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多模态体内分子遗传成像

Multimodality in vivo molecular-genetic imaging.

作者信息

Doubrovin Michael, Serganova Inna, Mayer-Kuckuk Philipp, Ponomarev Vladimir, Blasberg Ronald G

机构信息

Department of Neurology, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.

出版信息

Bioconjug Chem. 2004 Nov-Dec;15(6):1376-88. doi: 10.1021/bc0498572.

Abstract

Multimodality imaging is increasingly being used in molecular-genetic studies in small animals. The coupling of nuclear and optical reporter genes represents the beginning of a far wider application of this technology. Optical imaging and optical reporter systems are cost-effective and time-efficient, they require less resources and space than PET or MRI, and they are particularly well suited for small animal imaging and for in vitro assays to validate different reporter systems. However, optical imaging techniques are limited by depth of light penetration and scatter and do not yet provide optimal quantitative or tomographic information. These issues are not limiting for PET- or MRI-based reporter systems, and PET- and MRI-based animal studies are more easily generalized to human applications. Many of the shortcomings of each modality alone can be overcome by the use of dual- or triple-modality reporter constructs that incorporate the opportunity for PET, fluorescence and bioluminescence imaging. We optimistically expect that some form of tomographic, small animal optical imaging capability will be developed soon, and that this will provide the opportunity for the colocalization of optical signals to anatomical structures provided by tomographic CT and MR imaging.

摘要

多模态成像在小动物分子遗传学研究中的应用越来越广泛。核报告基因与光学报告基因的结合代表了这项技术更广泛应用的开端。光学成像和光学报告系统具有成本效益且省时,与PET或MRI相比,它们所需的资源和空间更少,并且特别适合小动物成像以及用于验证不同报告系统的体外分析。然而,光学成像技术受到光穿透深度和散射的限制,尚未提供最佳的定量或断层图像信息。这些问题对于基于PET或MRI的报告系统并非限制因素,并且基于PET和MRI的动物研究更容易推广到人类应用。通过使用结合了PET、荧光和生物发光成像机会的双模态或三模态报告构建体,可以克服每种单独模态的许多缺点。我们乐观地期望,某种形式的断层小动物光学成像能力将很快得到发展,这将为光学信号与断层CT和MR成像提供的解剖结构的共定位提供机会。

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