L. De Nardo

Shape memory polymer cellular solid design for medical applications

Shape memory polymers (SMPs) are an emerging class of active materials whose response can be easily tailored via modifications of the molecular parameters and optimization of the transformation processes. In this work, we originally demonstrated that a correct coupling of polymer transformation processes (co-extrusion with chemical blowing agents, salt co-extrusion/particulate leaching, solvent casting/particulate leaching) and SMPs allows one to obtain porous structures with a broad spectrum of morphological properties resulting in tunable thermo-mechanical and shape recovery properties. Such a wide range of properties could fulfil the specifications of medical applications in which the use of SMP-based foams can be envisaged.

Comparative evaluation and optimization of off-the-shelf cationic polymers for gene delivery purposes

Cationic polymers are amongst the most utilized non-viral vectors for gene transfer owing to their ability to condense and protect the genetic material within polyplexes and to ferry it into cells. Quite a number of parameters, both related to the features of the vectors themselves (e.g. degree of branching, molecular weight, polydispersity) and to polyplexes (e.g. nitrogen to phosphate ratio (N/P), dose of complexes delivered, complexation buffer, etc.), are known to affect transfection behaviour. Consequently, some substantial discrepancy found in raw materials and in-home protocols across laboratories account for some disagreement and conflicting data about their performance. Hereinafter we provide a thorough chemical-physical and in vitro biochemical characterization, comparison, and optimization of the most widely used, commercially sourced polymers used in transfection, namely linear polyethylenimines (lPEIs), branched PEIs (bPEIs), linear poly-L-lysines (lPLLs), and polyamidoamine dendrimers (dPAMAMs). By means of a stepwise approach, we pinpointed the most effective molecular weight and complexation conditions specific to each of them and correlated the physicochemical features of polyplexes with their transfection effectiveness. Besides, taking separately into account the effects on transfection of the plasmid dose delivered to cells, the cell seeding density and the volume of the culture medium, we highlited a range of optimal conditions roughly specific to each studied polymer. Finally, we coped with the effect of the variation of these three parameters at once on the transfection effectiveness of lPEI and bPEI and pinpointed an array of settings specifically optimized to attain truly superior performances.

Electrochemical surface modifications of titanium and titanium alloys for biomedical applications

Abstract: In this chapter the main issues related to surface modifications of titanium and titanium alloys in biomedical applications are discussed. Firstly the basic chemico-physical principles of electrochemical processes are considered, followed by a critical review of important results reported in this field. Finally, the latest advances in complex organic/inorganic surface preparation, based on electrochemical surface immobilisation of biomolecules, are presented.

Chitosan-Based Trilayer Scaffold for Multitissue Periodontal Regeneration:

Periodontal regeneration is still a challenge for periodontists and tissue engineers, as it requires the simultaneous restoration of different tissues—namely, cementum, gingiva, bone, and periodontal ligament (PDL). Here, we synthetized a chitosan (CH)–based trilayer porous scaffold to achieve periodontal regeneration driven by multitissue simultaneous healing. We produced 2 porous compartments for bone and gingiva regeneration by cross-linking with genipin either medium molecular weight (MMW) or low molecular weight (LMW) CH and freeze-drying the resulting scaffolds. We synthetized a third compartment for PDL regeneration by CH electrochemical deposition; this allowed us to produce highly oriented microchannels of about 450-µm diameter intended to drive PDL fiber growth toward the dental root. In vitro characterization showed rapid equilibrium water content for MMW-CH and LMW-CH compartments (equilibrium water content after 5 min >85%). The MMW-CH compartment degraded more slowly and provided significantly more resistance to compression (28% ± 1% of weight loss at 4 wk; compression modulus HA = 18 ± 6 kPa) than the LMW-CH compartment (34% ± 1%; 7.7 ± 0.8 kPa) as required to match the physiologic healing rates of bone and gingiva and their mechanical properties. More than 90% of all human primary periodontal cell populations tested on the corresponding compartment survived during cytocompatibility tests, showing active cell metabolism in the alkaline phosphatase and collagen deposition assays. In vivo tests showed high biocompatibility in wild-type mice, tissue ingrowth, and vascularization within the scaffold. Using the periodontal ectopic model in nude mice, we preseeded scaffold compartments with human gingival fibroblasts, osteoblasts, and PDL fibroblasts and found a dense mineralized matrix within the MMW-CH region, with weakly mineralized deposits at the dentin interface. Together, these results support this resorbable trilayer scaffold as a promising candidate for periodontal regeneration.

Dynamico-mechanical characterization of polymer biomaterials

Abstract Dynamic mechanical analysis (DMA) is a basic tool for the characterization of viscoelastic materials, particularly polymers. Applying an oscillatory force to a material, its response can be measured, calculating the viscosity and the stiffness related to temperature, time, or frequency. In addition, DMA can provide information on the thermal transitions of polymer-based systems. The present chapter provides the readers with notes on reasons for using DMA for polymeric biomaterials characterization. After a short overview on the main characteristics of the instrument, examples of possible characterizations performed on different polymers are reported, evidencing the test protocol and the possible outputs that can be obtained.

Chitosan strips with controlled micro-porosity to improve buccal mucoadhesion

Near-InfraRed-Spectroscopy (NIRS) is a neuroimaging method of brain cortical activity using low-energy optical radiation to detect local changes in (de)oxyhaemoglobin concentration. A methodology consisting of a raw signal preprocessing phase, followed by statistical analysis based on a general linear model, is currently being used to determine signal activity. The aim of this research is to define the median modification of the standard method usually used for the estimation of cortical activity from the NIRS signal and to verify its applicability in measuring motor tasks for patients with Parkinsons disease. Individual examinations were conducted in 10 cycles, during which finger tapping, and rest phases were alternating. Changes in oxyhaemoglobin concentration were calculated from the native NIRS signal using the modified Lambert-Beer equation. The signals were filtered in the 0.015–0.3 Hz band and fitted by the physiological response function of the brain tissue for each finger tapping cycle separately. The median value from the 10 cycles was then computed. Activity values obtained in individual subjects have been used in Brain Mapping visualizations. These describe motor task patterns during the ON and OFF deep brain stimulation of the subthalamic nucleus in Parkinsons disease, which demonstrates activation in accordance with the current state of knowledge in functional imaging.