pharmacokinateics Flashcards

1
Q

Dfine abosrption:

A

Transfer of drug from its site of administration to the blood stream.

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2
Q

define bioavailabilty:

A

Percentage of the administered dose of the drug that is
present in the systemic circulation in unchanged form.

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3
Q

passive diffusion is ;

A

-Driving force is
the concentration
gradient

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4
Q

passive diffusion features :

A

-No carrier
-Not saturable
-Low structural
specificity
-Lipid or aqueous
diffusion

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5
Q

Facilitated
diffusion

A

-Need specific carrier
-Saturable
-Not Energy dependent

-Drugs move from regions of high conc. To
regions of lower
conc.

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6
Q

Filtration

A

-Water soluble drugs and small sized ions
-Pass across water filled pores
-No energy
-According to osmotic or hydrostatic pressure

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7
Q

Active transport features

A

-Need specific
carrier
-Saturable
-Energy
dependent
-Drugs move
against
concentration
gradient

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8
Q

define endocytosis :

A

-Cell membrane folds in on itself engulfing substance in a vesicle

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9
Q

endocytosis is used mainly for

A

absorption of drug with high molecular weight

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10
Q

Ion-pair transport

A

-Highly lipophobic drugs combine reversibly with endogenous compound

to form neutral ion pair
complex that penetrate lipid membrane passive diffusion

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11
Q

Most substances, lipid or water soluble, cross……..
rates rapid in
comparison with their rates of passage across other body membrane.

A

capillary wall

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12
Q

major mechanism of passage
of drugs across most capillary endothelial Membrane,

A
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13
Q

Bulk flow of liquid occurs through intercellular pores in most capillary endothelial Membrane,
except:

A

CNS
through tight junction

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14
Q

(ionization constant) defined as

A

the ability or tendency of the drug to
ionise.

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