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作 者:徐缓[1] 尹朋朋[1] 于涛[1] 张伟[1] 王凯乾 邓意辉[3]
机构地区:[1]辽宁师范大学化学化工学院,辽宁大连116029 [2]大连富生天然药物开发有限公司,辽宁大连116600 [3]沈阳药科大学药学院,沈阳110016
出 处:《中国药房》2013年第1期57-60,共4页China Pharmacy
基 金:国家自然科学基金资助项目(No.81102394)
摘 要:目的:制备聚(2-乙基-2-噁唑啉)(PEOZ)修饰超氧化物歧化酶(SOD)模拟物脂质体的冻干制剂。方法:通过考察预冻方式、预冻时间、真空干燥时间及联合冻干保护剂的种类及比例等优化冻干工艺,并测定所制制剂的水化复溶时间、粒径和包封率。结果:以10%乳糖+1%甘露醇+10%海藻糖作为联合冻干保护剂,并以外加方式加入PEOZ修饰SOD模拟物脂质体中,快速冷冻5h,真空干燥30h,可得到外观光洁、平整的目标冻干制剂;其水化复溶时间为(10±1)s,粒径为(159.3±10.2)nm,包封率为86.25%(RSD=3.26%,n=6)。结论:该优化冻干工艺质量可控,重复性好。OBJECTIVE:To prepare freeze-dried preparation of poly(2-ethyl-2-oxazoline)(PEOZ)modified Superoxide dismutase(SOD)mimics liposomes.METHODS:The freeze-dried process of liposomes was investigated by investigating pre-freezing pattern,pre-freezing time,vacuum drying time,types and proportion of cryoprotectants.Re-dissolved time,particle size and entrapment efficiency of preparation were determined.RESULTS:The optimal technology:10% lactose+1% mannitol+10% trehalose as cryoprotectants were added into PEOZ modified SOD mimics liposomes,with rapid freezing for 5 h and vacuum drying for 30 h.The lyophilized preparation was prepared with smooth and complete appearance.Re-dissolved time was(10±1)s,particle size was(159.3±10.2)nm and entrapment efficiency was 86.25%(RSD=3.26%,n=6).CONCLUSION:The lyophilized technology is controllable in quality and reproducible.
关 键 词:聚(2-乙基-2-噁唑啉) 超氧化物歧化酶模拟物 脂质体 冻干保护剂 冻干制剂 包封率
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