期刊文献+

基于合成高分子的纳米药物载体的研究进展 被引量:2

Research Progress of Polymer-Based Nanoparticle Drug Carriers
下载PDF
导出
摘要 基于合成高分子的纳米微粒由于其良好的生物相容性、生物可降解性和粘膜粘附性等特点成为药物载体研究的热点。根据构建纳米药物载体的高分子聚合物结构的差异,将其分为:基于两亲聚合物的纳米微粒(胶团和囊泡)、脂质体、树枝状或超支化大分子、乳液聚合纳米微粒,并对上述纳米微粒作为药物载体在近年来的研究进展进行了归纳和总结,展望了其在药物缓释体系中的广阔应用前景。 Polymer-based nanoparticles have attracted more and more attentions as drug carriers in recent years because of their good biocompatibility, biodegradability and mucoadhesive ability. According to the poly-mer structures,the nanoparticles were divided into four types, including amphiphilic polymer-based nanoparti-cles (micelles and polymersomes),liposomes, dendrimers and nanoparticles prepared by emulsion polymeriza-tion. And then the research progress of the application of these polymer-based nanoparticles as drug carriers was summarized. And the broad application prospect of these polymer-based nanoparticle drug carriers in the drug controlled release system was looked forward to.
出处 《化学与生物工程》 CAS 2013年第3期6-9,20,共5页 Chemistry & Bioengineering
基金 陕西省教育厅科研计划资助项目(11JK0694) 西安医学院博士科研启动基金资助项目(2011DOC05) 陕西省教育厅产业化培育项目(08JC18) 陕西省卫生厅科研资助项目(2012D14)
关键词 高分子 纳米载体 药物控制释放 polymer nanopartiele carrier drug Controlled release
  • 相关文献

参考文献34

  • 1von Vlerken L E,Vyas T K,Amiji M M. Poly (ethylene glycol)- modified nanocarriers for tumor-targeted and intracellular delivery [J]. Pharm Res,2007,24(8) :1405-1414.
  • 2Maeda H,Sawa T, Konno T. Mechanism of tumor-targeted deliv- ery of macromolecular drugs, including the EPR effect in solid tumor and clinical overview of the prototype polymeric drug SMANCS[J]. J Control Release,2001,74(1-3) :47-61.
  • 3Brigger I,Dubernet C,Couveur P. Nanoparticles in cancer therapy and diagnosis[J]. Adv Drug Deliv Rev, 2002,54(5) : 631-651.
  • 4Xing J, Zhang D, Tan T. Studies on the oridonin-loaded poly(D, L- lactic acid) nanoparticles in vitro and in vivo[J]. Int J Biol Macro- mol,2007,40(2) :153-158.
  • 5王建新,张志荣.固体脂质纳米粒的研究进展[J].中国药学杂志,2001,36(2):73-76. 被引量:62
  • 6latrou H, Frielinghaus H, Hanski S, et al. Architecturally induced multiresponsive vesicles from well-defined polypeptides. Forma- tion of gene vehicles[J]. Biomacromolecules, 2007,8 (7) : 2173- 2181.
  • 7Ghoroghchian P P, Li G Z, Levine D H, et al. Bioresorbable vesi- cles formed through spontaneous self-assembly of amphiphilic po- ly(ethylene oxide)-block-polycaprolactone[J]. Macromolecules, 2006,39 : 1673-1675.
  • 8Napoli A, Boerakker M J, Tirelli N, et al. Glucose-oxidase based self-destructing polymeric vesicles [J]. Langmuir, 2004, 20 ( 9 ) 3487-3491.
  • 9Yu L L,Lu C,Wu L Z,et al. Photosensitive cross-linked block co- polymers with controllable release[J]. Photochemistry and Photo- biology, 2011,87 (3) : 646-652.
  • 10Lee J C M,Discher D E. Deformation-enhanced fluctuations in the red cell skeleton with theoretical relations to elasticity, con- nectivity,and spectrin unfolding[J]. Biophysical Journal, 2001, 81(6) :3178-3192.

二级参考文献16

  • 1Maia C S,Int J Pharm,2000年,196卷,2期,165页
  • 2Jenning V M,J Control Release,2000年,66卷,23期,115页
  • 3Yang S,Pharmacal Res,1999年,16卷,5期,751页
  • 4Muhlen A,Eur J Pharm Biopharm,1998年,45卷,2期,149页
  • 5Kristl J,Farm Vestin,1997年,48卷,12期,123页
  • 6Almeida A J,Int J Pharm,1997年,149卷,2期,255页
  • 7Heiata H,Int J Pharm,1997年,146卷,1期,123页
  • 8Roberta C,Int J Pharm,1997年,148卷,1期,47页
  • 9Muller R H,Pharm Ind,1997年,59卷,5期,423页
  • 10Muller R H,Int J Pharm,1996年,144卷,11期,115页

共引文献61

同被引文献5

引证文献2

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部