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Questions and Answers
What is one of the advantages of the oral route for drug delivery?
What is one of the advantages of the oral route for drug delivery?
- Larger surface area of the GI compared to other transmucosal routes (correct)
- Inability to use CR dosage forms to simplify dosing schedules
- Limited self-administration and invasiveness
- Reduced blood supply in the GI tract
Why is the specialized columnar epithelium of the GI tract conducive to drug absorption?
Why is the specialized columnar epithelium of the GI tract conducive to drug absorption?
- It allows for rapid absorption of drugs with appropriate physicochemical characteristics (correct)
- It is highly resistant to drug absorption
- It has a poor blood supply, leading to slow drug absorption
- It lacks absorptive properties, making it unsuitable for drug absorption
How does the rich blood supply of the GI mucosa contribute to drug delivery?
How does the rich blood supply of the GI mucosa contribute to drug delivery?
- It delays drug absorption due to reduced vascular surface
- It ensures rapid drug absorption and onset of action (correct)
- It leads to decreased drug effectiveness
- It has no impact on drug absorption
Why does the oral route allow for improved compliance?
Why does the oral route allow for improved compliance?
How do controlled-release (CR) dosage forms impact dosing schedules?
How do controlled-release (CR) dosage forms impact dosing schedules?
What characteristic makes the oral route usually the safest and least expensive route for drug delivery?
What characteristic makes the oral route usually the safest and least expensive route for drug delivery?
What is a significant benefit of the oral route for drug delivery?
What is a significant benefit of the oral route for drug delivery?
What is a function of the pancreatic enzymes in the small intestine?
What is a function of the pancreatic enzymes in the small intestine?
What is a role of the GI mucus layer in oral drug delivery?
What is a role of the GI mucus layer in oral drug delivery?
What is a limiting factor for oral drug delivery associated with the P-Glycoprotein Efflux Pump?
What is a limiting factor for oral drug delivery associated with the P-Glycoprotein Efflux Pump?
What pH range is observed in the duodenum along the GI tract?
What pH range is observed in the duodenum along the GI tract?
What is one of the roles of the pH of fluids along the GI tract in oral drug delivery?
What is one of the roles of the pH of fluids along the GI tract in oral drug delivery?
Which enzyme is found in the stomach?
Which enzyme is found in the stomach?
What is one function of the GI mucus layer?
What is one function of the GI mucus layer?
According to the Noyes-Whitney Rule, what is the fundamental principle for evaluation of the kinetics of drug release?
According to the Noyes-Whitney Rule, what is the fundamental principle for evaluation of the kinetics of drug release?
What are the units in which the rate of dissolution dM/dt can be expressed for most solids?
What are the units in which the rate of dissolution dM/dt can be expressed for most solids?
In which conditions is the dissolution of the solid said to be occurring under 'sink' conditions?
In which conditions is the dissolution of the solid said to be occurring under 'sink' conditions?
What is the effect of the prevailing concentration driving force (Cs - Ct) on the dissolution rate of the solid?
What is the effect of the prevailing concentration driving force (Cs - Ct) on the dissolution rate of the solid?
What was offered by Noyes and Whitney in 1897 as the fundamental principle for evaluation of the kinetics of drug release?
What was offered by Noyes and Whitney in 1897 as the fundamental principle for evaluation of the kinetics of drug release?
What does M represent in the Noyes-Whitney equation: M = (S)(Cs - Ct)(dM/dt)?
What does M represent in the Noyes-Whitney equation: M = (S)(Cs - Ct)(dM/dt)?
What is the ideal condition for the surface in the Noyes-Whitney equation?
What is the ideal condition for the surface in the Noyes-Whitney equation?
Which model assumes that the drug is dissolved uniformly from all surfaces of the particles?
Which model assumes that the drug is dissolved uniformly from all surfaces of the particles?
What relationship did Nernst and Brunner establish in their film theory?
What relationship did Nernst and Brunner establish in their film theory?
What type of methods are used to investigate the kinetics of drug release from controlled release formulations?
What type of methods are used to investigate the kinetics of drug release from controlled release formulations?
What does the Noyes-Whitney equation assume about the particles?
What does the Noyes-Whitney equation assume about the particles?
Which equation represents the relationship between the constant and the diffusion coefficient in Nernst and Brunner's film theory?
Which equation represents the relationship between the constant and the diffusion coefficient in Nernst and Brunner's film theory?
Which category of kinetic models describes the overall release of drug from dosage forms?
Which category of kinetic models describes the overall release of drug from dosage forms?
What are the number of kinetic models described for overall drug release?
What are the number of kinetic models described for overall drug release?
What assumption did Noyes-Whitney Equation make about the dissolution process?
What assumption did Noyes-Whitney Equation make about the dissolution process?
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