Surface modification of PLGA particles : the interplay between stabilizer, ligand size, and hydrophobic interactions

Therapeutic and diagnostic carriers can be functionalized with active targeters to induce tissue-specific delivery. However, the possible impact of adsorbed steric stabilizer such as the frequently used poloxamers (Pluronics) on surface modification of poly(D,L-lactide-co-glycolide) (PLGA) particles...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 26(2010), 3 vom: 02. Feb., Seite 1855-9
1. Verfasser: Ratzinger, Gerda (VerfasserIn)
Weitere Verfasser: Länger, Ursula, Neutsch, Lukas, Pittner, Fritz, Wirth, Michael, Gabor, Franz
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2010
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Fluorescent Dyes Immobilized Proteins Immunoglobulin G Ligands Poloxamer 106392-12-5 Polyglactin 910 34346-01-5 Cadaverine mehr... L90BEN6OLL Fluorescein TPY09G7XIR
Beschreibung
Zusammenfassung:Therapeutic and diagnostic carriers can be functionalized with active targeters to induce tissue-specific delivery. However, the possible impact of adsorbed steric stabilizer such as the frequently used poloxamers (Pluronics) on surface modification of poly(D,L-lactide-co-glycolide) (PLGA) particles has not been examined so far. Therefore, three model ligands of different molecular weights (653; 36,000; 155,000 g/mol) covering the size range of important targeters were conjugated to the surface of PLGA microparticles in the presence of different concentrations of Pluronic F68 (0.01-5%, w/v). Flow cytometry and fluorimetric quantification revealed for all tested ligands that high Pluronic concentrations decreased the coupling efficiency to a half or even one-third of that achieved in the absence of stabilizer. Moreover, the reduction strongly depends on the ligand size and its propensity for hydrophobic interactions. Apart from that, a high degree of particle aggregation was observed with Pluronic concentrations below 0.1% (w/v). Thus, a compromise has to be found, which combines sufficient stability with the best possible ligand coupling efficiency. For the studied system, 0.1% (w/v) turned out to be the optimum concentration of Pluronic F68
Beschreibung:Date Completed 24.03.2010
Date Revised 19.11.2015
published: Print
Citation Status MEDLINE
ISSN:1520-5827
DOI:10.1021/la902602z