1st module - basics Flashcards

1
Q

Pharmacotherapeutics

A

Area of pharmacology that refers to the use of specific drugs to prevent, treat, or diagnose a disease.

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2
Q

Pharmacokinetics

A

Study of how the body absorbs, distributes, metabolizes, and eliminates the drug.

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3
Q

Pharmacodynamics

A

The analysis of what the drug does to the body, including the mechanisms by which the drug exerts its effect on target tissues.

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4
Q

Chemical names

generic name

trade name

A

Specific compound’s structure

The official name, typically derived from chemical name

Brand name, assigned to compound by the company.

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5
Q

Dose response curve

A

Dosage range of which a drug is effective. Allows understanding for how much drug is needed to initiate an effect as well as plateau.

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6
Q

Potency

A

Potency helps understand at what dose are we able to produce a response.
A more potent drug may require less of a compound to produce a certain response.

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7
Q

Therapeutic index

A

toxic dose/effective dose , closer to 1 the more toxic it is, the further from 1 the less toxic it is

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8
Q

Different ways for drug to enter

A

(enteral -towards the GI)
Oral, sublingual, rectal
(Perenteral)
Inhalation, injection, topical, transdermal

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9
Q

Oral
Advantages and disadvantages

A

advantage: easy, safe, convenient
Disadvantage: limited or erratic absorption of some drugs
Chance of first pass inactivation in liver
Example, analgesics

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10
Q

Sublingual

A

advantages rapid onset, not subject to first pass inactivation
Disadvantages drug must be easily absorbed from oral mucosa

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11
Q

rectal

A

pros alternative to oral route, local effect on rectal tissues
Cons poor or incomplete absorption, chance of rectal irritation

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12
Q

inhalation

A

pros, rapid onset, direct application for respiratory disorders, large surface area for systemic absorption
Cons, chance of tissue irritations, patient compliance sometimes s problem

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13
Q

injection

A

pros, provides more direct administration to target tissues, rapid onset
Cons, chance of infection if sterility not maintained

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14
Q

topical

A

pros, local effects on surface of skin
Cons, only good in treated outer layers of skin

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15
Q

transdermal

A

pros, introduces drug into body without breaking the skin, can provide steady prolonged delivery via medicated patch
Cons, drug must be able to pass through dermal layers intact

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16
Q

Tissue permeability distribution

A

highly lipid soluble drugs can potentially reach several body compartments or cells
large non-lipid soluble compounds will likely remain in the tissue they’re administers
Specific tissues ex) blood-brain barrier: limits the movement of drugs into the CNS

17
Q

Blood flow distribution

A

Drugs circulating through the bloodstream have greater access to highly perfused tissues. Brain, Kidneys, and exercising skeletal muscle will receive more of the drug

18
Q

Binding to plasma proteins distribution

A

Drugs distribution will be limited as some of the drug will form bonds with the circulating proteins and will therefore have no therapeutic effect

19
Q

Binding to subcellular components distribution

A

Similar to binding to plasma proteins. Drugs may get “stuck” inside specific cells.

20
Q

Half life

A

the amount of time required for 50% of the drug remaining in the body to be eliminated

21
Q

Pharmodynamics

A

effect of drug

22
Q

pharmokinetics

A

how the drug moves around in the body

23
Q

surface receptors Link to

A

ion channels and directly to enzymes

24
Q

ion channels

A

Receptors directly involved in cellular response by acting as an ion pore which changes the membrane permeability.

ex) Ach binding opens a pore allowing for NA+ to depolarize
ex) GABA in CNS allows for Cl- to enter.

25
Directly to enzymes (interaction with drug)
Drugs and endogenous chemicals that bind to the receptor site can change the enzyme activity of the intracellular catalytic component <> altering the biochemical function within the cell. Drugs and endogenous chemicals that bind to the receptor site can change the enzyme activity of the intracellular catalytic component <> altering the biochemical function within the cell.
26
2nd messenger stuff
G proteins: proteins located on inner surface of cell’s membrane activated by binding guanine nucleotides. Substance binds to receptor -> receptor undergoes a shape change -> attaches to nearby G protein. -> G protein gets activated -> alters activity of enzyme/ion channel -> change in cell function
27
Affinity
amount of attraction between a drug and a receptor high affinity: binds readily to open receptor even if low concentration low affinity: may require higher drug concentration to bind. Allosteric modulators: regulator that when binding, alters affinity.
28
Selectivity
Selective: affects only one type of cell or tissue ex) cardioselective drug affects heart function with minimal response to GI or respiratory Allowed because of receptors structural and functional subgroups
29
Agonist vs antagonist
Agonist: a drug that can bidn to a receptor and initiate a change in the cell’s function. partial agonist Antagonist: drug will bind to receptor but will not have any effect on the cell. competitive vs non competitive
30
Receptor regulation
Overstimulation of receptors may lead to a decrease in receptor population. Prolonged decrease in stimulation can lead to increased receptor sensitivity.
31