Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9917727 | European Journal of Pharmaceutical Sciences | 2005 | 12 Pages |
Abstract
5,6-Dimethylxanthenone-4-acetic acid (DMXAA), a potent cytokine inducer, exhibited marked antitumor activity when given as multiple oral doses in mice. The aim of this study was to examine the transport of DMXAA and its acyl glucuronide (DMXAA-G) using the human Caco-2 cells. DMXAA was minimally metabolized by Caco-2 cells and both DMXAA and DMXAA-G were taken up to a minor extent by the cells. The permeability coefficient (Papp) values of DMXAA over 10-500 μM were 4 Ã 10â5 cm/s to 4.3 Ã 10â5 cm/s for both apical (AP) to basolateral (BL) and BL-AP transport, while the Papp values for the BL to AP flux of DMXAA-G were significantly greater than those for the AP to BL flux, with Rnet values of 4.5-17.6 over 50-200 μM. The BL to AP active efflux of DMXAA-G followed Michaelis-Menten kinetics, with a Km of 83.5 ± 5.5 μM, and Vmax of 0.022 ± 0.001 nmol/min. The flux of DMXAA-G was energy and Na+-dependent and MK-571 significantly (P < 0.05) inhibited its BL to AP flux, with an estimated Ki of 130 μM. These data indicate that the transport of DMXAA across Caco-2 monolayers was through a passive process, whereas the transport of DMXAA-G was mediated by MRP1/2.
Keywords
MRP5,6-dimethylxanthenone-4-acetic acidDMXAAAcyl glucuronidebasolateralP-gpTEERVmaxHBSSSRBCyPUGTHEPESIC50DMSOP-glycoproteinuridine diphosphate glucuronosyltransferaseApicaltumour necrosis factor-αIntestinal absorptionMichaelis-Menten constantdimethyl sulphoxideCaco-2 cellssulforhodamine BCytochrome P450Permeability coefficientTNF-αHanks’ balanced salt solutiontransepithelial electrical resistanceinhibition constantPappmultidrug resistance protein
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Authors
Shufeng Zhou, Xia Feng, Philip Kestell, James W. Paxton, Bruce C. Baguley, Eli Chan,