Abstract

AbstractMicrocapsules are a key class of microscale materials with applications in areas ranging from personal care to biomedicine, and with increasing potential to act as extracellular matrix (ECM) models of hollow organs, tissues, or biomolecular condensates. Such capsules are conventionally generated from non‐ECM materials including synthetic polymers. Here, robust microcapsules with controllable shell thickness from physically‐ and enzymatically‐crosslinked gelatin are fabricated, and a core–shell architecture is achieved by exploiting a liquid–liquid phase‐separated aqueous system in a one‐step microfluidic process. Microfluidic mechanical testing reveals that the mechanical robustness of thicker‐shell capsules could be controlled through modulation of the shell thickness. Furthermore, the microcapsules demonstrate environmentally‐responsive deformation, including buckling driven by osmosis and external mechanical forces. A sequential release of cargo species is obtained through the degradation of the capsules. Stability measurements show the capsules are stable at 37 °C for more than 2 weeks. Finally, through gel–sol transition, microgels function as precursors for the formation of all‐aqueous liquid–liquid phase‐separated systems that are two‐phase or multiphase. These smart capsules that can undergo phase transition are promising models of hollow biostructures, microscale drug carriers, and building blocks or compartments for active soft materials and robots.

Highlights

  • Artificial protein-based systems can be harnessed to form hydrogels and colloids at the microscale

  • We have shown mild and versatile gelation regimes capable of producing physically- and enzymatically crosslinked gelatin microgels as collagen substitutes with radial density gradients, and we have further shown that gelatin microgels that can undergo a gel–sol transition could act as precursors of all-aqueous LLPS systems.[6,20]

  • A gelatin/polyethylene glycol (PEG) liquid–liquid phase-separated system from Generally regarded as safe (GRAS) materials was chosen, in which the selected protein can be templated and crosslinked in a versatile and mild manner.[9,20,38,39]

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Summary

Introduction

Artificial protein-based systems can be harnessed to form hydrogels and colloids at the microscale. Www.advancedsciencenews.com www.advmatinterfaces.de smart microgels have prospects for applications in this context and more generally as environmentally-responsive carriers for catalysis, drug release, and sensing.[12,13,14,15,16,17,18] Compared to bulk gels, spherical microgels have higher specific surface area and can promote more rapid exchange of substance between the microgels and environment;[19,20] spherical droplets can highlight the liquid or liquid-like nature of the materials in another liquid.[5,6,21,22] Core–shell microgels present key advantages over homogeneous solid microgels, including the availability of both an outer and inner surface, and the ability to load the capsules with active ingredients Such core–shell structures have gained increasing interest as nature-inspired phase-flexible constructs which can be exploited as biocompatible 3D hollow scaffolds to simulate organoids or mini tissues with cavity configuration, multi-release models, hierarchical bioreactors, tailor-made cells, or selective membranes to separate biomolecules statically and dynamically together with other progressive approaches.[11,23,24,25,26]. LLPS of ECM proteins in aqueous environment can open up new application possibilities of advanced liquid material systems in biophysics, bioengineering, and biomedicine

Formation of the Microgels
Deformation of Microcapsules when Combining in Oil
Buckling by Osmosis
Buckling by Mechanical Pressure
Degradable Microcapsules as Drug Release Models
Conclusions
Experimental Section
Conflict of Interest
Data Availability Statement
Full Text
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