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Updated: Aug 14, 2026

Nanomechanics of Drug-target Interactions and Antibacterial Resistance Detection
Published on: October 25, 2013
Exploiting Bacterial Metabolism for Targeted Antimicrobial Release from Smart Nanocarriers
Jianhui Liu1, Jeremy Elias1, Xiaohong Wang2
1The ADA Forsyth Institute, Somerville, Massachusetts02143, United States.
Abstract:
Acidogenic and aciduric bacteria acidify their local microenvironment through carbohydrate metabolism, contributing to pathological microenvironment acidification in diseases, including dental caries, infection, and inflammation. We present a mesoporous silica nanoparticle platform equipped with surface-bound, pH-responsive gatekeepers that remain sealed at physiological pH yet rapidly release a drug payload under acidic conditions. This system converts a broad-spectrum antimicrobial into a selectively activated antimicrobial system: release is suppressed under neutral conditions and triggered when bacteria generate acid. In a human oral microbiome model, the nanoparticles selectively eradicate acid-producing bacteria, with metabolic acidification directly activating their own killing, as evidenced by simultaneous single-cell-scale fluorescence imaging of pH and viability. Mechanistic studies using proton NMR and contact angle measurements show that the gating mechanism relies on synergistic molecular interactions and hydrophilicity-hydrophobicity transitions. This work establishes an on-site antimicrobial strategy triggered by metabolic acidification for targeting microbes with undesirable metabolic features, thus paving the way toward more controlled infection therapies.
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