微气泡
体内分布
脾脏
链霉亲和素
病理
医学
超声波
氰基丙烯酸酯
流式细胞术
血管生成
体内
化学
癌症研究
内科学
放射科
生物素
免疫学
生物
胶粘剂
有机化学
图层(电子)
生物技术
生物化学
作者
Moritz Palmowski,Bernd Morgenstern,Peter Hauff,Michaël Reinhardt,Jochen Huppert,Mathias Mäurer,Eva C. Woenne,Sebastian Doerk,G. Ladewig,Juergen Jenne,Stefan Delorme,Lars Grenacher,Peter Hallscheidt,G. W. Kauffmann,Willi Semmler,Fabian Kießling
标识
DOI:10.1097/rli.0b013e31815a251b
摘要
To assess the pharmacodynamic behavior of cyanoacrylate, streptavidin-coated microbubbles (MBs) and to investigate their suitability for molecular ultrasound imaging.Biodistribution of MBs was analyzed in tumor-bearing mice using gamma-counting, immunohistochemistry, flow cytometry, and ultrasound. Further, vascular endothelial growth factor receptor 2-antibody coupled MBs were used to image tumor neovasculature.After 1 minute >90% of MBs were cleared from the blood and pooled in the lungs, liver, and spleen. Subsequently, within 1 hour a decent reincrease of MB-concentration was observed in the blood. The remaining MBs were removed by liver and spleen macrophages. About 30% of the phagocytosed MBs were intact after 48 hours. Shell fragments were found in the kidneys only. No relevant MB-accumulation was observed in tumors. In contrast, vascular endothelial growth factor receptor 2-specific MBs accumulated significantly within the tumor vasculature (P < 0.05).The pharmacokinetic behavior of streptavidin-coated cyanoacrylate MBs has been studied. In this context, the low amount of MBs in tumors after >5 minutes is beneficial for specific targeting of angiogenesis.
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