靶向输送血管系统中的药物。

Vladimir Muzykantov, Silvia Muro
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引用次数: 0

摘要

治疗药物的递送和效果仍不理想。大多数药物对它们的靶标没有亲和力。包括酶和遗传物质在内的生物疗法需要特定的亚细胞定位,这是无法自然实现的。内皮细胞位于血管管腔表面,是许多疾病的关键治疗靶点。细胞培养和动物模型的研究表明,使用靶向内皮细胞表面表达的特定分子的载体,可以实现靶向递送治疗药物到内皮细胞、进入内皮细胞和穿过内皮细胞。例如,细胞粘附分子是药物传递的有吸引力的靶标。合理设计药物传递系统(例如,选择最佳的几何形状和对特定表位的亲和力)提供了前所未有的药物传递参数控制水平,如药代动力学,血液循环,与选定的内皮细胞表型结合,锚定在细胞表面或内化到内皮,随后的细胞内寻址和作用的持续时间。我们在这里讨论了内皮靶向药物输送系统设计的关键方面,这些系统有可能转化为临床领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting delivery of drugs in the vascular system.

Delivery and effects of therapeutics remain suboptimal. Most drugs do not have affinity to their targets. Biotherapeutics including enzymes and genetic materials require specific sub-cellular addressing not attainable naturally. Endothelium, lining the luminal surface of blood vessels, represents a key therapeutic target in many diseases. Studies in cell culture and animal models revealed that targeted delivery of therapeutics to, into and across endothelium can be achieved using carriers targeted to specific molecules expressed on the surface of the endothelial cells. For example, cell adhesion molecules represent attractive targets for drug delivery. Rational design of the drug delivery systems (e.g., selection of optimal geometry and affinity to specific epitopes) provides an unprecedented level of control of such parameters of drug delivery as pharmacokinetics, circulation in blood, binding to selected endothelial cell phenotypes, anchoring on cell surface or internalization into the endothelium, subsequent intracellular addressing and duration of the effects. We discusse here key aspects of design of endothelium-targeted drug delivery systems with potential for translation into the clinical domain.

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