QUOTE(polaris91 @ May 29 2011, 04:28 PM)
hey folks i need some help from you guys regarding questions on pharmacokinetics...
-For rapidly dissolving oral dose forms of a drug, differences in rates
of dissolution markedly affect the plasma concentration-time profile,
when intestinal permeability is the rate-limiting step
is this statement correct ?
Assuming we're talking about passive diffusion across intestinal membranes..-For rapidly dissolving oral dose forms of a drug, differences in rates
of dissolution markedly affect the plasma concentration-time profile,
when intestinal permeability is the rate-limiting step
is this statement correct ?
Do you mean that the concentration gradient(across the membrane) is the rate-limiting step? ie: saturated vs. sink condition.
From what I understand, you can't alter intestinal permeability because it's natural/biological. What you can do however is alter the drug (Lipinski's rule of 5) such that it can permeate across the membranes better.
If we're talking about active transport, then substrate saturation becomes the rate-limiting factor..
May 30 2011, 01:34 AM

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