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注射用奥沙利铂纳米结构脂质载体冻干制剂的工艺优选 被引量:3

Optimization of Freeze-drying Process for Preparation of Oxaliplatin Loaded Nanostructured Lipid Carriers for Injection
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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.
出处 《医药导报》 CAS 北大核心 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)
关键词 奥沙利铂 纳米结构脂质载体 冻干保护剂 冻干制剂 Oxaliplatin Nanostructured lipid carriers Cryoprotectant Freeze-dried preparation
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  • 1Liu J, Hu W, Chen H B, et al. Isotretinoin-loaded solid lipidwith skin targeting for topical delivery [ J ]. Int J Pharm, 2007,328(2) :191-195.
  • 2KOBAYASHI Y, TAGAWA N, SAIKI K, et al. Studies on steroids in fetuses and neonates:identification of 16-dehy- dropregnenolone in the circulation of preterm neonates [ J ]. Biol Pharm Bull, 1994, 17 (11 ) :1501-1504.
  • 3LING Y Z,LI J S,KATO K,et al. Synthesis and in vitro ac- tivity of some epimeric 20 ct-hydroxy, 20-oxime and aziri- dine pregnene derivatives as inhibitors of human 17a- hydrxylase/C17,20-1yase and 5c-reductase [ J ]. Bioorg Med Chem, 1998, 6(10) :1683-1693.
  • 4PRATAP R, GUPTA R C, CHANDER R, et al. Method of treating hyperlipidemic and hyperglycemic conditions in mammals using pregnadienols and pregnadienones: EP, 99302556.8 [ P]. 2000-07-19.
  • 5SUN L X, FU W W, REN J, et al. Cytotoxic constituents from solanum lyratum [ J]. Arch Pharm Res, 2006, 29 (2) :135-139.
  • 6MA E L,ZHAO D M, LI Y C, et al. Activation of ATM- Chk2 by 16-dehydropregnenolone induces G1 phase arrest and apoptosis in HeLa cells [ J ]. J Asian Nat Prod Res, 2012,14(9) :817-825.
  • 7SURYAWANSHI S, WAHAJUDDIN, GUPTA R C, et al. Prechnical pharmacokinetics, dose proportionality, gender difference and protein binding study of 16-dehydropreg- nenolone, an antihyperlipidemic agent, in rats [ J ]. J Pharm Pharmaeol, 2011 , 63 ( 1 ) :41-48.
  • 8CHEN C J, HAND D, CAI C F, et al. An overview of li- posome lyophilization and its future potential [ J ]. J Control Release ,2010,142( 3 ) :299-311.
  • 9WANG T,WANG N, WANG T, et al. Preparation of submi- cron liposomes exhibiting efficient entrapment of drugs by freeze-drying water-in-oil emulsions [ J ]. Chem Phys Lip- ids,2011,164(2) :151-157.
  • 10谷东风,曾抗,李国锋,史毓杰,江中洪,杨莉.鬼臼毒素固体脂质纳米粒冻干粉的制备及理化性质考察[J].中国组织工程研究与临床康复,2008,12(10):1835-1838. 被引量:5

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