Basic Principles III Flashcards

1
Q

passive processes

A

simple diffusion, facilitated diffusion, filtration

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2
Q

active processes

A

active transport, micropinocytosis

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3
Q

weak electrolyte drugs

A

ionized forms do not diffuse, non-ionized forms diffuse and are lipid soluble. Follow the concentration gradient

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4
Q

weak acid drugs

A

will be in HA form in the stomach fluid (low pH), but when they diffuse to plasma (higher pH), will mainly be in H + A form

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5
Q

weak base drugs

A

will be in H + B form in stomach fluid (low pH), but when they diffuse to plasma, they will mainly be in the HB form

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6
Q

enteral administration

A

uses a portion of the GI tract

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7
Q

parenteral administration

A

does not use the GI tract

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8
Q

considerations for routes of administeration

A

planned use of medication, clinical setting (acute vs chronic), rapidity of onset of desired action, specific target organ that drug is intended to reach

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9
Q

oral advantages

A

easy, safe, self administered, cheap, prolonged absorption causes prolonged effect

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10
Q

oral disadvantages

A

may be too slow, unpredictable, and variable. May be too irritating or destroyed by gastric acids. May be completely metabolized on first pass through liver. Not available for comatose or vomiting patients

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11
Q

rectal advantages

A

useful for infants, coma, vomiting. Useful for bad tasting drugs. Useful for drugs destroyed in upper GI tract. Avoids liver. For local action in rectum

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12
Q

rectal disad

A

poor compliance. Absorption may be erratic. Possibility of rectal irritation

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13
Q

sublingual advantages

A

bypasses liver when first absorbed. Rapid absorption

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14
Q

sublingial diasadvan

A

must be soluble in saliva, not distasteful, have appropriate pKa for rapid absorption. Must be small tablets.

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15
Q

IV advantages

A

rapid effect, can watch response and titrate dose, all dose enters blood, good for when you cant do oral, good for irritating drugs or large volumes of drugs. Allows hypertonic solution to be administered

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16
Q

IV disadvan

A

cost, skill in administration, danger of infection, embolus formation, anaphylactic rxn, adverse cardiovascular effects if given too fast, painful

17
Q

intraarterial advantages

A

administration of radio-opaque material for visualization of circulatory tree. High concentration of drug going to local area when desirable.

18
Q

intraatertial disadvan

A

cost, skill in administration, danger of infection, embolus formation, anaphylactic rxn, adverse cardiovascular effects if given too fast, painful

19
Q

intramuscular advantages

A

when oral isnt avail, may be less variable absorption, may be less painful than subcutaneous, more rapid absorption than subcutaneous, possiblity of slowing absorption to prolong effect

20
Q

intramuscular disadvan

A

pain, sterile, posible local necrosis, lag period before onset, accidental injection in vein possible, not to be used after anticoag

21
Q

subcutaneous advantages

A

absorption usually slower than intramuscular, more prolonged effect

22
Q

subcutaneous disadvan

A

pain, sterile, posible local necrosis, lag period before onset, accidental injection in vein possible, not to be used after anticoag

23
Q

intrathecal advantages

A

when local effect on CNS required and other routes are unsatisfactory

24
Q

intrathecal disadvan

A

skill needed, danger of spinal cord injury

25
Q

topical advantages

A

for local action on or under skin/membrane. Non invasive

26
Q

topical disadvan

A

difficulty of absorption through skin. Danger of excessive absorption through membranes and systemic toxicity

27
Q

inhalation advantages

A

rapid absorption for systemic effect. High concentration attainable for local effect. Self administration possible

28
Q

inhalation disadvan

A

possible excessive absorption and systemic toxicity. Poor regulation of dosage, irritation of pulmonary tract

29
Q

bioavailability

A

fraction of dose available for biologic action. Measured by the area under the curve for the oral dose form vs. the IV dose form

30
Q

limiting step for oral drugs

A

usually dissolution

31
Q

factors affecting absorption in enteral drugs

A

form of drug, food in stomach, illness, blood flow

32
Q

factors affecting absorption in parenteral drugs

A

blood flow, head, cold, illness. Form of drug