Lecture 01 - Pharmacokinetics and Pharmacodynamics Flashcards

1
Q

What is pharmacology

A

studies the interactions between living organisms and chemicals that affect function

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2
Q

What is toxicology

A

examines undesirable effects of chemicals on living systems

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3
Q

What is pharmacodynamics

A

therapeutic and/or toxic actions of the drug on the body, receptor interactions, concentration-effect component

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4
Q

What is pharmacokinetics

A

effects of the body on the drug, dose-concentration component

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5
Q

What is pharmcogenetics

A

effects of genetics on how the drug is metabolized by the body and affects the body

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6
Q

Why are pharmacokinetics useful

A

to predict the effectiveness of different drugs or different dosage strategies as well as predicting blood levels in an individual under specific conditions

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7
Q

What is LADME

A

liberation, absorption, distribution, metabolism, elimination

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8
Q

What are metabolism and elimination together called

A

clearance

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9
Q

What is availability

A

a function of liberation and absorption

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10
Q

What effects liberation of a drug

A

formulation, ionization state, environmental pH

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11
Q

What effects absorption of a drug

A

gastrointestinal factors, physicochemical drug properties, transporters, route of administration

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12
Q

What is absorption

A

the drug moves from site of administration across cell membranes into the circulation

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13
Q

What is passive transport

A

diffusion from high to low, does not use ATP

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14
Q

What is active transport

A

movement from low to high, uses ATP

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15
Q

What is the charge state of a carboxcylic acid if pH<pKa

A

not ionized

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16
Q

What is the charge state of a carboxcylic acid if pH>pKa

A

ionized (negative charge)

17
Q

What is the charge state of an amine if pH<pKa

A

ionized (positive charge)

18
Q

What is the charge state of an amine if pH>pKa

19
Q

What is the AUC

A

area under the curve, the best indicator of total exposure to a dose of a pharmacological compound

20
Q

What is bioavailability

A

the amount of drug dose that reaches the circulation

21
Q

How is bioavailability estimated

A

drug dose and area under the curve from the plasma concentration vs. time plot

22
Q

What is first pass metabolism

A

intestinal and liver metabolism reduce bioavailability of an orally administered drug prior to the drug reaching circulation

23
Q

What is F

A

the bioavailability factor, the fraction of active dose that makes it to circulation

24
Q

What is S

A

the chemical form, the fraction of formulation that is the active form of the drug

25
What is distribution
the delivery of drug via the circulation to extravascular fluids and tissues in the body
26
What effects drug distribution
size of organ, tissue perfusion, drug binding to plasma proteins/tissues, and ability of drug to cross cell membranes
27
What Vd range indicates the drug is in the plasma
3-5
28
What Vd range indicates the drug is in the extracellular fluids
5-20
29
What Vd range indicates the drug is in the intracellular fluids
20-35
30
What Vd range indicates the drug is in deep storage
>40
31
What factors can effect Vd
drug solubility, plasma protein binding
32
What drugs does albumin bind to
acidic drugs, bilirubin, LCFA
33
What drugs does alpha one acid glycoprotein bind to
basic drugs
34
What drugs do lipoproteins bind to
cyclosporine, cholesterol, vitamins, steroid hormones
35
What drugs does transferrin bind to
iron
36
What drugs does ceruloplasmin bind to
copper
37
What effects the amount of free drug
acute phase reaction, hypoalbuminemia, uremia, overdose
38
Why is Vd important
determine whether dialysis of a drug is likely to be beneficial, estimate body burden of drug, calculate a loading dose