M1 L2 Flashcards

(26 cards)

1
Q

drug concentrations are sometimes expressed in ____

A

EXPONENTIAL FORM

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2
Q

____ are applied in many pharmacokinetic equations

A

LOGARITHMS

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3
Q

an important mathematical tool for analyzing drug movement quantitatively

A

CALCULUS

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4
Q

are used to relate the concentrations of drugs in various body organs over time

A

DIFFERENTIAL EQUATIONS

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5
Q

are used to model the cumulative therapeutic or toxic responses of drugs in the body

A

INTEGRAL EQUATIONS

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6
Q

a branch of calculus that involves finding the RATE at which a variable quantity is CHANGING

A

DIFFERENTIAL CALCULUS

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7
Q

the amount of drug DISSOLVING per unit time, typically in mg/s

A

RATE OF DISSOLUTION
dX / dt

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8
Q

tells how easily the drug molecules MOVE through the liquid

A

DIFFUSION COEFFICIENT

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9
Q

a ____ diffusion coefficient means the drug can spread out ____

A

HIGHER diffusion coefficient
spread out FASTER

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10
Q

the total EXPOSED AREA of the drug particles in contact with the liquid

A

SURFACE AREA

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11
Q

⬆️ particle size, ____ diffusion coefficient

A

⬇️

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12
Q

⬇️ Lipophilicity, ____ diffusion coefficient

A

⬇️

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13
Q

relationship of particle size and surface area

A

INDIRECT relationship

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14
Q

a ____ surface area means ____ dissolution

A

LARGER surface area
FASTER dissolution

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15
Q

the THICKNESS of the STAGNANT layer of liquid around the dissolving particle

A

DIFFUSION LAYER THICKNESS

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16
Q

A ____ layer means the drug can escape ____ into the bulk liquid

A

THINNER layer
escape FASTER

17
Q

the MAXIMUM concentration of drug that can dissolve in the solvent — like the DRUG’S LIMIT

A

SATURATION SOLUBILITY

18
Q

the CURRENT concentration of the drug in the surrounding solution

A

BULK CONCENTRATION

19
Q

if BULK concentration is CLOSE to saturation solubility, DISSOLUTION ____

20
Q

in pharmacokinetics, what is the DEPENDENT variable

A

amount of drug in the body

21
Q

in pharmacokinetics, which is considered to be the INDEPENDENT variable

22
Q

is the REVERSE of DIFFERENTIATION

23
Q

it is BREAKING a process down to look at the instantaneous process

A

DIFFERENTATION

24
Q

SUMS UP the information from small time intervals to give a total result over a larger time period

25
this will describe the **extent of absorption**
AREA UNDER THE CURVE
26
numerical method frequently used in pharmacokinetics to calculate the **AREA UNDER THE PLASMA** drug concentration versus time curve, called the **AREA UNDER THE CURVE (AUC)**
TRAPEZOIDAL RULE