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
What are some uses of pharmacokinetic models
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
What is the one-compartment model
Its used to simplify mathematics by assuming drug is given by rapid intravenous injection, a bolus, and is rapidly mixed
27
What is the two-compartment model
considering the body is a central compartment with rapid mixing and a peripheral compartment with slower distribution
28
What are examples of intersubject variability for pharmacokinetics
metabolism, and renal function
29
What are examples of intersubject variability for pharmacodynamics
receptor density, and underlying disease