ArticleMaterials today. Bio2025
pH-sensitive fibronectin nanogels combined with UTMD for anti-atherosclerosis treatment through anti-inflammatory and antioxidant effects.
Article in Materials today. Bio, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
4 citing papers in PubMed.
- Emerging Gel Technologies for Atherosclerosis Research and Intervention.Gels (Basel, Switzerland) · 2026Review
- Nanotechnology for atherosclerotic plaque stabilisation: bridging innovation and clinical practice.EBioMedicine · 2026Review
- Recent advances in polymer-based drug delivery systems for atopic dermatitis: enhancing therapeutic efficacy and outcomes.Materials today. Bio · 2025Review
- Engineered immune-driven theranostics for clinical cardiology.Military Medical Research · 2025Review
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The reactive oxygen species (ROS) and inflammatory factors secreted by macrophages play pivotal roles in all stages of atherosclerotic progression. Achieving targeted plaque localization while simultaneously reducing ROS levels to exert both anti-inflammatory and antioxidant effects remains a significant challenge. In this work, we developed a pH sensitive curcumin (Cur)-loaded fibronectin (FN) nanogels, combined with ultrasound-targeted microbubble destruction (UTMD) to enhance therapeutic efficacy via cavitation effects. The FN/FBA-PEG-FBA@Cur (denoted as FNC) nanogels demonstrated a targeted effect on atherosclerosis sites, attributed to the strong affinity between the RGD sequence on FN and the integrins highly expressed on the surface of plaque cells. Moreover, the Schiff base linkages in the nanogels respond to the acidic microenvironment within atherosclerosis plaques, leading to the controlled Cur release, which enable anti-inflammatory and antioxidant activity to attenuate plaque progression. Both
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Registered trials
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