Towards a practical Fourier transform infrared chemical imaging protocol for cancer histopathology

被引:164
作者
Bhargava, Rohit [1 ]
机构
[1] Univ Illinois, Beckman Inst Adv Sci & Technol, Dept Bioengn, Urbana, IL 61801 USA
关键词
Fourier transform infrared spectroscopy; FTIR imaging; infrared microscopy; prostate; histopathology; microspectroscopy;
D O I
10.1007/s00216-007-1511-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fourier transform infrared (FTIR) chemical imaging is a strongly emerging technology that is being increasingly applied to examine tissues in a high-throughput manner. The resulting data quality and quantity have permitted several groups to provide evidence for applicability to cancer pathology. It is critical to understand, however, that an integrated approach with optimal data acquisition, classification, and validation is necessary to realize practical protocols that can be translated to the clinic. Here, we first review the development of technology relevant to clinical translation of FTIR imaging for cancer pathology. The role of each component in this approach is discussed separately by quantitative analysis of the effects of changing parameters on the classification results. We focus on the histology of prostate tissue to illustrate factors in developing a practical protocol for automated histopathology. Next, we demonstrate how these protocols can be used to analyze the effect of experimental parameters on prediction accuracy by analyzing the effects of varying spatial resolution, spectral resolution, and signal to noise ratio. Classification accuracy is shown to depend on the signal to noise ratio of recorded data, while depending only weakly on spectral resolution.
引用
收藏
页码:1155 / 1169
页数:15
相关论文
共 76 条
[11]  
Bhargava R, 2007, NAT BIOTECHNOL, V25, P31
[12]   High throughput assessment of cells and tissues: Bayesian classification of spectral metrics from infrared vibrational spectroscopic imaging data [J].
Bhargava, Rohit ;
Fernandez, Daniel C. ;
Hewitt, Stephen M. ;
Levin, Ira W. .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2006, 1758 (07) :830-845
[13]  
Bhargava R, 2005, SHEFF ANALY CHEM, P1
[14]  
Boydston-White S, 1999, BIOSPECTROSCOPY, V5, P219, DOI 10.1002/(SICI)1520-6343(1999)5:4<219::AID-BSPY2>3.0.CO
[15]  
2-O
[16]   Minimization of optical non-linearities in Fourier transform-infrared microspectroscopic imaging [J].
Budevska, BO .
VIBRATIONAL SPECTROSCOPY, 2000, 24 (01) :37-45
[17]   Validation of tissue microarray technology in breast carcinoma [J].
Camp, RL ;
Charette, LA ;
Rimm, DL .
LABORATORY INVESTIGATION, 2000, 80 (12) :1943-1949
[18]   Molecular imaging of biological samples: Localization of peptides and proteins using MALDI-TOF MS [J].
Caprioli, RM ;
Farmer, TB ;
Gile, J .
ANALYTICAL CHEMISTRY, 1997, 69 (23) :4751-4760
[19]   Resolution limits for infrared microspectroscopy explored with synchrotron radiation [J].
Carr, GL .
REVIEW OF SCIENTIFIC INSTRUMENTS, 2001, 72 (03) :1613-1619
[20]  
CARTER MR, 1995, P SOC PHOTO-OPT INS, V2480, P380, DOI 10.1117/12.210892