Polylactic acid-phosphate glass composite foams as scaffolds for tissue engineering

Phosphate glass (PG) of the composition 0.46(CaO)-0.04(Na(2)O)- 0.5(P(2)O(5)) was used as filler in poly-L-lactic acid (PLA) foams developed as degradable scaffolds for bone tissue engineering. The effect of PG on PLA was assessed both in bulk and porous composite foams. Composites with various PG content (0, 5, 10, and 20 wt %) were melt-extruded, and either compression-molded or foamed through supercritical CO(2). Dynamic mechanical analysis on the bulk composites showed that incorporating 20 wt % PG resulted in a significant increase in storage modulus. Aging studies in deionized water in terms of weight loss, pH change, and ion release inferred that the degradation was due to PG dissolution, and dependent on the amount of glass in the composites. Foaming was only possible for composites containing 5 and 10 wt % PG, as an increase in PG increased the foam densities; however, the level of porosity was maintained above 75%. PLA-T(g) in the foams was higher than those obtained for the bulk. Compressive moduli showed no significant reinforcement with glass incorporation in either expansion direction, indicating no anisotropy. Biocompatibility showed that proliferation of human fetal bone cells was more rapid for PLA compared to PLA-PG foams. However, the proliferation rate of PLA-PG foams were similar to those obtained for foams of PLA with either hydroxyapatite or beta-tricalcium phosphate

Lichenological exploration of Algeria: historical overview and annotated bibliography, 1799-2013

yesDespite more than two centuries of almost uninterrupted surveys and studies of Algerian lichenology, the history and lichen diversity of Algeria are still poorly understood. During the preparation of a forthcoming checklist of Algerian lichens it was considered necessary to provide the present historical overview of lichenological exploration of the country from 1799 to 2013, supported by a reasonably comprehensive annotated bibliography of 171 titles

Viscerocutaneous form of loxoscelism and erythrocyte glucose-6-phosphate deficiency

In a period of time of five years, all patients who exhibited viscerocutaneous form of loxoscelism were investigated for erythrocyte glucose-6-phosphate deficiency, and in two patients out of seven it was found this deficiency. This finding suggests that this genetical enzyme deficiency could account for the hemolysis after Loxosceles bite, at least in some of the cases

Dissolution and bioactivity of a sol-gel derived borate glass in six different solution media

Sol-gel derived bioactive borate glasses (SGBGs) rapidly convert to hydroxycarbonated apatite (HCA) in simulated body fluid (SBF), in vitro. While previous studies have examined the influence of processing and composition on bioactivity, the effect of the in vitro dissolution media has not been well examined for these glasses. In this study, the mineral conversion of a SGBG substituted 45S5 Bioglass® formulation (“B46”, (46.1)B2O3-(26.9)CaO-(24.4)Na2O-(2.6)P2O5, mol%), was examined in six different dissolution media: SBF, tris(hydroxymethyl)aminomethane (TRIS, pH 7.4) buffer, Dulbecco’s phosphate buffered saline (PBS, 1X), Dulbecco’s Modified Eagle Medium (DMEM, 1X), 0.9% Saline (SAL), and deionized water (DIW) at 1.5 mg/mL for 10 min, 2h, and 1d. All media underwent a rapid increase in pH as a result of glass dissolution and ion release. B46 in SBF, TRIS, and PBS converted to HCA while B46 in DMEM, SAL, and DIW converted to calcite according to attenuated total reflectance-Fourier-transform infrared spectroscopy, X-ray diffraction, and scanning electron microscopy. The ratio of B46 to SBF was also examined at 3, 6, 12, and 24 mg/mL for 1d. These results help elucidate the dissolution and mineral conversion of borate glasses and help provide insights into optimizing pre-conditioning treatments for both in vitro and in vivo analyses

Highly Bioactive Sol-Gel-Derived Borate Glasses

Attributable to their low chemical durability, borate-based glasses have been demonstrated to convert rapidly to hydroxy-carbonated apatite (HCA), the inorganic component of bone. However, the effect of sol-gel processing on the bioactivity of borate-based glasses has not been investigated. In this study, the gel and glass forming abilities of six different borate-based glass formulations with borate content ranging from 36 to 61 mol % and based on a previously studied four component melt-derived glass system [(46.1)­B₂O₃–(26.9)­CaO–(24.4)­Na₂O–(2.6)­P₂O₅; mol %] were investigated. Compared to melt-quench, sol-gel processing fabricated nanoporous glass particles with at least 2 orders of magnitude greater values for specific surface areas and total pore volumes, which translated to dramatically higher aqueous interaction and ion release rates. Surprisingly, when immersed in simulated body fluid, HCA conversion was achieved in as little as 3 h for sol-gel derived borate based glasses, demonstrating a 25-fold increase in mineralization rate when compared to melt derived equivalents. The ability of the sol-gel derived borate-based glasses to rapidly convert to bone-like HCA holds promise in numerous potential tissue engineering applications, including the repair and augmentation of mineralized tissues