Surface modification of nanoparticles by PEO/PPO block copolymers to minimize interactions with blood components and prolong blood circulation in rats
- 30 September 1993
- journal article
- Published by Elsevier in Biomaterials
- Vol. 14 (11), 823-833
- https://doi.org/10.1016/0142-9612(93)90004-l
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- A new class of drug carriers: micelles of poly(oxyethylene)-poly(oxypropylene) block copolymers as microcontainers for drug targeting from blood in brainJournal of Controlled Release, 1992
- Sterie stabilization of microspheres with grafted polyethylene oxide reduces phagocytosis by rat Kupffer cells in vitroBiomaterials, 1991
- Size Analysis of a Block Copolymer-Coated Polystyrene LatexPublished by American Chemical Society (ACS) ,1991
- The effect of adsorbed coats of poloxamers 237 and 338 on the in vitro aggregation and in vivo distribution of polystyrene latex (PSL) particlesInternational Journal of Pharmaceutics, 1990
- Adsorption of fibrinogen on to polystyrene latex coated with the non-ionic surfactant, poloxamer 338Biomaterials, 1988
- Lipid Emulsions as Drug Delivery SystemsAnnals of the New York Academy of Sciences, 1987
- Surface characteristics and the interaction of colloidal particles with mouse peritoneal macrophagesBiomaterials, 1987
- The influence of emulsifying agents on the phagocytosis of lipid emulsions by macrophagesInternational Journal of Pharmaceutics, 1984
- Hydrodynamic thickness of adsorbed polymer layersMacromolecules, 1984
- The organ uptake of intravenously administered colloidal particles can be altered using a non‐ionic surfactant (Poloxamer 338)FEBS Letters, 1984