Surface modification of poly(lactide-co-glycolide) nanospheres by biodegradable poly(lactide)-poly(ethylene glycol) copolymers

• Published in: Pharmaceutical research Vol. 11; no. 12; p. 1800
• Main Authors: Stolnik, S, Dunn, S E, Garnett, M C, Davies, M C, Coombes, A G, Taylor, D C, Irving, M P, Purkiss, S C, Tadros, T F, Davis, S S
• Format: Journal Article
• Language: English
• Published: United States 01.12.1994
• Subjects: Animals; Chromatography; Drug Stability; Hydrogen-Ion Concentration; Lactates - administration & dosage; Lactates - pharmacology; Lactic Acid; Polyethylene Glycols - administration & dosage; Polyethylene Glycols - pharmacology; Polyglycolic Acid; Polylactic Acid-Polyglycolic Acid Copolymer; Polymers - chemistry; Polymers - pharmacokinetics; Rats; Rats, Wistar; Tissue Distribution
• ISSN: 0724-8741; 1573-904X
• DOI: 10.1023/a:1018931820564

The modification of surface properties of biodegradable poly(lactide-co- glycolide) (PLGA) and model polystyrene nanospheres by poly(lactide)-poly(ethylene glycol) (PLA:PEG) copolymers has been assessed using a range of in vitro characterization methods followed by in vivo studies of the nanospheres biodistribution after intravenous injection into rats. Coating polymers with PLA:PEG ratio of 2:5 and 3:4 (PEG chains of 5000 and 2000 Da. respectively) were studied. The results reveal the formation of a PLA:PEG coating layer on the particle surface resulting in an increase in the surface hydrophilicity and decrease in the surface charge of the nanospheres. The effects of addition of electrolyte and changes in pH on stability of the nanosphere dispersions confirm that uncoated particles are electrostatically stabilized, while in the presence of the copolymers, steric repulsions are responsible for the stability. The PLA:PEG coating also prevented albumin adsorption onto the colloid surface. The evidence that this effect was observed for the PLA:PEG 3:4 coated nanospheres may indicate that a poly(ethylene glycol) chain of 2000 Da can provide an effective repulsive barrier to albumin adsorption. The in vivo results reveal that coating of PLGA nanospheres with PLA:PEG copolymers can alter the biodistribution in comparison to uncoated PLGA nanospheres. Coating of the model polystyrene nanospheres with PLA:PEG copolymers resulted in an initial high circulation level, but after 3 hours the organ deposition data showed values similar to uncoated polystyrene spheres. The difference in the biological behaviour of coated PLGA and polystyrene nanospheres may suggest a different stability of the adsorbed layers on these two systems.