MICROBUBBLE ENZYME-LINKED IMMUNOSORBENT ASSAY FOR THE DETECTION OF TARGETED MICROBUBBLES IN IN VITRO STATIC BINDING ASSAYS

被引:4
|
作者
Wischhusen, Jennifer [1 ,2 ]
Padilla, Frederic [1 ,2 ]
机构
[1] INSERM, U1032, LabTAU, Lyon, France
[2] Univ Lyon, Lyon, France
来源
ULTRASOUND IN MEDICINE AND BIOLOGY | 2017年 / 43卷 / 07期
关键词
Targeted microbubbles; Microbubble quantification; Enzyme-linked immunosorbent assay; Static binding assays; Ultrasound molecular imaging; ULTRASOUND CONTRAST AGENTS; TUMOR ANGIOGENESIS; CANCER NEOVASCULATURE; ENDOTHELIAL-CELLS; EARLIER DETECTION; BREAST-CANCER; COLON-CANCER; ENHANCED US; MOUSE MODEL; P-SELECTIN;
D O I
10.1016/j.ultrasmedbio.2017.03.004
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
Targeted microbubbles (MBs) are ultrasound contrast agents that are functionalized with a ligand for ultrasound molecular imaging of endothelial markers. Novel targeted MBs are characterized in vitro by incubation in protein-coated wells, followed by binding quantification by microscopy or ultrasound imaging. Both methods provide operator-dependent results: Between 3 and 20 fields of view from a heterogeneous sample are typically selected for analysis by microscopy, and in ultrasound imaging, different acoustic settings affect signal intensities. This study proposes a new method to reproducibly quantify MB binding based on enzyme-linked immunosorbent assay (ELISA), in which bound MBs are revealed with an enzyme-linked antibody. MB-ELISA was adapted to in vitro static binding assays, incubating the MBs in inverted position or by agitation, and compared with microscopy. The specificity and sensitivity of MB-ELISA enable the reliable quantification of MB binding in a rapid, high-throughput and whole-well analysis, facilitating the characterization of new targeted contrast agents. (E-mail: frederic.padilla@inserm.fr) (C) 2017 World Federation for Ultrasound in Medicine & Biology.
引用
收藏
页码:1506 / 1519
页数:14
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