Kee Patrick H, Moody Melanie R, Huang Shao-Ling, Kim Hyunggun, Yin Xing, Peng Tao, Laing Susan T, Klegerman Melvin E, Rahbar Mohammad H, Vela Deborah, Genstler Curtis, Haworth Kevin J, Holland Christy K, McPherson David D
Department of Internal Medicine, The University of Texas Health Science Center at Houston, Houston, Texas.
Department of Bio-Mechatronic Engineering, Sungkyunkwan University, Suwon, Republic of Korea.
JACC Basic Transl Sci. 2019 Nov 28;5(1):1-11. doi: 10.1016/j.jacbts.2019.09.005. eCollection 2020 Jan.
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.
晚期支架内再狭窄仍然是一个重大问题。将裸金属支架植入小型猪的外周动脉,随后通过带有超声核心的血管内导管,将负载一氧化氮的可回声脂质体(ELIPs)和负载吡格列酮的抗细胞间黏附分子-1共轭ELIPs直接动脉内输注。超声辅助将ELIP制剂递送至支架植入的外周动脉可减轻内膜增生。将一氧化氮和吡格列酮(一种抗炎性过氧化物酶体增殖物激活受体-γ激动剂)以局部动脉粥样硬化靶向、超声触发的方式递送至支架植入动脉,有可能稳定支架诱导的内膜增生,并避免长期抗血小板治疗的需要。