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Retinoids - Advances in Basic Research and Therapy (Paperback, Softcover reprint of the original 1st ed. 1981)
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Retinoids - Advances in Basic Research and Therapy (Paperback, Softcover reprint of the original 1st ed. 1981)
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With the aromatic retinoic acid analog Tigason oral and intravenous
pharmacokinetic studies have been performed in 5 normal volunteers.
Simultaneous fitting of single i. v. and oral data to a
three-compartment model assuming first-order absorption was
possible. Using Nonlin parameter estimates of the single-dose data,
one is able to predict the decline in plasma levels of parent drug
following cessation of a 10 days multiple dosing regimen up to 24
hours. The model is however unable to predict a phase of prolonged
elimination observed beyond 24 hours. Moreover in 5 patients, who
underwent chronic therapy (8-15 months), substantial plasma levels
of both unchanged drug and main metabolite (corre sponding
carboxylic acid) were observed up to 140 days after cessation of
the therapy. An apparent half-life of elimination of 80-100 days
can be calculated. The drug appears to be stored at some yet
unknown storage site. Investigation of metabolism of Tigason in
rats and humans revealed 19 different bio transformation products
thus far, most of them appearing in the urine in low amounts (20010
of dose). A few of them (mainly the acid Ro 10-1670) after
conjugation to glucuronic acid are excreted in the bile in high
amounts (60-80% of dose). No drug appeared unchanged in the excreta
after i. v. administration to rats. References 1. Bollag W (1971)
Effects of vitamin A acid (NSC-122758) on transplantable and
chemically-induced tumors. Cancer Chemother Rep 55:53-58 2."
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