적혈구내 비용혈 약물봉입과 약물방출

Nonhemolytic entrapping method into red blood cells and its release pattern

  • 함성호 (원광대학교 의약자원연구센타, 약학대학) ;
  • 고건일 (원광대학교 의약자원연구센타, 약학대학) ;
  • 김재백 (원광대학교 의약자원연구센타, 약학대학) ;
  • 손동환 (원광대학교 의약자원연구센타, 약학대학)
  • Ham Seong ho (Medicinal Resources Research Center, and College of Pharmacy, Wonkwang University) ;
  • Ko Geon Il (Medicinal Resources Research Center, and College of Pharmacy, Wonkwang University) ;
  • Kim Jae Baek (Medicinal Resources Research Center, and College of Pharmacy, Wonkwang University) ;
  • Sohn Dong Hwan (Medicinal Resources Research Center, and College of Pharmacy, Wonkwang University)
  • 발행 : 1995.12.01

초록

Drug delivery by red cells was established to maintain the release of drugs in the blood. The entrapment method by amphotericin B was re-examined and evaluated for obtaining the suitable entrapping conditions without hemolysis. The amphotericin B treatment below $10{\mu}g/ml$ induced the non-hemolysis to entrap daunorubicin into red cells within 10min. Under these conditions intracellular ATP level was decreased as $18\%$. Membrane fluidity and the shape factor of red cells were maintained. To maintain intracellular ATP, ATP and sodium pyruvate were added during the entrapment procedure because hemolysis during the release test would reflect the loss of intracellular ATP that would be postulate the decrease of the viability invivo. Consequently, the addition of ATP in the reaction solution can raise the intracellular level of ATP.

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