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Author

Guohua Jiang

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Aug 2026

iRGD-targeted nanoliposomes for hypoxia-relieved sonodynamic and ferroptosis-enhanced chemodynamic combination cancer therapy.

Current clinical interventions for solid tumors are confronted with multiple prominent challenges, including intratumoral hypoxia, constitutively activated endogenous antioxidant defense systems, and inefficient tumor targeting. In this study, a multifunctional nanoliposome carrier is developed by co-encapsulation of hemoglobin (Hb), ferric citrate (FC), and chlorin e6 (Ce6), and surface-modified with the iRGD (CRGDKGPDC) peptide to facilitate active tumor targeting and enhance subsequent intratumoral penetration. Under ultrasound irradiation, the iRGD-targeted nanoliposomes can efficiently generate two distinct types of reactive oxygen species (ROS) to produce strong synergistic cytotoxicity against 4T1 breast cancer cells via separate pathways: singlet oxygen (1O₂) through the sonodynamic therapy (SDT) pathway, and hydroxyl radicals (·OH) through the chemodynamic therapy (CDT) pathway. In vivo experimental results show that tail vein injection (i.v.) of iRGD-targeted nanoliposomes combined with external ultrasound irradiation achieves can significantly enhance tumor growth inhibition, which is attributed to triggered on-demand drug release induced by ultrasound. The as-prepared iRGD-targeted nanoliposomes exhibit remarkable synergistic antitumor efficacy, inducing extensive tumor necrosis, apoptosis, and ferroptosis while causing minimal systemic side effects, demonstrating great application potential for future breast cancer therapy.

Runming Zhong, Yingzhe Wu, Yanzhen Lou et al. · 0 citations
Jul 2026

Borate‐Crosslinked Bioadhesives With Double Network Fabricated Using Dopamine‐Conjugated Gelatin and Polyvinyl Alcohol Incorporating Catechin Acid: Potential in Biomedical Applications

The hydrogel bio‐adhesive has demonstrated outstanding potential in regenerative wound care. Here, we prepared borate‐crosslinked bioadhesive hydrogels (PPGB) composed of dopamine‐conjugated gelatin (Gel‐DA), polyvinyl alcohol (PVA), and catechin acid. Scanning electron microscopy revealed an interconnected porous microstructure within the PPGB matrix. Rheological characterization confirmed typical viscoelastic solid behavior, favorable injectability, and excellent self‐healing capability, the latter of which was also supported by macroscopic observations. Antioxidant activity was validated through ABTS and DPPH radical scavenging assays. The PPGB adhesives exhibited strong adhesion to various material surfaces and moist organic tissues. Antibacterial testing demonstrated efficient activity against the typical Gram‐positive and Gram‐negative bacteria. Biocompatibility evaluation using CCK‐8 assays and DAPI/phalloidin staining of NIH 3 T3 fibroblasts exposed to hydrogel extracts indicated good cytocompatibility. Furthermore, a scratch wound healing assay confirmed enhanced cell migration. Collectively, these findings present a straightforward strategy for engineering multifunctional hydrogel bio‐adhesives with potential for biomedical applications.

Lei Nie, Letian Yan, Yaling Deng et al. · 0 citations
Open access Jul 2026

Composite Hydrogel Using Methacrylated Silk Fibroin and Mercaptolated Hyaluronic Acid with Encapsulating Zinc-Quercetin Nanozyme

Given the urgent need to regulate oxidative stress microenvironments in chronic wound healing, hydrogel dressings that simultaneously integrate antioxidant, antibacterial, mechanically adaptive, and biocompatible properties are highly desirable. In this study, a natural polymer-based composite hydrogel dressing loaded with zinc-quercetin nanozyme (Zn-Q) was designed. The gel skeleton was constructed via a dual network of photocrosslinked methacrylated silk fibroin (SilMA) and mercaptolated hyaluronic acid (HA-SH) via thiol-ene click chemistry, with the catalase (CAT)-like Zn-Q nanozyme encapsulated in situ within the network, thereby achieving synergy between chemical crosslinking and dynamic metal-polyphenol coordination. Systematic characterization revealed that Zn-Q nanozyme adopted a stable octahedral coordination configuration, and its continuous porous structure exposed abundant catalytically active sites. The composite hydrogels exhibited a highly interconnected, three-dimensional (3D) porous morphology, with swelling ratios that increased significantly with Zn-Q nanozyme content (up to around 1082%). Rheological and mechanical tests demonstrated that although incorporating the nanozyme reduced the storage modulus, the reversible physical crosslinks formed via hydrogen bonding and coordination interactions endowed the material with excellent tensile toughness and energy-dissipation capacity, exhibiting typical Mullins softening behavior. Functional evaluation showed that Zn-Q nanozyme conferred superior free radical scavenging capability to the hydrogels and exerted dose-dependent inhibition against both Staphylococcus aureus and Escherichia coli. Furthermore, the hydrogels exhibited favorable adhesion to various wet organs and heterogeneous material surfaces, with hemolysis rates below 5% and cell viability exceeding 100% after 3 days of culturing with fibroblasts, confirming their excellent hemocompatibility and cytocompatibility. This study provides an experimental basis for developing a new type of wound repair materials that integrate antioxidant, anti-infective, and mechanically adaptive properties, holding significant application potential in oxidative stress-related tissue repair fields.

Lei Nie, Xinran Li, Ru-Qiang Gong et al. · 0 citations