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The original particles of Lynestrenol with average size of 10 μm as a drug material were dissolved in supercritical CO2 and then expanded rapidly through a nozzle with 0.6 mm diameter.
The matrix fractions of the material were dissolved in toluene and the unaffected particles were harvested as a gel fraction which was levitated in fresh toluene as a dilute suspension.
Samples consisting of 50 mg of dry material were dissolved in 6 ml of nitric acid and 2 ml H2O2 (30%) and then heated at 180°C for 15 min.
The aqueous and methanol extracts of the plant material were dissolved in 10 ml of distilled water (dH2O) and that of chloroform was dissolved in 3 % Tween (T -80 prior T -80e actual expriorento the chloroform extractualilexperimentolve in dH2O.
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The material was dissolved in 5 ml water.
Both solutions were gently steered over a hot plate (<45 °C) until all solid material was dissolved.
The irradiated material was dissolved in HNO3, and then diluted in warm water.
The material was dissolved in phosphate buffered saline (PBS) aqueous solution and ethanol PBS mixtures.
The mineralized material was dissolved in 5 mL 0.1 M HNO3 and filtered on a 0.45 μm nylon membrane.
The bone material was dissolved in 4 mL concentrated analytical grade HNO3 (69%) and 2 mL concentrated analytical grade H2O2 (30%).
After the ampoule was crushed, it was moved to the hot cell containing the production panel (Fig. 2), where the target material was dissolved by repeated application of 6.5 mL 3.0 M HCl.
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