用于预防开放性手术后内膜增生的外膜周围给药
Periadventitial drug delivery for the prevention of intimal hyperplasia following open surgery.
作者信息
Chaudhary Mirnal A, Guo Lian-Wang, Shi Xudong, Chen Guojun, Gong Shaoqin, Liu Bo, Kent K Craig
机构信息
Department of Surgery, Wisconsin Institute for Medical Research, University of Wisconsin, 1111 Highland Ave, Madison, WI 53705, USA.
Department of Surgery, Wisconsin Institute for Medical Research, University of Wisconsin, 1111 Highland Ave, Madison, WI 53705, USA.
出版信息
J Control Release. 2016 Jul 10;233:174-80. doi: 10.1016/j.jconrel.2016.05.002. Epub 2016 May 12.
BACKGROUND
Intimal hyperplasia (IH) remains a major cause of poor patient outcomes after surgical revascularization to treat atherosclerosis. A multitude of drugs have been shown to prevent the development of IH. Moreover, endovascular drug delivery following angioplasty and stenting has been achieved with a marked diminution in the incidence of restenosis. Despite advances in endovascular drug delivery, there is currently no clinically available method of periadventitial drug delivery suitable for open vascular reconstructions. Herein we provide an overview of the recent literature regarding innovative polymer platforms for periadventitial drug delivery in preclinical models of IH as well as insights about barriers to clinical translation.
METHODS
A comprehensive PubMed search confined to the past 15years was performed for studies of periadventitial drug delivery. Additional searches were performed for relevant clinical trials, patents, meeting abstracts, and awards of NIH funding.
RESULTS
Most of the research involving direct periadventitial delivery without a drug carrier was published prior to 2000. Over the past 15years there have been a surge of reports utilizing periadventitial drug-releasing polymer platforms, most commonly bioresorbable hydrogels and wraps. These methods proved to be effective for the inhibition of IH in various animal models (e.g. balloon angioplasty, wire injury, and vein graft), but very few have advanced to clinical trials. There are a number of barriers that may account for this lack of translation. Promising new approaches including the use of nanoparticles will be described.
CONCLUSIONS
No periadventitial drug delivery system has reached clinical application. For periadventitial delivery, polymer hydrogels, wraps, and nanoparticles exhibit overlapping and complementary properties. The ideal periadventitial delivery platform would allow for sustained drug release yet exert minimal mechanical and inflammatory stresses to the vessel wall. A clinically applicable strategy for periadventitial drug delivery would benefit thousands of patients undergoing open vascular reconstruction each year.
背景
内膜增生(IH)仍然是外科血管重建治疗动脉粥样硬化后患者预后不良的主要原因。大量药物已被证明可预防内膜增生的发生。此外,血管成形术和支架置入术后的血管内药物递送已经实现,再狭窄发生率显著降低。尽管血管内药物递送取得了进展,但目前尚无适用于开放性血管重建的临床可用的外膜周围药物递送方法。在此,我们概述了近期关于在IH临床前模型中外膜周围药物递送的创新聚合物平台的文献,以及关于临床转化障碍的见解。
方法
对过去15年的外膜周围药物递送研究进行了全面的PubMed搜索。还对相关临床试验、专利、会议摘要和美国国立卫生研究院(NIH)资助奖项进行了额外搜索。
结果
大多数涉及无药物载体直接外膜周围递送的研究发表于2000年之前。在过去15年中,利用外膜周围药物释放聚合物平台的报道激增,最常见的是生物可吸收水凝胶和包裹物。这些方法在各种动物模型(如球囊血管成形术、钢丝损伤和静脉移植物)中被证明对抑制内膜增生有效,但很少有进展到临床试验阶段。有许多障碍可能导致这种缺乏转化的情况。将描述包括使用纳米颗粒在内的有前景的新方法。
结论
尚无外膜周围药物递送系统达到临床应用。对于外膜周围递送,聚合物水凝胶、包裹物和纳米颗粒具有重叠和互补的特性。理想的外膜周围递送平台应允许药物持续释放,同时对血管壁施加最小的机械和炎症应激。一种临床适用的外膜周围药物递送策略将使每年数千名接受开放性血管重建的患者受益。