An important physical characteristic in pharmacology is the fat-blood partition
ID: 964304 • Letter: A
Question
An important physical characteristic in pharmacology is the fat-blood partition coefficient. This is the equilibrium concentration of a drug in fatty tissues (a relatively oily phase) divided by the concentration of drug in blood (an aqueous phase). If the fat-blood partition coefficient is high, the majority of a drug will be transferred to fatty tissue during administration. The fat-blood partition coefficient of the anesthetic n-butyl 4-aminobenzoate is reported to be 575.4 at pH = 7.4. Calculate the free energy per mole to transport n-butyl 4- aminobenzoate from fatty tissue to blood. At pH = 7.4, n-butyl 4-aminobenzoate is not protonated, so you may assume that equations for uncharged species can be used.
Explanation / Answer
we know that
Free energy change = Delta G = -RTln P
P = paritition coefficeint
R = gas constant = 8.314
T = Temperature (assuming standard) = 298 K
So Free energy change = - 8.314 X 298 X 2.303 X log 575.4 = 15747.969 Joules
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