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Tracing molecular dephasing in biological tissue

机译:追踪生物组织中的分子移相

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摘要

We demonstrate the quantitative spectroscopic characterization and imaging of biological tissue using coherent time-domain microscopy with a femtosecond resolution. We identify tissue constituents and perform dephasing time (T_2) measurements of characteristic Raman active vibrations. This was shown in subcutaneous mouse fat embedded within collagen rich areas of the dermis and the muscle connective tissue. The demonstrated equivalent spectral resolution (<0.3cm~(-1)) is an order of magnitude better compared to commonly used frequency-domain methods for characterization of biological media. This provides with the important dimensions and parameters in biological media characterization and can become an effective tool in detecting minute changes in the bio-molecular composition and environment that is critical for molecular level diagnosis.
机译:我们证明了飞秒分辨率使用相干时域显微镜的生物组织的定量光谱表征和成像。我们确定组织成分并执行特征性拉曼主动振动的移相时间(T_2)测量。真皮和胶原纤维结缔组织的胶原蛋白丰富区域中嵌入的皮下小鼠脂肪中显示了这一点。与用于生物介质表征的常用频域方法相比,已证明的等效光谱分辨率(<0.3cm〜(-1))好一个数量级。这在生物介质表征中提供了重要的尺寸和参数,并可以成为检测生物分子组成和环境中微小变化的有效工具,而微小变化对于分子水平的诊断至关重要。

著录项

  • 来源
    《Applied Physics Letters》 |2017年第18期|183701.1-183701.4|共4页
  • 作者单位

    Department of Physics, University of Rhode Island, 2 Lippitt Road, Kingston, Rhode Island 02881, USA;

    Department of Physics, University of Rhode Island, 2 Lippitt Road, Kingston, Rhode Island 02881, USA;

    Department of Physics, University of Rhode Island, 2 Lippitt Road, Kingston, Rhode Island 02881, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
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