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Optical detection of meat spoilage using fluorescence spectroscopy with selective excitation wavelength.利用选择性激发波长的荧光光谱法进行肉品腐败的光学检测。
Appl Spectrosc. 2013 Feb;67(2):210-3. doi: 10.1366/12-06653.
3
Characterization and three-dimensional localization of cancerous prostate tissue using backscattering scanning polarization imaging and independent component analysis.使用背散射扫描偏振成像和独立成分分析对癌变前列腺组织进行特征描述和三维定位。
J Biomed Opt. 2012 Aug;17(8):081419. doi: 10.1117/1.JBO.17.8.081419.
4
Near infrared photonic finger imager for prostate cancer screening.近红外光子手指成像仪用于前列腺癌筛查。
Technol Cancer Res Treat. 2011 Dec;10(6):507-17. doi: 10.1177/153303461101000602.
5
Peptide coupling reagents, more than a letter soup.肽偶联试剂,远不止是一堆字母组合。
Chem Rev. 2011 Nov 9;111(11):6557-602. doi: 10.1021/cr100048w. Epub 2011 Aug 26.
6
Compensation-free, all-fiber-optic, two-photon endomicroscopy at 1.55 μm.在 1.55 μm 处实现无补偿、全光纤、双光子内窥成像。
Opt Lett. 2011 Apr 1;36(7):1299-301. doi: 10.1364/OL.36.001299.
7
Nuclear beta-catenin and CD44 upregulation characterize invasive cell populations in non-aggressive MCF-7 breast cancer cells.核β-连环蛋白和 CD44 的上调特征是在非侵袭性 MCF-7 乳腺癌细胞中的侵袭细胞群体。
BMC Cancer. 2010 Aug 10;10:414. doi: 10.1186/1471-2407-10-414.
8
A fiber-optic fluorescence microscope using a consumer-grade digital camera for in vivo cellular imaging.一种使用消费级数码摄像机的光纤荧光显微镜,用于活体细胞成像。
PLoS One. 2010 Jun 23;5(6):e11218. doi: 10.1371/journal.pone.0011218.
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J Bone Joint Surg Am. 2010 Jun;92(6):1453-61. doi: 10.2106/JBJS.I.00765.
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Evaluation of quantitative image analysis criteria for the high-resolution microendoscopic detection of neoplasia in Barrett's esophagus.评价高分辨率微内镜检测 Barrett 食管中肿瘤的定量图像分析标准。
J Biomed Opt. 2010 Mar-Apr;15(2):026027. doi: 10.1117/1.3406386.

合成染料偶联物以使用荧光显微镜观察癌细胞。

Synthesis of dye conjugates to visualize the cancer cells using fluorescence microscopy.

作者信息

Pu Yang, Tang Rui, Xue Jianpeng, Wang W B, Xu Baogang, Achilefu S

出版信息

Appl Opt. 2014 Apr 10;53(11):2345-51. doi: 10.1364/AO.53.002345.

DOI:10.1364/AO.53.002345
PMID:24787403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7328305/
Abstract

The clinical diagnosis of most cancers is based on evaluation of histology microscopic slides to view the size and shape of cellular nuclei and morphological structure of tissue. To achieve this goal for in vivo and in-deep tissues, near infrared dyes-bovine serum albumin and immunoglobulin G conjugates were synthesized. The spectral study shows that the absorption and fluorescence of the dye conjugates are in the "tissue optical window" spectral ranges between 650 and 900 nm. The internalization and pinocytosis of the synthesized compounds were investigated at cell level using fluorescence microscopy to obtain the optimal concentration and staining time.

摘要

大多数癌症的临床诊断是基于对组织学显微镜载玻片的评估,以观察细胞核的大小和形状以及组织的形态结构。为了在体内和深部组织中实现这一目标,合成了近红外染料-牛血清白蛋白和免疫球蛋白G缀合物。光谱研究表明,染料缀合物的吸收和荧光在650至900nm的“组织光学窗口”光谱范围内。使用荧光显微镜在细胞水平上研究了合成化合物的内化和胞饮作用,以获得最佳浓度和染色时间。