Preparing Method and Physico-chemical Characteristics of $Terfenadine-{\beta}-Cyclodextrin$ Inclusion Compound

테르페나딘-${\beta}$-시클로덱스트린 포접화합물의 제조방법 및 물리화학적 특성

  • Choi, Han-Gon (Central Research Laboratories, Dong-Wha Pharm. Ind., LTD.) ;
  • Ryu, Jei-Man (Central Research Laboratories, Dong-Wha Pharm. Ind., LTD.) ;
  • Yoon, Sung-June (Central Research Laboratories, Dong-Wha Pharm. Ind., LTD.)
  • 최한곤 (동화약품공업 (주) 중앙연구소) ;
  • 유제만 (동화약품공업 (주) 중앙연구소) ;
  • 윤성준 (동화약품공업 (주) 중앙연구소)
  • Published : 1997.09.20

Abstract

Terfenadine, antihistaminic drug, is poorly soluble in water. The purpose of this study is to investigate the possibility of using $terfenadine-{\beta}-cyclodextrin$ inclusion compound, instead of terfenadine, as the active substance of solid dosage form by improving the solubility, dissolution and anti-histaminic activity of terfenadine. The solubility and binding characteristics of $terfenadine-{\beta}-cyclodextrin$ complex in pH $1.2{\sim}6.8$ were investigated. Furthermore, the preparing method of $terfenadine-{\beta}-\;cyclodextrin$ inclusion compound was setting up and its physico-chemical characteristics such as DSC curve, solubility, dissolution and anti-histaminic activity were investigated. In conclusion, the solubility of terfenadine was increasing ${\beta}-cyclodextrin$ and with the decreasing pH. $Terfenadine-{\beta}-cyclodextrin$ inclusion compound, whose yield is almost 100%, was prepared by neutralization method. This inclusion compound was 200-times as soluble as terfenadine in pH 1.2-6.8. In addition, it had the faster dissolution and anti-histaminic activity than terfenadine. Therefore, it is used to the active substance of solid dosage form such as tablet and capsule in stead of terfenadine.

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