Pharmacy tutorial 2 Flashcards

1
Q

What are excipients?

A

An inactive substance that serves as the vehicle or medium for a drug or other active substance.

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

What can excipients be used for?

A
  • To aid manufacture of the medicine
  • Increase acceptability to the patient (improve flavour, fragrance or appearance)
  • Improve chemical or biological stability (eg. capsule so it can reach further down the GI tract)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is formulation?

A

The process of making a medicine containing a drug

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

List some formulations for oral route of administration

A
  • Tablets
  • Capsules
  • Syrups
  • Sublingual tablets
  • Powders
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

List the advantages of the oral route of administration

A
  • Allows self-medication
  • Does not require rigorously sterile preparations
  • Lower incidence of anaphylactic shock than IV
  • There is capacity to prevent complete absorption
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

List the disadvantages of oral route of administration

A
  • Innapropriate for some drugs (those altered by the pH of the stomach, or those that undergo first pass metabolism)
  • Requires patient compliance
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

List the advantages of IV route of drug administration

A
  • Rapid onset of action

- Avoids poor absorption from and destruction within the GI tract

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

List the disadvantages of IV drug administration

A
  • Slow injection necessary to avoid toxic bolus
  • Higher incidence of anaphylactic shock
  • Complications are possible (embolism, phlebitis and pain)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

List the advantages of inhalation drug administration

A
  • Ideal for small molecules and gases
  • Lungs have enormous SA
  • Simple diffusion
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

List the disadvantages of inhalation drug administration

A

Possible localised effect within the lung

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

List the advantages of intramuscular drug administration

A
  • High blood flow (into connective tissue reservoir in muscle block)
  • Increased during exercised
  • Enables depot therapy (prolongued absorption from a pellet, microcrystalline suspension or solution in oily vehicle)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

List the disadvantages of intramuscular drug administration

A

Possible infection and nerve damage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

List the advantages of subcutaneous injections

A

Local administration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

List the disadvantages of subcutaneous injections

A
  • Pain
  • Abscess
  • Tissue necrosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

List the advantages of percutaneous drug administration

A
  • Local application and action (across the skin)

- Lipid soluble compounds diffuse rapidly

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

List the disadvantages of percutaneous drug administration

A
  • Local irritation and skin reactions

- Alteration of skin structure

17
Q

List some agents that could be used as excipients

A
  • Lactose, glucose, starch

- Chalk (to make into a tablet large enough to pick up)

18
Q

Define bioavalability

A

The amount of a drug contained in a medicine that enters the systemic circulation unchanged after administration of the drug

19
Q

Why is bioavailability important?

A
  • Allows a drug to reach the site of action and have effect

- Enables medication to be delivered systemically

20
Q

When is bioavailability not important?

A
  • When administering a drug locally

- When converting a drug to an active prodrug

21
Q

How is bioavailability determined?

A

By comparing the areas under the plasma conc-time graph for the drug after IV administration and administration by the intended route

22
Q

List the factors that affect bioavailability

A
  • Physiochemical characteristics of the drug (ionisation)
  • GI pH
  • Passive/active transport
  • GI motility
  • Particle size of the drug
  • Physiochemical interaction between the drug and gut contents (may be degraded by the microbiome)
23
Q

List the available forms of aspirin

A
  • Aspirin tablets
  • Soluble aspirin
  • Enteric coated aspirin
24
Q

When would soluble aspirin be prefered?

A
  • When in need of immediate pain relief

- Tablets are longer acting

25
Define bioequivalence
Evidence that a new generic product behaves similar to existing products to ensure it will not cause clinical problems if substituted
26
Why is bioequivalence important?
A drug may have a narrow therapeutic window, so the concentration needs to be carefully monitored to prevent toxic effects
27
Give examples of drugs with narrow therapeutic windows
- Warfarin - Cancer drugs - Digoxin
28
Define first pass metabolism
Where the concentration of a dug is greatly reduced before reaching systemic circulation due to GI enzymes, bacteria and liver enzymes
29
How can good bioavailability be achieved for drugs with extensive first-pass metabolism
Administer by other methods, such as IV, sublingual, inhaler or cream
30
List some illnesses that could effect bioavailability of drugs
- Stomach ulcers - Hyper/hypomotility - Lack of transporters
31
When can 100% first pass metabolism of a drug be useful?
- Prodrugs | - GI tract conditions where the drug does not need to enter systemic circulation