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An Innovative Ultrasound Signal Processing Technique to Selectively Detect Nanosized Contrast Agents in Echographic Images

机译:一种创新的超声信号处理技术,可选择性地检测笔迹图像中的纳米造影剂

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The aim of this paper was to optimize the employment of a novel algorithm for acquisition and processing of medical ultrasound (US) signals to facilitate its clinical translation. The implemented procedure is dedicated to selective enhancement of nanoparticle (NP) contrast agents in echographic images and is based on the differences in US signal backscatter between NP-containing targets and more homogeneous objects. Previous preliminary studies verified the feasibility of this approach on silica nanospheres (SiNSs) dispersed at a constant volume concentration (0.7%) in agarose gel samples. The present extended these evaluations, addressing two issues of direct clinical interest: 1) safety: SiNSs were coated with a biocompatible layer made of polyethylene glycol (PEG) and the adopted NP volume concentration was reduced to 0.2%, which is in the nontoxic range and 2) reproducibility: a different phantom configuration was used, to verify the independence of algorithm performance from a specific target region shape. The obtained results demonstrated that the proposed method can be effectively applied to enhance the presence of PEG-coated SiNSs in the diameter range 160–660 nm at a low and biocompatible volume concentration: the combined employment of a phantom with a different geometry and a lower concentration of PEG-coated NPs, in fact, caused only slight variations in the suppression patterns of noncontrast echoes, without affecting the final diagnostic effectiveness of the investigated contrast detection scheme. This approach also provides specific advantages with respect to the available measurement techniques dedicated to the enhancement of targeted US contrast agents for molecular imaging purposes.
机译:本文的目的是优化采用一种新算法来采集和处理医学超声(US)信号,以促进其临床翻译。实施的过程专用于选择性增强超声图像中的纳米颗粒(NP)造影剂,并且基于含NP的目标与更均质物体之间US信号反向散射的差异。先前的初步研究证实了这种方法在琼脂糖凝胶样品中以恒定体积浓度(0.7%)分散的二氧化硅纳米球(SiNSs)上的可行性。本研究扩展了这些评估,解决了直接临床关注的两个问题:1)安全性:SiNSs涂有由聚乙二醇(PEG)制成的生物相容性层,并且所采用的NP体积浓度降低至0.2%,这在无毒范围内2)重现性:使用了不同的幻像配置,以验证算法性能与特定目标区域形状之间的独立性。获得的结果表明,所提出的方法可以有效地增强在低且生物相容的体积浓度下直径范围为160-660 nm的PEG包被的SiNS的存在:结合使用具有不同几何形状和更低体积的体模实际上,涂覆PEG的NP的浓度仅引起非对比回波抑制模式的微小变化,而不会影响所研究的对比检测方案的最终诊断效果。关于专用于增强用于分子成像目的的靶向美国造影剂的可用测量技术,该方法还提供了特定的优势。

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