Department of Dermatology, Erasmus MC, P.O. Box 2040, 3000 CA Rotterdam, The Netherlands.
J Biophotonics. 2011 Oct;4(10):721-30. doi: 10.1002/jbio.201100053. Epub 2011 Aug 15.
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.
在光动力疗法(PDT)期间对血管生理学进行光学监测可能有助于了解特定患者的治疗效果。然而,扩散光学技术未能观察到此处的变化,这可能是由于光学采样太深。因此,我们研究了使用差分路径长度光谱(DPS)来获得光化性角化病(AK)皮肤中血管生理学的浅表测量值。根据 AK 组织学样本的厚度,AK 特异性 DPS 询问深度选择高达 400 微米的深度。在光分档氨基酮戊酸-PDT 期间,分析反射光谱以获得血液体积和饱和度的定量估计。在 PDT 期间,血液体积显示出与病变特异性相关的显著变化,而饱和度在 PDT 期间仍然很高。这项研究表明,DPS 允许在皮肤 PDT 期间对浅表血液体积和饱和度进行光学监测。病变特异性的可变性支持剂量测量的需要。在 DPS 中,病变特异性的最佳询问深度可以根据病变厚度进行调整。