An oral coral-like resveratrol nanocomplex protects against dry eye disease through ocular and systemic redox homeostasis

Dry eye disease (DED) is a progressive ocular disorder in which chronic inflammation and oxidative stress synergistically damage ocular tissues and impair vision. While topical anti-inflammatory and artificial tears therapies are the standard treatment for DED, their long-term application is limited by adverse effects and poor patient compliance. Emerging evidence suggests that systemic redox dysregulation contributes to DED pathogenesis, highlighting the potential of oral antioxidant intervention as a disease-modifying strategy. However, the clinical translation of oral antioxidants has been constrained by poor bioavailability and rapid metabolic clearance. Herein, a coral-like resveratrol nanocomplex was fabricated with a composite natural carrier of sericin and dipotassium glycyrrhizinate through a simple pH-ultrasonic-shifting method in aqueous solution, enabling effective oral delivery of this potent polyphenolic antioxidant. This coral-like nanocomplex markedly enhanced gastrointestinal stability and systemic exposure of resveratrol, increasing oral bioavailability by approximately 6.62-fold and ocular accumulation by 2.49-fold. The nanocomplex exerted robust ocular and systemic antioxidant effects and protected against experimental DED in mice. Oral administration of this nanocomplex protected against benzalkonium chloride (BAC)-induced corneal epithelial damage, tear film dysfunction, and inflammatory responses. Mechanistically, the nanocomplex alleviated oxidative damage through ocular and systemic redox homeostasis. Rather than acting solely on the ocular surface, this orally nanomedicine may provide complementary therapeutic benefits through ocular and systemic redox regulation, while also being associated with modulation of gut microbiota and metabolic profiles. These findings support oral redox intervention as a promising complementary strategy for protecting against the DED, particularly for reducing the burden of prolonged topical treatment.

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Publication Details

Journal
Bioactive Materials
Published
2026-09-04
DOI
https://doi.org/10.1016/j.bioactmat.2026.08.039
Primary Topic
Ocular Surface and Contact Lens
Type
article
Field-Weighted Citation Impact
0.00

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article

An oral coral-like resveratrol nanocomplex protects against dry eye disease through ocular and systemic redox homeostasis

Mengzhen Xie, Yihan Guo, Jiayu Bao, Qingchen Cui et al.
Bioactive Materials
Ocular Surface and Contact Lens
article

An oral coral-like resveratrol nanocomplex protects against dry eye disease through ocular and systemic redox homeostasis

Mengzhen Xie, Yihan Guo, Jiayu Bao, Qingchen Cui, Ying Jie, Yaqiong Li, Qianru Wu, Lei Tian, Yunxiao Zang, Ziyu Liu
article en

Abstract

Dry eye disease (DED) is a progressive ocular disorder in which chronic inflammation and oxidative stress synergistically damage ocular tissues and impair vision. While topical anti-inflammatory and artificial tears therapies are the standard treatment for DED, their long-term application is limited by adverse effects and poor patient compliance. Emerging evidence suggests that systemic redox dysregulation contributes to DED pathogenesis, highlighting the potential of oral antioxidant intervention as a disease-modifying strategy. However, the clinical translation of oral antioxidants has been constrained by poor bioavailability and rapid metabolic clearance. Herein, a coral-like resveratrol nanocomplex was fabricated with a composite natural carrier of sericin and dipotassium glycyrrhizinate through a simple pH-ultrasonic-shifting method in aqueous solution, enabling effective oral delivery of this potent polyphenolic antioxidant. This coral-like nanocomplex markedly enhanced gastrointestinal stability and systemic exposure of resveratrol, increasing oral bioavailability by approximately 6.62-fold and ocular accumulation by 2.49-fold. The nanocomplex exerted robust ocular and systemic antioxidant effects and protected against experimental DED in mice. Oral administration of this nanocomplex protected against benzalkonium chloride (BAC)-induced corneal epithelial damage, tear film dysfunction, and inflammatory responses. Mechanistically, the nanocomplex alleviated oxidative damage through ocular and systemic redox homeostasis. Rather than acting solely on the ocular surface, this orally nanomedicine may provide complementary therapeutic benefits through ocular and systemic redox regulation, while also being associated with modulation of gut microbiota and metabolic profiles. These findings support oral redox intervention as a promising complementary strategy for protecting against the DED, particularly for reducing the burden of prolonged topical treatment.

Bioactive MaterialsVol. 68
Beijing Tongren Hospital (CN), Peking University (CN), State Key Laboratory of Natural and Biomimetic Drugs (CN)
Beijing Municipal Health Commission, Beijing Municipal Administration of Hospitals
Openalex Percentile: Top 8%
Ocular Surface and Contact Lens
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