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固体脂质纳米粒作为药物载体的研究进展 被引量:5

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机构地区 湖南省儿童医院
出处 《医学临床研究》 CAS 2008年第9期1701-1704,共4页 Journal of Clinical Research
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参考文献20

  • 1Mehnert W, Mader K. Solid lipid nanopartictes: Production, characterization and applications[J]. Adv Drug Del Rev, 2006,47(2-3) : 165-196.
  • 2Wrte G, Siekmann B, Bunjes H. Effect of drug loading on the transformation of vesicular into cubic nanopartictes during heat treatment of aqueous monootein/potoxame dispersions [J]. Fur J Pharm Biopharm , 2006, 63:128-133.
  • 3毛世瑞,王燕芝,纪宏宇,毕殿洲.微乳化技术制备固体脂质纳米粒[J].药学学报,2003,38(8):624-626. 被引量:38
  • 4Hu FQ, Hong Y; Yuan H. Preparation and charaterization of solid lipid nanopartictes containning peptide [ J]. Int J Pharm , 2006,273(2) : 29-35.
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  • 7Oner M,Wissing SA,Yener G, et al . Influence of surfactants on the physical stability of solid lipid nanoparticte(SLN)formulations[J]. Pharmazie ,2004,59(4) :331-338.
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二级参考文献29

  • 1王平全,陆国红,周贤飚,沈金芳,陈曙霞,梅尚文,陈美芳.苦参碱的人体药代动力学[J].药学学报,1994,29(5):326-329. 被引量:24
  • 2郭涛,储晓琴,宋洪涛,邓意辉,何进,孙学惠,颜鸣.静脉注射用大蒜油亚微乳的制备[J].中国药学杂志,2005,40(8):602-605. 被引量:17
  • 3何进,赵庆春,毕殿洲,刘宝庆.GC法测定大蒜油β─环糊精包合物中的大蒜素含量[J].药物分析杂志,1996,16(6):387-389. 被引量:15
  • 4庆慧.大蒜降血脂抗动脉粥样硬化的研究进展[J].中医研究,1997,10(1):50-52. 被引量:2
  • 5[1]Muller RH, Mehnert W, Lucks JS, et al. Solid lipid nanoparticles(SLN)-an alternative colloidal carrier system for controlled drug delivery [J]. Eur J Pharm Biopharm, 1995,41(1):62-69.
  • 6[2]De Vringer T, de Ronde HAG. Preparation and structure of a water-in-oil cream containing lipid nanoparticles [J]. J Pharm Sci, 1995,84(4):466-472.
  • 7[3]Schwarz C, Mehnert W, Lucks JS, et al. Solid lipid nanoparticles (SLN) for controlled drug delivery. I. Production, characterization and sterilization [J]. J Controlled Release, 1994,30(1):83-96.
  • 8[4]Yang SC, Lu LF, Cai Y, et al. Body distribution in mice of intraveneously injected camptothecin solid lipid nanoparticles and targeting effect on brain [J]. J Controlled Release, 1999,59(3):299-307.
  • 9[5]Annette M, Schwarz C, Mehnert W. Solid lipid nanoparticles(SLN) for controlled drug delivery-drug release and release mechanism [J]. Eur J Pharm Biopharm, 1998,45(2):149-155.
  • 10[6]Gasco MR. Method for producing solid lipid microspheres having a narrow size distribution [P]. US Pat: 5250236,1993-10-05.

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二级引证文献24

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