Question:
1 Dissolution rate of particles intended to dissolve; __ can increase the rate of drug dissolution and its bioavailability 2 Suspendability of particles intended to remain undissolved but uniformly dispersed in a __ 3 Uniform distribution of a drug substance in a powder mixture or solid dosage form to ensure __ 4 Penetrability of particles intended to be inhaled for deposition deep in the __ 5 Lack of grittiness of solid particles in dermal ointments, creams and ophthalmic preparations example
Author: Dwight ObillosAnswer:
1 Drug micronization 2 Liquid vehicle (e.g. fine dispersions have particles ~0.5 to 10 micrometers) 3 dose-to-dose content uniformity 4 respiratory tract (e.g. 1 to 5 micrometers) 5 (e.g. fine powders may be 50 to 100 micrometers in size)
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