drug administration Flashcards

1
Q

what are the stages drugs go through in the body?

A
administration
absorption
transport
clinical effect
metabolism
excretion
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2
Q

what are the advantages of oral drug administration?

A

socially acceptable

drug formulation can change onset and duration of action

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3
Q

what are the disadvantages of oral drug administration?

A
slow onset
variable absorption
-food interactions in GIT
-GI disease
-gastric acid may destroy drug
first-pass metabolism
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4
Q

what is first pass metabolism?

A

all blood from GIT drains to hepatic portal vein
-except sublingual and rectal veins
hepatic portal vein drains to LIVER
-liver metabolises contents
-drug only reaches systemic circulation after passing through the liver once
can inactivate or activate a proportion of the drug
-varies with liver disease & age

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5
Q

give an example of a drug that the liver metabolism inactivates

A
glyceryl trinitrate (GTN)
more needed by oral route to get desired clinical effect
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6
Q

give an example of a drug that the liver metabolism activates

A

valaciclovir aciclovir
makes an active form of an inactive drug
less needed by oral route

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7
Q

what are the advantages of IV/IM administration?

A

very rapid onset
predictable plasma levels
no 1st pass metabolism

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8
Q

what are the disadvantages of IV/IM administration?

A

allergic reactions more severe
short duration of action
access difficulties/self-medication
drug cost higher

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9
Q

what are the advantages of transdermal & subcutaneous administration?

A

no 1st pass metabolism
allergic reactions localised
prolonged action
-can be days with transdermal patches

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10
Q

what are the disadvantages of transdermal & subcutaneous administration?

A

very slow onset
self-medication possible
drug cost higher
effect will vary from person to person and site to site

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11
Q

what is bioavailability?

A

proportion of an ingested drug that is available for clinical effect

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12
Q

what is bioavailability modified by?

A
dosage form
route of administration
destruction in the gut
poor absorption
first pass metabolism
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13
Q

how are drugs distributed?

A

drug is dissolved in the blood and transported bound to carriers
-usually plasma protein albumin

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14
Q

what can happen when drugs bind to plasma proteins?

A

bound drug is inactive so can act as a reservoir
drug interactions possible by competitive binding
-warfarin & aspirin

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15
Q

what does the speed of diffusion into tissues from the blood depend on?

A

the blood flow to the area
the blood wall vessel barrier
active secretion of the drug into the tissue

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16
Q

what is the single compartment model?

A

drug behaves as if it is evenly distributed throughout the body

17
Q

what is the two compartment model?

A

drug behaves as if it is in equilibrium with dif tissues in the body

18
Q

what is volume of distribution?

A

some drugs actively secreted into tissues or fluid rather than simple diffusion

19
Q

why may dif parts of the body receive dif drug levels compared with plasma-compartment model?

A

drug selection may depend upon the preference of some drugs for some areas of the body
eg. vascular, tissues, CNS

20
Q

why do some drugs have significant lipid binding in the tissues?

A

slow release from accumulation-prolonged effect

eg. anaesthetic gas
- halothane, isofluorane