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The absolute bioavailability of levocarnitine from the two oral formulations of levocarnitine, calculated after correction for circulating endogenous plasma concentrations of levocarnitine, was 15.1 5.3% for levocarnitine tablets and 15.9 4.9% for levocarnitine oral solution USP

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New York (2013)

Braakhuis et al

The mechanism through which they are coupled is not obvious from our structures alone, though we hypothesise that the two glutamine residues previously identified as important for sodium-dependent transport 46 , Q180 and Q207, play a role in linking the Na + and carnitine sites