Pharmacology Flashcards

1
Q

what is meant by drug absorption

A

the process by which a drug enters the body from its site of administration

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2
Q

what is meant by drug distribution

A

the process by which a drug leaves the site of administration, enters the blood and subsequently the tissues perfused by the blood.

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3
Q

what is meant by drug metabolism

A

the process by which tissue enzymes (principally in the liver – hepatic metabolism) catalyze the chemical conversion of a frequently lipid soluble drug to an often less active and more polar form that is more readily excreted from the body

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4
Q

what is meant by drug excretion

A

the processes that remove the drug, or its metabolites, from the body (principally the kidneys – renal excretion)

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5
Q

what is meant by drug elimination

A

The linked processes of metabolism and excretion

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6
Q

what factors affect drug absorption

A

solubility

chemical stability

lipid to water partition coefficient

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7
Q

what is acids relationship with protons

A

donates protons

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8
Q

what is base’s relationship with protons

A

accepts protons

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9
Q

what does the degree of ionisation depend on in drugs

A

pKa of the drug

local pH

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10
Q

what can calculate Proportions of ionised and unionised drugs

A

the Henderson-Hasselbalch equation

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11
Q

what is the Henderson-Hasselbalch equation

A

pKa - pH = log(AH/A-)
for acid

pKa - pH = log(BH+/B)
for base

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12
Q

what facilities the absorption of weak acids

A

pH of the stomach lumen

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13
Q

where are bases readily absorbed

A

small intestines

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14
Q

what is oral availability

A

the fraction of drug that reaches the systemic circulation after oral ingestion

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15
Q

what is systemic availability

A

fraction that reaches the systemic circulation after absorption

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16
Q

what are ionised and unionised drugs distribution

A

if they are not bound to plasma protein (e.g. albumin, α1-acid glycoprotein) they can move freely by diffusion

17
Q

what are the only drugs that move readily by diffusion

A

unionised drugs