Encapsulation Strategy Matters: Pre- and Post-Loading of Macromolecules into Surface-Supported Microgels Formed via Vaterite Templates.

IF 9.1 Q2 CHEMISTRY, PHYSICAL
ACS Materials Au Pub Date : 2025-10-08 eCollection Date: 2025-11-12 DOI:10.1021/acsmaterialsau.5c00099
Deniya Joseph, Harrison Brown, Emmanuelle A B Konzi, Mehwish Khan, Dmitry Volodkin, Anna Vikulina
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引用次数: 0

Abstract

Calcium carbonate vaterite crystals have attracted increasing attention as sacrificial templates for forming polymer microgels. Vaterite's porous structure, biocompatibility, and eco-friendly synthesis make it ideal for biomedical applications. In this study, vaterite is grown on the surface, and surface-supported (ss)-microgels are formed by coating it with alternating layers of polyelectrolytes, sodium alginate (ALG), and poly-l-lysine (PLL), followed by core dissolution. Pre-loading (during vaterite synthesis) and post-loading (after microgel formation) of macromolecules are compared using dextran and its charged derivatives. Pre-loading proved to be more efficient, achieving up to 9% w/w encapsulation. Dextran adsorption follows the Langmuir model (ΔG = - 31.0 kJ/mol), while its derivatives follow the Freundlich model (1/n = 0.7-0.8), indicating intermolecular repulsion. Post-loading resulted in encapsulation levels below 1% w/w and exhibited pH-independent behavior. The microgels remained stable in acidic environments, but PLL degradation via trypsin enabled the sustained release of dextran. These findings clarify the mechanisms of macromolecular adsorption on ss-vaterite, highlight the importance of considering the loading strategy when designing microgels for specific applications, and support the use of ss-microgels for therapeutic delivery.

封装策略问题:大分子的预和后加载到表面支持的微凝胶通过维特利特模板形成。
碳酸钙水晶石晶体作为形成聚合物微凝胶的牺牲模板越来越受到人们的关注。Vaterite的多孔结构、生物相容性和环保合成使其成为生物医学应用的理想选择。在这项研究中,水晶石生长在表面,表面支撑(ss)微凝胶通过涂覆聚电解质,海藻酸钠(ALG)和聚赖氨酸(PLL)的交替层形成,然后核心溶解。用葡聚糖及其带电衍生物比较了大分子的预加载(在水晶石合成过程中)和后加载(在微凝胶形成后)。预加载被证明是更有效的,实现高达9% w/w的封装。右旋糖酐吸附遵循Langmuir模型(ΔG = - 31.0 kJ/mol),其衍生物遵循Freundlich模型(1/n = 0.7-0.8),表明分子间排斥。后加载导致包封水平低于1% w/w,并表现出与ph无关的行为。微凝胶在酸性环境中保持稳定,但通过胰蛋白酶降解PLL使葡聚糖得以持续释放。这些发现阐明了ss-vaterite上大分子吸附的机制,强调了在设计特定应用的微凝胶时考虑负载策略的重要性,并支持ss-微凝胶用于治疗递送。
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来源期刊
ACS Materials Au
ACS Materials Au 材料科学-
CiteScore
5.00
自引率
0.00%
发文量
0
期刊介绍: ACS Materials Au is an open access journal publishing letters articles reviews and perspectives describing high-quality research at the forefront of fundamental and applied research and at the interface between materials and other disciplines such as chemistry engineering and biology. Papers that showcase multidisciplinary and innovative materials research addressing global challenges are especially welcome. Areas of interest include but are not limited to:Design synthesis characterization and evaluation of forefront and emerging materialsUnderstanding structure property performance relationships and their underlying mechanismsDevelopment of materials for energy environmental biomedical electronic and catalytic applications
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