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作 者:邱立朋[1] 杨磊[1] 龙苗苗[1] 刘颖[2] 王东凯[1] 周晖[2]
机构地区:[1]沈阳药科大学药学院,110016 [2]中国医科大学附属第一医院药剂科,沈阳110001
出 处:《医药导报》2012年第11期1471-1473,共3页Herald of Medicine
基 金:辽宁省沈阳市科学技术计划项目(1091174-1-01)
摘 要:目的考察注射用奥沙利铂纳米结构脂质载体(OP-NLC)冻干粉末处方及工艺。方法通过单因素实验优选冻干制剂的处方工艺,并评价其制剂学性质。结果以5%甘露醇溶液作为冻干保护剂,确定最终的冻干工艺。冻干后制剂粒径(124±16)nm,Zeta电位-10.8 mV,包封率67.3%,与冻干前[粒径(115±17)nm,Zeta电位-16.0 mV,包封率72.6%]相比,无明显变化。结论在优选的冻干工艺条件下可制得稳定的奥沙利铂纳米结构脂质载体冻干制剂。Objective To investigate the freeze-drying formulations of oxaliplatin in oxaliplatin-loaded nanostuctured lipid carriers(OP-NLC) for injection.Methods The optimum freeze-drying preparation and techniques were established by single factor experiments and the characters were evaluated.Results The optimal freeze-drying technology was determined with 5% of mannitol as protective agent.No significant changes were found in the mean particle size,Zeta potential and EE%,which were(124±16) nm versus(115±17) nm,-10.8 mV versus-16.0 mV,and 67.3% versus 72.6% post-and pre-freeze-drying,respectively.Conclusion The stable freeze-drying preparation of OP-NLC could be prepared under the optimal condition.
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