Bioequivalence of Bambucol Tablet 10 mg to $Bambec^{(R)}$ Tablet 10 mg (Bambuterol Hydrochloride 10 mg)

밤벡$^{(R)}$ 정 10밀리그람(염산밤부테롤 10밀리그람)에 대한 밤부콜 정 10밀리그람의 생물학적동등성

  • Cho, Hea-Young (Clinical Trials Management Division, Korea Food and Drug Administration) ;
  • Choi, Ji-Hoon (College of Pharmacy and Institute of Bioequivalence and Bridging Study, Chonnam National University) ;
  • Yoo, Hee-Doo (College of Pharmacy and Institute of Bioequivalence and Bridging Study, Chonnam National University) ;
  • Lee, Yong-Bok (College of Pharmacy and Institute of Bioequivalence and Bridging Study, Chonnam National University)
  • 조혜영 (식품의약품안전청 임상제도과) ;
  • 최지훈 (전남대학교 약학대학 부속 생물학적동등성 및 가교시험연구소) ;
  • 류희두 (전남대학교 약학대학 부속 생물학적동등성 및 가교시험연구소) ;
  • 이용복 (전남대학교 약학대학 부속 생물학적동등성 및 가교시험연구소)
  • Received : 2010.10.08
  • Accepted : 2010.11.20
  • Published : 2010.12.31

Abstract

Bambuterol hydrochloride, dimethylcarbamic acid 5-[2-(1,1-dimethylethyl)amino-1-hydroxyethyl]-1,3-phenylene ester hydrochloride, is the prodrug of active ${\beta}_2$-adrenergic metabolite terbutaline. The purpose of the present study was to evaluate the bioequivalence of two bambuterol hydrochloride tablets, $Bambec^{(R)}$ tablet 10 mg (Yuhan Co., Ltd.) and Bambucol tablet 10 mg (Sam Chun Dang Pharm. Co., Ltd.), according to the guidelines of Korea Food and Drug Administration (KFDA). In vitro release of bambuterol from two bambuterol hydrochloride formulations was tested using KP VIII Apparatus II method with various dissolution media. Twenty eight healthy male Korean volunteers, $23.86{\pm}1.65$ years in age and $68.98{\pm}9.58$ kg in body weight, were divided into two groups and a randomized $2{\times}2$ cross-over study was employed. After two tablets containing 10 mg as bambuterol hydrochloride were orally administered, blood samples were taken at predetermined time intervals, and the concentrations of bambuterol in serum were determined using column switching HPLC with UV detector. The dissolution profiles of two formulations were similar in all tested dissolution media. The pharmacokinetic parameters such as $AUC_t$, $C_{max}$ and $T_{max}$ were calculated, and ANOVA test with K-BE Test 2002 was utilized for the statistical analysis of the parameters using logarithmically transformed $AUC_t$, $C_{max}$ and untransformed $T_{max}$. The results showed that the differences between two formulations based on the reference drug, $Bambec^{(R)}$, were -8.10%, -3.82% and 12.65% for $AUC_t$, $C_{max}$ and $T_{max}$, respectively. There were no sequence effects between two formulations in these parameters. The 90% confidence intervals using logarithmically transformed data were within the acceptance range of log 0.8 to log 1.25 (i.e., log 0.8093~log 1.0302 and log 0.8564~log 1.1280 for $AUC_t$ and $C_{max}$, respectively). Thus, the criteria of the KFDA bioequivalence guideline were satisfied, indicating Bambucol tablet 10 mg was bioequivalent to $Bambec^{(R)}$ tablet 10 mg.

Keywords

References

  1. Rosenborg J, Larsson P, and Nyberg L. Pharmacokinetics of bambuterol during oral administration of plain tablets and solution to healthy adults. Br J Clin Pharmacol 2000; 49: 199-206.
  2. Nyberg L, Rosenborg J, Weibull E, et al., Pharmacokinetics of bambuterol in healthy subjects. Br J Clin Pharmacol 1998; 45: 471-8.
  3. 생물학적동등성시험기준, (식품의약품안전청고시, 제 2002-60호).
  4. Lee YJ, Kim YG, Lee MG, et al., Analysis of bioequivalence study using log-transformed model. Yakhakhoeji 2000; 44: 308-14.
  5. 의약품임상시험관리기준, (식품의약품안전청고시, 제 1999-67호).
  6. Wannerberg O, and Persson B. Liquid chromatographic method for the determination of bambuterol hydrochloride and related compounds. J Chromatogr 1988; 435: 199-203. https://doi.org/10.1016/S0021-9673(01)82175-0
  7. Cho HY, Park CH, and Lee YB. Direct and simultaneous analysis of loxoprofen and its diastereometric alcohol metabolites in human serum by on-line column switching liquid chromatography and its application to a pharmacokinetic study. J Chromatogr B Analyt Technol Biomed Life Sci 2006; 835: 27-34. https://doi.org/10.1016/j.jchromb.2006.02.058
  8. Falco PC, Hernandez RH, and Cabeza AS. Column-switching techniques for high-performance liquid chromatography of drugs in biological samples. J Chromatogr 1993; 619: 177-90. https://doi.org/10.1016/0378-4347(93)80107-F
  9. 생물학적동등성시험기준, (식품의약품안전청고시, 제 2010-43호).