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Buckypapers (50 100 mg) were cut into small pieces approximately 5 mm2 to load into a porosimeter cell.
Curcumin-loaded electrospun mats, each 50 mg, were cut and after sterlization by UV-lamp and were placed in 5 mL of bacterial solution.
Patches (14 mg) were cut into 30 equal sized squares representing 0.45 mg of nicotine using a razor blade.
Liver pieces (100 mg) were cut and weighed.
The tissue samples (17.0 ± 4.7 mg) were cut to fit the rotor.
Cubes 3×3×3mm with approximate mass of ~30 mg were cut from histological specimens collected during necropsies.
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A biopsy of approximately 750 1000 mg was cut into small pieces using a surgical blade followed by washing in Tyrode's solution (in mmol/L: NaCl 137, KCl 5.4, MgCl2 0.5, CaCl2 1.8, Na-HEPES 11.8, and glucose 10; pH 7.4) for 10 minutes.
Each frozen ovarian specimen (100 mg) was cut into several small pieces about 3 mm in size.
A 3-mm thick and 3-cm long hair sample, weighing 5 6 mg, was cut close to the scalp from the posterior vertex area of the head.
Testis tissue (200 mg) was cut into small pieces and homogenized in 1.8 mL ice-cold saline buffer (1 : 9, wt/v) using Ultra-Turrax (T8, IKA-labortechnik Staufen, Germany) to get testicular homogenates at the concentration of 0.1 g/mL.
Each sample (15.1 ± 2.8 mg) was cut to fit a 30 μl leak-proof disposable insert (Bruker Biospin Corp ,USA) and added phosphate buffered saline (PBS, 3 μl) in D2O containing trimethylsilyl tetradeuteropropionic acid (TSP, 98.2 mM) for chemical shift referencing.
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