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环糊精-药物复合纳米粒子的制备及其控制释放研究进展 被引量:7

Research Advance in Preparation of Nanoparticles Based on Cyclodextrins and Their Applications in Controlled Drug Release Behaviors
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摘要 从直接法、小分子键合、星形、树枝状和超支化环糊精大分子胶束及水凝胶、超分子组装7方面论述了环糊精-药物纳米复合体的制备,认为扩散控制、溶胀控制和化学控制是环糊精-药物纳米复合体主要的释放机理。结合释放机理,指出具有超分子结构的复合体系可望成为智能靶向释放领域的主导。 The preparation of CDs-drug nanoparticle is summarized from aspects including non-covalent inclusion, covalent conjugate, micelles inclusion of CDs polymer and supramolecular assembly in nano size. Star-shape, dendritic and hyperbranched-CD polymers and CD hydrogel-drug inclusions are described in details. Mechanism of drug controlled release is elucidated in diffusion, target controlled and swelling controlled routes. Combination to drug release mechanisms, CDs-drug complexes integrated supramolecular structure is desired to guide in smart target controlled release.
出处 《材料导报》 EI CAS CSCD 北大核心 2010年第5期136-140,共5页 Materials Reports
基金 国家自然科学基金(基金号20674060)
关键词 环糊精 纳米粒子 药控释放 两亲性 包合 cyclodextrins, nanoparticles, drug controlled release, amphiphilicity, inclusion
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参考文献48

  • 1Helena Dodziuk. Cyclodextrins and their complexes [M]. Weinheim: Wiley Vch Verlag Gmbh & Co. Kgaa, 2006 : 31.
  • 2Jun Li, Xian Jun Loh. Cyelodextrin-based supramolecular architectures: Syntheses, structures, and applications for drug and gene delivery[J]. Adv Drug Delivery Rev, 2008,60 (9) :1000.
  • 3Breslow R,Yang Z, Ching R, et al. Sequence selective binding of peptides by artificial receptors in aqueous solution[J]. J Am Chem Soc,1998,120(14):3536.
  • 4Hirayama F, et al. Cyclodextrin-based controlled drug release system [J]. Adv Drug Delivery Rev, 1999,36(1):125.
  • 5Kumaresh S Soppimath, et al. Microspheres as floating drugdelivery systems to increase gastric retention of drugs [J]. Drug Metab Rev, 2001, 33(2): 149.
  • 6Costas Kaparissides, et al. Recent advances in novel drug delivery systems [J]. J Nano Online, 2006, 2:1.
  • 7Dominique Duchene, Gilles Ponchel, Denis Wouessidjewe, et al. Cyclodextrins in targeting application to nanoparticles [J]. Adv Drug Delivery Rev, 1999, a6(1) :29.
  • 8Lemos-Senna E, Wouessidjewe D, Lesieur S, et al. Preparation of amphiphilie eyelodextrin nanospheres using the emulsification solvent evaporation method. Influence of the surfactant on preparation and hydrophobic drug loading [ J]. Int J Pharm, 1998,170(1) :119.
  • 9Erem Memisoglu, et al. Non-surfactant nanospheres of progesterone inclusion complexes with amphiphilic β-cyclodextrins [J]. Inte J Pharm,2003,251(1-2): 143.
  • 10Erem Memisoglu, Bilensoy A, Atilla Hincal. Sterile, injectable cyclodextrin nanoparticles: Effects of gamma irradiation and autoclaving [J]. Int J Pharm, 2006 , 311(1-2) : 203.

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