drug absorption Flashcards

1
Q

what is the pharmaceutical process ?

A

getting the drug into the patient

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2
Q

what is it called when u ‘get the drug to the site of action in the patient’?

A

pharmokinetic process

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3
Q

what determines pharmokinetics ?

A

ADME

absorption
distribution
metabolism
elimination

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4
Q

define absorption

A

movement of UNCHANGED drug from its site of administration to the systemic circulation

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5
Q

what is the pharmacodynamic process

A

producing the correct pharmacological effect with the drug

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6
Q

what is the therapeutic process ?

A

producing the intended therapeutic response

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6
Q

be familiar with the 9 drug application routes

A

IV & IM (intravenously ,muscularly
rectal
sublingual (under the tongue)
topical
transdermal (skin patch)
inhilation/nasal

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7
Q

what is meant by therapeutic range

A

the range of blood over which a drug is active

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8
Q

what happens if drug conc is above or below the therapeutic range ?

A

if its above then toxicity ocurs

if below then insufficient pharmocological effects occur

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9
Q

what is therapeutic Index (TI)

A

a comparison of drug concentration

compares the dose that causes therapeutic effects against the dose that causes toxicity

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10
Q

what 2 things must you consider concerning the rate of oral absorption of a drug

A

the amount of drug entering the systemic circulation

the speed at which it happens

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11
Q

what is Tmax and Cmax?

A

Tmax- time at which maximum concentration occurs

Cmax- maximum concentration of drug in the body

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12
Q

where does the Tmax and Cmax occur in the body

A

in systemic circulation

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13
Q

what is the AUC? and what does it show

A

area under curve (of a tmax & cmax curve)
the amount of drug reaching circulation

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14
Q

state the effect on increasing dose & root adminintration on Cmax and Tmax

A

increases Cmax

no effect on Tmax

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15
Q

define bioavailability

A

amount of drug reaching circulation

16
Q

What method of drug administration has 100% bioavailability?

A

intravenous drugs

17
Q

What 3 factors effect Bioavailability?

A

-solubility (hydrophobic and small drugs easily pass through membrane therefore bioavailability increases & vice versa)

-formulation (environment it gets absorbed in)

-first pass metabolism

18
Q

What 3 gastrointestinal effects alter bioavailability?

A

-food
-illness & disease
-gut motility

19
Q

define first pass metabolism

A

when a drug goes into the gastrointestinal tract before reaching the systemic circulation

20
Q

what drug administration goes through first pass metabolism

A

oral administration

21
Q

what does passive diffusion rely on ?

A

degree of ionisation
solubility (hydrophobic and small)

22
Q

can ionised and unionised drugs pass the membrane

A

ionised drugs cannot as theyre are not lipid soluble

unionised ones can

23
Q

What is the henderson-hasselbach equation show?

A

relationship between local Ph and drug ionisation

pH = pKa + log10

24
Q

how does ph affect drug ionisation?

A

small ph change would have a significant change to drug ionisation

(for example an acid drug will ionise in an alkaline environment)

25
Q

explain active absorption

A

occurs against conc graident and needs carriers & energy

26
Q

give example of drugs moved by active absorbance

A

potassium, sodium,calcium,iron

also levodopa

27
Q

Explain Facilitated Diffusion

A

moves along conc gradient
uses carriers and NO ENERGY

28
Q

give 3 examples of drugs moved by facilitated diffusion

A

-amino acids
-vitamins
-monosaccharides

29
Q

what drives the flow across membrane

A

osmotic or hydrostatic pressure

30
Q

state the effects food and ilness have on drug absorption

A

food and illness can enhance or repair absorption of some drugs

31
Q

Descrive Intravenous drug administration:

A

100% bioavailability
Avoids 1st pass metabolism

32
Q

Describe Topical drug Administration:

A

Can achieve local or systemic effects
Can achieve controlled, sustained doses of drugs
Avoids 1st pass metabolism

33
Q

Descrive Inhalation drug administration:

A

Drug delivered directly to site
Rapid effect
Small doses needed
Reduced adverse effects
Metabolised in lungs so only 5-10% is absorbed. (little systemic effecT)

34
Q

How is drug metabolised in first pass metabolism?

A

by enzymes in the gut lumen and wall

by enzymes in the liver (hepatic enzymes)

35
Q

Pka value should be closest to the ph when choosing ur answer, true or false

A

true

36
Q

what is drug therapy

A

to achieve efficacy without toxicity

37
Q

why do most drugs not ionise completly in water

A

cus theyre weak bases or acids