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The screw samples were implanted into the tibial bone defects.
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In the cadaver study by Soin et al. [35], both the suture-button and the screw fixation samples were tested until failure.
To have better control over the thermomechanical history, instead of a reciprocating screw, the samples were prepared by extruding supercooled melt through capillary die.
Individual factors important for implant fixation were identified using a model system with an experimental design in which cylindrical or screw-shaped samples were embedded in thermosetting polymers, in order to eliminate biological variation.
Turbidity of the resultant NEs given in a nephelometric turbidity unit (NTU) was measured using a turbidimeter (TurbiDirect, Lovibond, U.K). Turbidity measurements were performed on the NEs stored in screw capped sample vials.
The two layers were then allowed to separate, and an aliquot of organic layer was pipetted out in a screw-capped sample vial.
A visualization technique known as 'screw pullouts' was used to directly observe the state of granulation along the screw length and samples were collected from each screw segment for particle size and porosity analysis.
Except for the PLLA and titanium control samples, no screw was fully integrated in the surrounding bone tissue.
During the experiment, one (EP) and two (IP) abutment screws out of seven samples were fractured.
Scanning electron microscopy of a 95/5 wt% PS/HDPE blend provided Dn values of 500 and 270 nm in the twin-screw extruded and pulverized samples, respectively.
Screw-cap tube chromatin samples were treated with micrococcal nuclease to generate mononucleosomes.
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