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A drug can not generally have an oral bioavailability value higher than its value for f H , and oral bioavailability can equal f H only when all of the drug escapes from the GI tract and is able to enter the portal circulation (i.e

50 L of 100 mM/L 3,5 dichloro-2-hydroxy benzene sulfonate in phosphate buffer (pH 7) was used as a chromogen, and 500 L of 4-amino antipyrine peroxidase preservatives were added to 50 L of the sample or standard, and 500 L of chromogen and 500 L deionized water were added to 50 L of the blank sample

Silymarin and its components are inhibitors of -glucuronidase

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