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跨膜梯度法制备羟苯磺酸铵-盐酸阿霉素脂质体 被引量:1

Loading of doxorubicin hydrochloride into liposomes by ammonium dobesilate transmembrane gradient method
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摘要 目的:以2,5-二羟基苯磺酸铵形成脂质体内外水相跨膜梯度,主动装载盐酸阿霉素。方法:以2,5-二羟基苯磺酸铵溶液为水化介质制备空白脂质体。通过透析法建立空白脂质体跨膜梯度。超滤法结合离子对-高效液相色谱法(IP-HPLC)测定空白脂质体外水相2,5-二羟基苯磺酸铵浓度。将已建立梯度的空白脂质体与盐酸阿霉素溶液50℃孵育20min制备盐酸阿霉素脂质体。结果:脂质体平均粒径约为106.4nm,包封率为28.54%。结论:可以通过建立2,5-二羟基苯磺酸铵跨膜梯度来制备盐酸阿霉素脂质体。 Objective Ammonium dobesilate was used to form transmembrane gradient to load doxorubicin hydrochloride (DOX) into liposomes. Methods:The lipid mixture was hydrated by 80 mmol·L-1 ammonium dobesilate to form liposomes. Ammonium dobesilate transmembrane gradient was obtained by dialysis method. The concentration of extraliposomal ammonium dobesilate was determined by ion-pair-HPLC method. The DOX solution was incubated with blank liposomes having transmembrane gradient at 50 ℃ for 20 minutes. Results:The average particle size of the liposomes was 106.4 nm. The entrapment efficiency of DOX liposomes determined by ultraviolet spectrophotometry was 28.54%. Conclusion:Ammonium dobesilate transmembrane gradient can be used to load DOX into liposomes.
出处 《中国药剂学杂志(网络版)》 2009年第4期260-265,共6页 Chinese Journal of Pharmaceutics:Online Edition
关键词 药剂学 脂质体 盐酸阿霉素 2 5-二羟基苯磺酸铵 跨膜梯度载药 pharmaceutics liposome doxorubicin hydrochloride ammonium dobesilate transmembrane gradient
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