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Questions and Answers
What does the Noyes-Whitney equation describe?
What does the Noyes-Whitney equation describe?
- The rate of dissolution of tablet dosage forms in gastric fluids
- The rate of solubilization of drugs in the diffusion layer
- The rate of chemical reaction in drug dissolution
- The rate of dissolution of spherical particles when the dissolution process is diffusion-controlled (correct)
What does the Noyes-Whitney equation include as a parameter for the rate of dissolution?
What does the Noyes-Whitney equation include as a parameter for the rate of dissolution?
- Diffusion coefficient of drug (correct)
- Molecular size of the drug
- Buffer capacity of the GI fluids
- Viscosity of luminal contents
Which apparatus is a very versatile device for the in vitro assessment of release characteristics of solid oral dosage forms?
Which apparatus is a very versatile device for the in vitro assessment of release characteristics of solid oral dosage forms?
- Apparatus 4 (Flow-Through Cell)
- Apparatus 3 (Reciprocating Cylinder) (correct)
- Apparatus 2 (Paddle Apparatus)
- Apparatus 1 (Basket Apparatus)
What is the standard flow rate for the Flow-Through Cell apparatus?
What is the standard flow rate for the Flow-Through Cell apparatus?
In the dissolution procedure for immediate-release dosage forms, where should the specimen be withdrawn from?
In the dissolution procedure for immediate-release dosage forms, where should the specimen be withdrawn from?
What is the main difference between solubility and dissolution?
What is the main difference between solubility and dissolution?
Which factor is NOT known to affect the dissolution rate of drugs?
Which factor is NOT known to affect the dissolution rate of drugs?
Why is slow dissolution of solid drugs associated with poor performance in vivo?
Why is slow dissolution of solid drugs associated with poor performance in vivo?
What does in vitro bioavailability refer to?
What does in vitro bioavailability refer to?
What does in vivo evaluation of oral dosage forms involve?
What does in vivo evaluation of oral dosage forms involve?