Effect of Cilostazol on the Pharmacokinetics of Simvastatin in Healthy Subjects

• Published in: BioMed research international Vol. 2019; no. 2019; pp. 1 - 6
• Main Authors: Ko, Jae-Wook, Ghim, Jong-Lyul, Huh, Wooseong, Kim, Seokuee, Jung, Jin Ah, Kim, Jung-Ryul, Shin, Jae-Gook
• Format: Journal Article
• Language: English
• Published: Cairo, Egypt Hindawi Publishing Corporation 01-01-2019; Hindawi; Hindawi Limited
• Subjects: Acids; Adult; Cholesterol; Chromatography, Liquid; Cilostazol - administration & dosage; Clinical Study; Cytochrome P-450 CYP3A - genetics; Drug dosages; Drug Interactions; Drug therapy; Enzymes; Female; Healthy Volunteers; Humans; Laboratories; Lipids; Liquid chromatography; Male; Mass spectrometry; Mass spectroscopy; Metabolism; Metabolites; Nitric oxide; Pharmacokinetics; Pharmacology; Simvastatin; Simvastatin - administration & dosage; Simvastatin - analogs & derivatives; Simvastatin - blood; Simvastatin - pharmacokinetics; Statins; Substrates; Vital signs
• ISSN: 2314-6133; 2314-6141
• DOI: 10.1155/2019/1365180

Purpose. We evaluated potential drug-drug interactions between cilostazol and simvastatin, both CYP3A substrates, in healthy subjects. Methods. An open-label, two-period, fixed-sequence clinical study was conducted. Seventeen subjects were given a single oral dose of simvastatin 40 mg on day 1 and multiple oral doses of cilostazol 100 mg twice daily on days 2 to 5 followed by a single dose of cilostazol and simvastatin on day 6. Plasma concentrations of simvastatin and its active metabolite, simvastatin acid, were measured using liquid chromatography-tandem mass spectrometry for pharmacokinetic assessment. Moreover, serum lipid profiles under fasting conditions were determined. Results. The geometric mean ratios of the area under the plasma concentration-time curve from time zero to time infinity of simvastatin combined with cilostazol to that of simvastatin alone were 1.64 (90% CI, 1.38-1.95) for simvastatin and 1.31 (1.04-1.66) for simvastatin acid. In addition, coadministration with cilostazol significantly increased the maximum concentration of simvastatin and simvastatin acid, up to 1.8-fold and 1.6-fold, respectively. However, the effects of a single dose of simvastatin on serum lipid profiles were not affected notably when simvastatin was coadministered with cilostazol. Conclusions. Multiple doses of cilostazol increased the systemic exposure of simvastatin and simvastatin acid following a single dose of simvastatin.