Department of Pharmacology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104-6068, USA.
Semin Thromb Hemost. 2010 Apr;36(3):332-42. doi: 10.1055/s-0030-1253455. Epub 2010 May 20.
The endothelium is one of the key targets for pharmacological interventions in oxidative stress and thrombosis, two conditions that are notoriously difficult to treat due to limited efficacy and precision of action of current drugs. Design of molecular and nano-devices that deliver potent antioxidant and antithrombotic therapeutic enzymes to the endothelium holds promise to improve the potency, localization, timing, specificity, safety, and mechanistic precision of these interventions. In particular, cell adhesion molecules expressed on the surface of resting and pathologically altered endothelial cells can be used for drug delivery to the endothelial surface (preferable for thrombolytics) and into intracellular compartments (preferable for antioxidants). Drug delivery platforms including protein conjugates, recombinant fusion constructs, and stealth polymer carriers designed to target these drugs to endothelium are reviewed in this article.
内皮细胞是氧化应激和血栓形成中药物干预的关键靶点之一,由于现有药物的疗效和作用精度有限,这两种情况的治疗一直非常困难。设计将强效抗氧化和抗血栓治疗酶递送至内皮细胞的分子和纳米器件有望提高这些干预措施的效力、定位、时间、特异性、安全性和机制精度。特别是,在静止和病理改变的内皮细胞表面表达的细胞黏附分子可用于将药物递送至内皮表面(更适合溶栓药物)和细胞内隔室(更适合抗氧化剂)。本文综述了旨在将这些药物靶向内皮细胞的蛋白质缀合物、重组融合构建体和隐形聚合物载体等药物递送平台。