ArticleBiology direct2026
4-phenylbutyric acid-loaded mesoporous silica nanoparticles alleviate endoplasmic reticulum stress and reduce intraocular pressure in glaucoma model.
Article in Biology direct, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
purposeTo develop a mesoporous silica nanoparticle-based delivery system for 4-phenylbutyric acid (4-PBA) and evaluate its potential to alleviate endoplasmic reticulum (ER) stress and improve mutant myocilin (MYOC)-associated glaucoma. MATERIALS AND
methodsWe synthesized hollow/snowflake-like mesoporous silica nanoparticles loaded with 4-PBA (mSiO₂-PBA) for drug loading and release. Cellular uptake and cytotoxicity were evaluated in human corneal epithelial cells (HCECs) and human trabecular meshwork cells (HTMCs). The effects of mSiO₂-PBA on mutant MYOC secretion and ER stress-associated proteins were assessed by Western blot analysis. In Tg-MYOC
resultsmSiO₂-PBA exhibited efficient cellular uptake and favorable biocompatibility in vitro. Treatment with mSiO₂-PBA enhanced mutant MYOC secretion and reduced ER stress-associated KDEL-positive proteins in HTMCs. Following topical administration, mSiO₂-PBA achieved ocular penetration and exposure in trabecular meshwork tissue. In Tg-MYOC
conclusionsmSiO₂-PBA represents a promising nanoparticle-based delivery platform for 4-PBA in MYOC-associated glaucoma. By promoting mutant MYOC secretion and alleviating ER stress, mSiO₂-PBA demonstrated therapeutic efficacy in vitro and in vivo, supporting its potential as a nanotherapeutic strategy for MYOC-associated glaucoma.
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