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Self-Assembled Multilayered Concentric Supraparticle Architecture
Agasthya Suresh1,2,3, Dhananjay Suresh1, Zhaohui Li1
1Department of Radiology, University of Missouri, Columbia, MO, 65212, USA.
Advanced Materials (Deerfield Beach, Fla.)
|April 26, 2025
Summary
Researchers developed Self-Assembled Multilayered Supraparticles (SAMS) using gold nanoparticles, lipidoid, and gelatin. These novel supraparticles show promise for efficient in vivo delivery of therapeutic payloads like siRNA and mRNA.
Area of Science:
- Nanotechnology and Materials Science
- Biomedical Engineering
- Drug Delivery Systems
Background:
- Supraparticles (SPs) are emerging as versatile platforms for catalysis, photonics, and medicine due to their unique properties.
- Synthesizing novel SPs with complex internal structures presents a significant challenge in materials science.
- Existing SPs often lack the intricate architectures required for advanced applications, particularly in nanomedicine.
Purpose of the Study:
- To introduce a novel class of Self-Assembled Multilayered Supraparticles (SAMS) with complex internal structures.
- To investigate the synergistic interactions between gold nanoparticles, lipidoid, and gelatin in SAMS formation.
- To evaluate the potential of SAMS as a platform for efficient in vivo delivery of therapeutic nucleic acids.
Main Methods:
- Fabrication of SAMS through a synergistic three-way interaction involving gold nanoparticles, lipidoid, and gelatin.
- Characterization of SAMS structure, including concentric lamellar spherical architecture, interlayer spacing (3.5 ± 0.2 nm), and diameter (156.8 ± 56.6 nm).
- Analysis of physical and chemical factors influencing SAMS formation, such as nanoparticle size, lipidoid chain length, and surface chemistry.
Main Results:
- Successful synthesis of SAMS with controlled multilayered spherical structures.
- Demonstration that SAMS formation is critically dependent on nanoparticle size, lipidoid chain length, and surface chemistry.
- Efficient in vivo delivery of labile payloads, including siRNA, achieving dose-dependent gene silencing, with potential for mRNA delivery.
Conclusions:
- This work introduces a novel supraparticle structure (SAMS) and a new interaction phenomenon for their formation.
- SAMS exhibit tunable properties influenced by physical and chemical factors, enabling precise control over interparticle interactions.
- SAMS demonstrate significant potential as an advanced nanomedicine platform for effective in vivo nucleic acid delivery.
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