基于激光的分子数据采集技术

Y. Kistenev, A. Borisov, D. Vrazhnov
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摘要

检验许多疾病的“金标准”是对活检样本进行组织病理学分析。活组织检查是提取细胞或组织进行检查。后者的缺点是耗时和侵入性。在癌症检测中,由于癌细胞可能通过手术区域的血液或淋巴管异化,因此有很高的转移风险。“光学活检”一词已进入生物医学光学领域的常用术语。这个术语内部不一致,因为“活组织检查”特指组织切除,而“光学”的含义是不切除组织。无论如何,“光学活检”通常被理解为光学测量,通常是一种光谱学,以无创(或微创)在体内进行实时诊断。根据所分析的诊断试剂,光学活检通常分为呼吸活检、液体活检和组织活检。光学活检可以作为一种诊断工具或揭示特定的(病理)生理机制。后者与特定化合物的基于化学的鉴定有关。但由于特异性较低,单个分子化合物很难作为特定疾病的生物标志物。通过控制一组分子生物标志物(谱),可以进行可靠的诊断。生物标记谱的概率区分可以通过模式识别方法进行,这形成了评估可接受诊断准确性的基础。在临床环境中,基于化学分析的个体分子生物标志物鉴定并不是严格必要的;此外,请注意大多数分子生物标志物的生化起源是未知的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Laser-based Molecular Data-Acquisition Technologies
A “gold standard” for the verification of many diseases is histopathology analysis of a biopsy sample. A biopsy is the extraction of cells or tissues for examination. The latter’s disadvantages are that it is time consuming and invasive. In cancer detection, there is a high risk of metastasis due to the cancer cells possible dissimilation through blood or lymph vessels from the region of surgery. The term “optical biopsy” has entered into common usage in the field of biomedical optics. This term has internal inconsistency because “biopsy” refers specifically to tissue removal, whereas the implication of “optical” is that tissue is not removed. Regardless, “optical biopsy” is commonly understood as optical measurements, often a kind of spectroscopy, to noninvasively (or minimally invasively) perform in vivo and real-time diagnosis. Depending on an analyzed diagnostic agent, the optical biopsy is often divided into breath biopsy, liquid biopsy, and tissue biopsy. Optical biopsy can be used as a diagnostic tool or to reveal specific (patho-) physiological mechanisms. The latter is connected with the chemical-based identification of particular compounds. But an individual molecular compound hardly serves as a biomarker of a specific disease due to low specificity. Reliable diagnostics is possible through the control of a group (profile) of molecular biomarkers. Probabilistic discrimination of biomarker profiles can be conducted by a pattern-recognition approach, which forms the basis for assessing acceptable diagnostic accuracy. The chemical analytical-based identification of individual molecular biomarkers is not strictly necessary in a clinical setting; also, note that the biochemical origin of most molecular biomarkers is unknown.
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