Lecture 1 Flashcards

1
Q

What is PK

A

Pharmacokinetics. What the body does to the drug.. the fate of the molecule. ADME

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2
Q

What is PD

A

Pharmacodynamics. What the drug does to the body… the biological effect/ Efficacy

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3
Q

What is the A in ADME

A

Absorption. the passage of a drug from its site of administration into the systemic circulation

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4
Q

What is the D is ADME

A

Distribution. the movement of drug from site of absorption to site of action and the site of metabolism or excretion

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5
Q

What is the M is ADME

A

Metabolism. Irreversible alteration of drug chemistry

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6
Q

What is the E is ADME

A

Excretion. Passage of drug or metabolites out of the body

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7
Q

Examples of excretion in ADME

A

Renal and Biliary pathways

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8
Q

Examples of Metabolism in ADME

A

Hepatic, oxidation, reduction, and conjugation

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9
Q

examples of distribution in ADME

A

Perfusion, permeability, and binding

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10
Q

examples of absorption is ADME

A

dosage form, site, chemical and biological interactions

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11
Q

High drug concentrations is toxic or subtherapeutic?

A

Toxic

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12
Q

Low drug concentrations are toxic or subtherapeutic

A

sub therapeutic

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13
Q

How is whole blood obtained

A

Venous punction, contains and anticoagulant such as heparin or EDTA

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14
Q

How is Serum Obtained

A

WHole blood is allowed to clot and the clot is removed

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15
Q

How is plasma obtained

A

Centrifugation of nonclotted whole blood that contains an anticoagulant

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16
Q

Components of whole blood

A

All the cellular and protein elements of blood

17
Q

Components of Serum

A

Does not contain cellular elements, fibrinogen or the other clotting factors

18
Q

Components of plasma

A

Noncellular liquid fraction of the whole blood, contains all the proteins and clotting factors

19
Q

What is AUC, and what does it find

A

The area under the Curve describes the exposure of drugs to the body

20
Q

What is MTC

A

Minimum toxic concentration, a Concentration that you have to be careful to not go above

21
Q

What is MEC

A

Minimum effective concentration. A concentration that you have to reach so you can see therapeutic effect

22
Q

What is a therapeutic window

A

The useful range of concentration over which a drug is therapeutically beneficial

23
Q

How should you change dosing for a drug with narrow therapeutic windows

A

Smaller and more frequent doses. A different method of administration

24
Q

How should you change dosing for a drug with a slow elimination rate

A

One large initial dose, followed by smaller doses

25
Q

What are some uses of pharmacokinetic models

A

Predicting plasma tissue and urine drug levels with any dose regimen, calculating optimum dosage regimen for each patient, estimating the possible accumulation of drugs and or metabolites, etc

26
Q

What is the one-compartment model

A

Its used to simplify mathematics by assuming drug is given by rapid intravenous injection, a bolus, and is rapidly mixed

27
Q

What is the two-compartment model

A

considering the body is a central compartment with rapid mixing and a peripheral compartment with slower distribution

28
Q

What are examples of intersubject variability for pharmacokinetics

A

metabolism, and renal function

29
Q

What are examples of intersubject variability for pharmacodynamics

A

receptor density, and underlying disease