CH 3 PHARMACOKINETICS Flashcards

1
Q

The process by which drug molecules move from their site of administration to the blood; movement of nutrients and other substances form the alimentary canal to the circulation:

A

Absorption

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2
Q

The ability of some tissues to attract, accumulate, and store drugs in high concentrations relative to other tissues:

A

Affinity

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3
Q

Network of capillaries in the CNS that inhibits many chemicals and drugs form gaining access to the brain:

A

Blood-brain barrier

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4
Q

The movement of a chemical from an area of higher concentration to an area of lower concentration:

A

Diffusion

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5
Q

The transport of drugs throughout the body after they are absorbed:

A

Distribution

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6
Q

Complex that is formed when a drug that binds reversibly to a plasma protein, particularly albumin, that makes the drug unavailable for distribution to its site of action:

A

Drug-protein complexes

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7
Q

Administration of drugs orally or through nasogastric or gastrostomy tubes:

A

Enteral route

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8
Q

Tablets that have a hard, waxy coating designed to dissolve in the alkaline environment of the small intestine:

A

Enteric-coated

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9
Q

Recycling of drugs and other substances by the circulation of bile through the intestine and liver:

A

Enterohepatic recirculation

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10
Q

Process by which a drug increases the activity of the hepatic microsomal enzymes:

A

Enzyme induction

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11
Q

The process of removing substances from the body:

A

Excretion

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12
Q

Tablets or capsules designed to dissolve very slowly, resulting in a longer duration of action for the medication; also called long-acting sustained release:

A

Extended release

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13
Q

Special anatomic barrier that inhibits many chemicals and drugs from entering the fetus:

A

Fetal-placental barrier

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14
Q

Mechanism whereby drugs are absorbed, enter in to the hepatic portal circulation, and are inactivated by the liver before they reach the general circulation:

A

First-pass effect

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15
Q

As it relates to pharmacotherapy, liver enzymes that metabolize drugs as well as nutrients and other endogenous substances; sometimes called the P-450 system:

A

Hepatic microsomal enzyme system

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16
Q

Multiple, similar forms of an enzyme that perform slightly different metabolic functions:

A

Isozymes

17
Q

Relatively large dose of a drug given at the beginning of treatment to rapidly obtain a therapeutic response:

A

Loading dose

18
Q

Amount of drug that keeps the plasma drug concentration in the therapeutic range:

A

Maintenance doses

19
Q

The process used by the body to chemically change a drug molecule; also called biotransformation:

A

Metabolism

20
Q

Amount of drug required to produce a therapeutic effect:

A

Minimum effective concentration

21
Q

Study of drug movement throughout the body:

A

pharmacokinetics

22
Q

The length of time required for the plasma concentration of a drug to decrease by one half after administration:

A

Plasma half-life (t 1/2)

23
Q

Drugs that become more active after they are metabolized:

A

Prodrugs

24
Q

Drug that is metabolized by a CYP enzyme:

A

Substrate

25
Q

Practice of monitoring plasma levels of drugs that have low safety profiles and using the data to predict drug action or toxicity:

A

Therapeutic drug monitoring

26
Q

Dosage that produces the desired effects of a drug:

A

Therapeutic range

27
Q

Medications applied to the skin or the membranous linings of the eye, ear, nose, respiratory tract, urinary tract, vagina, and rectum:

A

Topical route

28
Q

Level of drug that results in serious adverse effects:

A

Toxic concentration

29
Q

Topical delivery method that uses patches that contain a specified amount of medication that is released over a specified time period:

A

Transdermal patches