Specific targeting of ultrasound contrast agent (USCA) for diagnostic application: an in vitro feasibility study based on SAW biosensor

被引:19
作者
Joseph, S
Gronewold, TMA
Schlensog, MD
Olbrich, C
Quandt, E
Famulok, M
Schirner, M
机构
[1] Schering AG, Res Dept, CRBA, DG&RP, D-13342 Berlin, Germany
[2] Caesar, Dept Aptamer Biosensors, D-53175 Bonn, Germany
[3] Univ Bonn, Kekule Inst Org Chem & Biochem, D-53121 Bonn, Germany
关键词
surface acoustic wave sensor; love-wave sensor; specific targeting; ultrasound contrast agent; tumor; EDB-fibronectin;
D O I
10.1016/j.bios.2004.07.014
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The present study described a new strategy to examine the interaction between the targeted ultrasound contrast agent (USCA) and its target under flow conditions with a surface acoustic wave (SAW) transducer. The sensing principle is based on the measurement of the phase change on the sensing element upon the binding of specific biomolecules. Love-wave biosensor array was consisting of sensor elements and reference elements. The sensor elements have been prepared by coating the sensor surface with tumor marker EDB-fibronectin by means of SAM technique and carbodiimide chemistry. Reference elements were left blank or coated with fibronectin and used to eliminate thermal drift, unspecific binding, and turbulence from injection of liquids by calculating the differential phase shift with respect to the sensor elements. The binding of targeted USCA to the sensor surface was constantly recorded by monitoring the phase shift on the sensor element. The binding of targeted USCA generated a high phase shift on the sensor elements, but almost no change on the reference elements. Control experiments using non-targeted and isotype-targeted USCA confirmed the specificity of binding due to anti-EDB-fibronectin scFv-antibody-fragment-EDB-fibronectin antigen interaction. The suitability of the SAW technique to monitor the specific binding behavior of targeted micron-sized USCA in real time has been well established. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:1829 / 1835
页数:7
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