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and being in the blood is not the same as being in those tissues,
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and you're right.
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It's hard to measure those concentrations in individual tissues
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and so we define bioavailability as the fraction of a drug dose
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that gets into the blood.
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Now, why wouldn't we do intravenous administration for everything?
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Because if it is fast, usually you don't want to wait for--
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you want the drug to act as rapidly as possible
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and you'd like all the drug molecules to be bioavailable,
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you would like all of them to be useful.
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So, why don't we use intravenous administration all the time?
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Well, it probably is obvious that not--that it's not so easy to do.