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Male Wistar rats (7-9 weeks of age) fasted overnight were used. Each compound of 17k, 21e, and 6 was dissolved in 0.5% hydroxypropylmethyl-cellulose and administered orally at a dose of 10 μmol/kg. At pre-administration and at 0.5, 1, 2, 3, 5, 7, and 9 h after administration, 0.1 mL of blood was collected from the jugular vein. After centrifugation, 10 μL of plasma was diluted 10-fold using buffer (0.003% Brij-35 containing PBS). 20 μL of the diluted plasma was used instead of 20 μL of the test substrate for the determination of DPP-IV inhibitory activity by fluorescence as described above.
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