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CHEMISTRY-A EUROPEAN JOURNAL · 2025 ·Vol. 31 ·期 12 ·e202404538 · IF 3.7

Development of pH-Responsive SA/PEGDA/AS-POSS Hydrogels via Michael Addition for Controlled Drug Release and Enhanced Mechanical Properties

Yang Meng,Wen Li,Lingji Zhang,Mario Berrettoni,Hongzhong Zhang,Xiaojing Zhang

Graphical This study develops pH-responsive SA/PEGDA/AS-POSS hydrogels through Michael addition reactions to achieve controlled drug release and enhanced mechanical properties. The hydrogels exhibit tunable swelling and degradation behaviors under various pH conditions, demonstrating their potential for targeted drug delivery. These hydrogels offer promising prospects for biomedical applications, providing efficient drug loading, controlled release, and improved mechanical strength. In this study, thiolated sodium alginate (SA) and hydrophilic, polymerizable Janus-type polyhedral oligomeric silsesquioxane (AS-POSS) are synthesized by introducing thiol and sulfonic acid groups, respectively. A series of pH-responsive SA/PEGDA/AS-POSS nanocomposite hydrogels are successfully prepared through Michael addition reactions between the thiol groups of thiolated sodium alginate and the double bonds in the molecular chains of AS-POSS and poly(ethylene glycol) diacrylate (PEGDA). This reaction proceeds rapidly under physiological conditions without requiring initiators or catalysts. As the content of AS-POSS increases, the pore size within the hydrogel decreases, and the network structure becomes denser, with significant improvements in mechanical properties. The hydrogel exhibits excellent pH sensitivity, showing lower swelling in acidic media compared to neutral media, and undergoing hydrolysis and losing stability in alkaline media. Moreover, the incorporation of AS-POSS significantly enhances the drug-loading capacity (85.7 %) and encapsulation efficiency (72.1 %) of doxorubicin (DOX). The drug is released faster in weakly acidic environments, with a cumulative release rate reaching 80.4 %, demonstrating excellent targeting and controlled release properties. Cytotoxicity tests show that the SA/PEGDA/AS-POSS hydrogel has good biocompatibility and exhibits effective tumor-killing ability, indicating its great potential as a drug carrier with promising applications in biomedical materials.

研究领域: 生物材料 · 药剂学 · 高分子化学
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JOURNAL OF APPLIED POLYMER SCIENCE · 2024 ·Vol. 141 ·期 30 ·e55692 · IF 2.7

Exploring drug release performance of hollow-structured CS/SA/POSS composite gel spheres employing hydrophilic polymerizable AS-POSS as crosslinker

Yang Meng,Mengke Shi,Wenbo Feng,Lingji Zhang,Hongzhong Zhang,Xiaojing Zhang

This study prepares a series of hollow-structured CS/SA/POSS composite gel spheres with a diameter of ~2.5 mm by using hydrophilic Janus-type polyhedral oligomeric silsesquioxane (AS-POSS) as a crosslinking agent in combination with sodium alginate and chitosan via electrostatic adsorption/free radical polymerization. As the content of POSS increases, the wall thickness of the gel spheres also increases from 20 to 30 μm, leading to a more compact and smooth wall structure in the polymerized CS/SA/POSS composite gel spheres. Additionally, the introduction and polymerization of POSS significantly enhance the stability, drug loading rate, and entrapment rate of the gel spheres, providing them with improved drug release capabilities. For hydrophilic drug doxorubicin, the loading rate and encapsulation rate reach 41.2% and 79.9%, respectively, while for the hydrophobic drug ibuprofen, they are 14.7% and 76.3%. Compared to some previously reported drug-loaded gel materials, the gels prepared in this study demonstrate relatively higher drug loading performance. Thus, these hollow-structured CS/SA/POSS composite gel spheres hold promise as innovative drug carriers in the biomedical field.

研究领域: 材料科学 · 生物医学工程
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