupling agents. Covalent immobilization of fibrinogen onto poly(vinylidene fluoride) surface leads to a more stable protein-modified polymer surface. Non-cytotoxic plasma-based coating technology has the ability to covalently immobilize bioactive molecules for surface modification of some biomaterials that mainly could be achieved by the immobilization of proteins such as fibrinogen that triggers desirable cellular responses. The fibrinogen-modified poly(vinylidene fluoride) materials showed increased cell viability of fibroblasts. Cell viability was enhanced by plasma-activated fibrinogen coatings onto poly(vinylidene fluoride) surface, this being more significant if coating was linked further by a coupling reaction. Hence, they could be good candidates for biomedical applications.

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Novel biocompatible and antimicrobial composites based on poly(lactic acid) (PLA), hydrolyzed collagen (HC) and silver nanoparticles (AgNPs) were prepared by melt processing. Tributyl o-acetyl citrate (ATBC) was used as plasticizer, for improving the processability of PLA. The influence of HC and AgNPs on the PLA bionanocomposites was investigated in terms of biocompatibility, antifungal activity and water contact angle measurements. Surface morphology by SEM and the identification of AgNPs by UV-Vis were also presented. The investigated bionanocomposites exhibited the characteristic plasmonic effect of silver nanoparticles. All composites showed a high degree of biocompatibility. Sample containing HC 5 wt.% and AgNPs showed a significant antifungal property, inhibiting fungal adhesion and mature biofilm development. The increased hydrophilicity determined by contact angle analysis for the PLA/HC10/AgNPs composite did no contributed significantly to improving of anti-adherence effect. 10 wt.% HC promoted fungal colonization and mature biofilm development.

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The present work reports on the biocompatibility of poly (3-hydroxybutyrate) and poly (3-hydroxybutyrateco-3-hydroxyvalerate) loaded with bacterial cellulose and microcrystalline cellulose via melt processing. Biocompatibility was tested by physico-chemical and in vitro methods. Physico-chemical tests of biocomposites, such as reducing substances, acidity, alkalinity, absorbance by UV/VIS, residue on evaporation were performed on aqueous extract. The cell viability was evaluated by MTT assay. Cell morphology evaluation of cell culture treated with composites was visualized by light microscopy. Also, thermal properties of biocomposites were investigated by DSC analysis. The obtained results have shown good biocompatibility of all biocomposites.

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Poly(vinyl chloride) (PVC) is the most widely used material for the production of medical devices such as intravenous fluid bags and tubing, enteral feeding, dialysis equipment and catheters. Despite of their numerous advantages, the plastic medical devices are non biodegradable and prone to microbial colonization causing biofilm associated infections which are difficult to treat and tend to chronicisation. A possible solution to surpass these limitations could be the fabrication of new biodegradable polymeric materials with optimized biocompatibility and antimicrobial properties. In this regard, biodegradable polymeric materials, such as poly(epsilon-caprolactone) (PCL), poly(DL-lactic acid) (PLA) etc. have been considered the most desirable solution from the environment management point of view. In this paper, Alg(1%) Zn, Alg(2%) Zn, Alg(3%) Zn compounds were obtained from sodium alginate (AlgNa) crosslinked with ZnCl2. Antimicrobial activity of the AlgZn compounds was assessed by the microdilutions and the diffusion methods, towards Gram-positive and Gram-negative bacterial strains (reference and clinical isolates). The Alg(3%) Zn compound was selected as antimicrobial agent to obtain the biocomposites encoded: PLA/PCL/AlgZn0.1 and PLA/PCL/AlgZn0.3. The PLA/PCL sample was used as control. Antibiofilm activity against Staphylococcus xylosus, cytotoxic effect on mammalian cells and thermal analysis by DSC were investigated for the obtained biocomposites. The obtained results show that the addition of the Alg(3%) Zn compound in the biocomposites decreased the glass transition temperature as well as the degree of crystallinity both of the PCL and PLA components in samples. Although the results suggest that the biocomposites containing Alg(3%) Zn did not inhibit the staphylococcal colonization and mature biofilm formation, the high degree of biocompatibility of blends leads to conclusion that these materials could be used for the development of novel bioactive and biodegradable polymeric materials with medical applications.

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