Bioinspired Diffusion-Limited Silicification in Coacervate Assemblies Enables Smart Nanotoroids for Deep and Sensitive Tumor Penetration
Controlling the self-assembly of mesoporous materials beyond equilibrium remains a fundamental challenge. Conventional templating systems form ordered structures through energy-minimizing coassembly but lack the kinetic and spatial freedom required to produce asymmetric or topologically complex architectures. Here, we report a bioinspired coacervate-directed silicification strategy that enables diffusion-limited and spatially asymmetric condensation within soft templates, yielding ordered hexagonal mesoporous nanotoroids. In this system, poly(acrylic acid) (PAA) electrostatically associates with the cationic surfactant cetyltrimethylammonium bromide (CTAB), driving liquid-liquid phase separation and forming disc-like coacervate assemblies. Reaction-diffusion imbalance across the inner and outer interfaces within these templates induces asymmetric silicification, driving an interior collapse and toroidal self-transformation. By tuning PAA concentration, the diffusion-condensation kinetics can be precisely modulated, allowing programmable control over collapse dynamics and final topology, with enlarged central cavities (14-71 nm) and reduced rim thickness (15-35 nm). These nanotoroids exhibit uniform sub-100 nm size, high surface area (846 m<sup>2</sup> g<sup>-1</sup>), and abundant mesopores (∼2.0 nm). The nanotoroids (rim thickness ∼15 nm, height ∼40 nm) display markedly prolonged blood circulation, enhanced tumor accumulation (+173%), improved vascular extravasation, and deeper intratumoral penetration, while reducing hepatic and splenic uptake by 19% and 14%, respectively, compared with spherical analogues. These combined advantages translate into potent antitumor efficacy in both subcutaneous and spinal metastasis models. This work establishes a new paradigm for sol-gel topology control by bridging reaction-diffusion dynamics with bioinspired silicification based on the chemistry of LLPS (liquid-liquid phase separation), thereby unlocking the untapped biomedical potential of toroidal topologies that were rarely accessible.
Authors
- Peng Pei (ORCID: https://orcid.org/0000-0002-9616-5066)
- Miao Yan (ORCID: https://orcid.org/0000-0002-0546-6630)
- Shan Zhou (ORCID: https://orcid.org/0000-0002-6476-3280)
- Qingyan Chen
- Jinqiang Wang (ORCID: https://orcid.org/0000-0002-0048-838X)
- Hui Zeng (ORCID: https://orcid.org/0009-0007-2578-4090)
- Liping Jiang
- Tianyi Liu
- Zhen Gu
- Lei Zhou
- Fei Han
- Jian Dong
- Biao Kong
- Xunbin Wei
Institutions
- Yong In University (KR)
- National University of Singapore (SG)
- Chinese Academy of Sciences (CN)
- Peking University (CN)
- Harbin Institute of Technology (CN)
- Fudan University (CN)
- UNSW Sydney (AU)
- Shanghai Liangyou (China) (CN)
- Beijing National Laboratory for Molecular Sciences (CN)
- Department of Physics, Mathematics and Informatics (BY)
- Quzhou University (CN)
- Zhongshan Hospital (CN)
- Kindeva Drug Delivery (United States) (US)
- Ministry of Education (ET)
- Collaborative Innovation Center of Chemistry for Energy Materials (CN)
- Beijing Advanced Sciences and Innovation Center (CN)
- Zhejiang University (CN)
- Ministry of Industry and Information Technology (CN)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-03-23
- DOI
- https://doi.org/10.1021/jacs.5c22993
- Primary Topic
- Mesoporous Materials and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00