Analytical Chemistry· 2026Q1
Dual-Functional Fluorescent Nanoprobe Tracks Lipid Droplet Accumulation and Superoxide Anion in Early Atherosclerotic Lesions
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- Q1SCImago
- 2026year
Short summary
A novel dual-functional fluorescent nanoprobe, LDN-O, simultaneously images lipid droplet accumulation and superoxide anion production in early atherosclerosis, showing these markers increase with oxidized LDL stimulation and are elevated in mouse models.
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Key points
- A dual-functional fluorescent nanoprobe, LDN-O, was created for simultaneous imaging of lipid droplets and superoxide anions.
- In vitro experiments showed LDN-O is sensitive and specific for both targets.
- LDN-O revealed a positive correlation between lipid droplets, superoxide anions, and oxidized LDL stimulation in foam cell formation.
- Ex vivo imaging in mouse models showed elevated lipid droplets and superoxide anions in atherosclerotic aortas, particularly in those with steatohepatitis.
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Abstract
Abstract As the primary risk factor for cardiovascular events, early diagnosis of atherosclerosis (AS) is essential for reducing their incidence. Abnormal accumulation of lipid droplets (LDs) and excessive production of superoxide anion (O2•–) are key synergistic drivers that promote the early progression of AS. This study developed a dual-functional fluorescent nanoprobe, termed LDN-O, for simultaneous imaging and assessment of changes in LDs and O2•– levels during the onset and progression of AS. LDN-O was fabricated via nanoprecipitation to encapsulate two responsive molecules: LDB-O-ME enables high-fidelity targeted imaging of LDs, while LN-SF-O allows highly selective detection of O2•–. In vitro experiments confirmed that LDN-O exhibits excellent sensitivity and specificity for both targets. Dynamic monitoring with LDN-O revealed that during foam cell formation, the levels of LDs and O2•– were positively correlated with the duration of oxidized low-density lipoprotein (ox-LDL) stimulation, providing direct experimental evidence for understanding the intrinsic drivers driving early pathological progression in AS. Ex vivo imaging of aortas was further performed in mouse models of early-stage AS and in a combined model of AS with steatohepatitis. The results showed that LDs and O2•– levels in aortic tissue were significantly higher in the model groups than in the control group, with an even more pronounced increase in the group with concurrent steatohepatitis. Overall, LDN-O enables visualization of lipid deposition and oxidative stress in early AS, offering a new strategy for its early diagnosis.
The authors' abstract, as published at the source. Analytical Chemistry, 2026 · DOI ↗
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Field: Biochemistry (Biochemistry, Genetics and Molecular Biology)
BiochemistryBiochemistry, Genetics and Molecular Biology