Baran Timothy M, Foster Thomas H
Department of Imaging Sciences, University of Rochester Medical Center, Rochester, New York, 14642.
Lasers Surg Med. 2013 Oct;45(8):542-50. doi: 10.1002/lsm.22166. Epub 2013 Aug 23.
We developed a method for the recovery of intrinsic fluorescence from single-point measurements in highly scattering and absorbing samples without a priori knowledge of the sample optical properties. The goal of the study was to demonstrate accurate recovery of fluorophore concentration in samples with widely varying background optical properties, while simultaneously recovering the optical properties.
Tissue-simulating phantoms containing doxorubicin, MnTPPS, and Intralipid-20% were created, and fluorescence measurements were performed using a single isotropic probe. The resulting spectra were analyzed using a forward-adjoint fluorescence model in order to recover the fluorophore concentration and background optical properties.
We demonstrated recovery of doxorubicin concentration with a mean error of 11.8%. The concentration of the background absorber was recovered with an average error of 23.2% and the scattering spectrum was recovered with a mean error of 19.8%.
This method will allow for the determination of local concentrations of fluorescent drugs, such as doxorubicin, from minimally invasive fluorescence measurements. This is particularly interesting in the context of transarterial chemoembolization (TACE) treatment of liver cancer.
我们开发了一种方法,可在无需预先了解样品光学特性的情况下,从高散射和吸收性样品的单点测量中恢复固有荧光。本研究的目的是证明在背景光学特性差异很大的样品中准确恢复荧光团浓度,同时恢复光学特性。
制备了含有阿霉素、锰-四苯基卟啉(MnTPPS)和20% 脂质乳剂的组织模拟体模,并使用单个各向同性探头进行荧光测量。使用正向-伴随荧光模型分析所得光谱,以恢复荧光团浓度和背景光学特性。
我们证明了阿霉素浓度的恢复,平均误差为11.8%。背景吸收剂的浓度恢复平均误差为23.2%,散射光谱恢复平均误差为19.8%。
该方法将允许通过微创荧光测量来确定荧光药物(如阿霉素)的局部浓度。在肝癌的经动脉化疗栓塞(TACE)治疗背景下,这一点尤其有趣。