Synthesis of Pegylated Immunonanoparticles
暂无分享,去创建一个
H. Lee | F. Calon | W. Pardridge | J. Olivier | R. Huertas
[1] D. Putnam,et al. Poly(lactic acid)-poly(ethylene glycol) nanoparticles as new carriers for the delivery of plasmid DNA. , 2001, Journal of controlled release : official journal of the Controlled Release Society.
[2] パードリッジ、ウィリアム、エム.. Non-invasive gene targeting to the brain , 2001 .
[3] C Vigneron,et al. Protein C-loaded monomethoxypoly (ethylene oxide)-poly(lactic acid) nanoparticles. , 2001, International journal of pharmaceutics.
[4] Masao Kato,et al. Sugar-Installed Polymer Micelles: Synthesis and Micellization of Poly(ethylene glycol)−Poly(d,l-lactide) Block Copolymers Having Sugar Groups at the PEG Chain End , 1999 .
[5] S. Stolnik,et al. COLLOIDAL STABILITY AND DRUG INCORPORATION ASPECTS OF MICELLAR-LIKE PLA-PEG NANOPARTICLES , 1999 .
[6] D. Bazile,et al. Comparison of the safety profiles of PLA50 and Me.PEG-PLA50 nanoparticles after single dose intravenous administration to rat , 1999 .
[7] Ruxandra Gref,et al. Protein encapsulation within polyethylene glycol-coated nanospheres. I. Physicochemical characterization. , 1998, Journal of biomedical materials research.
[8] A. Petit,et al. Protein encapsulation in biodegradable amphiphilic microspheres. I. Polymer synthesis and characterization and microsphere elaboration , 1998 .
[9] Anderson,et al. Biodegradation and biocompatibility of PLA and PLGA microspheres. , 1997, Advanced drug delivery reviews.
[10] J. Huwyler,et al. Receptor mediated delivery of daunomycin using immunoliposomes: pharmacokinetics and tissue distribution in the rat. , 1997, The Journal of pharmacology and experimental therapeutics.
[11] Robert Langer,et al. PEG-coated nanospheres from amphiphilic diblock and multiblock copolymers: Investigation of their drug encapsulation and release characteristics1 , 1997 .
[12] C. Booth,et al. Association and surface properties of diblock copolymers of ethylene oxide and DL-lactide in aqueous solution , 1997 .
[13] J. Huwyler,et al. Brain drug delivery of small molecules using immunoliposomes. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[14] R. Müller,et al. The controlled intravenous delivery of drugs using PEG-coated sterically stabilized nanospheres. , 1995, Advanced drug delivery reviews.
[15] Michel Veillard,et al. Non-stealth (poly(lactic acid/albumin)) and stealth (poly(lactic acid-polyethylene glycol)) nanoparticles as injectable drug carriers , 1995 .
[16] W. Pardridge,et al. Vector-mediated delivery of a polyamide ("peptide") nucleic acid analogue through the blood-brain barrier in vivo. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[17] D. Bazile,et al. Stealth Me.PEG-PLA nanoparticles avoid uptake by the mononuclear phagocytes system. , 1995, Journal of pharmaceutical sciences.
[18] W. Pardridge,et al. Use of neutral avidin improves pharmacokinetics and brain delivery of biotin bound to an avidin-monoclonal antibody conjugate. , 1994, The Journal of pharmacology and experimental therapeutics.
[19] V. Torchilin,et al. Biodegradable long-circulating polymeric nanospheres. , 1994, Science.
[20] W. Pardridge,et al. Transport of recombinant CD4 through the rat blood-brain barrier in vivo. , 1992, The Journal of pharmacology and experimental therapeutics.
[21] A. Gabizon,et al. Sterically stabilized liposomes: improvements in pharmacokinetics and antitumor therapeutic efficacy. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[22] G. Spenlehauer,et al. Interactions of poly(lactic acid) and poly(lactic acid-co-ethylene oxide) nanoparticles with the plasma factors of the coagulation system. , 1997, Biomaterials.
[23] W. Simons. The Sadtler handbook of proton NMR spectra , 1978 .