全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
海洋科学  2006 

壳聚糖在药物缓释中的研究进展

, PP. 85-89

Full-Text   Cite this paper   Add to My Lib

Abstract:

References

[1]  石玲,胡利平,孙秀珍.壳聚糖的安全性研究[J].中国海洋药物,2000,19(1):25-28.
[2]  曾名勇.几种甲壳质衍生物在医药上的应用[J].中国海洋药物,1995,14(1):49-52.
[3]  Liu L S,Liu S Q,Ng S Y,et al.Controlled release of interleukin-2 for tumour immunotherapy using alginate/chitosan porous microspheres[J].Journal of Controlled Release,1997,43(1):65-74.
[4]  Jameela S R,Kumary T V,Lal A V,et al.Progesterone-loaded chitosan microspheres:a long acting biodegradable controlled delivery system[J].Journal of Controlled Release,1998,52(1-2):17-24.
[5]  Hejazi R,Amiji M.Stomach-specific anti-H pylori therapy Ⅰ:preparation and characterization of tetracycline-loaded chitosan microspheres[J].International Journal of Pharmaceutics,2002,235(1-2):87-94.
[6]  Mi F L,Shyu S S,Chen C T,et al.Porous chitosan microsphere for controlling the antigen release of Newcastle disease vaccine:preparation of antigen-absorbed microspheres and in vitro release[J].Biomaterials,1999,20(17):1 603-1 612.
[7]  Ganza-González A,Anguiano-Igea S,Otero-Espinar G J,et al.Chitosan and chondroitin microspheres for oral-administration controlled release of metoclopramide[J].European Journal of Pharmaceutics and Biopharmaceutics,1999,48(2):149-155.
[8]  Alonso M J,Vila-Jato J L.Development of new chitosan-cellulose multicore microparticles for controlled drug delivery[J].European Journal of Pharmaceutics and Biopharmaceutics,1998,45:49-56.
[9]  Jameela S R,Jayakrishnan A.Glutaraldehyde cross-linked chitosan microspheres as a long acting biodegradable drug delivery vehicle:studies on the in vitro releases of mitoxantrone and in vivo degradation of microspheres in rat muscle[J].Biomaterials,1995,16(10):769-775.
[10]  Conti B M,Genta I T.A proposed new method for the cross-linking of chitosan microsphere[J].Drug Delivery,1998,5(2):87.
[11]  Abd M D,Hameed E L,Kellaway I W.Preparation and in vitro characterization of mucoadhesive polymeric microspheres as intra-nasal delivery system[J].European Journal of Pharmaceutics and Biopharmaceutics,1997,44:53-60.
[12]  Genta I,Perugini P,Conti B,et al.A multiple emulsion method to entrap a lipophilic compound into chitosan microspheres[J].International Journal of Pharmaceutics,1997,152(2):237-246.
[13]  Berthold A,Cremer K,Kreuter J.Preparation and characterization of chitosan microspheres as drug carrier for prednisolone sodium phosphate as model for anti-inflammatory drugs[J].Journal of Controlled Release,1996,39(1):17-25.
[14]  He P,Davis S S,Illum L.Chitosan microspheres prepared by spruy drying[J].International Journal of Pharmaceutics,1999,187(1):53-65.
[15]  Huang Y C,Yeh M K,Chiang C H.Formulation factors in preparing BTM-chitosan microspheres by spray drying method[J].International Journal of Pharmaceutics,2002,242(1-2):239-242.
[16]  Mi F L,Wong T B,Shyu S S,et al.Chitosan microspheres:modification of polymeric chem-physical properties of spray-dried microspheres to control the release of antibiotic drug[J].Journal of Applied Polymer Science,1999,71:747-759.
[17]  Ribeiro A J,Neufeld R J,Arnaud P,et al.Microencapsulation of lipophilic drugs in chitosan-coated alginate microspheres[J].International Journal of Pharmaceutics,1999,187(1):115-123.
[18]  Illum L,Jorgensen H,Bisgaard H,et al.Bioadhensive microspheres as a potential nasal drug delivery system[J].International Journal of Pharmaceutics,1987,39:189-199.
[19]  He P,Davis S S,Illum L.Chitosan microspheres prepared by spray drying method[J].European Journal of Pharmaceutical Sciences,1996,4(1):173.
[20]  梁桂媛,方华丰,刘志伟.5-氟尿嘧啶壳聚糖微球的制备[J].广东药学院学报,2000,16(1):7-10.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133