Skala Melissa C, Palmer Gregory M, Zhu Changfang, Liu Quan, Vrotsos Kristin M, Marshek-Stone Crystal L, Gendron-Fitzpatrick Annette, Ramanujam Nirmala
Department of Biomedical Engineering, University of Wisconsin, 1550 Engineering Drive, Madison, WI 53706, USA.
Lasers Surg Med. 2004;34(1):25-38. doi: 10.1002/lsm.10239.
The first objective of this study was to evaluate the performance of fluorescence spectroscopy for diagnosing pre-cancers in stratified squamous epithelial tissues in vivo using two different probe geometries with (1) overlapping versus (2) non-overlapping illumination and collection areas on the tissue surface. Probe (1) and probe (2) are preferentially sensitive to the fluorescence originating from the tissue surface and sub-surface tissue depths, respectively. The second objective was to design a novel, angled illumination fiber-optic probe to maximally exploit the depth-dependent fluorescence properties of epithelial tissues.
STUDY DESIGN/MATERIALS AND METHODS: In the first study, spectra were measured from epithelial pre-cancers and normal tissues in the hamster cheek pouch and analyzed with a non-parametric classification algorithm. In the second study, Monte Carlo modeling was used to simulate fluorescence measurements from an epithelial tissue model with the angled illumination probe.
An unbiased classification algorithm based on spectra measured with probes (1) and (2), classified pre-cancerous and normal tissues with 78 and 94% accuracy, respectively. The angled illumination probe design provides the capability to detect fluorescence from a wide range of tissue depths in an epithelial tissue model.
The first study demonstrates that fluorescence originating from sub-surface tissue depths (probe (2)) is more diagnostic than fluorescence originating from the tissue surface (probe (1)) in the hamster cheek pouch model. However in general, it is difficult to know a priori the optimal probe geometry for pre-cancer detection in a particular epithelial tissue model. The angled illumination probe provides the capability to measure tissue fluorescence selectively from different depths within epithelial tissues, thus obviating the need to select a single optimal probe design for the fluorescence-based diagnosis of epithelial pre-cancers.
本研究的首要目的是评估荧光光谱法在体内诊断分层鳞状上皮组织癌前病变的性能,使用两种不同的探头几何结构,(1)组织表面的照明和采集区域重叠,以及(2)非重叠。探头(1)和探头(2)分别对源自组织表面和亚表面组织深度的荧光具有优先敏感性。第二个目的是设计一种新型的、角度照明光纤探头,以最大程度地利用上皮组织的深度依赖性荧光特性。
研究设计/材料与方法:在第一项研究中,从仓鼠颊囊中的上皮癌前病变和正常组织测量光谱,并用非参数分类算法进行分析。在第二项研究中,使用蒙特卡罗建模来模拟使用角度照明探头从上皮组织模型进行的荧光测量。
基于用探头(1)和(2)测量的光谱的无偏分类算法,对癌前组织和正常组织的分类准确率分别为78%和94%。角度照明探头设计能够检测上皮组织模型中广泛组织深度的荧光。
第一项研究表明,在仓鼠颊囊模型中,源自亚表面组织深度(探头(2))的荧光比源自组织表面(探头(1))的荧光更具诊断性。然而,一般来说,很难事先知道在特定上皮组织模型中用于癌前检测的最佳探头几何结构。角度照明探头能够选择性地测量上皮组织内不同深度的组织荧光,从而无需为基于荧光的上皮癌前病变诊断选择单一的最佳探头设计。