Distinct endocytosis and immune activation of poly(lactic-co-glycolic) acid nanoparticles prepared by single- and double-emulsion evaporation

Author:

Pusch Lennart1ORCID,Brox Regine1ORCID,Scheuer Karl2ORCID,Yokosawa Tadahiro3ORCID,Wu Mingjian3ORCID,Zubiri Benjamin Apeleo3ORCID,Spiecker Erdmann3ORCID,Jandt Klaus D.24ORCID,Fischer Dagmar5ORCID,Hackstein Holger1ORCID

Affiliation:

1. Department of Transfusion Medicine & Hemostaseology, University Hospital Erlangen, Krankenhausstraße 12, Erlangen, 91054, Germany

2. Department of Materials Science & Technology, Otto Schott Institute of Materials Research, Friedrich Schiller University Jena, Löbdergraben 32, Jena, 07743, Germany

3. Institute of Micro- & Nanostructure Research (IMN) & Center for Nanoanalysis & Electron Microscopy (CENEM), Interdisciplinary Center for Nanostructured Films (IZNF), Friedrich-Alexander-University Erlangen-Nürnberg, Cauerstraße 3, Erlangen, 91058, Germany

4. Jena Center for Soft Matter (JCSM), Friedrich Schiller University Jena, Philosophenweg 7, Jena, 07743, Germany

5. Friedrich-Alexander-University Erlangen-Nürnberg, Cauerstraße 4 (Haus 6), Erlangen, 91058, Germany

Abstract

Background: Poly(lactic-co-glycolic) acid (PLGA) nanoparticles can be prepared by emulsion-solvent-evaporation from o/w and w1/o/w2 emulsions. Aims: To elaborate similarities and differences regarding mechanical, morphological and physicochemical properties, as well as endocytosis and dose-dependent immune responses by primary human leukocytes between nanoparticles prepared by these two methods. Methods: Fluorescently labeled as well as TLR agonist (R848)-loaded PLGA nanoparticles were prepared via both single- and double-emulsion solvent evaporation. Results: Particles prepared by both methods were similar in chemical composition and surface charge but exhibited slight differences in size and morphology. Pronounced differences were found for loading, dissolution and mechanical properties. The particles were differently endocytosed by monocytes and induced qualitatively and quantitatively different immune responses. Conclusions: Variations in nanoparticle preparation can affect particle-derived immunological characteristics.

Funder

SFB Transregio 94 “Innate Immunity of the lung”

Collaborative Research Center SFB 1278 “PolyTarget”

Deutsche Forschungsgemeinschaft

Publisher

Future Medicine Ltd

Subject

Development,General Materials Science,Biomedical Engineering,Medicine (miscellaneous),Bioengineering

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