Background: Atheroregression becomes an attractive target for cardiovascular treatment. Some clinical trials have demonstrated that intensive therapy with rosuvastatin or recombinant ApoA-I Milano can partially reduce the total atheroma volume (TAV) up to 6.38 mm<sup>3</sup> or 14.1 mm<sup>3</sup> respectively. Our previous bench studies of selected nanotechnologies documented TAV reduction up to unprecedented 79.4 mm<sup>3</sup>. Methods: The completed observational three arms (n=180) first-in-man trial (the NANOM FIM trial) assessed (NCT01270139) the safety and feasibility of two delivery techniques for nanoparticles (NP), and plasmonic photothermal therapy (PPTT). Patients were assigned to receive either (1) nano-intervention with delivery of silica-gold NP in bioengineered on-artery patch (n=60), or (2) nano-intervention with delivery of silica-gold iron-bearing NP with targeted micro-bubbles or stem cells using magnetic navigation system (n=60) versus (3) stent implantation (n=60). The primary outcome was TAV at 12 months. Results: The mean TAV reduction at 12 months in nano group was 60.3 mm<sup>3</sup> (SD 39.5; min 41.9 mm<sup>3</sup>, max 94.2 mm<sup>3</sup>; p<0.05) up to mean 37.8% (95% CI: 31.1%, 51.7%; p<0.05) plaque burden. The analysis of the event free survival of the ongoing clinical follow-up shows the significantly lower risk of cardiovascular death in nano group when compared with others (91.7% vs 81.7% and 80% respectively; p<0.05) with no cases of the target lesion-related complications. Conslusions: PPTT using silica-gold NP associated with significant regression of coronary atherosclerosis.

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doi.org/10.4172/2157-7439.1000160, hdl.handle.net/1765/85009
Journal of Nanomedicine and Nanotechnology
Erasmus MC: University Medical Center Rotterdam

Kharlamov, A. N., Tyurnina, A. E., Veselova, V. S., Novoselova, O. S., Filatova, A. S., Kovtun, O. P., … Gabinsky, J. L. (2013). Plasmonics for treatment of atherosclerosis: Results of NANOM-FIM trial. Journal of Nanomedicine and Nanotechnology, 4(1). doi:10.4172/2157-7439.1000160