Emulsion-templated formation of poly(N-isopropylacrylamide):surfactant mixed shells by thermo-enhanced interfacial complexation

TL;DR

This paper introduces a thermo-enhanced interfacial complexation method using thermoresponsive PNIPAM to create robust, functionalized capsule shells for biomolecule encapsulation, advancing biotechnological delivery systems.

Contribution

It presents a novel thermo-responsive interfacial complexation technique to form and strengthen capsule shells with potential for biomolecule delivery.

Findings

Thermo-triggered polymer layer enrichment observed.

Formation of gel-like mixed shells with nanoparticles.

Compatible with protein encapsulation under mild conditions.

Abstract

The encapsulation of fragile biomacromolecules is crucial for many biotechnological applications but remains challenging. Interfacial complexation (IC) in water-in-oil emulsions turned out to be an efficient process for the formation of protective polymer layers at the surface of capsule-precursor water droplets. We propose to further enhance this IC process by introducing thermoresponsive poly(N-isopropylacrylamide) (PNIPAM) strands in the interfacial polymer layer. In this work, we implement surfactant-polymer IC in water-in-fluorocarbon oil emulsions between a water-soluble poly(L-lysine)-g-poly(N-isopropylacrylamide) cationic copolymer (PLL-g-PNIPAM) and an oil-soluble anionic surfactant. We demonstrate that the thermal collapse transition of PNIPAM strands triggers an enrichment of the polymer layer initially formed by IC. This process is leveraged to irreversibly segregate water-soluble nanoparticles in the interfacial polymer layer, resulting in gel-like mixed shells. We demonstrate that this thermo-enhancement of conventional IC is a promising approach for the formation, strengthening and functionalization of capsule shells. As implemented in mild conditions, thermo-enhanced IC is additionally compatible with the encapsulation of proteins, paving the way for new delivery systems of biomacromolecules.