3.8 Article

Nonresonant CARS Imaging of Porous and Solid Silicon Nanoparticles in Human Cells

期刊

ACS BIOMATERIALS SCIENCE & ENGINEERING
卷 8, 期 10, 页码 4185-4195

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsbiomaterials.1c00771

关键词

coherent anti-Stokes Raman scattering (CARS); porous silicon; bioimaging; nanoparticles; nonlinear optical imaging

资金

  1. Russian Science Foundation [19-72-10131]
  2. Academy of Finland [317042, 331151]
  3. University of Helsinki Research Funds
  4. Helsinki Institute of Life Science Funds
  5. Sigrid Juselius Foundation
  6. Russian Foundation for Basic Research [20-015-00157, 190345, 181301]

向作者/读者索取更多资源

Coherent anti-Stokes Raman scattering (CARS) is a powerful optical method for rapid visualization of biological objects. In this study, efficient nonresonant CARS imaging of silicon nanoparticles (SiNPs) in human cells was demonstrated. SiNPs can be visualized without specific labels due to their high third-order nonlinear susceptibility. CARS microscopy provides localization of SiNPs within biological structures at the cellular level and can be used to monitor various bioprocesses.
Coherent anti-Stokes Raman scattering (CARS), a nonlinear optical method for rapid visualization of biological objects, represents a progressive tool in biology and medicine to explore cells and tissue structures in living systems and biopsies. In this study, we report efficient nonresonant CARS imaging of silicon nanoparticles (SiNPs) in human cells as a proof of concept. As both bulk and porous silicon exhibit a high third-order nonlinear susceptibility, chi(3), which is responsible for the CARS intensity, it is possible to visualize the SiNPs without specific labels. Porous and solid SiNPs were obtained from layers of porous and nonporous silicon nanowires and mesoporous silicon. Electron microscopy and Raman spectroscopy showed that porous SiNPs consisted of similar to 3 nm silicon nanocrystals (nc-Si) and pores, whereas solid nanoparticles comprised similar to 30 nm nc-Si. All types of SiNPs were nontoxic at concentrations up to 500 mu g/mL after 24 h of incubation with cells. We demonstrated that although nc-Si possesses a distinguished narrow Raman band of about 520 cm-1, it is possible to detect a high CARS signal from SiNPs in the epi-direction even in a nonresonant regime. 3D CARS images showed that all types of studied SiNPs were visualized as bright spots inside the cytoplasm of cells after 3-6 h of incubation because of the contrast provided by the high third-order nonlinear susceptibility of SiNPs, which is 1 x 104 to 1 x 105 times higher than that of water and typical biological media. Overall, CARS microscopy can provide localization of SiNPs within biological structures at the cellular level and can be a powerful tool for in vitro monitoring of silicon-based drug delivery systems or use SiNPs as labels to monitor various bioprocesses inside living cells.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据