体内
叶酸受体
自体荧光
体内分布
荧光
医学
药代动力学
体外
对比度(视觉)
分子生物学
赫拉
核医学
病理
生物物理学
癌症
化学
药理学
癌细胞
光学
内科学
生物
生物化学
物理
生物技术
作者
Elizabeth De Jesus,Jane Keating,Sumith A. Kularatne,Jack Jiang,Ryan Judy,Jarrod D. Predina,Shuming Nie,Philip S. Low,Sunil Singhal
出处
期刊:International Journal of Molecular Imaging
[Hindawi Limited]
日期:2015-09-28
卷期号:2015: 1-10
被引量:83
摘要
Background. Intraoperative imaging can identify cancer cells in order to improve resection; thus fluorescent contrast agents have emerged. Our objective was to do a preclinical comparison of two fluorescent dyes, EC17 and OTL38, which both target folate receptor but have different fluorochromes. Materials. HeLa and KB cells lines were used for in vitro and in vivo comparisons of EC17 and OTL38 brightness, sensitivity, pharmacokinetics, and biodistribution. In vivo experiments were then performed in mice. Results. The peak excitation and emission wavelengths of EC17 and OTL38 were 470/520 nm and 774/794 nm, respectively. In vitro, OTL38 required increased incubation time compared to EC17 for maximum fluorescence; however, peak signal-to-background ratio (SBR) was 1.4-fold higher compared to EC17 within 60 minutes (p < 0.001). Additionally, the SBR for detecting smaller quantity of cells was improved with OTL38. In vivo, the mean improvement in SBR of tumors visualized using OTL38 compared to EC17 was 3.3 fold (range 1.48-5.43). Neither dye caused noticeable toxicity in animal studies. Conclusions. In preclinical testing, OTL38 appears to have superior sensitivity and brightness compared to EC17. This coincides with the accepted belief that near infrared (NIR) dyes tend to have less autofluorescence and scattering issues than visible wavelength fluorochromes.
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