• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

使用油浸法进行折射率和脉冲展宽特性的表征及其对在 1700nm 窗口激发的三光子显微镜的影响。

Refractive index and pulse broadening characterization using oil immersion and its influence on three-photon microscopy excited at the 1700-nm window.

机构信息

Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen, China.

Shenzhen Key Laboratory of Marine Bioresource and Eco-Environmental Science, Guangdong Engineering Research Center for Marine Algal Biotechnology, College of Life Science and Oceanography, Shenzhen University, Shenzhen, China.

出版信息

J Biophotonics. 2019 Feb;12(2):e201800263. doi: 10.1002/jbio.201800263. Epub 2018 Oct 5.

DOI:10.1002/jbio.201800263
PMID:30239164
Abstract

Three-photon microscopy excited at the 1700-nm window enables deep-tissue penetration. However, the refractive indices of commonly used immersion oils, and the resultant pulse broadening are not known, preventing imaging optimization. Here, we demonstrate detailed characterization of the refractive index, pulse broadening and distortion for excitation pulses at this window for commonly used immersion oils. On the physical side, we uncover that absorption, rather than material dispersion, is the main cause of pulse broadening and distortion. On the application side, comparative three-photon imaging results indicate that 1600-nm excitation yields 5 times higher three-photon signal than 1690-nm excitation.

摘要

三光子显微镜在 1700nm 窗口激发,实现了深层组织穿透。然而,常用浸没油的折射率以及由此产生的脉冲展宽尚不清楚,这阻碍了成像的优化。在这里,我们展示了对常用浸没油在该窗口的激发脉冲的折射率、脉冲展宽和失真的详细特性。从物理方面来看,我们揭示了脉冲展宽和失真的主要原因是吸收,而不是材料色散。在应用方面,比较三光子成像结果表明,1600nm 激发产生的三光子信号比 1690nm 激发高 5 倍。

相似文献

1
Refractive index and pulse broadening characterization using oil immersion and its influence on three-photon microscopy excited at the 1700-nm window.使用油浸法进行折射率和脉冲展宽特性的表征及其对在 1700nm 窗口激发的三光子显微镜的影响。
J Biophotonics. 2019 Feb;12(2):e201800263. doi: 10.1002/jbio.201800263. Epub 2018 Oct 5.
2
Deep-brain three-photon microscopy excited at 1600 nm with silicone oil immersion.1600nm 激发的硅酮油浸深脑三光子显微镜。
J Biophotonics. 2019 Jun;12(6):e201800423. doi: 10.1002/jbio.201800423. Epub 2019 Mar 13.
3
Deep-skin multiphoton microscopy in vivo excited at 1600 nm: A comparative investigation with silicone oil and deuterium dioxide immersion.1600nm 激发的深层皮肤多光子显微镜体内成像:硅油和重水浸没的比较研究。
J Biophotonics. 2021 Oct;14(10):e202100076. doi: 10.1002/jbio.202100076. Epub 2021 Jun 29.
4
Order-of-magnitude multiphoton signal enhancement based on characterization of absorption spectra of immersion oils at the 1700-nm window.基于对1700纳米窗口浸油吸收光谱的表征实现数量级多光子信号增强。
Opt Express. 2017 Mar 20;25(6):5909-5916. doi: 10.1364/OE.25.005909.
5
The effects of spherical aberration on multiphoton fluorescence excitation microscopy.球差对多光子荧光激发显微镜的影响。
J Microsc. 2011 May;242(2):157-65. doi: 10.1111/j.1365-2818.2010.03449.x. Epub 2010 Oct 11.
6
Deep-Brain 3- and 4-Photon Fluorescence Imaging of Subcortical Structures Labeled by Quantum Dots Excited at the 2200 nm Window.2200纳米窗口激发的量子点标记的皮层下结构的深部脑三光子和四光子荧光成像
ACS Nano. 2023 Feb 28;17(4):3686-3695. doi: 10.1021/acsnano.2c10724. Epub 2023 Feb 17.
7
Coherence-Gated Sensorless Adaptive Optics Multiphoton Retinal Imaging.相干门控无传感器自适应光学多光子视网膜成像。
Sci Rep. 2016 Sep 7;6:32223. doi: 10.1038/srep32223.
8
In Vivo Deep-Brain Structural and Hemodynamic Multiphoton Microscopy Enabled by Quantum Dots.基于量子点的在体大脑结构和血液动力学多光子显微镜技术
Nano Lett. 2019 Aug 14;19(8):5260-5265. doi: 10.1021/acs.nanolett.9b01708. Epub 2019 Jul 8.
9
The effects of refractive index heterogeneity within kidney tissue on multiphoton fluorescence excitation microscopy.肾脏组织内的折射率不均匀性对多光子荧光激发显微镜的影响。
J Microsc. 2011 May;242(2):148-56. doi: 10.1111/j.1365-2818.2010.03448.x. Epub 2010 Sep 27.
10
Beyond the 1/Tp limit: two-photon-excited fluorescence using pulses as short as sub-10-fs.超越 1/Tp 极限:使用短至亚 10 飞秒的脉冲进行双光子激发荧光。
J Biomed Opt. 2009 Sep-Oct;14(5):054041. doi: 10.1117/1.3253388.

引用本文的文献

1
Three-photon excited fluorescence imaging in neuroscience: From principles to applications.神经科学中的三光子激发荧光成像:从原理到应用
Front Neurosci. 2023 Feb 20;17:1085682. doi: 10.3389/fnins.2023.1085682. eCollection 2023.
2
The frontier of live tissue imaging across space and time.活组织成像在时空上的前沿。
Cell Stem Cell. 2021 Apr 1;28(4):603-622. doi: 10.1016/j.stem.2021.02.010.