Department of Pharmaceutical Sciences, College of Pharmacy, University of Michigan, 428 Church St., Ann Arbor, MI 48109, USA.
Department of Pharmacology, University of Michigan Medical School, 1150 W. Medical Center Dr., Room 2220D, Medical Sciences Research Building III, Ann Arbor, MI 48109, USA.
Sci Adv. 2020 Dec 4;6(49). doi: 10.1126/sciadv.abd0130. Print 2020 Dec.
Antiplatelet agents offer a desirable approach to thrombosis prevention through the reduction of platelet reactivity. However, major bleeding events greatly attenuate the clinical outcomes of most antithrombotic agents. Therefore, the development of safer and more effective strategies to prevent vascular occlusion and avoid bleeding is urgently needed. A reconstituted nanoparticle, synthetic high-density lipoprotein (sHDL), which mimics the native HDL, has been established as clinically safe and is easily manufactured on a large scale. In this study, we propose that the delivery of the antiplatelet drug ML355, a selective inhibitor of 12(S)-lipoxygenase (12-LOX), by sHDL will efficiently inhibit thrombosis by targeting ML355 to the intended site of action, improving the pharmaceutical profile and harnessing the innate antithrombotic efficacy of the sHDL carrier. Our data show that ML355-sHDL exhibits more potent inhibition of thrombus formation in both small arterioles and larger arteries in mice without impairing the normal hemostasis in vivo.
抗血小板药物通过降低血小板反应性提供了一种理想的血栓预防方法。然而,大出血事件大大降低了大多数抗血栓药物的临床效果。因此,迫切需要开发更安全、更有效的策略来预防血管阻塞和避免出血。一种重建的纳米颗粒,即合成高密度脂蛋白(sHDL),模拟天然 HDL,已被证明在临床上是安全的,并且可以大规模轻松生产。在这项研究中,我们提出通过 sHDL 输送抗血小板药物 ML355(12-脂氧合酶(12-LOX)的选择性抑制剂),将 ML355 靶向作用部位,从而有效抑制血栓形成,改善药物特性并利用 sHDL 载体的固有抗血栓作用。我们的数据表明,ML355-sHDL 在不损害体内正常止血的情况下,在小鼠的小动脉和较大动脉中更有效地抑制血栓形成。