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神经外科手术显微镜的光学特性:定量荧光和 PpIX 光漂白评估。

Optical Characterization of Neurosurgical Operating Microscopes: Quantitative Fluorescence and Assessment of PpIX Photobleaching.

机构信息

Department of Neurosurgery, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona, USA.

RGB Optics, Lake Forest Park, WA, USA.

出版信息

Sci Rep. 2018 Aug 22;8(1):12543. doi: 10.1038/s41598-018-30247-6.

Abstract

Protoporphyrin IX (PpIX) induced by 5-aminolevulinic acid (5-ALA) is increasingly used as a fluorescent marker for fluorescence-guided resection of malignant gliomas. Understanding how the properties of the excitation light source and PpIX fluorescence interact with the surgical microscope is critical for effective use of the fluorescence-guided tumor resection technique. In this study, we performed a detailed assessment of the intensity of the emitted blue light and white light and the light beam profile of clinical grade operating microscopes used for PpIX visualization. These measurements revealed both recognized fluorescence photobleaching limitations and unrecognized limitations that may alter quantitative observations of PpIX fluorescence obtained with the operating microscope with potential impact on research and clinical uses. We also evaluated the optical properties of a photostable fluorescent standard with an excitation-emission profile similar to PpIX. In addition, we measured the time-dependent dynamics of 5-ALA-induced PpIX fluorescence in an animal glioma model. Finally, we developed a ratiometric method for quantification of the PpIX fluorescence that uses the photostable fluorescent standard to normalize PpIX fluorescence intensity. This method increases accuracy and allows reproducible and direct comparability of the measurements from multiple samples.

摘要

原卟啉 IX(PpIX)在 5-氨基酮戊酸(5-ALA)的诱导下,被越来越多地用作荧光引导切除恶性脑胶质瘤的荧光标记物。了解激发光源的特性和 PpIX 荧光如何与手术显微镜相互作用,对于有效利用荧光引导肿瘤切除技术至关重要。在这项研究中,我们详细评估了用于 PpIX 可视化的临床级手术显微镜发出的蓝光和白光的强度以及光束轮廓。这些测量结果揭示了公认的荧光光漂白限制以及可能改变通过手术显微镜获得的 PpIX 荧光定量观察的未被认识到的限制,这可能对研究和临床应用产生影响。我们还评估了具有与 PpIX 相似激发-发射谱的光稳定荧光标准的光学特性。此外,我们测量了动物脑胶质瘤模型中 5-ALA 诱导的 PpIX 荧光的时变动力学。最后,我们开发了一种用于 PpIX 荧光定量的比率法,该方法使用光稳定荧光标准来归一化 PpIX 荧光强度。该方法提高了准确性,并允许对来自多个样本的测量进行可重复且直接的比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8f/6105612/13d59937f2ed/41598_2018_30247_Fig1_HTML.jpg

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