Organic–Inorganic Multilayer Microcarriers with Superior Mechanical Properties for Potential Active Delivery in Fast-Moving Consumer Goods
This study introduces an eco-friendly approach to fabricating superstrong, core-shell, composite microcapsules, offering a sustainable alternative to traditional insoluble microplastic-based materials like melamine-formaldehyde. These microcapsules were engineered with a thick CaCO3 shell formed via crystal ripening in the presence of water-soluble poly(acrylic acid), encasing a hexylsalicylate oil core armoured by hydrophilic SiO2 nanoparticles. An additional polydopamine layer was deposited via oxidative auto-polymerisation at pH 8.5 for improved structural and surface properties of the resulting microcapsules. These microcapsules (D3,2=8.8±0.3 μm) were spherical, with a relatively smooth surface, and exhibited unique mechanical properties, which are essential to broaden their applications in industry. Remarkably, compression tests showed a mean rupture stress of 73.5±5.0 MPa, which dramatically surpasses any other inorganic/synthetic microcarrier reported in literature. In addition, only 10-20% of the core active was released within 2 hours into a mixed water-propanol medium used as an accelerated release test, where the solubility of the active oil is high, with full release over 3 days. Herein, we also propose a novel pathway-specific binding constant (PSBC) that describes the strong interaction between Ca2+ ions and polyacrylic acid, in connection with their stoichiometric ratio. Overall, these microcapsules hold promise for multiple fast-moving consumer goods, where maximising the mechanical strength of microcapsules for encapsulation of valuable functional actives is paramount; this includes but is not limited to energy storage, household, agrochemical, personal care, and healthcare applications.
Publication Details
- Journal
- Apollo (University of Cambridge)
- Published
- 2025-02-19
- DOI
- https://doi.org/10.17863/cam.115925
- Primary Topic
- Calcium Carbonate Crystallization and Inhibition
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Engineering and Physical Sciences Research Council