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It is known that mechanical stimulation, in the form of fluid perfusion or mechanical strain, enhances cell differentiation and overall tissue formation.
Results indicate that the distribution of shear stress induced by fluid perfusion is very dependent on pore distribution within the scaffold.
The results of this study have demonstrated that fluid perfusion can result in a higher cell density in the scaffold region closed to the outlet, while cell density distribution under mechanical compression was similar with static condition.
After baseline measurements and blood sampling, 500 cc of fluids were given over 30 mn and hemodynamic measurement were performed at the end of fluid perfusion.
The MR image is dependent on a few factors, including the proton density of the tissue, longitudinal and transverse relaxation times of the tissue, vascular flow of the fluid, perfusion of the fluid, diffusion of the fluid, and chemical spectroscopy [77].
Isotonic perfusion fluid (Perfusion Fluid CNS; M-Dialysis, Stockholm, Sweden) was pumped through the system at a flow rate of 0.3 μL/minute.
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Study solutions were prepared daily using artificial cerebrospinal fluid (aCSF) perfusion fluid (Harvard Apparatus, Holliston, MA) and sterile syringes.
We detected BPA-GA and deconjugated BPA in the fetus and amniotic fluid after perfusion.
The membrane was perfused with perfusion fluid (PER, 147 mmol/L NaCl, 4 mmol/L KCl, 2.3 mmol/L CaCl2; CMA Microdialysis AB, Solna, Sweden) or 0.9% NaCl solution at flow rates of 1 2 µL/min using a CMA402 microdialysis pump (CMA Microdialysis).
We must balance the alleged benefits of fluids (improved perfusion) with the potential harm (tissue edema).
The catheter was perfused with CNS perfusion fluid at 0.3 μl min−1 using a CMA106 pump.
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