Exam 4: Pharmacology Basics Flashcards

1
Q

What 5 things are included in pharmacodynamics?

A
  1. Site of action
  2. Mechanism of action
  3. Receptor binding
  4. Postreceptor effects
  5. Chemical interactions
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What 3 things can affect pharmacodynamics?

A
  1. Disease/Disorder
  2. Age
  3. Drug-Drug interactions
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the 3 subtypes of receptors?

A
  1. Enzymes
  2. Ion channels
  3. Membrane receptors
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are the 4 types of chemical interactions that cause drugs to bind?

A
  1. Electrostatic interactions (intermolecular forces)
  2. Hydrophobic interactions
  3. Covalent bonding
  4. Stereospecific interactions
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are the 3 drug properties we look for?

A
  1. Affinity
  2. Efficacy
  3. Potency
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What 2 types of categories do drugs have? Which one do we prefer?

A
  1. Competitive PREFERRED
  2. Non-competitive
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What 4 things do pharmacokinetics help us understand better?

A
  1. Drug administration
  2. Therapeutic dosing
  3. Time intervals between drug dosing
  4. Toxic dosing
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What are the 2 main methods of drug administration?

A
  1. Enteral (oral) - through the intestines
  2. Parenteral (not oral) - not through the intestines
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Which 5 ways can drugs be administered?

A
  1. Enteral/oral
  2. Intramuscular
  3. Subcutaneously
  4. Intravenously
  5. Inhalation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Define bioavailability

A

How much of the administered drug is actually absorbed

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What 8 things affect bioavailability?

A
  1. Molecular weight of drug
  2. Drug formulation
  3. Drug stability (especially pH sensitivity)
  4. First pass metabolism
  5. Blood flow
  6. Gastric emptying
  7. Intestinal motility
  8. Drug interactions
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What 6 things influence distribution?

A
  1. Blood
  2. Total body water
  3. Extracellular fluids
  4. Lymphatic fluids
  5. Cerebrospinal fluids
  6. Protein-binding
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What 2 common processes are used for metabolism?

A
  1. Hydrolysis
  2. REDOX reactions
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the 4 main routes of excretion?

A
  1. Kidneys (majority of drugs)
  2. Feces
  3. Lungs
  4. Sweat
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is the main area for metabolism?

A

Liver

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

When do most drugs fail?

A

During the discovery phase

17
Q

90% of drugs fail in the ____ testing

A

clinical

18
Q

What is the Lipinskri Rule of 5

A
  1. Hydrogen bond donors/acceptors cannot be more than 10 combined
  2. Molecular weight target is less than 500 Daltons
  3. Partition coefficient (cLogP) should be less than 5
  4. Structural alerts
19
Q

What type of bonding increases the affinity of a drug?

A

Hydrogen bonding

20
Q

What are the 5 types of structural alerts?

A
  1. Aromatic anilines
  2. Nitroaromatics
  3. Aliphatic halides
  4. Polycyclic aromatic hydrocarbons
  5. Thiophenes
21
Q

What is drug efficacy directly related to?

A

Concentration of drug at the site of action