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1) I am completeing some research regarding the impact of folate on the PKT
profile of PHT. I have use 3 methods MM, True & DDCl. I use DDCl
clinically as it provides me with greater predictability particularly
as my practice is predominantly ambulatory and hence po.
a1) Does anyone have experience with DDCl, I would like to work on
the model as there are definite holes in the equation.
b) Each method gives a diff Km although Vmax is stable across the 3
methods. Does one publish using all 3 methods or just True.
2) Is there anyone doing ant PKT work using Delphi as a programming
language, I am having problems getting a 2 BCM termination sequence
to reach extinction. I seem to be picking up problems passing
parameters into the functions.
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