Module 1: Section 4 Flashcards

(38 cards)

1
Q

ADME

A

absorption, distribution, metabolism, exertion (determines concentration of drug in blood, determined concentration of drug at site of action.

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2
Q

routes of administration

A

topical, eternal, parental

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3
Q

topical

A

on skin, through skin, inhalation

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4
Q

enernal

A

admin via GI tract - mouth, rectum, sublingual (tounge), buccal(cheek)

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5
Q

Parental

A

intravenous, intramuscular, subcutaneous

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6
Q

systemic

A

something that affects the whole body or multiple organ systems

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7
Q

on skin

A

skin conditions

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8
Q

transdermal

A

nicotine patch, conveinent, steady supply of drug (no frequent oral dosing), bypasses enymes of stomach, intestine, liver , - but expensive and can cause loacal irritation

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9
Q

Inhalation

A

rapidly absorbed from lungs. administered through lungs for local and systemic affects - anesthetics, steroids for lung disease. qauntity of drug is small, less required. But requires proper use by patient

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10
Q

enternal

A

enter blood through GI tract. when absorbed in GI, goes to liver. liver has enzymes that decrease amount of active drug ledt to enter general circulation - First pass effect

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11
Q

Enternal - mouth

A

how most drugs administered. most convientent, least expensice, non invasive, self administered BUT variable absorption bc differences in intestinal mobility and disease

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12
Q

Enternal - Rectum

A

systemic or local effect, use for patinets who are vomiting, less invasive for comatose, digestive enzymes bypassed. BUT limited number of medication this way, absorption is slow, incomplete, variable

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13
Q

Enternal - Sublingual and Buccal

A

enzyme of stomach, intestines, liver all bypassed BUT not all adequettly absorbed and drug may be swollowed

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14
Q

Paretnal - Intravenous

A

immediate effect. used for drugs that are porrly absorbed as long as they can be made into a solution of purified water. response is irreversable - highets risk for drug interactions. requires significant human resources + sterile peperations free of fever producting substansaes (pyrogens)

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15
Q

parental - Intramuscular

A

injected deep in msucle. volume of drug is limited to 2-3 ml for adult

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16
Q

Parental - subcutantous

A

injected in deepest layer of skin. allows for modificaon of drug preperarions to contol timing of release from injection site

17
Q

bioavailability

A

the fraction of an administered dose that reached the systemic circulation (blood) in active form

18
Q

Bioavailability - topical

A

rapid to slow, 5 -100%

19
Q

Bioavailability - enternal

A

mouth - slow 30 -1 hour (5-100%)
rectum - slow and incomplete (30-100%)
Under tounge - rapid 1-2 min (30-100%)
cheek - intermediate 3-4 min - 30-100)

20
Q

Bioavailability - parenteral

A

IV -15-30 sec - 100
Muscle - 10 - 20 min - 75-100
under skin - 15-30 min - 74-100

21
Q

absorption

A

movement of drug from site of administration into blood

22
Q

distribution

A

movement of a drug from the blood to the site of action and other tissues. most drugs reach all tissues and organs +target site. concentration in equilibrium. is concentration in blood drops below concentration at any site, drug move from that site to the blood to maintin equillibrium. greater the blood flow to an orgen, the more rapidly drugs reach that organ and vice versa.

23
Q

distribution and termination

A

distribtution can result in termination of the theraputic effect for some drugs

24
Q

thiopentnal

A

Iv absorption, concentration is high, high in brain, patient falls asleep. concentraiton in muscle and fat increases , concentration in blood decreases, causes frug to leave brain and move into bloos. as concentration in brain decreases, patient awakens

25
metabolism - biotransformation
conversion of drug into different chemical compound in order to eliminate. product of metabolis, called metabolites.to be eliminated by kidney, drug must be water soluable. most drugs converted to water souable. mostly occurs in liver but also kidneys, intestines, lungs, skin etc
26
biotransformation reactions
p450, phase 1, phase 2, excretion
27
p450
enzyme capable of biotransfroming drug. found in tissues bu high in liver. cytochrome p450 family do majority of biotransformatinos for drugs
28
biotransformation - phase 1
add or unmask functional froup. prepare for addition of large water soluable molecule in phase 2. adding a handle for the molecule to be attached
29
biotransformation - phase 2
adds large water soluable moiety (glucronic acid or sulfate) - kidneys can now excrete
30
biotransformation - excreation
excreted by kidneys. last step
31
excretion by
kidneys, GI tract (poop), lungs (eg alchol) breat milk, saliva and sweat
32
half life
time needed for the liver and kidney to remove half the drug from the body
33
factors for drug response variation
genetic, environmental, disease states, altered psychilogical states, presence of other drugs
34
drug response variation - genetic
variability in receptors to which drug binds and body handles and eliminates drugs. variability in activity of enzymes - ex metabolism of alcohol
35
drug response variation - environment
certain chemicals increase enzymes - eliminate drug more rapidly
36
drug response variation - disease state
drug response variation - alter way body reacts ex. liver disease = slower metabolic rate
37
drug response variation - altered physiochological state
elderly more suseptible to drug acting on CNS. liver and kidney function decreasing as age. Pregannsy
38
drug response variation - other drugs present
one drug might change biological effect of a second dryg