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. Author manuscript; available in PMC: 2011 Aug 1.
Published in final edited form as: Mol Pharm. 2010 Aug 2;7(4):1342–1347. doi: 10.1021/mp100036b

Figure 1.

Figure 1

Uptake of pramipexole and TEA into hOCT1-MDCK and mock cells. A, Pramipexole uptake did not differ between hOCT1-MDCK cells and mock cells over a 5–200 μM pramipexole concentration range. Pramipexole permeability into mock cell monolayers was a low 1.21 (±0.06) ×10−7 cm/sec. B, TEA uptake into hOCT1-MDCK cells was higher than uptake into mock cells over a 14.3–570 μM TEA concentration range. Error bars denote SEM.