Arzneimittelforschung 2012; 62(03): 123-127
DOI: 10.1055/s-0031-1298004
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Relative Bioavailability of Two 5-mg Montelukast Sodium Chewable Tablets: A Single Dose, Randomized, Open-Label, 2-Period Crossover Comparison in Healthy Korean Adult Male Volunteers

H. T. Kim*
1   Department of Medicine/Gastroenterology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Gangnam-gu, Seoul, Republic of Korea
,
Y.-K. Song*
2   College of Pharmacy, Seoul National University, Gwanak-gu, Seoul, Republic of Korea
,
S. D. Lee
3   BioInfra Co. Ltd., Youngtong-gu, Suwon, Republic of Korea
,
Y. Park
4   College of Pharmacy, Inje University, Gyungnam, Republic of Korea
,
C.-K. Kim
4   College of Pharmacy, Inje University, Gyungnam, Republic of Korea
› Author Affiliations
Further Information

Publication History

received 09 August 2011

accepted 18 November 2011

Publication Date:
19 January 2012 (online)

Abstract

Montelukast sodium, cysteinyl leukotriene receptor 1 specific antagonist, has been marketed in Korea for the treatment of bronchial asthma and allergic rhinitis. The aim of this study was to compare the pharmacokinetics and relative bioavailability of a test and reference formulation of montelukast 5-mg chewable tablets in healthy Korean male volunteers to meet KFDA regulatory criteria for marketing of the new generic formulation. This study was designed as a single-dose, 2-treatment, and 2-period crossover trial with 32 healthy volunteers. Each subject was randomly assigned to receive the test (Dong-Kook Montelukast Sodium Chewable Tablet 5 mg®) or reference (Singulair Chewable Tablet 5 mg®) formulation. The tablet was chewed 20 times, and then swallowed with 240 mL of water. Plasma concentrations of montelukast up to 24 h after the dose were determined using a validated UPLC-MS/MS method, and the bioequivalence between the 2 formulations was assessed by statistical analysis of mean ratios of log-transformed AUC0–24h and Cmax. No period or sequence effects were detected. The AUC0–24h was 1 835 ng·h/mL for the test formulation, and 1 930 ng·h/mL for the reference formulation. The respective values of AUC0–∞ were 1 917 and 2 015 ng·h/mL. The Cmax of the test and reference products (247 and 283 ng/mL, respectively) reached at 2.25 and 2.72 h, respectively. Then, they gradually decreased with the mean terminal t1/2 of 5.25 and 5.30 h for the test and reference products, respectively. The 90% CIs for the ratio of log-transformed AUC0–24h and Cmax for the test and reference formulations were 0.92–0.99 and 0.83–0.91, respectively. No adverse events were reported in this study. This single dose study found that the test and reference products met the regulatory criteria for bioequivalence in these fasting healthy Korean male volunteers.

*

*  These authors contributed equally to the work presented here, therefore should be recognized as equivalent authors.


 
  • References

  • 1 Montelukast sodium – substance summary [Internet] National Library of Medicine (US): [cited 2011 Nov 30]. [about 2 screen]. Available from http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=search&db=pcsubstance&term=%22151767-02-1%22[Synonym]%2023663996[standardizedcid]
  • 2 SINGULAIR Label information [Internet] Merck & Co., Inc: US Food and Drug Administration (US); 2011 April 27. Available from: http://www.accessdata.fda.gov/drugsatfda_docs/label/2011/020829s057,020830s059,021409s034lbl.pdf
  • 3 Graff GR, Weber A, Wessler-Starman D et al. Montelukast pharmacokinetics in cystic fibrosis. J Pediatr 2003; 142: 53-56
  • 4 Korea Food and Drug Administration Regulation on drug product authorization, declaration, and review (KFDA notification No. 2009-17) 2009
  • 5 Nation RL, Sansom LN. Bioequivalence requirements for generic products. Pharmac Ther 1994; 62: 41-55
  • 6 Smith GA, Rawls CM, Kunka RL. An automated method for the determination of montelukast in human plasma using dual-column HPLC analysis and peak height summation of the parent compound and its photodegradation product. Pharm Res 2004; 21: 1539-1544
  • 7 Sripalakit P, Maphanta S, Saraphanchotiwitthaya A. Bioequivalence study of two generic formulations of 10 mg montelukast tablets in healthy Thai male volunteers. Int J Clin Pharmacol Ther 2010; 48: 628-632
  • 8 Knorr B, Hartford A, Li X et al. Bioequivalence of the 4-mg oral granules and chewable tablet formulations of montelukast. Arch Drug Inf 2010; 3: 37-43
  • 9 Challa BR, Awen BZ, Chandu BR et al. Method development and validation of montelukast in human plasma by HPLC couples with ESI-MS/MS: application to a bioequivalence study. Sci Pharm 2010; 78: 411-422
  • 10 Korea Food and Drug Administration . Guidance document for bioequivalence study. 2008;
  • 11 Papp R, Luk P, Mullett WM et al. A rapid and sensitive method for the quantitation of montelukast in sheep plasma using liquid chromatography/tandem mass spectrometry. J Chromatogr B 2007; 858: 282-286
  • 12 US Food and Drug Administration. Guidance for industry: Bioanalytical method validation. 2001;
  • 13 Korea National Institute of Toxicological Research. Bioanalytcal Method Validaton 2003;
  • 14 Lee YJ, Kim YG, Lee MG et al. Analysis of bioequivalence study using a log- transformed model [in Korean]. Yakhak Hoeji 2000; 44: 308-314
  • 15 US Food and Drug Administration . Guidance for industry: Bioavailability and bioequivalence studies for orally administered drug products. 2003;
  • 16 Gandhi M, Aweeka F, Greenblatt RM et al. Sex differences in pharmacokinetics and pharmacodynamics. Annu Rev Pharmacol Toxicol 2004; 44: 499-523