Pharmacokinetics 1 Flashcards

1
Q

what are the 7 routes of drug administration?

A
\+ oral
\+ sublingual
\+ inhalation
\+ topical
\+ transdermal
\+ intramuscular (IM)
\+ intravenous (IV)
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2
Q

what are the advantages and disadvantages of the oral route?

A

A: convenient

D: first-pass effect, many variables and barriers

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3
Q

what are the advantages and disadvantages of the sublingual route?

A

A: no first-pass effect

D: inconvenient, small dose limit, taste

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4
Q

what are the advantages of the inhalation route?

A

A: fast, rapid delivery to blood

D: requires special properties of drug (atomised. vaporised)

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5
Q

what are the advantages and disadvantages of the topical route?

A

A: convenient, localised

D: only local

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6
Q

what are the advantages and disadvantages of the transdermal route?

A

A: prolonged release

D: skin very effective barrier

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7
Q

what are the advantages and disadvantages of the intramuscular route?

A

A: rapid for aqueous

D: painful, requires trained personnel

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8
Q

what are the advantages and disadvantages of the intravenous route?

A

A: direct, total dose, rapid

D: requires professional, infection risk, rapid response

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9
Q

what are examples of polar aqueous media?

A

+ blood plasma
+ cytosol
+ interstitial fluid

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10
Q

what are examples of non-polar media?

A

+ interior of lipid bilayer

+ fat

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11
Q

what are the basic drugs, from strongest to weakest?

A
\+ amphetamine
\+ atropine
\+ noradrenaline
\+ codeine
\+ diazepam
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12
Q

what are the acid drugs from strongest to weakest?

A
\+ penicillins
\+ aspirin
\+ warfarin
\+ phenytoin
\+ paracetamol
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13
Q

what are some non-selective muscarinic ACh receptor agonists?

A

+ pilocarpine

+ bethanechol

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14
Q

what are clinical uses of pilocarpine?

A

+ constriction (miosis)
+ glaucoma (to decrease IOP)
+ xerostomia (following head/neck radiotherapy)

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15
Q

what factors affect drug distribution?

A
\+ degree of drug ionisation
\+ lipid solubility
\+ pH of compartments
\+ cardiac output and blood flow
\+ capillary permeability
\+ plasma protein binding
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16
Q

in relation to pharmacokinetics, what are the criteria of (L)ADME

A
(Liberation)
Adsorption
Distribution
Metabolism
Excretion