Pharmacokinetics Flashcards

1
Q

Pharmacokinetics

A

How he body affects the absorption of a drug and how that drug moves through the body.

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2
Q

5 stages of pharmacokinetics

A
Liberation
Absorption
Distribution
Metabolism
Excretion
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3
Q

Liberation

A

The release of the drug from its dosage form

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4
Q

Absorption

A

The movement of drug from the site of administration to the blood circulation

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5
Q

Distribution

A

The process by which drug diffuses or is transferred from intravascular space to extravascular space

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6
Q

Metabolism

A

The chemical conversion or transfomation of drugs into compounds which are easier to eliminate

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7
Q

Excretion

A

The elimination of unchanged drug or metabolite from the body via renal, biliary, or pulmonary processes.

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8
Q

Types of liberation

A

Immediate: medicine is formulated to release the medicinal drug without delay

Delayed: the medicine is formulated to release medicinal drug sometime after it is taken

Extended: the medicine is formulated to make the drug available over an extended period allowing a reduction in dosing frequency.

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9
Q

Routes of administration

A

Enteral
Parenteral
Mucous membranes
Topical/transdermal

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10
Q

First pass metabolism

A

Term used for the hepatic metabolism of a pharmacological agent when it is absorbed from the gut and delivered to the liver via the portal circulation

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11
Q

Bioavailability

A

Quantity of drug reaching systemic circulation/ quantity of drug administered

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12
Q

Enteral routes

A

Oral

Rectal

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13
Q

Parenteral routes

A

IV
IT
IM
SQ

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14
Q

Factors affecting drug absorption

A
Administration route
Rate of dissolution of tablet
Drug formulation
Physical factors
Diffusion
Transport
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15
Q

FIcks law

A

Fick’s law describes passive movement of molecules down its concentration gradient

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16
Q

If pH < pKa

A

Protonated form dominates

Weak acids exposed to low pH diffuse across cell membranes, but weak bases do not

17
Q

If pH > pKa

A

Ionized form dominates

18
Q

pH trapping

A

Weak acid in a highly acidic environment –> largely protonated

In blood, a majority now exists in ionized form and cannot diffuse back to GI, trapping it in the blood

19
Q

Vd values

A

Vd < 0.071 L/Kg indicate the drug is mainly in the ciruclatory system

Vd > 0.071 L/Kg indicates the drug is most likely well distributed