Bioequivalence of Terbina Tablet to Lamisil Tablet (Terbinafine 125 mg)

라미실 정(테르비나핀 125 mg)에 대한 터비나 정의 생물학적 동등성

  • Kim, Soo-Jin (College of Pharmacy and Research Institute of Drug Development, Chonnam National University) ;
  • Jeong, In-Seong (Pharmaceutical Manufacturing Team, Chong Kun Dang) ;
  • Cho, Hea-Young (College of Pharmacy and Research Institute of Drug Development, Chonnam National University) ;
  • Shim, Young-Sun (College of Pharmacy and Research Institute of Drug Development, Chonnam National University) ;
  • Jeong, Tae-Jin (College of Pharmacy and Research Institute of Drug Development, Chonnam National University) ;
  • Oh, In-Joon (College of Pharmacy and Research Institute of Drug Development, Chonnam National University) ;
  • Moon, Jai-Dong (Medical School, Chonnam National University) ;
  • Lee, Yong-Bok (College of Pharmacy and Research Institute of Drug Development, Chonnam National University)
  • 김수진 (전남대학교 약학대학/약품개발연구소) ;
  • 정인성 (종근당 제제팀) ;
  • 조혜영 (전남대학교 약학대학/약품개발연구소) ;
  • 심영순 (전남대학교 약학대학/약품개발연구소) ;
  • 정태진 (전남대학교 약학대학/약품개발연구소) ;
  • 오인준 (전남대학교 약학대학/약품개발연구소) ;
  • 문재동 (전남대학교 의과대학) ;
  • 이용복 (전남대학교 약학대학/약품개발연구소)
  • Published : 2000.06.20

Abstract

Terbinafine is an orally active antifungal agent as it inhibits the fungal enzyme squalene epoxidase, which is important in the early biosynthetic pathway of ergosterol. This leads to abnormal development of the fungal cell membrane. Bioequivalence of two terbinafine tablets, $Lamisil^{TM}$ (Novartis Korea Ltd.) and $Terbina^{TM}$ (Korean Drug Co., Ltd.), was evaluated according to the guidelines of Korea Food and Drug Administration (KFDA). Sixteen normal male volunteers, $23.56{\pm}1.75$ years old and $65.60{\pm}8.54\;kg$ of body weight, were divided into two groups and a randomized $2{\times}2$ cross-over study was employed. After one tablet containing 125 mg of terbinafine was orally administered, blood was taken at predetermined time intervals and the serum concentrations of terbinafine were determined using an HPLC method with UV detector. The pharmacokinetic parameters $(AUC_t,\;C_{max}\;and\;T_{max})$ were calculated and ANOVA test was utilized for the statistical analysis of parameters. The results showed that the differences in $AUC_t,\;C_{max}\;and\;T_{max}$ between two tablets based on $Lamisil^{TM}$, tablet were -2.53%, -2.98% and 8.13%, respectively. The powers $(1-{\beta})$ for $AUC_t,\;C_{max}\;and\;T_{max}$ were 85.21%, 98.21% and 93.11%, respectively. Minimum detectable differences $({\Delta})$ at ${\alpha}=0.1\;and\;1-{\beta}=0.8$ were all less than 20%. The 90% confidence intervals were all within ${\pm}20%$. All the parameters above met the criteria of KFDA for bioequivalence, indicating that $Terbina^{TM}$ tablet is bioequivalent to $Lamisil^{TM}$ tablet.

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