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For the experiments the prepared semi-solid samples were extruded under isothermal condition and with 5 different ram speeds.
The samples were extruded to approximately 32 × 7 mm cross-sectional profiles, and tested for physico-mechanical properties.
The samples were extruded, subsequently injection-moulding processed into standard dog-bone specimens, and finally tested for physico-mechanical properties.
To prepare unilamellar liposome vesicles, samples were extruded 21 times through a 200 nm polycarbonate filter (Liposofast, Avestin, Ottawa, Canada).
The samples were extruded ten times using 200 and 400 nm polycarbonate membranes to obtain unilamellar liposomes.
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Samples of moist porcelain paste were extruded through dies of 30 and 50 mm diameter.
Polymer samples containing various amounts of oxygen were extruded without stabilizer and in the presence of a hindered phenolic antioxidant.
Aqueous solutions of dextran (core solution), sodium alginate (sample solution) and CaCl2 (sheath solution) were extruded simultaneously from the inner, intermediate and outer cylinders, respectively.
While limited in sample size, the teeth had root fillings that were extruded beyond the apex (47 %) or flush with the radiographic apex (53 %).
Liposomes were extruded to a similar size (125 ± 20 nm) to exosome samples (120 ± 54 nm) and have equivalent particle concentrations as measured by a NanoSight NS300 (data not shown).
Technicians stored all sealed sample cores on wet ice (4°C) before transport to the University of Michigan Environmental and Water Resources Engineering laboratories, where they were extruded, separated into strata by depth, and composited across cores.
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