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Design and characterization of targeted ultrasound microbubbles for diagnostic use.

机译:用于诊断用途的目标超声微泡的设计和表征。

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摘要

Targeted ultrasound (US) contrast agents represent, because of their size (1 to 5 mum), a unique class of diagnostic imaging agents enabling true vascular imaging of conditions like inflammation and tumor angiogenesis. The objective of this study was to develop technology for preparing targeted microbubbles with binding and acoustic properties compatible with diagnostic use. Phosphatidylcholine (PC) was shown to represent the most favorable wall material. Various thiolated peptide binders were effectively conjugated to PC-based microbubbles containing maleimide functionalized lipids (95:5) without the need for biotin-streptavidin or antibody technology. By optimizing the technology, specific targeting of the inflammatory target E-selectin and the angiogenic target VEGFR2 in the presence of 100% serum was achieved. Increased phospholipid chain length from 18 carbons to 22 carbons improved the stability of the microbubbles during US exposure, without compromising binding or acoustic properties.
机译:靶向超声(US)造影剂由于其尺寸(1至5微米)而代表一类独特的诊断成像剂,可对诸如炎症和肿瘤血管生成等病症进行真正的血管成像。这项研究的目的是开发用于制备具有与诊断用途兼容的结合和声学特性的靶向微泡的技术。磷脂酰胆碱(PC)被证明是最有利的壁材料。无需生物素-链霉亲和素或抗体技术,就可以将各种硫醇化的肽结合剂有效地偶联到含有马来酰亚胺官能化脂质(95:5)的PC基微泡上。通过优化技术,可以在100%血清存在的情况下特异性靶向炎症目标E-选择蛋白和血管生成目标VEGFR2。磷脂链长度从18个碳增加到22个碳可改善微泡在美国暴露期间的稳定性,而不会影响结合或声学性能。

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