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Monoclonal antibody-based optical molecular imaging probes; considerations and caveats in chemistry, biology and pharmacology

机译:基于单克隆抗体的光学分子成像探针;化学,生物学和药理学方面的注意事项和注意事项

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The monoclonal antibody (mAb) has proven to be a good platform for designing specific molecular imaging probes due to its superior binding specificity. Several optical imaging probes have been developed for surgical navigation in patients and are in early phase clinical trials. However, an inherent limitation of using the mAb is its pharmacokinetics which result in a prolonged circulating half-life and slow clearance from the body. This results in undesirable target to background ratios during imaging. In this review, we first describe the mAb as a platform material for optical probe design and then discuss optimizing the design of monoclonal antibody-based optical molecular imaging probes by focusing on chemistry, biology and pharmacology.
机译:单克隆抗体(mAb)具有优越的结合特异性,已被证明是设计特定分子成像探针的良好平台。已经开发了几种光学成像探针用于患者的手术导航,并且处于早期临床试验中。但是,使用mAb的固有局限性是其药代动力学,这会导致循环半衰期延长和从体内清除缓慢。这导致成像期间不期望的目标与背景之比。在本综述中,我们首先将mAb描述为用于光学探针设计的平台材料,然后通过重点研究化学,生物学和药理学来讨论优化基于单克隆抗体的光学分子成像探针的设计。

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