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Influence of laser parameters and staining on femtosecond laser-based intracellular nanosurgery
Femtosecond (fs) laser-based intracellular nanosurgery has become an important tool in cell biology, albeit the mechanisms in the so-called low-density plasma regime are largely unknown. Previous calculations of free-electron densities for intracellular surgery used water as a model substance for bi...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Optical Society of America
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3017989/ https://www.ncbi.nlm.nih.gov/pubmed/21258492 http://dx.doi.org/10.1364/BOE.1.000587 |
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author | Kuetemeyer, K. Rezgui, R. Lubatschowski, H. Heisterkamp, A. |
author_facet | Kuetemeyer, K. Rezgui, R. Lubatschowski, H. Heisterkamp, A. |
author_sort | Kuetemeyer, K. |
collection | PubMed |
description | Femtosecond (fs) laser-based intracellular nanosurgery has become an important tool in cell biology, albeit the mechanisms in the so-called low-density plasma regime are largely unknown. Previous calculations of free-electron densities for intracellular surgery used water as a model substance for biological media and neglected the presence of dye and biomolecules. In addition, it is still unclear on which time scales free-electron and free-radical induced chemical effects take place in a cellular environment. Here, we present our experimental study on the influence of laser parameters and staining on the intracellular ablation threshold in the low-density plasma regime. We found that the ablation effect of fs laser pulse trains resulted from the accumulation of single-shot multiphoton-induced photochemical effects finished within a few nanoseconds. At the threshold, the number of applied pulses was inversely proportional to a higher order of the irradiance, depending on the laser repetition rate and wavelength. Furthermore, fluorescence staining of subcellular structures before surgery significantly decreased the ablation threshold. Based on our findings, we propose that dye molecules are the major source for providing seed electrons for the ionization cascade. Consequently, future calculations of free-electron densities for intracellular nanosurgery have to take them into account, especially in the calculations of multiphoton ionization rates. |
format | Text |
id | pubmed-3017989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Optical Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-30179892011-01-21 Influence of laser parameters and staining on femtosecond laser-based intracellular nanosurgery Kuetemeyer, K. Rezgui, R. Lubatschowski, H. Heisterkamp, A. Biomed Opt Express Cell Studies Femtosecond (fs) laser-based intracellular nanosurgery has become an important tool in cell biology, albeit the mechanisms in the so-called low-density plasma regime are largely unknown. Previous calculations of free-electron densities for intracellular surgery used water as a model substance for biological media and neglected the presence of dye and biomolecules. In addition, it is still unclear on which time scales free-electron and free-radical induced chemical effects take place in a cellular environment. Here, we present our experimental study on the influence of laser parameters and staining on the intracellular ablation threshold in the low-density plasma regime. We found that the ablation effect of fs laser pulse trains resulted from the accumulation of single-shot multiphoton-induced photochemical effects finished within a few nanoseconds. At the threshold, the number of applied pulses was inversely proportional to a higher order of the irradiance, depending on the laser repetition rate and wavelength. Furthermore, fluorescence staining of subcellular structures before surgery significantly decreased the ablation threshold. Based on our findings, we propose that dye molecules are the major source for providing seed electrons for the ionization cascade. Consequently, future calculations of free-electron densities for intracellular nanosurgery have to take them into account, especially in the calculations of multiphoton ionization rates. Optical Society of America 2010-08-10 /pmc/articles/PMC3017989/ /pubmed/21258492 http://dx.doi.org/10.1364/BOE.1.000587 Text en ©2010 Optical Society of America http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially. |
spellingShingle | Cell Studies Kuetemeyer, K. Rezgui, R. Lubatschowski, H. Heisterkamp, A. Influence of laser parameters and staining on femtosecond laser-based intracellular nanosurgery |
title | Influence of laser parameters and staining on femtosecond laser-based
intracellular nanosurgery |
title_full | Influence of laser parameters and staining on femtosecond laser-based
intracellular nanosurgery |
title_fullStr | Influence of laser parameters and staining on femtosecond laser-based
intracellular nanosurgery |
title_full_unstemmed | Influence of laser parameters and staining on femtosecond laser-based
intracellular nanosurgery |
title_short | Influence of laser parameters and staining on femtosecond laser-based
intracellular nanosurgery |
title_sort | influence of laser parameters and staining on femtosecond laser-based
intracellular nanosurgery |
topic | Cell Studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3017989/ https://www.ncbi.nlm.nih.gov/pubmed/21258492 http://dx.doi.org/10.1364/BOE.1.000587 |
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