drug absorption Flashcards

1
Q

what is the pharmacokinetic process

A

getting the drug to the site of action

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2
Q

what is the pharmacodynamic process

A

producing the correct pharmacological effect

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3
Q

what are the 4 basic factors that determine drug pharmacokinetics
(ADME)

A

Absorption
Distribution
Metabolism
Elimination

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4
Q

define pharmacokinetics

A

the science of the rate of movement of drugs within a biological system

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5
Q

what does pharmacokinetics allow the understanding of

A

dosage, drug administration, drug handling, patient variability, potential for harm

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6
Q

what do most drugs require to have biological action

A

enter the blood stream and be distributed to a site of action

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7
Q

methods of administration of drugs

A

oral, IV (not absorbed), subcutaneous, intramuscular, other GI (sublingual, rectal), inhalation, nasal, transdermal

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8
Q

define absorption

A

the process of movement of unchanged drug from the site of administration to the systemic circulation

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9
Q

regarding absorption, what 2 factors is there always a correlation between

A

plasma concentration of the drug and the therapeutic response

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10
Q

Tmax

A

time to peak concentration of the drug, depends on how acute the symptoms are to be treated

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11
Q

Cmax

A

peak concentration of the drug

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12
Q

AUC

A

area under the drug concentration-time curve, represents the amount of drug which reaches the systemic circulation and is used to work out bioavailability

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13
Q

during which point do we want Cmax to occur within

A

the therapeutic window

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14
Q

what would cause an earlier Tmax

A

a more rapid rate of absorption

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15
Q

what impact does dose have on Tmax and Cmax

A

doesnt effect Tmax but does increase Cmax

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16
Q

Define therapeutic range

A

the range of concentrations over which a drug is active
below this = insufficient or no pharmacological action
above this = toxicity

17
Q

what is the therapeutic index

A

a measure of the range at which a drug is safe and active

18
Q

what is the bioavailability of a drug given IV

A

100%

19
Q

what factors affect bioavailability

A

formultion, ability of the drug to pass physiological barriers, GI effects, route of administration, first pass metabolism

20
Q

how does formulation affect bioavailability

A

some medications are prepared in slow release preparations, capsules break down faster than tablets

21
Q

what can alter the ability of drugs to cross physiological barriers

A

particle size, lipid solubility (blood-brain/ovary barrier, placenta etc), pH, ionisation

22
Q

why can lipid soluble drugs have significant side effects

A

they can bypass lipid membranes e.g. cannabis

23
Q

how do GI effects alter bioavailability

A

motility: speed of gastric absorption affects the speed at which the drug reaches the side of aborption (most drugs are absorbed in small intestine), can be affected by other drugs, food/drink and illnesses
food: can enhance or impair absorption
illness: malabsorption can increase/decrease rate of absorption, migraine reduces rate of stomach emptying and therefore rate of absorption of analgesic drugs

24
Q

how does route of administration affect bioavailability

A

by mouth will get into the blood faster than rectally

25
Q

first pass metabolism and its effects on bioavailability

A
  • Varies markedly between individuals and increases during pregnancy
    • Metabolism of drug prior to reaching systemic circulation, can be a limit on oral route for some drugs (oral route not useable - insulin), gut lumen (acid, enzymes), gut wall (metabolic enzymes), liver (hepatic enzymes). These factors can be changed by drugs and disease
26
Q

subcutaneous/intramuscular drug administration

A

can change the rate of absorption from these sites with different physical properties of formulation, depends on blood flow to site, needs small volume, avoids first pass metabolism, some drugs not well absorbed from this route (water soluble better)

27
Q

sublingual/buccal drug administration

A

sublingual absorption from the buccal mucosa bypasses first pass metabolism which will inactivate the drug, drugs given this way enter the circulation directly e.g. GTN for angina

28
Q

rectal drug administration

A

bypasses first pass metabolism, absorption tends to be slow, often used for drugs that cause stomach irritation or local conditions

29
Q

inhalation/nasal administration

A

absorption depends on the type of delivery system, particle size and patient technique. Better for volatile agents, can be metabolism in the lungs. Relatively rapid action, about 5-10% absorbed. Most commonly used for asthma, allows dosage to be reduces. Usually used for topical effect or to avoid problems of oral absorption e.g. nausea

30
Q

transdermal drug administration

A

avoids first pass metabolism, can provide controlled released, few substances well absorbed, need to be non-irritant

31
Q

what factors need to be taken into consideration when determining the mode of administration for a drug

A
  • purpose and site of drug action (local, first pass metabolism)
  • disease effects
  • patient’s ability to take the medicine
  • speed of action
  • reliability of absorption