Monitoring blood volume and saturation using superficial fibre optic reflectance spectroscopy during PDT of actinic keratosis

被引:11
作者
Middelburg, Tom A. [1 ]
Kanick, Stephen C. [2 ]
de Haas, Ellen R. M. [1 ]
Sterenborg, Henricus J. C. M. [2 ]
Amelink, Arjen [2 ]
Neumann, Martino H. A. M. [1 ]
Robinson, Dominic J. [1 ,2 ]
机构
[1] Erasmus MC, Dept Dermatol, NL-3000 CA Rotterdam, Netherlands
[2] Erasmus MC, Dept Radiat Oncol, Ctr Opt Diagnost & Therapy, NL-3000 CA Rotterdam, Netherlands
关键词
treatment monitoring; blood; saturation; ALA-PDT; dosimetry; spectroscopy; PHOTODYNAMIC THERAPY; PATH-LENGTH; PROTOPORPHYRIN-IX; RAT ESOPHAGUS; TURBID MEDIA; FLUENCE RATE; HUMAN SKIN; FLUORESCENCE; SCATTERING; IRRADIANCE;
D O I
10.1002/jbio.201100053
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Optically monitoring the vascular physiology during photodynamic therapy (PDT) may help understand patient-specific treatment outcome. However, diffuse optical techniques have failed to observe changes herein, probably by optically sampling too deep. Therefore, we investigated using differential path-length spectroscopy (DPS) to obtain superficial measurements of vascular physiology in actinic keratosis (AK) skin. The AK-specific DPS interrogation depth was chosen up to 400 microns in depth, based on the thickness of AK histology samples. During light fractionated aminolevulinic acid-PDT, reflectance spectra were analyzed to yield quantitative estimates of blood volume and saturation. Blood volume showed significant lesion-specific changes during PDT without a general trend for all lesions and saturation remained high during PDT. This study shows that DPS allows optically monitoring the superficial blood volume and saturation during skin PDT. The patient-specific variability supports the need for dosimetric measurements. In DPS, the lesion-specific optimal interrogation depth can be varied based on lesion thickness. [GRAPHICS] Experimental setup of differential path-length spectroscopy.
引用
收藏
页码:721 / 730
页数:10
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