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In vivo 3D quantitative analysis of the mouse embryonic brain with a 38 MHz annular array and coded excitation

机译:具有38 MHz环形阵列和编码激发的小鼠胚胎大脑的体内3D定量分析

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During mammalian embryogenesis the central nervous system (CNS) is the first organ to develop, and it dynamically evolves well into the postnatal stages. Magnetic resonance imaging (MRI) has traditionally been the modality of choice to visualize and analyze abnormal in vivo and fixed sample CNS phenotypes in the adult and late stage embryonic mouse. Extending these techniques for in vivo imaging of the the early stages of mouse embryo CNS will be a technical challenge for MRI with the current state of coil technology. High-frequency ultrasound imaging systems have become an important complimentary, non-invasive imaging modality which can image small structures at resolutions comparable to those of microMRI. Previous work reported on the development of a 38 MHz annular array imaging system and demonstrated its capabilities to extend the depth of field and increase the signal-to-noise ratio over traditional fixed-focus imaging transducers. Here the array system was extended by implementation of coded excitation and respiratory gating to develop an imaging protocol which has permitted the in vivo and in utero acquisition of complete volumetric datasets in about 2 minutes. After validating our protocol, we acquired volumetric datasets from 78 mouse embryos spanning embryonic days 10 to 13. The high-quality images enabled us to segment out the complete neuroanatomy of the mouse CNS and to perform statistical analysis of the CNS development.
机译:在哺乳动物胚胎发生过程中,中枢神经系统(CNS)是第一个发育的器官,它动态地进化到产后阶段。传统上,磁共振成像(MRI)是可视化和分析成年和晚期胚胎小鼠体内和固定样本CNS表型异常的模式。扩展这些技术以对小鼠胚胎中枢神经系统的早期进行体内成像,在当前线圈技术的现状下,将是MRI的一项技术挑战。高频超声成像系统已成为一种重要的补充性,非侵入性成像方式,可以以与microMRI相当的分辨率成像小型结构。先前的工作报道了38 MHz环形阵列成像系统的开发,并证明了其具有扩展景深和增加信噪比的能力,优于传统的定焦成像换能器。在这里,通过实施编码激发和呼吸门控扩展了阵列系统,以开发一种成像方案,该方案已允许在大约2分钟内在体内和子宫内采集完整的体积数据集。验证我们的方案后,我们从10到13天胚胎的第78天中获取了78个小鼠胚胎的体积数据集。高质量的图像使我们能够划分出小鼠CNS的完整神经解剖结构,并对CNS的发育进行统计分析。

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