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Acellular dermal matrix was placed when prosthetic coverage with autologous tissue could not be achieved.
The composite core (matrix) was placed in the center of a plexiglass cylinder, with the annulus between the core and the cylinder wall serving as the fracture.
For the animals of group 3 the lyophilized 1.5% hyaluronan thiomer matrix was placed into the chondral defect before it was filled up with HA gel.
Then, the solution was cast on a clean glass petri dish and the glass fiber matrix was placed to get immersed in the solution before drying in the oven for 24 h at 80 °C.
To produce the ceramic bars this matrix was placed on a glass plate, and thin wax layers were poured, in order to prevent distortion, until the complete filling with a slight excess that was removed with a sharp instrument.
In each case, one seeded matrix was provided magnetic stimulation at 160 rpm (2.6 Hz) whereas the other matrix was placed outside the magnetic field.
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The magnet has a dominant role in a high gradient magnetic separator; it provides the passage for the magnetic field and the working space where the matrix is placed to produce magnetic gradients and magnetic forces high enough to capture magnetic particles from the slurry.
Two layers of a PRF matrix were placed on top of the implant.
The three different matrices were placed into a microcentrifuge tube and stored at a relative humidity (RH) of 22% for three days at 20°C in the dark.
An offset address represented by 1r, vis located at the r th (0 ≤ r ≤ jp-1) row of the parity check H-matrix and v th (0 ≤ v ≤ k-1) column in which k circulant permutation sub-matrices are placed.
Dried matrices were placed in DMEM and their fluid capacity was calculated (n = 8) [ 41]: (1) Hydrophilicity = wet weight − dry weight dry weight.
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