Basic Pharmacology Flashcards

1
Q

What are drugs

A
  • any substance that alters the physiology of the body but is not a food or nutrient
  • usually derived from compounds found in plants
  • definition often accounts for the intention of the user
  • examples
    • vitamin C in pills = drugs
    • vitamin C in fruit/veg = not drug
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2
Q

Psychoactive drugs

A
  • aka psychotropic drugs
  • act upon CNS to alter brain function resulting in changes to perception, mood, consciousness and behaviour
  • may be used recreationally
    • or as entheogens for ritual or spiritual purposes
    • or therapeutically
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3
Q

Formulation

A
  • trade name refers to formulation
    • the way the medicine is made
  • includes both active ingredient and excipients (non active ingredients)

-drugs with exact same ingredients could have very different psychoactive properties due to different formulations

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4
Q

Describing drug doses

A
  • doses: mg/kg (body weight)
  • concentration at site of action
  • TD50: median toxic does
    • undesirable effects
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5
Q

Therapeutic index

A
  • TI=LD50/ED50
  • higher number = safer drug
  • alcohol has lowest TI
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6
Q

Potency

A
  • more potent drug produces effect at lowest dose

- heroine vs morphine

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7
Q

Efficacy

A

-maximum effect a drug will produce that is desirable

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8
Q

Synergistic effects

A
  • potentiation
  • the whole is greater than the sum of the parts
  • greater than additive effect
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9
Q

Over effects

A
  • combination of substances produce something different than either substance alone
  • Ayahausca effect
    • DMT = Harmine = profound hallucinations
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10
Q

Pharmacodynamics

A

What the drug does to the body

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11
Q

Pharmocokinetics

A

What the body does to the drug

  • routes of administration
  • absorption
  • distribution
  • excretion/elimination
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12
Q

Subcutaneous injection

A
  • absorption rate dependent on blood flow to injection site
  • tends to be slow
  • provide even sustained delivery over time
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13
Q

Intramuscular

A
  • slower absorption than iv
  • faster than sc
  • usually to deltoid or gluteus
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14
Q

Intraparetoneal

A
  • directly into organs

- common in lab animals

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15
Q

Other injection methods

A
  • IVC
    • intracerebroventricular
    • into ventricles
    • brain and capital cord surrounded by CSF
    • ICV injections directly into ventricle via cannula
    • bypass BBB
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16
Q

Factors that influence absorption from injection site

A
  • temp
    • heat increases blood flow
  • once in blood drug must pass through walls of capillaries in order to enter circulation
    • drug diffuses through pores
17
Q

Intranasal administration

A
  • enters nasal cavity in mucosa membrane then diffuses into blood
  • some enters lungs
  • some runs down into stomach
  • further away from heart so slower reaction time than inhalation
18
Q

Oral administration

A
  • some absorption from stomach but mostly from small intestine
  • tissue made of cells surrounds by bilipid membrane
  • rate of absorption controlled by ability of drug molecules to dissolve in lipids
    • lipid solubility
    • high lipid solubility = easily dissolved = faster onset of effects
19
Q

Lipid solubility

A
  • olive oil partition coefficient
  • when a drug is dissolved in a mixture of oil and water, different proportions of the drug will end up dissolved in the oil and water
  • high partition coefficient means that most of drug will end up in oil
    • high lipid solubility
  • low coefficient mean that most will end up in water
    • low lipid solubility
  • high lipid soluble drugs can diffuse through membrane and be absorbed from small intestine
  • low lipid solubility diffuse slowly into blood from small intestine
  • when molecule of a drug have an electric charge (IONIZED) they are NOT lipid soluble at all