Test 1 Flashcards

(73 cards)

1
Q

What is pharmacology?

A

Study of biochemical and physiological effects of drugs

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2
Q

What is pharmacodynamics?

A

study of the cellular and molecular interactions of drugs with their targets

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3
Q

What is pharmaceutical toxicology?

A

study of harmful or toxic effects of drugs

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4
Q

What is pharmacokinetics?

A

study of factors that control the concentration-time relationship of drug at various sites in the body (what the body does to the drug)

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5
Q

What is medical chemistry?

A

study of drug design to optimize pharmacokinetics and pharmacodynamics and synthesis

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6
Q

What is pharmaceutics?

A

study and design of drug formulation and optimum delivery, stability, pharmacokinetics and patient acceptance.

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7
Q

What is pharmacogenomics?

A

study of influence of genetic variation on drug response in patients

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8
Q

What is the most effective way of excretion?

A

Urine

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9
Q

What is a drug?

A

Any substance used in diagnosis, treatment, and prevention of a disease

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10
Q

What are the 4 types of drugs?

A
  1. Synthetic
  2. Semi-Synthetic
  3. Naturally Occurring
  4. Mixture
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11
Q

What are some natural drug sources?

A

Plants, animals, and minerals

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12
Q

What are some examples of plants?

A

seaweed, castor oil, resins

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13
Q

What are some examples of animals?

A

insulin, cod liver oil, pepsin

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14
Q

What source do vaccines come from?

A

Animals

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15
Q

How are minerals used in drugs?

A

As they occur in nature and combined with other ingredients

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16
Q

What are the components of an ideal drug?

A
  1. Has desirable effects
  2. Has no side effects
  3. Reaches to its target with right amount @ right time
  4. Remains at the site of action for necessary period of time
  5. Rapidly eliminates from body when no longer needed
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17
Q

What are drug receptors made up of?

A

Protiens

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18
Q

What are some side effects of a drug binding to an unintended target?

A

Toxicity

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19
Q

What is the most effective means of drug administration?

A

IV

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20
Q

What is the most common means of drug administration?

A

Oral

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21
Q

What is the second most common means of drug administration?

A

Intramuscular

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22
Q

What are some means of drug administration?

A

Buccal, sublingual, gastric, intradermal, rectal and vaginal, respiratory inhalants, subcutaneous, topical, epidural, spinal

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23
Q

What happens during Phase 1 of new drug development?

A

testing on small number of healthy volunteers

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24
Q

What does phase 1 test?

A

Safety, toxicity, and pharmacokinetics

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25
What happens during Phase 2?
Drug trials with small number of patients with disease of interest
26
What does Phase 2 test?
Assesses treatment efficacy, optimal dosing and adverse effects
27
What happens during phase 3?
drug is used on larger # of patients
28
What does phase 3 test?
compares current treatment to the current standard of care
29
What happens during phase 4?
post-market surveillance of drugs effects
30
What does phase 4 test?
detects rare or long term effects; can it stay on the market?
31
When is a drug taken off the market?
When toxicity outweighs the benefit
32
What is the only drug administered subQ?
Insulin
33
Why do we not administer more drugs by subQ?
skin irritation
34
What do drug actions depend on?
1. physiochemical properties 2. Chemical properties 3. sterochemistry
35
What are some biochemical barriers?
transport proteins, enzymes, and receptors
36
How does a drug increase or decrease cellular functions?
by acting on its receptors
37
What are some regulatory protein targets?
receptor, ion channels, enzymes, and transporters
38
What is an example of a receptor?
Zyrtec. Antihistamine that targets histamine to prevent allergic reactions
39
What is an example of an ion channel?
Lidocaine. blocks sodium channels to prevent sensation of pain. Local anesthetics
40
What is an example of an enzyme?
Celebrex. blocks COX-2 enzyme to prevent production of inflammatory substances (prostaglandins)
41
What is the enzyme COX-2 responsible for?
transition from phospholipids to prostaglandins
42
What is an example of a transporter?
Prozac. blocks the removal of serotonin to elevate mood
43
What is a ligand?
Ion/molecule that binds to the protein receptor to carry out physiological effect
44
What is an example of an endogenous ligand?
Neurotransmitters
45
What is a exogenous ligand?
Drug
46
What is the body's own pain killer called?
Endorphin
47
What does endorphin do?
acts on special receptors to reduce pain
48
What are the 3 kinds of protein-ligand binding?
1. Hydrogen Bonding 2. Ionic reaction 3. Hydrophobic interaction
49
What is pharmacophore?
needed for binding of drug to their targets and producing a biological response
50
Examples of pharmacophore?
1. Vector groups 2. Carrier groups 3. Vulnerable groups
51
What are vector groups?
physiochemical properties of the molecule
52
What are carrier groups?
control absorption, distribution, and excretion
53
What are vulnerable groups?
determine metabolism
54
What does complementarity determine?
strength of bonding
55
What does physiochemical complementarity deal with?
physical/chemical
56
What does steric complementarity deal with?
size
57
What is hydrogen bonding?
bonding between opposite poles of molecules
58
What are van der Waals forces?
intermolecular forces other than ionic or covalent bonds
59
What is steric complementarity?
determines 3D shape and size that fit into the shape of the targets
60
What are sterorisomers?
molecules that have the same molecular formula but different spatial arrangement
61
What is chirality?
geometric property of a molecule not being superimposed with its mirror image
62
What is bioisosterism?
The application of isosterism of drugs
63
What does bioisosterism allow?
change in drug structure and functions and improve the drug effect
64
How does ionization effect drug intake?
structure and function
65
What do buffers do?
prevent a change in pH when H+ ions are added to or removed from a solution
66
What is the major extracellular buffer?
HCO3-
67
What is the major intracellular buffer?
hemoglobin
68
How do buffers work?
minimizes the pH change
69
When do weak acids become more non-ionized?
when H+ increases (pH decreases)
70
When do weak bases become more non-ionized?
when H+ decreases (pH increases)
71
WHen do weak acids become more ionized?
When H+ decreases (pH increases)
72
When do weak bases become more ionized?
When H+ increases (pH decreases)
73
What form can only cross the membrane?
non-ionized