Polymerized solid lipid nanoparticles for oral or mucosal delivery of therapeutic proteins and peptides

作者: Kollipara Koteswara Rao

DOI:

关键词:

摘要: The present invention encompasses lipid nano/micro particles, which have been modified, preferably on their surface, to contain a molecule or ligand, targets the particles specific site. also use of modified for oral delivery drugs and antigen systems.

参考文章(7)
Alberto Bernareggi, Paolo Gasco, Maria Rosa Gasco, Nanoparticle formulations of platinum compounds ,(2005)
Yelena V. Grinkova, Timothy H. Bayburt, Natanya R. Civjan, Mary A. Schuler, Stephen James Grimme, Ilia G. Denisov, Stephen G. Sligar, Membrane scaffold proteins ,(2005)
Ashwath Jayagopal, Eric Sussman, V. Prasad Shastri, Functionalized solid lipid nanoparticles and methods of making and using same ,(2005)
Na Zhang, Qi N. Ping, Gui H. Huang, Wen F. Xu, Investigation of lectin-modified insulin liposomes as carriers for oral administration. International Journal of Pharmaceutics. ,vol. 294, pp. 247- 259 ,(2005) , 10.1016/J.IJPHARM.2005.01.018
Na Zhang, Qineng Ping, Guihua Huang, Wenfang Xu, Yanna Cheng, Xiuzhen Han, Lectin-modified solid lipid nanoparticles as carriers for oral administration of insulin. International Journal of Pharmaceutics. ,vol. 327, pp. 153- 159 ,(2006) , 10.1016/J.IJPHARM.2006.07.026