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Indocyanine green–enhanced imaging of antigen-induced arthritis with an integrated optical imaging/radiography system†

机译:集成光学成像/放射成像系统的吲哚菁绿增强抗原诱导的关节炎成像†

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ObjectiveTo evaluate a combined indocyanine green–enhanced optical imaging/radiography system for the detection of arthritic joints in a rat model of antigen-induced arthritis.MethodsArthritis of the knee and ankle joints was induced in 6 Harlan rats, using peptidoglycan–polysaccharide polymers. Three rats served as untreated controls. Optical imaging of the knee and ankle joints was done with an integrated optical imaging/radiography system before and up to 24 hours following intravenous injection of 10 mg/kg indocyanine green. The fluorescence signal intensities of arthritic and normal joints were compared for significant differences, using generalized estimating equation models. Specimens of knee and ankle joints were further processed and evaluated by histology.ResultsImmediately after administration, indocyanine green provided a significant increase in the fluorescence signal of arthritic joints compared with baseline values (P 0.05). The fluorescence signal of arthritic joints was significantly higher compared with that of nonarthritic control joints at 1–720 minutes after intravenous injection (P 0.05). Fusion of indocyanine green–enhanced optical imaging and radiography allowed for anatomic coregistration of the inflamed tissue with the associated joint. Hematoxylin and eosin staining confirmed marked synovial inflammation of arthritic joints and the absence of inflammation in control joints.ConclusionIndocyanine green–enhanced optical imaging is a clinically applicable tool for detection of arthritic tissue. Using relatively high doses of indocyanine green, long-term enhanced fluorescence of arthritic joints can be achieved. This may facilitate simultaneous evaluations of multiple joints in a clinical setting. Fusion of indocyanine green–enhanced optical imaging scans with radiography increases anatomic resolution.
机译:目的评估结合吲哚菁绿增强的光学成像/放射成像系统在抗原性关节炎大鼠模型中检测关节炎关节的方法。方法使用肽聚糖-多糖聚合物在6只Harlan大鼠中诱发膝关节和踝关节关节炎。三只大鼠作为未治疗的对照。在静脉注射10 mg / kg吲哚菁绿之前和之后的24小时内,使用集成的光学成像/放射成像系统对膝盖和踝关节进行光学成像。使用广义估计方程模型,比较了关节炎和正常关节的荧光信号强度是否存在显着差异。结果给药后立即,吲哚菁绿使关节炎关节的荧光信号显着高于基线值(P <0.05)。静脉注射后1–720分钟,关节炎关节的荧光信号显着高于非关节炎对照组的荧光信号(P <0.05)。吲哚菁绿增强的光学成像和放射线照相术融合在一起,可以使发炎的组织与相关关节解剖融合。苏木精和曙红染色证实关节炎关节明显滑膜发炎,而对照关节无炎症。结论吲哚菁绿增强光学成像是一种可用于临床检测关节炎组织的工具。使用相对高剂量的吲哚菁绿,可以实现关节炎关节的长期增强荧光。这可以促进在临床环境中同时评估多个关节。吲哚菁绿增强的光学成像扫描与射线照相术的融合可提高解剖分辨率。

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