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Tensile strength of the interface between hydroxyapatite (HA) and bone was tested. Scanning electron microscopy was used to observe the tensile failure mode and the morphological change of hydroxyapatite ceramic surface in bone. The porosity of hydroxyapatite is 14% and pore size less than 2 microns. After 2 weeks of implantation, the tensile strength of the interface is 0.72 MPa. After 4, 8, and 16 weeks, the average tensile strength stayed at 1.5 MPa. SEM showed that tensile failure occurred at the HA-bone interface at the second week, but after 4 weeks, the failure occurred between HA particles within the bulk, and not at the HA-bone interface. Calcified tissue was directly deposited on the HA ceramic surface and exits also in the micropores. Near the interface, sintered necks among HA ceramic particles were subjected to biodegradation.

Auger electron spectroscopy was used to investigate the relative concentration of the calcium impurity at the external and fracture surfaces of a dense alumina after in vivo exposure for 6, 12, and 23 weeks. The Ca concentration at the external surface initially decreased, reached a minimum at 12 weeks, and increased thereafter. These results, were compared with the flexural strength, which decreased nearly linearly from 6 to 23 weeks.

Ceramic pelletes (in Al2O3 92% and in calcium aluminate) implanted into the muscles of rabbits for varying periods of time, and samples of similar material, not implanted but mixed with organic substances, have been analyzed by means of thermal differential analysis (TDA). Which hydrated calcium aluminates are formed from implants after contract with the tissue fluid, has been established. It has also been ascertained that the ceramic implants absorb organic substances from the tissue fluid, which, from a first evaluation, seem to be composed of simple molecules. The results of this initial inquiry have provided positive indications of the utility of TDA to assist in elucidating the phenomena that occur between implant and tissue.

Disk-shaped implants of spinel, alumina, mullite, zircon, a cast Co-Cr-Mo alloy, and ultra-high molecular weight polyethylene (UHMWPE), were implanted in the paraspinalis muscle of 12 adult, male, white New Zealand rabbits. Prior to implantation the implants were characterized with respect to size and shape, weight and surface roughness. After periods of 1 month, 2 months, and 4 months, the rabbits were sacrificed and the tissue specimens were retrieved with the implants still intact. Histological examination of the tissues surrounding the implants along with changes in the size and shape, weight, and surface roughness of the implants were used as criteria for evaluating these materials for implant purposes. No surfaces degradation of any of the materials was detected using scanning electron microscopy. Fibrous tissue seemed to adhere to the UHMWPE implants more than any other material used in this study. Large amounts of fibrous tissue were also found to adhere to the cast Co-Cr-Mo alloy implants. The histological results indicated that within the limits of this investigation, the biocompatibility of the ceramic materials used in this study compared favorably with the clinically used Co-Cr-Mo alloy implants and the UHMWPE implants.

Pellets of well-characterized microporous hydroxyapatite (HA) ceramic were implanted in hamsters in two nonosseous sites: (1) in the fatty tissue of the gingival crease, far from bony tissue and (2) in intraperitoneal sites. The implants in site 1 were placed directly in contact with tissues, cells, and extracellular fluids while the implants in site 2 were placed in special chambers made of plexiglass cylinders covered in both ends with millipore filters, preventing contact with tissues and cells, but not with extracellular fluids. The hamsters were sacrificed and the implants recovered after 8, 16, 30, 150, and 365 days. The pellets were characterized using x-ray diffraction, infrared absorption, thermogravimetry, scanning and transmission electron microscopy, and calcium and phosphate analyses before and after implantation. Physicochemical analyses of HA ceramic implants before and after implantation demonstrated the formation of new material which was significantly different from the HA ceramic in terms of the following: (a) morphology (size of shape) of crystals; (b) intimate association of the inorganic phase of the new material with an organic phase similar to inorganic/organic association in bone; (c) the inorganic phase of the new material is a CO3-apatite, similar to that of bone, while the HA in ceramic is CO3-free; (d) electron diffraction of apatite of new material is similar to that of bone apatite. This study also demonstrated that the new material associated with the HA ceramics implanted in two different nonosseous sites were identical in spite of the differences in their microenvironment (cellular and acellular).

This article addresses three aspects of the mechanical and biological properties of bioreactive glasses. First, it describes the composition and the relationship between the composition and bonding and its influence on the bone bonding mechanism and the rate of bond formation. Second, the mechanical properties of bioglass are dealt with. It is shown that the approaches to use bioglass in highly stressed applications, have met with various degrees of success. Third, the issue of the effect of loading on the glass properties and, above all, on the glass bonding properties is discussed.

Sixteen ceramic specimens were implanted in the femur of mature rhesus monkeys. The specimens consisted of four groups of a basic calcium aluminate composition with additions of 5, 10, 15 and 20 wt% phosphorous pentoxide (P2O5). The increasing amounts of P2O5 caused variations in the resorption rate, microstructure and surface characteristics of the implant. The influence of these variables on bone and tissue growth within and about the implant was investigated. After sacrifice the ceramic-bone specimens were studied by a tetracycline-based histological analysis, scanning electron microscopy and energy dispersive analysis. The results indicate an increase in mesenchymal cell proliferation, fibrous and bone tissue formation at the ceramic tissue interface and within the implant with increasing concentrations of P2O5. The results obtained from the study did not furnish sufficient evidence to differentiate between the direct chemical influence the increasing P2O5 had on osseous tissue formation or the indirect influence that may have resulted from its effect on the ceramic microstructure and morphology.

The in vivo biocompatibility of metals coated with several different types of ceramics [alumina (alpha-Al2O3), titanium oxide (TiO2), titanium nitride (TiN), and hydroxyapatite (HAP)] was investigated. These composites had been devised for the purpose of incorporation into the stem of a total hip prosthesis. The materials were inserted into the mid-diaphyseal region of the femurs of adult dogs, and follow-up quantitative histological comparisons were performed for a period of up to 96 weeks. HAP-coated composites showed the best biocompatibility.