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pharm 2060 MT 1 - 2

Mary Nguyen English 35 cards

Cards in this deck (35)

  1. 1pharmacokineticsthe study of drug movement in the body
    what the body does to the drug
  2. 2absorptionthe movement of the drug from the site of administration into the blood
    det how quickly the drug effect will occur
    the amt of drug absorption determines how intense the effect of the drug will be
  3. 3factors affecting absorption (5)rate of dissolution
    SA
    blood flow
    lipid solubility
    pH partitioning
    activity of drug transport proteins
  4. 4rate of dissolutionhow fast it dissolves in solution
    drugs must dissolve before they can be absorbed
  5. 5surface areaie stomach has rugae folds
    itnestine has villi
    villi that line the intestine make the SA very large
  6. 6blood flowdrug absorption is fastest in areas w high blood flow b/c high BF maintains conc grad
    exercise increases blood flow --> can inc drug absorption
    blood flow is decreased in heart failure, severe hypotension, hypothermia and circulatory shock
  7. 7lipid solubilitycan cross PM but hydrophilic can't
  8. 8pH partitioningdrug absorption is greater when there's a difference between the pH at the site of administration and the blood such that the drug is ionized in the blood
  9. 9activity of drug transport proteinuptake drug transporters increase the absorption of drugs
    efflux drug transporters decrease the absorption of drugs
  10. 108 major routes of administrationsoral
    sublingual
    rectal
    intravenous
    subcutaneous
    intramuscular
    pulmonary
  11. 11enteralroutes of administration that involve the GI tract: oral, rectal
  12. 12parenteralroutes of administration that do not involve the GI tract: intravenous, intramuscular, subcutaneous
  13. 13other routes of administration (other than enteral, parenteral)sublingual, transdermal, pulmonary
  14. 14intestine v stomach for oral absorptionintestine has larger SA so drug absorption greater in intestine
    even weak acids b/c the stomach (stomach = acidic) is covered in a thick layer of mucous
  15. 15pharmaceutical phaseoccurs after the patient swallows a tablet
    involves the disintegration of the tablet and the dissolution of the drug
    if drug does not completely disintegrate, or does not go into soln, absorption is reduced
  16. 16gastric emptyinggastric emptying is the movement of stomach contents into the intestine
    things that inc the rate of gastric emptying also inc the rate of drug absorption
  17. 17factors that increase gastric emptyingempty stomach
    cold water
    lay down right side
    high osmolality feeding (tube feed)
    taking prokinetic drug (inc GI motility)
  18. 18factors that decrease gastric emptyinghigh fat meal
    heavy exercise
    lying down on left side
    taking a drug that inhibits the vagus nerve (anticholinergic)
  19. 19enteric coatingspecial coating that prevents drug dissolution in the acidic environment of the stomach
    will dissolve in alkaline duodenum
  20. 20bioavailabilityfraction of a dose of drug that reaches the systemic circulation unchanged -- influenced by: drug formulation, route of administration, degree of metabolism
  21. 21order of bioavailabilityaqueous soln is most
    syrup
    suspension
    chewable tablet
    granules
    capsules
    compressed tablet
    enteric coated tablets
    time release capsules
  22. 22sublingualplacing drugs under tongue --> absorbed across the oral mucosa
    venous drainage from oral mucosa to the superior vena cava --> heart
    these avoid first pass metabolism thru the liver ***
    in order to be absorbed, drugs must be lipophilic and uncharged
  23. 23transdermalproblem b/c not all drugs penetrate hte skin
    drugs must be lipophilic enough to penetrate the skin, but hydrophilic enough to dissolve into the extracellular fluid
    ideal transdermal preparations have some degree of lipophilicity and some degree of hydrophilicty and are usually small
  24. 24transdermal preparationsusually: patches, ointments, sprays, lotions
    transdermal administration provides constant plasma drug levels w minimal peaks and troughs
    tolerance may develop unless drug-free periods are enforced --> remove for 6-10 hours a day
  25. 25factors affecting transdermal absorptionthickness of skin
    hydration (more = better)
    hair follicles (more = better)
    application area
    integrity of the barrier (psoriasis, burned inc absorption)
  26. 26rectaluseful when unconscious or vomitting
    50% bypasses liver
    inserted as a suppository --> dissolves and drug crosses rectal mucosa
  27. 27intravenousdrug is injected directly into a peripheral vein
    most commonly used veins: back of hand, median cubital vein @ elbow
    can be bolus or IV Drip
    IV bolus: single dose over short time
    IV drip: continuous infusion over long time (usually diluted)
  28. 28advantages of intravenousno barriers to absorption, bioavailability 100%
    allows precise control of the drug dosage and duration of action
    allows administration of poorly soluble drugs that must be diluted in a large volume
    allows injection of drugs that are irritants (ie chemo) --> can be injected slowly so they are diluted in the blood
  29. 29disadvantages of intravenousexpensive, invasive, inconvenient
    drug can't be removed once injected
    risk of infection and fluid overload
    risk of injecting wrong formulation (IM instead of IV)
  30. 30subcutaenousdrug is injected beneath the skin into the subcutaneous tissue
    only barrier is the capillary wall
    irritant drugs must not be injected subcutaneously as this will cause severe pain and tissue sloughing
    primary det of rate of absorption: blood flow, water solubility
  31. 31intramusculardrug injected directly into muscle tissue
    absorption is det by the ability of the drug to pass thru fenestrations in the capillary wall
    primary et of rate of absorp: blood flow, water solubility
  32. 32advantages of intramuscularcan be used for poorly soluble drugs
    can use to administer depot preparations (where it is slowly absorbed over time)
  33. 33disadvantages of intramuscularpain or discomfort
    may cause local tissue or nerve damage if the injection is done improperly
  34. 34how blood flow affects intramuscular absorptionblood flow: diff dep on which muscle is used for injection
    deltoid > vastus lateralis > gluteal
    exercise increases blood flow --> may inc absorption for IM drugs
    blood flow may be dec in heart failure, severe hypotension and hypothermia
  35. 35pulmonarygaseous and volatile drugs can be inhaled and absorbed into the blood thru the pulmonary epithelium
    absorption is v rapid due to large surface area of lung
    if pulmonary disease, drug is delivered to its site of action which is a major advantage
    drugs such as general anaesthetics used in surgery are also often administered by the pulmonary route of administration

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Flashcards on pharm 2060 MT 1 - 2 , created by Mary Nguyen on 10/02/2016.
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Mary Nguyen
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