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作 者:董晓东[1] 邓英杰[1] 陈超[1] 曹永仓[1] 崔丽莉[1] 王晓宇[1]
出 处:《中国新药杂志》2010年第12期1075-1079,共5页Chinese Journal of New Drugs
基 金:国家自然科学基金(30672555)
摘 要:目的:制备灯盏花素阳离子脂质体和普通脂质体并对其相关性质进行考察。方法:采用薄膜分散法制备灯盏花素脂质体;以包封率为指标,通过正交试验对处方进行优化。考察灯盏花素普通脂质体和阳离子脂质体的体外释放行为。结果:制备的灯盏花素阳离子脂质体性质稳定,包封率为(76.42±1.973)%,平均粒径为(186±35)nm,Zeta电位为(48.9±9.83)mV。灯盏花素普通脂质体和阳离子脂质体的释放过程的拟合方程分别为lnln[1/(1-Q)]=0.7797lnt-2.3187(r=0.9739)和lnln[1/(1-Q)]=0.3553lnt-3.197(r=0.9899)。结论:确定了最优处方,制备得到包封率较高且状态稳定的灯盏花素阳离子脂质体。Objective:To prepare breviscapine cationic liposomes and ordinary liposomes,optimize the formulation and investigate characteristics of the liposomes. Methods:The breviscapine liposomes were prepared by thin-film dispersion method. With the entrapment efficiencies as references,the formulation was optimized by the orthogonal design. The in vitro release profiles of the liposomes were determined. Results:The prepared cationic liposomes were stable with the mean size of (186±35) nm,the Zeta potential of (48.9±9.83) mV and the entrapment efficiencies (76.42±1.973)%. The fitting equations of the release profiles of both kinds of liposomes were lnln^[1/(1-Q)]=0.779 7ln^t-2.318 7(r=0.973 9) and lnln^[1/(1-Q)]=0.355 3ln^t-3.197(r=0.989 9),relatively. Conclusions:We have optimized formulation and obtained the stable and uniform breviscapine cationic liposomes.
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