Drug Res (Stuttg) 2014; 64(6): 296-300
DOI: 10.1055/s-0033-1357190
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Pharmacokinetics of Niacin, Simvastatin and their Metabolites in Healthy Chinese Subjects after Single and Multiple Doses of a Fixed Dose Combination Tablet of Niacin Extended Release/Simvastatin

M. Liu
1   Department of Clinical Pharmacology, Aerospace Center Hospital, Beijing, P. R. China
,
X. L. Wang
1   Department of Clinical Pharmacology, Aerospace Center Hospital, Beijing, P. R. China
,
D. Zhang
1   Department of Clinical Pharmacology, Aerospace Center Hospital, Beijing, P. R. China
,
M. Yang
1   Department of Clinical Pharmacology, Aerospace Center Hospital, Beijing, P. R. China
,
J. Han
1   Department of Clinical Pharmacology, Aerospace Center Hospital, Beijing, P. R. China
,
Y. N. Zhang
1   Department of Clinical Pharmacology, Aerospace Center Hospital, Beijing, P. R. China
,
Z. L. Wang
1   Department of Clinical Pharmacology, Aerospace Center Hospital, Beijing, P. R. China
,
H. C. Liu
1   Department of Clinical Pharmacology, Aerospace Center Hospital, Beijing, P. R. China
› Author Affiliations
Further Information

Publication History

received 27 May 2013

accepted 23 September 2013

Publication Date:
23 October 2013 (online)

Preview

Abstract

Objective: A fixed dose combination tablet of niacin extended release (ER)/simvastatin was recently developed in China. This study was designed to assess and compare the pharmacokinetics of niacin, simvastatin and their metabolites in healthy Chinese subjects after single and multiple doses administration.

Methods: From day 1 to day 7, 12 Chinese subjects were given a tablet every day at approximately 10 p.m. Serial blood samples were collected. Niacin and nicotinuric acid (NUA) in plasma, niacin, NUA, N-methylnicotinamide (MNA) and N-methyl-2-pyridone-5-carboxamide (2PY) in urine, simvastatin and simvastatin acid in plasma were determined by LC/MS/MS methods. Pharmacokinetic parameters on days 1 and 7 were compared.

Results:The main pharmacokinetic parameters for the single and multiple doses were as ­follows: Niacin: Tmax were 3.8±1.5 h and 3.9±2.0 h; Cmax were 2 091±1 315 ng/ml and 2 323±1 542 ng/ml; AUC0-t were 4 123.88±3 138.48 ng ∙ h/ml and 4 385.98±3 127.05 ng ∙ h/ml. NUA: Tmax were 4.7±1.7 h and 3.8±1.5 h; Cmax were 1 057±549 ng/ml and 1 087±470 ng/ml; AUC0-t were 4 012.49±2 168.68 ng ∙ h/ml and 4 040.45±1 886.57 ng ∙ h/ml. Simvastatin: Tmax were 1.8±1.0 h and 2.5±2.5 h; Cmax were 3.15±1.67 ng/ml and 4.87±4.11 ng/ml; AUC0-t were 9.03±5.10 ng ∙ h/ml and 17.63±13.93 ng ∙ h/ml. Simvastatin acid: Tmax were 5.8±1.7 h and 6.5±1.4 h; Cmax were 4.22±2.10 ng/ml and 9.30±8.09 ng/ml; AUC0-t were 34.65±16.89 ng ∙ h/ml and 61.62±46.41 ng ∙ h/ml. Urine Recovery rate of total niacin: (40.55±7.38)% and (62.87±12.04)%.

Conclusion: Compared with those after a single dose, pharmacokinetics of niacin and NUA was similar; total urine recovery of niacin was higher; exposure to simvastatin and simvastatin acid were higher following multiple doses.