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Updated: Jun 13, 2025

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Double Emulsion Generation Using a Polydimethylsiloxane PDMS Co-axial Flow Focus Device
Published on: December 25, 2015
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Engineering sequential liquid-liquid phase separation and affinity partitioning for compartmentalization and
Weijiang Wang1, Wentao Sun2, Futai Du1
1School of Pharmacy, Qingdao University, Qingdao 266021, China.
Journal of Colloid and Interface Science
|June 11, 2025
Summary
This study introduces a novel strategy for creating advanced biomaterials using sequential liquid-liquid phase separation (LLPS) and affinity partitioning, enabling precise control over core-shell structures for enhanced therapeutic applications.
Area of Science:
- Biomaterials Science
- Chemical Engineering
- Physical Chemistry
Background:
- Liquid-liquid phase separation (LLPS) is crucial for biological processes and biomaterial design, enabling the formation of distinct liquid compartments.
- Current LLPS methods for core-shell structures often require external agents or multiple steps, limiting control over functionalization.
- Achieving precise spatial and temporal control over compartmentalization and functionalization in biomaterials remains a significant challenge.
Purpose of the Study:
- To develop an integrated strategy for spatiotemporal compartmentalization and functionalization of all-aqueous emulsion drops.
- To engineer sequential LLPS and affinity partitioning for controlled core-shell microstructure formation without exogenous agents.
- To enable simultaneous functionalization of discrete core and shell regions for sophisticated biomaterial functions.
Main Methods:
- Leveraged intrinsic concentration gradients in all-aqueous emulsion drops to induce osmotic pressure gradients.
- Engineered spontaneous, sequential LLPS for controlled compartmentalization and stable core-shell microstructure formation.
- Utilized affinity partitioning, inspired by intracellular mechanisms, for precise distribution of functional components.
Main Results:
- Achieved spatiotemporal control over LLPS-based compartmentalization without exogenous agents or multi-step processing.
- Generated stable core-shell microstructures with precise spatial and temporal control over component distribution.
- Demonstrated simultaneous functionalization of core and shell regions, leading to enhanced therapeutic performance in a wound healing model.
Conclusions:
- Established a versatile strategy for developing advanced biomaterials with sophisticated core-shell architectures.
- The developed approach offers precise spatiotemporal control over compartmentalization and functionalization.
- The biomaterials show significant potential for therapeutic applications, as evidenced by improved wound healing outcomes.
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