应用于生命科学的数字全息显微技术的进展与展望

P. Marquet, J. Kuhn, D. Boss, P. Jourdain, P. Magistretti, N. Pavillon, C. Depeursinge
{"title":"应用于生命科学的数字全息显微技术的进展与展望","authors":"P. Marquet, J. Kuhn, D. Boss, P. Jourdain, P. Magistretti, N. Pavillon, C. Depeursinge","doi":"10.1109/WIO.2010.5582513","DOIUrl":null,"url":null,"abstract":"Digital holographic microscopy (DHM) is a technique that allows obtaining, from a single recorded hologram, quantitative phase image of living cell with interferometric accuracy. Specifically the optical phase shift induced by the specimen on the transmitted wave front can be regarded as a powerful endogenous contrast agent, depending on both the thickness and the refractive index of the sample. The quantitative phase images allow the derivation of highly relevant cell parameters, including dry mass density and spatial distribution. Thanks to a decoupling procedure, cell thickness and intracellular refractive index can be measured separately. Consequently, cell morphology, shape as well as cell membrane fluctuations can be accurately monitor. As far as red blood cell are considered, Mean corpuscular volume (MCV) and mean corpuscular hemoglobin concentration (MCHC), two highly relevant clinical parameters, have been measured non-invasively at a single cell level. The DHM nanometric axial and microsecond temporal sensitivities have permitted to measure the red blood cell membrane fluctuations (CMF) over the whole cell surface. In addition, the development of live-cell multimodality microscope combining fluorescence with digital holographic microscopy is presented. The biophysical cell parameters derived from the quantitative phase information in combination with the numerous different specific fluorescent cellular probes allow to this multimodality microscope to address various important issues in cell biology.","PeriodicalId":201478,"journal":{"name":"2010 9th Euro-American Workshop on Information Optics","volume":"15 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2010-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Progress and perspectives in digital holographic microscopy applied to life sciences\",\"authors\":\"P. Marquet, J. Kuhn, D. Boss, P. Jourdain, P. Magistretti, N. Pavillon, C. Depeursinge\",\"doi\":\"10.1109/WIO.2010.5582513\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Digital holographic microscopy (DHM) is a technique that allows obtaining, from a single recorded hologram, quantitative phase image of living cell with interferometric accuracy. Specifically the optical phase shift induced by the specimen on the transmitted wave front can be regarded as a powerful endogenous contrast agent, depending on both the thickness and the refractive index of the sample. The quantitative phase images allow the derivation of highly relevant cell parameters, including dry mass density and spatial distribution. Thanks to a decoupling procedure, cell thickness and intracellular refractive index can be measured separately. Consequently, cell morphology, shape as well as cell membrane fluctuations can be accurately monitor. As far as red blood cell are considered, Mean corpuscular volume (MCV) and mean corpuscular hemoglobin concentration (MCHC), two highly relevant clinical parameters, have been measured non-invasively at a single cell level. The DHM nanometric axial and microsecond temporal sensitivities have permitted to measure the red blood cell membrane fluctuations (CMF) over the whole cell surface. In addition, the development of live-cell multimodality microscope combining fluorescence with digital holographic microscopy is presented. The biophysical cell parameters derived from the quantitative phase information in combination with the numerous different specific fluorescent cellular probes allow to this multimodality microscope to address various important issues in cell biology.\",\"PeriodicalId\":201478,\"journal\":{\"name\":\"2010 9th Euro-American Workshop on Information Optics\",\"volume\":\"15 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2010-07-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2010 9th Euro-American Workshop on Information Optics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/WIO.2010.5582513\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2010 9th Euro-American Workshop on Information Optics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/WIO.2010.5582513","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

数字全息显微镜(DHM)是一种可以从单个记录的全息图中获得活细胞定量相位图像的技术,具有干涉测量精度。具体来说,试样在透射波前引起的光学相移可被视为一种强大的内源对比剂,它取决于试样的厚度和折射率。定量相位图像可以推导出高度相关的细胞参数,包括干质量密度和空间分布。通过解耦程序,可以分别测量细胞厚度和细胞内折射率。因此,细胞形态、形状以及细胞膜的波动都能得到准确的监测。就红细胞而言,平均血球容积(MCV)和平均血球血红蛋白浓度(MCHC)这两个高度相关的临床参数已在单细胞水平上进行了无创测量。DHM 的纳米级轴向灵敏度和微秒级时间灵敏度允许测量整个细胞表面的红细胞膜波动 (CMF)。此外,还介绍了结合荧光和数字全息显微镜的活细胞多模态显微镜的开发情况。从定量相位信息中得出的细胞生物物理参数与多种不同的特异性荧光细胞探针相结合,使这种多模态显微镜能够解决细胞生物学中的各种重要问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Progress and perspectives in digital holographic microscopy applied to life sciences
Digital holographic microscopy (DHM) is a technique that allows obtaining, from a single recorded hologram, quantitative phase image of living cell with interferometric accuracy. Specifically the optical phase shift induced by the specimen on the transmitted wave front can be regarded as a powerful endogenous contrast agent, depending on both the thickness and the refractive index of the sample. The quantitative phase images allow the derivation of highly relevant cell parameters, including dry mass density and spatial distribution. Thanks to a decoupling procedure, cell thickness and intracellular refractive index can be measured separately. Consequently, cell morphology, shape as well as cell membrane fluctuations can be accurately monitor. As far as red blood cell are considered, Mean corpuscular volume (MCV) and mean corpuscular hemoglobin concentration (MCHC), two highly relevant clinical parameters, have been measured non-invasively at a single cell level. The DHM nanometric axial and microsecond temporal sensitivities have permitted to measure the red blood cell membrane fluctuations (CMF) over the whole cell surface. In addition, the development of live-cell multimodality microscope combining fluorescence with digital holographic microscopy is presented. The biophysical cell parameters derived from the quantitative phase information in combination with the numerous different specific fluorescent cellular probes allow to this multimodality microscope to address various important issues in cell biology.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信