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MD23 Oral dosage forms III

Mer Scott 8 questions

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  1. 1Advatanges of controlled release:
    • Frequency of dosing [blank_start]reduced[blank_end] (improve patient [blank_start]compliance[blank_end] especially for [blank_start]chronic[blank_end] conditions)
    • Improve residence time for drugs with short [blank_start]half lives[blank_end]
    • Optimise release conditions to maintain [blank_start]drug stability[blank_end]
    • Mimic IV infusion with a more zero order, [blank_start]uniform release[blank_end] and effect
    1. Areduced
    2. Bcompliance
    3. Cchronic
    4. Dhalf lives
    5. Edrug stability
    6. Funiform release
  2. 2Monolithic matrix systems - diffusion controlled release:
    1. Lipid matrix
    Drug in [blank_start]solid, hydrophobic[blank_end] matrix. Channelling [blank_start]agents[blank_end] allow water in, and drug to [blank_start]diffuse[blank_end] out. Higuchi release profile.
    2. Insoluble polymer matrix
    Drug is dissolved or dispersed in a [blank_start]porous insoluble polymer[blank_end] matrix.
    3. Hydrophilic matrix
    Water soluble drug in [blank_start]swellable polymer[blank_end]. Two diffusion steps ([blank_start]water in and drug out)[blank_end]. Gel formation, then gel [blank_start]erosion[blank_end].
    1. Asolid, hydrophobic
    2. Bagents
    3. Cdiffuse
    4. Dporous insoluble polymer
    5. Eswellable polymer
    6. Fwater in and drug out)
    7. Gerosion
  3. 3Mixed size particles with variable coating thickness contribute to a steady release profile.
    1. ATrue
    2. BFalse
  4. 4Choose the incorrect statement about the mucous later of the GIT.
    1. AMade up of glycoproteins
    2. B95% water by weight
    3. CPositively charged at physiological pH
    4. DMucus turnover 50 - 250 min
  5. 5A mucoadhesive delivery system increases absorption because it avoids enzyme degradation.
    1. ATrue
    2. BFalse
  6. 6If the pH is higher than the drug pKa they will adhere together strongly.
    1. ATrue
    2. BFalse
  7. 7Site-specific delivery is advantageous when the drug has a [blank_start]narrow[blank_end] therapeutic window, is [blank_start]unstable[blank_end] in the GIT, or [blank_start]local[blank_end] delivery is needed.
    - Methods of site-specific delivery for the stomach(<[blank_start]7mm[blank_end] evacuated and
    >[blank_start]15mm[blank_end] prolongs retention):
    1. Superporous hydrogel
    Fast, [blank_start]super swelling[blank_end] system that is mechanically [blank_start]strong[blank_end] but biodegradable over time.
    2. Expandable systems
    Many types eg [blank_start]accordion[blank_end] pill for levodopa release to treat Parkinson's.
    1. Anarrow
    2. Bunstable
    3. Clocal
    4. D7mm
    5. E15mm
    6. Fsuper swelling
    7. Gstrong
    8. Haccordion
  8. 8We may want to give site-specific drug delivery to the colon to treat colon cancer, Crohn's disease, or ulcerative colitis. The colon has a small ([blank_start]0.2 metres squared[blank_end]) surface area, a [blank_start]wide[blank_end] lumen, and no [blank_start]villi[blank_end]. However in the colon drugs will have a [blank_start]prolonged[blank_end] residence time, there are [blank_start]reduced[blank_end] enzyme secretions, and it is responsive to [blank_start]absorption enhancers[blank_end]. It may be possible to use [blank_start]cleavage[blank_end] release by utilising the enzymes specific to colon [blank_start]bacteria[blank_end]. [blank_start]Prodrugs[blank_end] are therefore a viable option. Must be cautious when co-administering with [blank_start]antibiotics[blank_end] which could kill gut microflora.
    1. A0.2 metres squared
    2. Bwide
    3. Cvilli
    4. Dprolonged
    5. Ereduced
    6. Fabsorption enhancers
    7. Gcleavage
    8. Hbacteria
    9. IProdrugs
    10. Jantibiotics

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Description
PHCY211 (Medicines) Quiz on MD23 Oral dosage forms III, created by Mer Scott on 24/05/2018.
Author
Mer Scott
Language
English
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