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DF16 Drug Partioning

Mer Scott 4 preguntas

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Preguntas del test (4)

  1. 1Partioning is the distribution of solutes between [blank_start]immiscible[blank_end] solvents — S(water) ⇄ S(oil).
    The solute distributes in a [blank_start]definite concentration ratio[blank_end] known as the [blank_start]partition coefficient[blank_end]. (K or P)
    K = [blank_start][oil]eq[blank_end] / [blank_start][water]eq[blank_end]
    1. Aimmiscible
    2. Bdefinite concentration ratio
    3. Cpartition coefficient
    4. D[oil]eq
    5. E[water]eq
  2. 2The partition coefficient indicates the relative lipophilic/hydrophilic character of a compound. Low K indicates a [blank_start]hydrophilic[blank_end] compound, high K indicates a [blank_start]lipophilic[blank_end] compound.
    1. Ahydrophilic
    2. Blipophilic
  3. 3True partition coefficient (K): the coefficient when all drug is in the [blank_start]unionised[blank_end] form (pH independent!)
    Apparent partition coefficient (K’): the coefficient that applies when some of the drug in the [blank_start]aqueous[blank_end] phase is [blank_start]ionised[blank_end] as a result of the pH
    1. Aunionised
    2. Baqueous
    3. Cionised
  4. 4Preservatives as an example:
    Preservatives prevent growth of microorganisms in the [blank_start]aqueous[blank_end] phase, and are often weak electrolytes. The problem is that preservatives [blank_start]partition[blank_end] between the aqueous and the oil phase. We therefore want to keep it in the [blank_start]unionised[blank_end] form so it is active.
    1. Aaqueous
    2. Bpartition
    3. Cunionised

Información

Descripción
(Formulation) PHCY211 Test sobre DF16 Drug Partioning, creado por Mer Scott el 30/04/2018.
Idioma
English
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