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Ligands Designed for Targeting Nanoparticles Differentiate Normal and Atherosclerotic Tissue

机译:设计用于靶向纳米颗粒的配体区分正常和动脉粥样硬化组织

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The ability to target specific tissues, normal and disease-state, is a critical component for developing nano-scale particles that can detect, analyse, and deliver drugs to the desired location. This study has demonstrated that antibody-based ligands can be used to differentially bind endothelium in the disease-state, i.e. atherosclerotic plaque. Future studies extending from this research will explore the binding potential of ligands to other disease-state endothelial markers, such as inflammatory, thrombogenic, and cell-cell/cell-extracellular matrix adhesion markers. This targeting approach is particularly relevant to nanoparticle design, since it provides both a vascular pathway and disease-specific target for their localization and subsequent detection in vivo.
机译:靶向特异性组织,正常和疾病状态的能力是用于开发纳米​​级颗粒可以检测,分析和递送药物到所需位置的关键组分。该研究表明,抗体基配体可用于差异地在疾病状态下结合内皮,即动脉粥样硬化斑块。从该研究延伸的未来研究将探讨配体与其他疾病状态内皮标记物的结合潜力,例如炎症,血栓形成和细胞 - 细胞/细胞 - 细胞外基质粘附标记。这种靶向方法与纳米粒子设计特别相关,因为它为其定位和随后的体内检测提供了血管途径和疾病特异性靶标。

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