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超声造影剂的靶向性。一项体外可行性研究。

Targeting of ultrasound contrast material. An in vitro feasibility study.

作者信息

Klibanov A L, Hughes M S, Marsh J N, Hall C S, Miller J G, Wible J H, Brandenburger G H

机构信息

Mallinckrodt Medical Imaging Division, St. Louis, MO 63134, USA.

出版信息

Acta Radiol Suppl. 1997;412:113-20.

PMID:9240089
Abstract

PURPOSE

It would be beneficial to design a targetable microbubble ultrasound contrast agent that would selectively bind to the areas of interest in the body and enhance the target organ in the ultrasound examination.

MATERIAL AND METHODS

We have studied the feasibility of targeting in a model system. We used avidin and biotin as a model ligand-receptor pair. Avidin was adsorbed on the surface of polystyrene, and biotin derivative was attached to microbubble shells. After removal of unincorporated biotin from the microbubbles, they were allowed to come in contact with avidin-coated or albumin-coated plastic. Unbound bubbles were washed by a stream of water.

RESULTS

Binding of microbubbles to the surface occurred selectively in the areas where avidin layer was deposited. Binding of microbubbles to avidin layer was dependent on the amount of biotin incorporated in the microbubble shell. Presence of free biotin blocked targeting completely. Acoustic studies were performed using a custom-built ultrasound measurement apparatus and an ultrasound medical imaging system. Microbubble-coated areas of the plastic dish were clearly visualized with ultrasound imaging. A strong backscattered signal was obtained for microbubble surface densities as low as 3%.

CONCLUSION

Microbubbles have been selectively targeted via a ligand-receptor system in vitro. Firm binding of microbubbles to avidin-coated surface has been achieved. Microbubbles deposited on the target were visualized with ultrasound imaging systems.

摘要

目的

设计一种可靶向的微泡超声造影剂,使其能够选择性地结合到体内的感兴趣区域,并在超声检查中增强目标器官,这将是有益的。

材料与方法

我们在一个模型系统中研究了靶向的可行性。我们使用抗生物素蛋白和生物素作为模型配体-受体对。抗生物素蛋白吸附在聚苯乙烯表面,生物素衍生物连接到微泡壳上。从微泡中去除未结合的生物素后,让它们与涂有抗生物素蛋白或白蛋白的塑料接触。未结合的气泡用水流冲洗。

结果

微泡与表面的结合选择性地发生在抗生物素蛋白层沉积的区域。微泡与抗生物素蛋白层的结合取决于微泡壳中掺入的生物素量。游离生物素的存在完全阻断了靶向作用。使用定制的超声测量装置和超声医学成像系统进行了声学研究。塑料培养皿上涂有微泡的区域通过超声成像清晰可见。对于低至3%的微泡表面密度,获得了强烈的反向散射信号。

结论

微泡已在体外通过配体-受体系统实现了选择性靶向。微泡已实现与抗生物素蛋白包被表面的牢固结合。沉积在目标上的微泡通过超声成像系统可见。

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