Exam 2 - Controlled Drug Delivery Flashcards

(29 cards)

1
Q

Describe temporal dosing & give examples

A

dosing over time

  • sustained release: delayed, extended
  • pulsatile release
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2
Q

Describe spatial dosing & give examples

A

looking for a particular directed targeting drug delivery (ex. nuclear pharmaceuticals, goal for local delivery)

  • systemic
  • local
  • targeted
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3
Q

Give examples of a drugs that used a diffusion-reservoir system

A

ocusert

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4
Q

Give examples of a diffusion-controlled system

A

reservoir devices
matrix devices

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5
Q

Define diffusion-controlled systems

A

drug diffusion through the polymer network is the rate-limiting step

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6
Q

Explain the mechanism of matrix (monolithic) systems

A
  • drug and matrix former are not physically separated
  • drug release depends on the device geometry
  • larger concentration of drugs initially → slower concentration of drugs over time
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7
Q

Describe when a matrix (monolithic) system should NOT be used as the drug release system

A

NOT the most effective mechanism to release a drug if the drug does not take a long time to get into the therapeutic window and is narrow to maintain

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8
Q

List potential advantages of controlled drug delivery

A
  • maintain optimum drug concentration
  • improve efficiency of treatment with less amount of drug
  • minimize side effects
  • less frequent administration (ex: concerta)
  • increase patient convenience and compliance with dosing regimen (adherence)
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9
Q

List disadvantages of controlled drug delivery

A
  • relatively high production costs
  • leakage of drug mass (dose dumping) → DO NOT CHEW
  • difficult to stop drug release
  • biocompatibility of the delivery system? (once swallowed, you cannot stop drug)
  • necessity of surgical operation
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10
Q

Describe the release mechanism of reservoir devices (diffusion-controlled release systems)

A

the drug is released at a constant rate over time (when a drug is passing through that membrane, you get a constant drug release)

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11
Q

Describe the release mechanism of matrix devices (diffusion-controlled release systems)

A

the membrane thickness is essentially changing over time (how the drug has to diffuse through the system will increase because the drug at the surface does not have to diffuse nearly as far as the drug further into the matrix)

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12
Q

List types of dissolution-controlled release systems

A

encapsulated
matrix

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13
Q

Describe encapsulated dissolution-controlled release systems

A
  • when the drug dissolves, your body immediate releases the drug
  • you either get FULL drug release or NO drug release
  • the thickness of the membrane determines how quickly the drug will be released
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14
Q

Describe matrix dissolution-controlled release systems

A
  • aka erodible drug system (as the matrix erodes, it releases drug under that particular mechanism)
  • the rate controlling membrane itself or the matrix system will actually dissolve
  • the surface area and the thickness of dissolution layer DOES change, unlike other systems
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15
Q

Describe full drug release in encapsulated dissolution-controlled release systems

A

as that matrix slowly dissolves and breaks apart, the polymer membrane dissolves

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16
Q

Explain how the membrane thickness of a encapsulated dissolution-controlled systems

A

thin membrane: quick release

thick membrane: slow release

17
Q

List types of osmotic controlled-release systems

A
  • one chamber device
  • two chamber device
  • reverse osmosis
  • film coating

osmotic systems are independent of the pH in the system (regardless where in the body)

18
Q

Describe osmotic controlled-release systems

A

allowing water to pass thru the membrane. as water passes thru the membrane, it forces the drug out of a compartment

19
Q

Describe one-chamber osmotic controlled-release systems

A

easier to make

semi-permeable membrane that allows only water to pass through

you start with an initial concentration of drug that will slowly decrease overtime as water goes in, and overtime the drug will be pushed out (diluted drug)

20
Q

Describe advantages of two-chamber osmotic controlled-release systems

A

water is going thru the system at a constant rate

the drug is not diluted by water, drug is also going thru system at a constant rate

21
Q

Describe disadvantages of two-chamber osmotic controlled-release systems

A

more complex to make (making it more expensive)

22
Q

Describe the reverse osmosis osmotic controlled-release system

A

by concentrating all the ions, you force all the pure water out of the system

23
Q

Describe film coating osmotic controlled-release system

A
  • permeable for water
  • not permeable for drugs or excipients
  • rigid: resist the hydrostatic pressure → push out the drug
24
Q

Give a simple description of erosion-controlled release systems

A

when drug is dissolved, drug is released

25
Explain erosion-controlled release systems
- initial release phase is controlled by diffusion of drug molecules that are on the surface / have access to the surface via pores in the microsphere matrix - sustained release: determined by the erosion of the polymer - as the polymer erodes, entrapped drug molecules are released from the delivery matrix
26
Describe swelling controlled-release systems
- not changing the matrix - as the water permeates into the matrix, we’ve allowed matrix to swell - as drug swells → drug diffuses out
27
Describe how to increase the drug-release rate in swelling controlled-release systems
when the length of the diffusion pathways increase, it causes a decreasing drug-concentration gradient
28
Describe how to decrease the drug-release rate in swelling controlled-release systems
the mesh size of polymer network increases, causing there to be increasing drug diffusivities in the polymer network
29
Describe lupron depot as a drug release control system/product
constant release over time via injectable microspheres