THE ROLE OF SECONDARY ION MASS-SPECTROMETRY (SIMS) IN BIOLOGICAL MICROANALYSIS - TECHNIQUE COMPARISONS AND PROSPECTS

被引:40
作者
LINTON, RW
GOLDSMITH, JG
机构
[1] Department of Chemistry, University of North Carolina, Chapel Hill
关键词
SIMS MICROSCOPY; BIOLOGICAL MICROANALYSIS; MICROPROBE TECHNIQUES;
D O I
10.1016/0248-4900(92)90021-R
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The virtues and limitations of SIMS ion microscopy are compared with other spectroscopic techniques applicable to biological microanalysis, with a special emphasis on techniques for elemental localization in biological tissue (electron, X-ray, laser, nuclear, ion microprobes). Principal advantages of SIMS include high detection sensitivity, high depth resolution, isotope specificity, and possibilities for three-dimensional imaging. Current limitations, especially in comparison to X-ray microanalysis, center on lateral spatial resolution and quantification. Recent SIMS instrumentation advances involving field emission liquid metal ion sources and laser post-ionization will help to minimize these limitations in the future. The molecular surface analysis capabilities of static SIMS, especially with the new developments in commercial time-of-flight spectrometers, are promising for application to biomimetic, biomaterials, and biological tissue or cell surfaces. However, the direct microchemical imaging of biomolecules in tissue samples using SIMS will be hindered by limited concentrations, small analytical volumes, and the inefficiencies of converting surface molecules to structurally significant gas phase ions. Indirect detection using elemental or isotopically tagged molecules, however, shows considerable promise for molecular imaging studies using SIMS ion microscopy.
引用
收藏
页码:147 / 160
页数:14
相关论文
共 210 条
[21]  
BERRY JP, 1984, NICKEL HUMAN ENV, V53, P153
[22]  
Bouquegneau J.M., 1984, P147
[23]   LOW-TEMPERATURE ASHING PRECONCENTRATION FOR ELEMENTAL LOCALIZATION IN BIOLOGICAL SOFT-TISSUES BY ION MICROSCOPY [J].
BRENNA, JT ;
MORRISON, GH .
ANALYTICAL CHEMISTRY, 1984, 56 (14) :2791-2797
[24]   IONIZATION PROBABILITY VARIATIONS DUE TO MATRIX IN ION MICROSCOPIC ANALYSIS OF PLASTIC-EMBEDDED AND ASHED BIOLOGICAL SPECIMENS [J].
BRENNA, JT ;
MORRISON, GH .
ANALYTICAL CHEMISTRY, 1986, 58 (08) :1675-1680
[25]  
BRENNA JT, 1984, MICROBEAM ANAL, V19, P265
[26]  
BRENNA JT, 1986, SPRINGER SER CHEM PH, V44, P124
[27]  
BRENNA JT, 1985, MICROBEAM ANAL, V20, P123
[28]   CHANGES IN I-127 MICE THYROID-FOLLICLE STUDIED BY ANALYTICAL ION MICROSCOPY - A KEY FOR THE COMPREHENSION OF AMIODARONE-INDUCED THYROID-DISEASES [J].
BRIANCON, C ;
HALPERN, S ;
TELENCZAK, P ;
FRAGU, P .
ENDOCRINOLOGY, 1990, 127 (03) :1502-1509
[29]   A MICROCOMPUTER BASED DIGITAL IMAGING-SYSTEM FOR ION MICROANALYSIS [J].
BRYAN, SR ;
WOODWARD, WS ;
GRIFFIS, DP ;
LINTON, RW .
JOURNAL OF MICROSCOPY-OXFORD, 1985, 138 (APR) :15-28
[30]   AN AUTOMATED-METHOD FOR HIGH DYNAMIC-RANGE SECONDARY ION IMAGE DEPTH PROFILING [J].
BRYAN, SR ;
LINTON, RW ;
GRIFFIS, DP .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS, 1986, 4 (05) :2317-2322