TTT method [NCA / SHAM]

posted by hiren379 – India, 2012-07-11 14:53 (5081 d 08:12 ago) – Posting: # 8930
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❝ Please avoid SMS spelling in your messages on this forum.


sorry as I am new to this forum

❝ Let me replace multicompartmental with multiphasic, then ?


Then how can you assume monophasic when calculating Kel for extra vascular drug administration. May be when you are calculating Kel for a tablet distribution is still on??

❝ 1. F*** R2


Strongly with you for this

❝ 2. I don't assume instantaneous distribution or monophasic elimination without looking at the PK profiles for each subject.

❝ (Also look at Helmut's first message in this same thread).


I also believe in this

So I think conclusion is that manual selection coupled with statistical method is best irrespective of dosage form....
Is it OK?

Now if I am using this + I know that my drug is having instantaneous distribution then still I should go for manual linearity finding. Will it not be bias???

:confused::confused:

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