Late in-stent restenosis remains a significant problem. Bare-metal stents were implanted into peripheral arteries in miniature swine, followed by direct intra-arterial infusion of nitric oxide-loaded echogenic liposomes (ELIPs) and anti-intercellular adhesion molecule-1 conjugated ELIPs loaded with pioglitazone exposed to an endovascular catheter with an ultrasonic core. Ultrasound-facilitated delivery of ELIP formulations into stented peripheral arteries attenuated neointimal growth. Local atheroma-targeted, ultrasound-triggered delivery of nitric oxide and pioglitazone, an anti-inflammatory peroxisome proliferator-activated receptor-γ agonist, into stented arteries has the potential to stabilize stent-induced neointimal growth and obviate the need for long-term antiplatelet therapy.
Keywords: ELIP, echogenic liposome; ICAM, intercellular adhesion molecule; IVUS, intravascular ultrasound; NO, nitric oxide; PGN, pioglitazone; SPDP, 3-(2-pyridyldithio propionic acid)-N-hydroxysuccinimide ester; atherosclerosis; in-stent restenosis; nitric oxide; pioglitazone; ultrasound contrast agent.
© 2020 The Authors.