Gasper Warren J, Jimenez Cynthia A, Walker Joy, Conte Michael S, Seward Kirk, Owens Christopher D
From the Departments of Vascular Surgery (W.J.G., J.W., M.S.C., C.D.O.) and Pathology (C.A.J.), University of California, San Francisco; and Mercator MedSystems, Inc, San Leandro, California (K.S.).
Circ Cardiovasc Interv. 2013 Dec;6(6):701-9. doi: 10.1161/CIRCINTERVENTIONS.113.000195. Epub 2013 Nov 12.
Endovascular interventions on peripheral arteries are limited by high rates of restenosis. Our hypothesis was that adventitial injection of rapamycin nanoparticles would be safe and reduce luminal stenosis in a porcine femoral artery balloon angioplasty model.
Eighteen juvenile male crossbred swine were included. Single-injury (40%-60% femoral artery balloon overstretch injury; n=2) and double-injury models (endothelial denudation injury 2 weeks before a 20%-30% overstretch injury; n=2) were compared. The double-injury model produced significantly more luminal stenosis at 28 days, P=0.002, and no difference in medial fibrosis or inflammation. Four pigs were randomized to the double-injury model and adventitial injection of saline (n=2) or 500 μg of nanoparticle albumin-bound rapamycin (nab-rapamycin; n=2) with an endovascular microinfusion catheter. There was 100% procedural success and no difference in endothelial regeneration. At 28 days, nab-rapamycin led to significant reductions in luminal stenosis, 17% (interquartile range, 12%-35%) versus 10% (interquartile range, 8.3%-14%), P=0.001, medial cell proliferation, P<0.001, and fibrosis, P<0.001. There were significantly fewer adventitial leukocytes at 3 days, P<0.001, but no difference at 28 days. Pharmacokinetic analysis (single-injury model) found rapamycin concentrations 1500× higher in perivascular tissues than in blood at 1 hour. Perivascular rapamycin persisted ≥8 days and was not detectable at 28 days.
Adventitial nab-rapamycin injection was safe and significantly reduced luminal stenosis in a porcine femoral artery balloon angioplasty model. Observed reductions in early adventitial leukocyte infiltration and late medial cell proliferation and fibrosis suggest an immunosuppressive and antiproliferative mechanism. An intraluminal microinfusion catheter for adventitial injection represents an alternative to stent- or balloon-based local drug delivery.
外周动脉的血管内介入治疗受到再狭窄高发生率的限制。我们的假设是,在猪股动脉球囊血管成形术模型中外膜注射雷帕霉素纳米颗粒是安全的,并能减少管腔狭窄。
纳入18只幼年雄性杂交猪。比较了单次损伤模型(40%-60%股动脉球囊过度扩张损伤;n = 2)和双次损伤模型(在20%-30%过度扩张损伤前2周进行内皮剥脱损伤;n = 2)。双次损伤模型在28天时产生的管腔狭窄明显更多,P = 0.002,而在中层纤维化或炎症方面无差异。4只猪被随机分配到双次损伤模型,并通过血管内微输注导管在外膜注射生理盐水(n = 2)或500 μg纳米颗粒白蛋白结合雷帕霉素(nab-雷帕霉素;n = 2)。手术成功率为100%,内皮再生无差异。在28天时,nab-雷帕霉素导致管腔狭窄显著降低,分别为17%(四分位间距,12%-35%)和10%(四分位间距,8.3%-14%),P = 0.001,中层细胞增殖降低,P < 0.001,纤维化降低,P < 0.001。在3天时,外膜白细胞明显减少,P < 0.001,但在28天时无差异。药代动力学分析(单次损伤模型)发现,在1小时时,血管周围组织中的雷帕霉素浓度比血液中的高1500倍。血管周围的雷帕霉素持续≥8天,在28天时检测不到。
在猪股动脉球囊血管成形术模型中,外膜注射nab-雷帕霉素是安全的,并显著降低了管腔狭窄。观察到早期外膜白细胞浸润以及晚期中层细胞增殖和纤维化的减少,提示存在免疫抑制和抗增殖机制。用于外膜注射的腔内微输注导管是基于支架或球囊的局部药物递送的一种替代方法。