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靶向超声微泡的设计与特性研究及其在诊断中的应用。

Design and characterization of targeted ultrasound microbubbles for diagnostic use.

机构信息

Omegatri AS, Oslo, Norway.

出版信息

Ultrasound Med Biol. 2011 Jan;37(1):136-50. doi: 10.1016/j.ultrasmedbio.2010.10.010.

Abstract

Targeted ultrasound (US) contrast agents represent, because of their size (1 to 5 μm), 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.

摘要

靶向超声(US)对比剂因其尺寸(1 至 5 μm)而成为独特的一类诊断成像剂,可真正实现炎症和肿瘤血管生成等疾病的血管成像。本研究的目的是开发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。已证明磷脂酰胆碱(PC)是最有利的壁材料。各种巯基化肽结合物可有效地与马来酰亚胺功能化脂质(95:5)的基于 PC 的微泡结合,而无需使用生物素-链霉亲和素或抗体技术。通过优化该技术,在存在 100%血清的情况下,成功实现了对炎症靶标 E-选择素和血管生成靶标 VEGFR2 的特异性靶向。增加磷脂酰胆碱的碳链长度从 18 个碳原子增加到 22 个碳原子,可改善微泡在超声暴露期间的稳定性,而不会影响结合或声学特性。

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