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오메프라졸과 $gamma$-시클로덱스티린과의 복합체 형성 및 제제학적 특성
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  • 오메프라졸과 $gamma$-시클로덱스티린과의 복합체 형성 및 제제학적 특성
  • Interaction between Omeprazole and $gamma$-Cyclodextrin
저자명
이계주,김은영
간행물명
약학회지
권/호정보
1995년|39권 2호|pp.175-184 (10 pages)
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대한약학회
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정기간행물|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

The interaction of omeprazole(OMP) with $gamma$-cyclodextrin($gamma$-CyD) was investigated by solubility study and the complexation was confirmed by means of UV/VIS spectrophotometer, circular dichroism, differential scanning calorimeter, and $^{1}$H nuclear magnetic resonance spectra. The stability, dissolution rate, and partition coefficient of the complex were measured. The results present that the benzimidazole moiety and a part of pyridine ring containing sulfur atom of OMP might be included into the cavity of $gamma$-CyD and the formation type of inclusion complex appeared to be B$_{s}$. The stoichiometric ratio of OMP to $gamma$-CyD in the complex was found to be 1:1 and the stability constant of the complex found to be 97.1 M$^{-1}$. And the dissolution rate of OMP was markedly increased by inclusion complex formation with $gamma$-CyD, and so it was above 90% in 5 min. from solid complex. Oil to water partition coefficient of OMP-$gamma$-CyD complex was 60, which is significantly higher than that of OMP itself, 36.4. The degradation rate constant of OMP were greater than OMP-$gamma$-CyD complex in aqueous solutions of various pHs, and the half lives of OMP and OMP-$gamma$-CyD at pH 9 were 279.2 and 509.9 days, respectively, showing that the complex was more stable than OMP, therefore it was thought that OMP was stabilized by inclusion formation with $gamma$-CyD.