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PHRM 4200: Biopharmaceutics Exam Study Guide.

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PHRM 4200: Biopharmaceutics Exam Study Guide. Define biopharmaceutics. - Answerthe study of how the physicochemical properties of drugs, dosage forms, and route of administration affect the rate and extent of drug absorption liberation and dissolution - Answersolid state - solution The drug must be ___ to be absorbed. - Answerin solution Define bioavailability. - Answerthe rate and extent of therapeutically active drug reaching the systemic circulation F - Answerbioavailability absolute F - AnswerIV reference relative F - Answercompare formulation to a recognized standard (ex. market product or topical vs oral) Cmax - Answerpeak plasma concentration of drug Tmax - Answertime at the Cmax Where can the rate of absorption be found? - Answerbefore the Cmax/Tmax Where can the rate of elimination be found? - Answerafter the Cmax/Tmax AUC - Answerarea under the curve; extent of absorption Where can the extent of absorption be found? - Answerarea under the curve ka - Answerabsorption rate K - Answerelimination rate; partition What is the equation for the plasma vs time curve? - AnswerdX/dt = kaXa - KX What happens when ka is increased? - Answerelimination: same rate Tmax: decreases ©FYNDLAY. 2 Cmax: increases AUC: same What happens to K when ka is increased? - Answerstays the same (same elimination rate) What happens to Tmax when ka is increased? - Answerdecreases (reaches Cmax faster) What happens to Cmax when ka is increased? - Answerincreases What happens to the extent of absorption when ka is increased? - Answerstays the same (AUC is equal) Rate of drug change in body = - Answerrate in - rate out true dose - Answerthe drug available to exert its effect (not the drug swallowed) What can cause a drug to have low bioavailability? - Answer- does not dissolve easily - does not readily pass across biological membranes - extensively metabolized during absorption process Variable bioavailability may produce - - Answervariable exposures What are the physicochemical factors affecting bioavailability? - Answersolubility, solid state, MW, polarity, lipophilicity, permeability, ionization, chemical stability, particle size What are the physiological factors affecting bioavailability? - Answerabsorption mechanism, gastric residence time, intestinal motility, blood flow, disease, GI degradation, gastric pH, metabolism What are the biopharmaceutical factors affecting bioavailability? - Answer- route of admin, dosage form, excipients, drug interactions, dose, food Which route of admin is metabolized in the liver? - Answeroral, but not all drugs (some rectal) Do all oral drugs undergo first pass metabolism? - Answerno There are differences in bioavailability in drugs with the same dosage form, but - - Answerdifferent routes of admin (ex. oral vs IM) There are differences in bioavailability of drugs with same route of admin, but - - Answerdifferent types of dosage forms (ex. capsule vs suspension) There are differences in bioavailability of drugs with same dosage form and route of admin, but - - Answerdifferent formulations (ex. different tablets)

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Voorbeeld van de inhoud

©FYNDLAY.



PHRM 4200: Biopharmaceutics Exam Study
Guide.


Define biopharmaceutics. - Answer✔✔the study of how the physicochemical properties of
drugs, dosage forms, and route of administration affect the rate and extent of drug absorption
liberation and dissolution - Answer✔✔solid state -> solution

The drug must be ___ to be absorbed. - Answer✔✔in solution
Define bioavailability. - Answer✔✔the rate and extent of therapeutically active drug reaching
the systemic circulation
F - Answer✔✔bioavailability

absolute F - Answer✔✔IV reference
relative F - Answer✔✔compare formulation to a recognized standard (ex. market product or
topical vs oral)
Cmax - Answer✔✔peak plasma concentration of drug

Tmax - Answer✔✔time at the Cmax
Where can the rate of absorption be found? - Answer✔✔before the Cmax/Tmax

Where can the rate of elimination be found? - Answer✔✔after the Cmax/Tmax

AUC - Answer✔✔area under the curve; extent of absorption
Where can the extent of absorption be found? - Answer✔✔area under the curve

ka - Answer✔✔absorption rate

K - Answer✔✔elimination rate; partition
What is the equation for the plasma vs time curve? - Answer✔✔dX/dt = kaXa - KX

What happens when ka is increased? - Answer✔✔elimination: same rate
Tmax: decreases


1

, ©FYNDLAY.


Cmax: increases
AUC: same
What happens to K when ka is increased? - Answer✔✔stays the same (same elimination rate)

What happens to Tmax when ka is increased? - Answer✔✔decreases (reaches Cmax faster)

What happens to Cmax when ka is increased? - Answer✔✔increases
What happens to the extent of absorption when ka is increased? - Answer✔✔stays the same
(AUC is equal)
Rate of drug change in body = - Answer✔✔rate in - rate out

true dose - Answer✔✔the drug available to exert its effect (not the drug swallowed)
What can cause a drug to have low bioavailability? - Answer✔✔- does not dissolve easily
- does not readily pass across biological membranes
- extensively metabolized during absorption process
Variable bioavailability may produce - - Answer✔✔variable exposures

What are the physicochemical factors affecting bioavailability? - Answer✔✔solubility, solid
state, MW, polarity, lipophilicity, permeability, ionization, chemical stability, particle size
What are the physiological factors affecting bioavailability? - Answer✔✔absorption mechanism,
gastric residence time, intestinal motility, blood flow, disease, GI degradation, gastric pH,
metabolism
What are the biopharmaceutical factors affecting bioavailability? - Answer✔✔- route of admin,
dosage form, excipients, drug interactions, dose, food
Which route of admin is metabolized in the liver? - Answer✔✔oral, but not all drugs (some
rectal)
Do all oral drugs undergo first pass metabolism? - Answer✔✔no
There are differences in bioavailability in drugs with the same dosage form, but - -
Answer✔✔different routes of admin (ex. oral vs IM)
There are differences in bioavailability of drugs with same route of admin, but - -
Answer✔✔different types of dosage forms (ex. capsule vs suspension)
There are differences in bioavailability of drugs with same dosage form and route of admin, but -
- Answer✔✔different formulations (ex. different tablets)



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