Authors: Ana Maria Minarelli Gaspar, Sybele Saska, J. Jimenez, L.R. da Cunha, P.D.A. Bolini, Claudinete V. Leal, L. Morejón-Alonso, R. García Carrodeguas, A. López-Bravo, Cecília A.C. Zavaglia
Abstract: The biological behavior of a new bioactive material composed of calcium-deficient
hydroxyapatite, octacalcium phosphate, and β-tricalcium phosphate was investigated by in vitro
indirect and direct cytotoxicity, cell adhesion and proliferation tests, and by in vivo subcutaneous
and bone implantation in rats. The results of the in vitro studies showed that the material is
biocompatible and no cytotoxic. Slightly poorer initial cell adhesion and lower cell proliferation
than in control was observed, which were attributed to the reactivity and roughness of the material
surface. In vivo results showed that the material is biodegradable and bioactive in bone tissue, but
only biocompatible and partially biodegradable in soft tissue.
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Authors: R. García Carrodeguas, Antonio de Aza, J. Jimenez, P.N. De Aza, P. Pena, A. López-Bravo, S. De Aza
Abstract: In this work a new kind of CaSiO3-doped α-Ca3(PO4)2 ceramic materials, with
compositions lying outside the field of the Ca3(PO4)2 solid solution in the system Ca3(PO4)2-
CaSiO3, were obtained and some of their properties, relevant for bone repairing, were studied in
vitro. Crystalline α-Ca3(PO4)2 solid solution and minor amounts of non-equilibrium residual glass
were the only phases in the materials containing 2 and 5 wt% of CaSiO3. α-Ca3(PO4)2, crystalline
eutectic-like phase and residual glass were observed for sample containing 15 and 20 wt% of
CaSiO3. The mechanical strength improved for all the doped ceramics with regard to un-doped
Ca3(PO4)2. The release of ionic Ca and Si in simulated physiological conditions increased with the
content of CaSiO3 and favored α-Ca3(PO4)2 surface transformation. The soluble components
extracted from the CaSiO3-doped α-Ca3(PO4)2 bioceramics were not cytotoxic to human fibroblastlike
cells. Initial cell adhesion onto the surface of the materials seemed to be partially hindered by
surface reactivity and remodeling, however those cells adhered to the experimental bioceramics
were viable and proliferated normally.
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Authors: Luis M. Rodríguez-Lorenzo, M. Fernandez, J. Parra, Blanca Vázquez, A. López-Bravo, Julio San Román, Kārlis A. Gross, Gail I. Anderson
Abstract: Bisphosphonates (BP) are drugs currently administered orally to treat diseases
characterised by an excessive bone resorption. Alternative and more efficient delivery routes and
more potent compounds are being investigated. Three implantable delivery systems, which allow
the controlled release of therapeutic agents from the device core, are examined in this paper. (4-
(aminomethyl) benzene) bisphosphonic acid (ABBP) was incorporated on
Ca8.8Na0.8(PO4)4.8(CO3)1.2(OH)0.4F1.6 particles by refluxing the powder in a 60 mmol suspension in
acetone at 60°C for 5 hours. 4-aminophenyl acetic bisphosphonate monosodium salt (APBP) and 1-
H-indole-3-acetic bisphosphonate monosodium (IBP) were loaded on Ca10(PO4)6(OH)1F1 ceramic
bodies by stirring the ceramic bodies in 0.04M BP solutions. Injectable acrylic cements based on
self-curing formulations of methyl methacrylate (MMA) and vitamin E were loaded with APBP and
IBP. The incorporation of ABBP was confirmed by MAS-NMR spectroscopy. Modified powder
shows two different phosphorous environments, the first one at 2.91 ppm can be assigned to the
apatite base and the second one at 18.0 ppm has to be attributed to the phosphonic group of the
ABBP. The IBP addition on ceramic surfaces did not decrease the number of osteoclast colonies
and appeared to improve the performance of the HA as a surface for osteoblast culture. A
therapeutic dosage of APBP and IBP can be achieved from acrylic cements that showed lack of
toxicity and an increased cellular activity and proliferation.
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Authors: Luis M. Rodríguez-Lorenzo, R. García-Carrodeguas, M.A. Rodríguez, S. De Aza, J. Jiménez, A. López-Bravo, M. Fernandez, Julio San Román
Abstract: Synthetic pseudowollastonite (psW) and a nanostructured copolymer made of a biostable component, Poly(ethylmethacrylate) (PEMA) and a bioresorbable component, vinylpyrrolidone (VP) are used in this work for the preparation of a new family of bone substitutes that allow osseointegration and mechanical stability. Composites are prepared by bulk polymerization of the desired composition in 15 mm diameter cylindrical plastic moulds. Polymerization was induced
thermally at 50°C using 1wt% azobis(isobutyronitrile) (AIBN) as free-radical initiator. The moulds were filled to a height of 100 mm and 1 mm height discs were cut with a diamond saw. Specimens with a ceramic/polymer ratio 58/42, 33/67,17/83 and 0/100 were obtained. Compression stress in the range 39-59 MPa and elastic modulus between 2.64 and 4.14 GPa are obtained where the
greater values correspond to the specimens prepared with a 60% ceramic load. Degradation in SBF produces a porous nanostructure in the polymeric component indicating microdomains of different solubility and the formation of an apatite-like layer on the surface of the wollastonite component.
All the compositions assayed present a biocompatibility at least of the level or even superior than the Thermanox® control used.
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