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10.1007/s40261-016-0386-y

http://scihub22266oqcxt.onion/10.1007/s40261-016-0386-y
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suck abstract from ncbi


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pmid26951201      Clin+Drug+Investig 2016 ; 36 (ä): 443-52
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  • In Vitro and In Vivo Interaction Studies Between Lesinurad, a Selective Urate Reabsorption Inhibitor, and Major Liver or Kidney Transporters #MMPMID26951201
  • Shen Z; Yeh LT; Wallach K; Zhu N; Kerr B; Gillen M
  • Clin Drug Investig 2016[]; 36 (ä): 443-52 PMID26951201show ga
  • Background and Objectives: Lesinurad is a selective uric acid reabsorption inhibitor (SURI) under investigation for the treatment of gout. This study elucidated the interaction of lesinurad with major liver and kidney transporters in vitro and evaluated the drug?drug interactions (DDIs) of lesinurad and atorvastatin, metformin, and furosemide in clinical studies. Methods: Lesinurad interaction with membrane transporters was evaluated in validated transporter-expressing cell systems and analyzed by liquid scintillation counting. Healthy male subjects (ages 18?65 years; body mass index 18?32 kg/m2) received atorvastatin (40 mg; n = 28) with or without lesinurad 200 or 400 mg, or received metformin (850 mg; n = 12) or furosemide (40 mg; n = 11) with or without lesinurad 400 mg. Plasma concentrations of each concomitant drug were determined by validated liquid chromatography with tandem mass spectrometry methods. Results: Lesinurad interacted in vitro with OATP1B1, OCT1, and OAT1/3 transporters. Co-administration of lesinurad 200 mg did not significantly alter plasma exposure (maximum concentration [Cmax] and area under the concentration?time curve [AUC]) of total atorvastatin (atorvastatin + hydroxyl-metabolites) or atorvastatin, while co-administration of lesinurad 400 mg increased the Cmax of total atorvastatin and atorvastatin by 17?26 %, but had no effect on AUC. Co-administration of lesinurad 400 mg had no effect on the plasma exposure of metformin. Furosemide plasma AUC was reduced by 31 % in the presence of lesinurad 400 mg, but furosemide renal clearance and diuretic activity were unchanged. Conclusions: No clinically relevant DDIs were observed between lesinurad and substrates of major liver or kidney transporters.
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