The surface of solvent cast chitosan membranes was modified using a two-step procedure. Oxygen plasma treatment was used at the first activation step followed by vinyl monomer graft polymerization. Two monomers were used in order to compare the influence of different functional groups on cell adhesion and proliferation; acrylic acid (AA) was used to introduce carboxyl groups and vinyl sulfonic acid (VSA) was used as a source of sulfonic groups. The surface chemistry/energy changes were characterized by means of X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR-ATR), and contact angle measurements. Additionally, alterations in the surface morphology were investigated by scanning electron microscopy (SEM). XPS analyses confirmed the polymer grafting on the surface; an S 2s peak appears in the VSA survey spectrum and an O-CLO peak emerges in the C 1s high resolution spectrum after AA grafting. Moreover, contact angle measurements showed an increment in the values of the surface energy polar and Lewis base components for all treated samples, confirming the introduction of additional polar groups by the modification processes. FTIR-ATR spectra showed no significant difference between treated and original materials. These results confirmed that only the very top (a few angstroms) surface layer, but not the bulk of the material, was modified. The effect of modification on the adhesion and proliferation of osteoblast-like cells was studied on a preliminary basis. Direct contact tests were performed using a human osteosarcoma cell line (SaOs-2). Cell morphology (optical microscopy and SEM) and cell viability (MTS test) were evaluated for untreated and surface modified membranes. The results revealed that both plasma treatment, and the presence of sulfonic groups on the surface of chitosan membranes, improve SaOs-2 adhesion and proliferation when compared to untreated or AA-grafted membranes. This effect was strongly related to the polar and Lewis basic components of the total surface energy.

Chitosan biocompatibility is often associated with the structural similarities with glycosaminoglycans (GAGs). Although all of the GAGs are built from repeating disaccharide units and some of them contain N-glucosamine (the main hexosamine in the chitosan backbone), all of them also contain negatively charged functional groups. These charged units are believed to have a crucial role for the formation of proteoglycans and hence for key biochemical processes/signaling related to cell functionality and survival. Lack of these groups in chitosan structure could be the reason for the previously observed poor cell adhesion to this material. Herein, we report that plasma induced grafting of negatively charged phosphonic groups can induce remarkably distinguishable cell response and significantly improve the adhesion, proliferation and viability of osteoblast cells. The proposed plasma induced polymerization is a very simple and versatile method and can be easily adapted to other materials and different negatively charged units.

A commonly applied strategy in the field of tissue engineering (TE) is the use of temporary three-dimensional scaffolds for supporting and guiding tissue formation in various in vitro strategies and in vivo regeneration approaches. The interactions of these scaffolds with highly sensitive bioentities such as living cells and tissues primarily occur through the material surface. Hence, surface chemistry and topological features have principal roles in coordinating biological events at the molecular, cellular and tissue levels on timescales ranging from seconds to weeks. However, tailoring the surface properties of scaffolds with a complex shape and architecture remains a challenge in materials science. Commonly applied wet chemical treatments often involve the use of toxic solvents whose oddments in the construct could be fatal in the subsequent application. Aiming to shorten the culture time in vitro (i.e. prior the implantation of the construct), in this work we propose a modification of previously described bone TE scaffolds made from a blend of starch with polycaprolactone (SPCL). The modification method involves surface grafting of sulfonic or phosphonic groups via plasma-induced polymerization of vinyl sulfonic and vinyl phosphonic acid, respectively. We demonstrate herein that the presence of these anionic functional groups can modulate cell adhesion mediated through the adsorbed proteins (from the culture medium). Under the conditions studied, both vitronectin adsorption and osteoblast proliferation and viability increased in the order SPCL << sulfonic-grafted SPCL < phosphonic-grafted SPCL. The results revealed that plasma-induced polymerization is an excellent alternative route, when compared to the commonly used wet chemical treatments, for the surface functionalization of biodevices with complex shape and porosity.

The quantitative detection of viable pathogen load is an important tool in determining the degree of infection in animals and contamination of foodstuffs. Current conventional culture methods are limited in their ability to determine these levels in Mycobacterium avium subspecies paratuberculosis (MAP) due to slow growth, clumping and low recoverability issues. The principle goal of this study was to evaluate a novel culturing process (TiKa) with unique ability to stimulate MAP growth from low sample loads and dilutions. We demonstrate it was able to stimulate a mean 29-fold increase in recoverability and an improved sensitivity of up to three logs when compared with conventional culture. Using TiKa culture, MAP clumping was minimal and produced visible colonies in half the time required by standard culture methods. Parallel quantitative evaluation of the TiKa culture approach and qPCR on MAP loads in tissue and gut mucosal samples from a MAP vaccine-challenge study, showed good correlations between colony counts (cfu) and qPCR derived genome equivalents (Geq) over a large range of loads with a 30% greater sensitivity for TiKa culture approach at low loads (two logs). Furthermore, the relative fold changes in Geq and cfu from the TiKa culture approach suggests that non-mucosal tissue loads from MAP infected animals contained a reduced proportion of non-viable MAP (mean 19-fold) which was reduced significantly further (mean 190-fold) in vaccinated “reactor” calves. This study shows TiKa culture equates well with qPCR and provides important evidence that accuracy in estimating viable MAP load using DNA tests alone may vary significantly between samples of mucosal and lymphatic origin.

A series of random terpolymers composed of N-isopropylacrylamide (NIPAAm), 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS), and N-tert-butylacrylamide (NTBAAm) monomers were synthesized by free radical polymerization. The molar fraction of the negatively charged monomer (AMPS) was maintained constant (0.05) for all studied terpolymer compositions. Turbidity measurements were used to evaluate the influence of the relative amount of NIPAAm and NTBAAm, polymer concentration, and solution ionic strength on the cloud point and redissolution temperatures (macroscopic phase separation). Dynamic light scattering (DLS) was employed to elucidate some aspects regarding the molecular scale mechanism of the temperature-induced phase separation and to determine the low critical solution temperature (LCST). The aqueous solutions of terpolymers remained clear at all studied temperatures; turbidity was only observed in the presence of NaCl. The cloud point temperature (CPT) determined by turbidimetry was found to be systematically much higher than the LCST determined by DLS; nanosized aggregates were observed at temperatures between the LCST and the CPT. Both CPT and LCST decreased when increasing the molar ratio of NTBAAm (increased hydrophobicity). It was found that above a critical molar fraction of NTBAAm (0.25-0.30) the aggregation rate suddenly decreased. Polymers with NTBAAm content lower than 0.25 showed a fast macroscopic phase separation, but the formed large aggregates are disaggregating during the cooling ramp at temperatures still higher than the LCST. On the contrary, polymers with NTBAAm contents above 0.30 showed a slow macroscopic phase separation, and the formed large aggregates only redissolved when LCST was reached. These differences were explained on the basis of a delicate balance between the electrostatic repulsion and the hydrophobic attractive forces, which contribute cooperatively to the formation of metastable nanosized aggregates.

Osteoporosis represents a major health problem in terms of compromising bone strength and increasing the risk of bone fractures. It can be medically treated with bisphosphonates, which act systemically upon oral or venous administration. Further, bone regenerative treatments in osteoporotic conditions present a challenge. Here, we focused on the development of a synthetic bone substitute material with local diminishing effects on osteoporosis. Composites were created using calcium phosphate cement (CPC; 60 wt%) and polylactic-co-glycolic acid (PLGA; 40 wt%), which were loaded with alendronate (ALN). In vitro results showed that ALN-loaded CPC/PLGA composites presented clinically suitable properties, including setting times, appropriate compressive strength, and controlled release of ALN, the latter being dependent on composite degradation. Using a rat femoral condyle bone defect model in osteoporotic animals, ALN-loaded CPC/PLGA composites demonstrated stimulatory effects on bone formation both within and outside the defect region.

In this study, we investigated the fundamental relationship between the physicochemical characteristics of antibiotics and the kinetics of their release from gelatin nanospheres. We observed that antibiotics of high molecular weight (colistin and vancomycin) were released in a sustained manner from oppositely charged gelatin carriers for more than 14 d, as opposed to antibiotics of low molecular weight (gentamicin and moxifloxacin) which were released in a burst-like manner. The release kinetics of positively charged colistin strongly correlated with the rate of the enzymatic degradation of gelatin. To elucidate the differences among release kinetics of antibiotics, we explored the mechanism of interactions between antibiotics and gelatin nanospheres by monitoring the kinetics of release of antibiotics as a function of pH, ionic strength, and detergent concentrations. These studies revealed that the interactions between antibiotics and gelatin nanospheres were mainly dominated by (i) strong electrostatic forces for colistin; (ii) strong hydrophobic and electrostatic forces for vancomycin; (iii) weak electrostatic and hydrophobic forces for gentamicin; and (iv) weak hydrophobic forces for moxifloxacin. These results confirm that release of antibiotics from gelatin nanospheres strongly depends on the physicochemical characteristics of the antibiotics.

Peptide arrays on cellulose are a powerful tool to investigate peptide interactions with a number of different molecules, for examples antibodies, receptors or enzymes. Such peptide arrays can also be used to study interactions with whole cells. In this review, we focus on the interaction of small antimicrobial peptides with bacteria. Antimicrobial peptides (AMPs) can kill multidrug-resistant (MDR) human pathogenic bacteria and therefore could be next generation antibiotics targeting MDR bacteria. We describe the screen and the result of different optimization strategies of peptides cleaved from the membrane. In addition, screening of antibacterial activity of peptides that are tethered to the surface is discussed. Surface-active peptides can be used to protect surfaces from bacterial infections, for example implants.