Lorenzo Pio Serino

A Semi-Degradable Composite Scaffold for Articular Cartilage Defects

Few options exist to replace or repair damaged articular cartilage. The optimal solution that has been suggested is a scaffold that can carry load and integrate with surrounding tissues; but such a construct has thus far been elusive. The objectives of this study were to manufacture and characterize a nondegradable hydrated scaffold. Our hypothesis was that the polymer content of the scaffold can be used to control its mechanical properties, while an internal porous network augmented with biological agents can facilitate integration with the host tissue. Using a two-step water-in-oil emulsion process a porous polyvinyl alcohol (PVA) hydrogel scaffold combined with alginate microspheres was manufactured. The scaffold had a porosity of 11-30% with pore diameters of 107-187 μm, which readily allowed for movement of cells through the scaffold. Alginate microparticles were evenly distributed through the scaffold and allowed for the slow release of biological factors. The elastic modulus (Es ) and Poissons ratio (υ), Aggregate modulus (Ha ) and dynamic modulus (ED ) of the scaffold were significantly affected by % PVA, as it varied from 10 to 20% wt/vol. Es and υ were similar to that of articular cartilage for both polymer concentrations, while Ha and ED were similar to that of cartilage only at 20% PVA. The ability to control scaffold mechanical properties, while facilitating cellular migration suggest that this scaffold is a potentially viable candidate for the functional replacement of cartilage defects.

Urease loaded alginate microspheres for blood purification

In this paper a device, based on urease-loaded microspheres, is presented. The first task of this work was the optimization of a procedure for the alginate microspheres realization, having a radius as close as possible to the optimal one necessary to achieve the maximum enzyme exploitation. This optimal radius was calculated theoretically through a mathematical model which describes the concentration of substrate (urea) inside the microspheres on the assumption of a diffusion-reaction mechanism. The enzyme-loaded microspheres were successfully tested in a prototypal device aimed at the depletion of urea from a circulating fluid simulating blood flow: the results showed that urea concentration in the circulating fluid drops down to less than 25% of the initial value after 5 h.

PVA-Based Scaffolds for the Repair of Musculoskeletal Soft Tissue

The objective of this study was to design a partly-degradable scaffold to repair cartilage defects. The scaffold, based on poly(vinyl alcohol), PVA, was intended to maintain long-term mechanical integrity and to facilitate cell proliferation via bioactive agent release from contained microparticles, made from either alginate, ALG or poly(lactic-co-glycolic acid), PLGA. The aim of this study was to characterize the morphological features and mechanical behaviour of composite scaffolds as a function of microparticle type and percent content. Our hypothesis was that the dynamic mechanical properties (Dynamic Modulus and Phase Angle) of the composite scaffold would not be affected by microparticle type, but that Dynamic Modulus would increase as a function of increased microparticle content. Scanning Electron Microscopy confirmed that the manufacturing process homogenously dispersed microspheres within the scaffolds. For pure PVA samples Dynamic Modulus ranged from 66±3 kPa at 0.01 Hz to 83±3 kPa at 50 Hz. As ALG microsphere content increased from 25% to 75%, Dynamic Modulus ranged from 92±5 kPa at 0.01 Hz to 153±19 kPa at 50 Hz. As the microsphere content increased from 25% to 75% PLGA, Dynamic Modulus ranged from 85±9 kPa at 0.01 Hz, to 157±16 kPa at 50 Hz. As expected, Dynamic Modulus increased with increasing test frequencies. For pure PVA specimens Phase Angle ranged from 4.3±0.8 degrees at 0.01 Hz to 12±1.2 degrees at 50 Hz. Phase Angle was not affected by microsphere content. In conclusion, the addition of microspheres affected the dynamic mechanical behavior, in particular Dynamic Modulus, of PVA scaffolds. However, the dynamic mechanical properties were not affected by the polymer from which the microspheres were manufactured. These findings suggest that microsphere type can be chosen to optimize the inclusion of bioactive factors, without detrimentally affecting the mechanical properties of the composite scaffold. It also suggests that % content of included microspheres can be used to modulate the mechanical properties of the scaffold at time zero.Copyright

Erratum to: Gelatine/PLLA sponge-like scaffolds: morphological and biological characterization

This article was mistakenly published twice, both in print and online. The publication details are as follows: DOI 10.1007/s10856-006-0594-8 was published online on December 3, 2006, and was printed in volume 17, number 12, December 2006, pages 1211–1217. DOI 10.1007/s10856-007-0127-0 was published online on February 3, 2007, and was printed in volume 18, number 7, July 2007, pages 1399–1405. The official publication date of this article is that associated with DOI 10.1007/s10856-006-0594-8: December 3, 2006. This was a Publisher’s error.