Analysis of long range correlations due to coherent light scattering from in-vitro cell arrays using angle-resolved low coherence interferometry

被引:18
作者
Pyhtila, John W. [1 ]
Ma, Hongwei [1 ]
Simnick, Andrew J. [1 ]
Chilkoti, Ashutosh [1 ]
Wax, Adam [1 ]
机构
[1] Duke Univ, Dept Biomed Engn, Fitzpatrick Ctr Photon, Durham, NC 27708 USA
关键词
low coherence interferometry; scattering measurements; cell arrays;
D O I
10.1117/1.2209561
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Angle-resolved low coherence interferometry (a/LCl) enables depth-resolved measurements of scattered light that can be used to recover subsurface structural information, such as the size of cell nuclei. Measurements of nuclear morphology, however, can be complicated by coherent scattering between adjacent cell nuclei. Previous studies have eliminated this component by applying a window filter to Fourier transformed angular data, based on the justification that the coherent scattering must necessarily occur over length scales greater than the cell size. To fully study this effect, results of experiments designed to test the validity of this approach are now presented. The a/LCl technique is used to examine light scattered by regular cell arrays, created using stamped adhesive micropatterned substrates. By varying the array spacing, it is demonstrated that cell-to-cell correlations have a predictable effect on light scattering distributions. These results are compared to image analysis of fluorescence micrographs of the cell array samples. The a/LCI results show that the impact of coherent scattering on nuclear morphology measurements can be eliminated through data filtering. (c) 2006 Society of Photo-Optical Instrumentation Engineers.
引用
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页数:7
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