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딜라트렌 정 12.5밀리그람(카르베딜롤 12.5밀리그람)에 대한 카딜란 정 12.5밀리그람의 생물학적동등성

Bioequivalence of Cadilan Tablet 12.5 mg to Dilatrend® Tablet 12.5 mg (Carvedilol 12.5 mg)

  • 김세미 (전남대학교 약학대학 부속 생물학적동등성 및 가교시험연구소) ;
  • 신새벽 (전남대학교 약학대학 부속 생물학적동등성 및 가교시험연구소) ;
  • 김주환 (전남대학교 약학대학 부속 생물학적동등성 및 가교시험연구소) ;
  • 권인호 (전남대학교 약학대학 부속 생물학적동등성 및 가교시험연구소) ;
  • 김용희 (전남대학교 약학대학 부속 생물학적동등성 및 가교시험연구소) ;
  • 이상노 (전남대학교 약학대학 부속 생물학적동등성 및 가교시험연구소) ;
  • 조혜영 (국립독성과학원) ;
  • 이용복 (전남대학교 약학대학 부속 생물학적동등성 및 가교시험연구소)
  • Kim, Se-Mi (College of Pharmacy, Institute of Bioequivalence and Bridging Study, Chonnam National University) ;
  • Shin, Sae-Byeok (College of Pharmacy, Institute of Bioequivalence and Bridging Study, Chonnam National University) ;
  • Kim, Ju-Hwan (College of Pharmacy, Institute of Bioequivalence and Bridging Study, Chonnam National University) ;
  • Kwon, In-Ho (College of Pharmacy, Institute of Bioequivalence and Bridging Study, Chonnam National University) ;
  • Kim, Yong-Hee (College of Pharmacy, Institute of Bioequivalence and Bridging Study, Chonnam National University) ;
  • Lee, Sang-No (College of Pharmacy, Institute of Bioequivalence and Bridging Study, Chonnam National University) ;
  • Cho, Hea-Young (General Pharmacology Team, Pharmacological Research Department, NITR, KFDA) ;
  • Lee, Yong-Bok (College of Pharmacy, Institute of Bioequivalence and Bridging Study, Chonnam National University)
  • 발행 : 2008.12.20

초록

Carvedilol, is a nonselective $\beta$-blocking agent and it also has vasodilating properties that are attributed mainly to its blocking activity at ${\alpha}_1$-receptors. The purpose of the present study was to evaluate the bioequivalence of two carvedilol tablets, $Dilatrend^{(R)}$ tablet 12.5 mg (Chong Kun Dang Pharmaceutical Co., Ltd.) and Cadilan tablet 12.5 mg (KyungDong Pharmaceutical. Co., Ltd.), according to the guidelines of the Korea Food and Drug Administration (KFDA). The release of carvedilol from the two carvedilol formulations in vitro was tested using KP VIII Apparatus II method with pH 4.5 dissolution medium. Thirty two healthy male subjects, $25.00{\pm}3.09$ years in age and $70.71{\pm}11.35\;kg$ in body weight, were divided into two groups and a randomized $2{\times}2$ cross-over study was employed. After a single tablet containing 12.5 mg as carvedilol was orally administered, blood samples were taken at predetermined time intervals and the concentrations of carvedilol in serum were determined using HPLC with fluorescence detector. The dissolution profiles of two formulations were similar in the tested dissolution medium. The pharmacokinetic parameters such as $AUC_t$, $C_{max}$ and $T_{max}$ were calculated and ANOVA test 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, $Dilatrend^{(R)}$ tablet 12.5 mg, were 4.66%, 8.33% and -7.45% 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 (e.g., $\log\;0.9823{\sim}\log\;1.1042$ and $\log\;1.0132{\sim}\log\;1.1875$ for $AUC_t$ and $C_{max}$, respectively). Thus, the criteria of the KFDA bioequivalence guideline were satisfied, indicating Cadilan tablet 12.5 mg was bioequivalent to $Dilatrend^{(R)}$ tablet 12.5 mg.

키워드

참고문헌

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피인용 문헌

  1. Preparation and Dissolution Properties of Oral Controlled Release Formulation Containing Carvedilol vol.11, pp.7, 2010, https://doi.org/10.5762/KAIS.2010.11.7.2451