PTB lecture 1 Flashcards

1
Q

Therapeutic effect

A

desired effect determined by drug substance and dosage form by which the drug is administered (and structure)

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2
Q

Pharmacokinetics

A

How the body affects the drug (what does the body do with the drug after the drug is administered)

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3
Q

ADME

A

absorption, distribution, metabolism, excretion

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4
Q

absorption

A

uptake of the drug in the systemic blood circulation

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5
Q

distribution

A

the distribution of the drug to the different compartments (fluid, organs) of the body

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6
Q

metabolism

A

the chemical conversion of a drug substance by the body to different active/inactive substances (mostly by enzymes)

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7
Q

excretion

A

the removal of the drug or its metabolites from the body (via urine, bile, sweat, breath)

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8
Q

most direct route of drug administration

A

intravenous injection (bioavailability = 100%)

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9
Q

clearance (Cl)

A

the blood or plasma volume which is cleared from all drug per unite of time (ml/min)

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10
Q

Volume of distribution (Vd)

A

the apparent volume in which the drug is dissolved after administration and distribution (L/kg)

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11
Q

Vd =/< body volume

A

no concentration of the drug in organs, fluids or tissues

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12
Q

Vd > body volume

A

concentration of the drug is organs, fluids or tissues

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13
Q

Tmax

A

point in time where the maximum concentration (Cmax) of a drug is in the blood

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14
Q

pharmaceutical availability

A

fraction of a total amount of the drug that is present in the dosage form that will dissolve in the fluid of the GI tract (the fraction that dissolves)(no ME)

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15
Q

bioavailability

A

the total amount of an administered drug that reaches the systemic blood circulation in an unchanged way. (ADM) PA - fraction that was unable to pass the absorptive membrane and fraction that was metabolized

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16
Q

fick’s first law

A

mass flux per unit of surface ≈ D(dc/dx)

17
Q

para-cellular uptake

A

passive transport via tight junctions (ic spaces/aqueous pores)

18
Q

trans-cellular uptake

A

passive or active transport through the cell (transporter: P glycoprotein = PGP)

19
Q

BCS class 1

A

high permeability, high solubility

20
Q

BCS class 2

A

high permeability, low solubility

21
Q

BCS class 3

A

low permeability, high solubility

22
Q

BCS class 4

A

low permeability, low solubility

23
Q

DN < 0.1

A

no effect of solubility on absorption rate

24
Q

DN > 10

A

solubility will affect absorption rate and bioavailability

25
Q

DN = 0.1 - 10

A

solubility may affect absorption rate and bioavailability