Microfluidically Produced Microcapsules with Amphiphilic Polymer Conetwork Shells

Author:

Velasquez Sara T. R.123ORCID,Belluati Andrea12ORCID,Tervoort Elena4ORCID,Mattich Iacopo4ORCID,Hertel Brigitte5,Russell Sam123ORCID,Gouveia Micael G.23ORCID,Grysan Patrick6ORCID,Mugemana Clément67ORCID,Studart André R.34ORCID,Bruns Nico123ORCID

Affiliation:

1. Department of Chemistry Technical University of Darmstadt Peter‐Grünberg‐Straße 4 64287 Darmstadt Germany

2. Department of Pure and Applied Chemistry University of Strathclyde Thomas Graham Building, 295 Cathedral Street Glasgow G1 1XL UK

3. Swiss National Center of Competence in Research Bio‐Inspired Materials Fribourg Switzerland

4. Complex Materials Department of Materials ETH Zürich Vladimir‐Prelog‐Weg 5 Zürich 8093 Switzerland

5. Department of Biology Technical University of Darmstadt Schnittspahnstraße 3 64287 Darmstadt Germany

6. Materials Research and Technology Luxembourg Institute of Science and Technology 5 Avenue des Hauts‐Fourneaux Esch‐sur‐Alzette L‐4362 Luxembourg

7. Adolphe Merkle Institute University of Fribourg Chemin des Verdiers 4 Fribourg 1700 Switzerland

Abstract

AbstractMicrocapsules with an aqueous core can be conveniently prepared by water‐in‐oil‐in‐water double emulsion microfluidics. However, conventional shell materials are based on hydrophobic polymers or colloidal particles. Thus, these microcapsules feature a hydrophobic shell impermeable to water‐soluble compounds. Capsules with semipermeable hydrogel shells have been demonstrated but may exhibit poor mechanical properties. Here, amphiphilic polymer conetworks (APCNs) based on poly(2‐hydroxyethyl acrylate)‐linked by‐polydimethylsiloxane (PHEA‐l‐PDMS) are introduced as a new class of wall materials in double emulsion microcapsules. These APCNs are mechanically robust silicone hydrogels that are swellable and permeable to water and are soft and elastic when dry or swollen. Therefore, the microcapsules can be dried and rehydrated multiple times or shrunken in sodium chloride salt solutions without getting damaged. Moreover, the APCNs are permeable for hydrophilic organic compounds and impermeable for macromolecules. Thus, they can be loaded with macromolecules or nanoparticles during microfluidic formation and with organic molecules after capsule synthesis. The microcapsules serve as microreactors for catalytically active platinum nanoparticles that decompose hydrogen peroxide. Finally, the surface of the APCN microcapsules can be selectively functionalized with a cholesterol‐based linker. Concluding, APCN microcapsules could find applications for the controlled delivery of drugs, as microreactors for synthesis, or as scaffolds for synthetic cells.

Funder

National Science Foundation

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Wiley

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