Key result
GSNPD nanoparticles ablate pro-inflammatory macrophages and curb photothermal therapy-induced inflammation in vitro.
Why the study?
Does GSNPD nanoparticle therapy improve macrophage ablation and reduce inflammation in in vitro models of atherosclerosis?
Does GSNPD nanoparticle therapy improve macrophage ablation and reduce inflammation in in vitro models of atherosclerosis?
GSNPD nanoparticles offer a novel dual approach of photothermal ablation and NO-mediated anti-inflammation for targeted atherosclerosis treatment in preclinical models.
Introduction: Photothermal therapy (PTT) is attracting increasing attention in treating atherosclerotic plaques. However, PTT can induce inflammatory responses, in turn stimulating the regeneration of atherosclerosis and hindering subsequent therapy. Methods: /RSNO/DS, GSNPD) for the synergistic treatment of atherosclerosis through PTT and anti-inflammation effects was developed. The preparation and characterization of GSNPD, their cellular toxicity, photothermal conversion and targeted ablation efficiency, anti-inflammation and ROS scavenging effect, as well as the inhibition of foam cell formation were studied in vitro. Results: The experimental results showed that the fabricated GSNPD NPs displayed positive effects on anti-atherosclerosis by pro-inflammatory macrophages ablation, NO production and ROS scavenging. Discussion: GSNPD NPs were designed to effectively and accurately ablate pro-inflammatory macrophages by recognizing and targeting to SR-A overexpressed on the activated macrophages of arterial plaques via PTT, and simultaneous inhibit the PTT-induced inflammation through the laser-activated NO release in situ. This match of therapeutic agents and inhibitors not only achieves good therapeutic effects but also minimizes side effects as much as possible, which may provide an effective way for PTT-based treatment of atherosclerosis.
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Lu et al. (2025) studied Atherosclerosis. GSNPD nanoparticles was evaluated on Pro-inflammatory macrophages ablation, NO production, ROS scavenging, and inhibition of foam cell formation. GSNPD nanoparticles effectively ablated pro-inflammatory macrophages and inhibited photothermal therapy-induced inflammation via NO release and ROS scavenging in vitro.
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