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The clinical results for calcium orthophosphate-coated implants reveal that they have much longer life times after implantation than uncoated devices, and therefore, they are particularly beneficial for younger patients (Capello et al. 1997).
The study was motivated by increased use of dynamic loading, in vitro, for early stimulation of tissue engineered cartilage, and the need to understand the effects of loading, in vivo, at early times after implantation of constructs.
First, we monitored tumor growth in vivo by magnetic resonance imaging (MRI) at different times after implantation.
The driver electronics must be powered at all times after implantation.
Tumour-infiltrating lymphocytes (TIL) were isolated and purified by successive passage over Sephadex G-10 columns and their cytotoxic activity in vitro compared with that of lymphoid cells from normal rats and from tumour-bearers at different times after implantation.
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The number of proinflammatory CD68+ (M1-like) macrophages declined with time after implantation, but for the NRX implants in the late phase of inflammation their number increased again, caused by different material properties.
Inside the open-type cage, trabecular architectural anisotropy and apatite orientation significantly increased with time after implantation.
The retrieval case obtained some time after implantation showed new bone formation had occurred around the threads onto the HA coating.
All cells inside a tissue engineering construct die within a short period of time after implantation of the construct because vascularization and establishment of connections to the recipient circulatory system is a time consuming process.
The estimates are interpreted as the probability of the prosthesis surviving until a nominated time after implantation.
Biopsies (n = 70) were classified by their time after implantation: before 18 months of follow-up or after longer than 18 months of follow-up.
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