Pharmacokinetic Alteration of Paclitaxel by Ferulic Acid Derivative
Keyword(s):
P-glycoprotein (P-gp) is known to be involved in multidrug resistance (MDR) and modulation of pharmacokinetic (PK) profiles of substrate drugs. Here, we studied the effects of synthesized ferulic acid (FA) derivatives on P-gp function in vitro and examined PK alteration of paclitaxel (PTX), a well-known P-gp substrate drug by the derivative. Compound 5c, the FA derivative chosen as a significant P-gp inhibitor among eight FA candidates by in vitro results, increased PTX AUCinf as much as twofold versus the control by reducing PTX elimination in rats. These results suggest that FA derivative can increase PTX bioavailability by inhibiting P-gp existing in eliminating organs.
1985 ◽
Vol 3
(3)
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pp. 311-315
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1987 ◽
Vol 5
(9)
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pp. 1452-1460
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2015 ◽
Vol 2015
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pp. 1-10
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Keyword(s):
2020 ◽
Vol 17
(10)
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pp. 1270-1282
Keyword(s):
2012 ◽
Vol 2012
◽
pp. 1-11
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2019 ◽
Vol 11
(16)
◽
pp. 2095-2106
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Keyword(s):
Reversal of P-glycoprotein-mediated multidrug resistance and pharmacokinetics study in rats by WYX-5
2017 ◽
Vol 95
(5)
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pp. 580-585
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Keyword(s):