Some practical considerations about the effects of radiation damage on hydrated cells imaged by X-ray fluorescence microscopy

被引:21
作者
Fayard, B. [1 ]
Salome, M. [1 ]
Takemoto, K. [2 ]
Kihara, H. [2 ]
Susini, J. [1 ]
机构
[1] European Synchrotron Radiat Facil, F-38043 Grenoble, France
[2] Kansai Med Univ, Dept Phys, Osaka 5731136, Japan
关键词
X-ray microscopy; Radiation damage; Synchrotron; Fluorescence; BLOOD-CELLS; BIOLOGICAL-MATERIALS; PHASE-CONTRAST; VANADIUM; ACCUMULATION; TOMOGRAPHY; RESOLUTION; ASCIDIANS; APOPTOSIS; COPPER;
D O I
10.1016/j.elspec.2008.11.003
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
X-ray fluorescence (XRF) microscopy features unique capabilities which make it well suited for biological investigations. Its high sensitivity together with high spatial resolution and penetration depth provide a unique tool for trace elements analysis in heterogeneous samples. Like most of the X-ray based techniques, radiation damage sets hard limits on the ultimate performance. Although the interactions between matter and photons are well described from a physics point-of-view, there is a lack of experimental data, in particular for XRF imaging mode. in this context, this work proposes a practical approach in addressing the limits set by radiation damage to X-ray fluorescence imaging in the case of hydrated and unfixed cells at room temperature. We find that the maximum dose tolerated by ascidian blood cells is 10(5) Gy. A simple theoretical model allowed the minimal closes required for a good image contrast to be determined for various experimental schemes. The results are consistent with the experimental observation on ascidian blood cells which exemplifies the peculiar case of highly concentrated samples (> 10,000 ppm) at room temperature. The same simple model predict; that in the case of the detection of high Z trace elements in cryo-preserved cells, the relative detection limit set by radiation damage is below 0.1 ppm at a spatial resolution of 100 nm. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:19 / 24
页数:6
相关论文
共 36 条
[1]  
Abraham-Peskir JV, 2000, CELL MOL BIOL, V46, P1045
[2]   Advanced analytical techniques: platform for nano materials science [J].
Adams, F ;
Van Vaeck, L ;
Barrett, R .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 2005, 60 (01) :13-26
[3]   Soft X-ray radiation-damage studies in PMMA using a cryo-STXM [J].
Beetz, T ;
Jacobsen, C .
JOURNAL OF SYNCHROTRON RADIATION, 2003, 10 :280-283
[4]  
Belyakov OV, 1999, INT J RADIAT BIOL, V75, P985, DOI 10.1080/095530099139746
[5]   Synchrotron hard x-ray microprobe:: Fluorescence imaging of single cells [J].
Bohic, S ;
Simionovici, A ;
Snigirev, A ;
Ortega, R ;
Devès, G ;
Heymann, D ;
Schroer, CG .
APPLIED PHYSICS LETTERS, 2001, 78 (22) :3544-3546
[6]  
CHAMPION C, 1999, THESIS U P M CURIE P
[7]   A single low dose of X-rays induces high frequencies of genetic instability (aneuploidy) and heritable damage (apoptosis), dependent on cell type and p53 status [J].
Crompton, NEA ;
Shi, YQ ;
Wuergler, F ;
Blattmann, H .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2002, 517 (1-2) :173-186
[8]  
DELRIO MS, 1997, SPIE P, V3152, P148
[9]   X-ray fluorescence microscopy reveals large-scale relocalization and extracellular translocation of cellular copper during angiogenesis [J].
Finney, Lydia ;
Mandava, Suneeta ;
Ursos, Lyann ;
Zhang, Wen ;
Rodi, Diane ;
Vogt, Stefan ;
Legnini, Daniel ;
Maser, Jorg ;
Ikpatt, Francis ;
Olopade, Olufunmilayo I. ;
Glesne, David .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (07) :2247-2252
[10]   The vanadium environment in blood cells of Ascidia ceratodes is divergent at all organismal levels:: an XAS and EPR spectroscopic study [J].
Frank, P ;
Carlson, RMK ;
Carlson, EJ ;
Hodgson, KO .
JOURNAL OF INORGANIC BIOCHEMISTRY, 2003, 94 (1-2) :59-71