Facile Fabrication of Multifunctional Metal-Phenolic Network Nanoparticles for Bacterial Keratitis Treatment

keratitis model, EGCG-Zn-VAN NPs combined potent bactericidal efficacy with effective modulation of the oxidative and inflammatory milieu. Notably, despite delivering a substantially lower antibiotic dose (∼14.9 μg/mL), the nanoparticle formulation significantly outperformed a clinical standard-of-care comparator (5% free vancomycin), achieving >95% reduction of MRSA burden and suppressing pro-inflammatory cytokines (IL-1β, IL-6, TNF-α) toward near-baseline levels. Quantitative histomorphometry confirmed that treatment led to the preservation of corneal transparency, epithelial integrity, and physiological stromal thickness. These outcomes arise from the cooperative interplay between vancomycin and the ROS-scavenging EGCG-Zn network, establishing EGCG-Zn-VAN NPs as a versatile, stimuli-responsive nanotherapeutic platform capable of addressing both microbial burden and host pathology. This platform provides a promising dose-sparing strategy for the clinical management of drug-resistant bacterial keratitis and other inflammation-associated ocular infections.

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Publication Details

Journal
Molecular Pharmaceutics
Published
2026-04-17
DOI
https://doi.org/10.1021/acs.molpharmaceut.6c00108
Primary Topic
Ocular Infections and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

Facile Fabrication of Multifunctional Metal-Phenolic Network Nanoparticles for Bacterial Keratitis Treatment

Chen Qin, Quankui Lin, Yajia Wang, Wenjing Zhu et al.
Molecular Pharmaceutics
Ocular Infections and Treatments
article

Facile Fabrication of Multifunctional Metal-Phenolic Network Nanoparticles for Bacterial Keratitis Treatment

Chen Qin, Quankui Lin, Yajia Wang, Wenjing Zhu, Hao Chen, Mengting Wang, Pengfei Cheng
article en

Abstract

keratitis model, EGCG-Zn-VAN NPs combined potent bactericidal efficacy with effective modulation of the oxidative and inflammatory milieu. Notably, despite delivering a substantially lower antibiotic dose (∼14.9 μg/mL), the nanoparticle formulation significantly outperformed a clinical standard-of-care comparator (5% free vancomycin), achieving >95% reduction of MRSA burden and suppressing pro-inflammatory cytokines (IL-1β, IL-6, TNF-α) toward near-baseline levels. Quantitative histomorphometry confirmed that treatment led to the preservation of corneal transparency, epithelial integrity, and physiological stromal thickness. These outcomes arise from the cooperative interplay between vancomycin and the ROS-scavenging EGCG-Zn network, establishing EGCG-Zn-VAN NPs as a versatile, stimuli-responsive nanotherapeutic platform capable of addressing both microbial burden and host pathology. This platform provides a promising dose-sparing strategy for the clinical management of drug-resistant bacterial keratitis and other inflammation-associated ocular infections.

Molecular PharmaceuticsVol. 23(5)
New England College of Optometry (US), Wenzhou Medical University (CN)
Zhejiang Provincial Outstanding Youth Science Foundation
Openalex Percentile: Top 16%
Ocular Infections and Treatments
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