Pharmacokinetics Flashcards

1
Q

What is a drug?

A

A substance used for treatment, relief, diagnosis or prophylaxis of a disease

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2
Q

What are the 3 sources where drugs can come from?

A

Plant
Animal
Mineral

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3
Q

How do enteral drugs enter the body?

A

Anything involving digestive tract. Mouth to rectum

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4
Q

Where do parenteral drugs go?

A

Avoids the gut so any route other than via gastrointestinal tract

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5
Q

Give examples of parenteral drugs? ( not through digestive tract )

A

Transdermal - patches
Implantation
Intramuscular - muscle
Intrathecal - spine ( epidural )

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6
Q

What does TOP TIPS stand for?

A

Tropical, oral, parenteral, transdermal, inhalation & subcutaneous ( under the skin )

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7
Q

What is a subcutaneous drug?

A

Applied under the skin

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8
Q

What is the pharmacokinetic phase?

A

ADME

Absorption
Distribution
Metabolism
Excretion

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9
Q

Absorption across cell membranes involves what transports?

A

Passive - no energy required. Movement from a high to low concentration

Active - energy is required. Drugs move against the concentration gradient

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10
Q

Factors that may affect the absorption of drugs across the GI tract?

A

Drug preparation - how quickly it disintegrates

Interaction - pH of stomach contents, food and other drugs

Physiological factors - how quickly the drug is moved through the digestive tract

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11
Q

How does blood flow to a tissue affect distribution?

A

Drugs will reach higher concentrations in tissues which have a good blood supply eg, Brain. However, reduced flow to tissues and organs will affect distributions eg, blood brain barrier

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12
Q

Some substances blocked from entering the brain tissue?

A

Toxins, some drugs and specific bacteria

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13
Q

What is the first pass effect?

A

The effect liver metabolism has upon the drug during its first passage through the liver and in particular how much of the drug is inactivated

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14
Q

If taken orally, where is the tablet absorbed across??

A

The wall of the stomach and / or the small intestine

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15
Q

What is biotransformation?

A

The conversion of molecules from one form to another within an organism, often associated with change in pharmacological activity

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16
Q

What are the main organs involved in elimination of drugs?

A

But, Skin, Lungs, Salivary grands, sweat glands, breast milk and Kidneys

17
Q

What is bioavailability?

A

Describes the fraction of administers dose of the drug that reaches the systemic circulation

18
Q

How much bioavailability of a drug is there when it’s administer intravenously ( vein )?

A

100%

19
Q

Why does propranolol have a bioavailability of 25%?

A

Because 75/85% is metabolised via 1st oasis effect ( metabolised by liver ) if taken orally before it can reach the circulation

20
Q

Why is morphine usually given via intramuscular injection?

A

Takes longer for plasma concentration to reach and it lasts longer

21
Q

What does onset mean?

A

Time from administration to when the therapeutic effect occurs

22
Q

What is a modified release?

A

Designed to slowly release drug into the gastrointestinal tract over a period of time

23
Q

What is a therapeutic range?

A

Optimum plasma level in which it has its therapeutic effect

24
Q

What is a therapeutic window for a drug?

A

Describes the levels in plasma which a drug can act

25
Q

What organs are most likely to be affected by drug toxicity?

A

Liver and kidneys

26
Q

Name a withdrawal symptom that can be experience when stopping opioids ( heroin and morphine ) after a long period of time?

A

Headaches

27
Q

Pharmacokinetics is?

A

How the body handles the drug

28
Q

Tolerance is?

A

A decrease in pharmacological effect when a drug is given repeatedly

29
Q

Modified release predations are designed to?

A

Slowly release drug over a period of time

30
Q

What happens to the drug in the liver?

A

Metabolic processes will convert the drug into a more water-soluble compound by increasing its polarity

31
Q

Name a drug sourced by a plant origin?

A

Digoxin