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利用吖啶橙的荧光可视化效应进行小鼠软组织骨肉瘤的体外光动力图像检测。

Extracorporeal photodynamic image detection of mouse osteosarcoma in soft tissues utilizing fluorovisualization effect of acridine orange.

作者信息

Satonaka Haruhiko, Kusuzaki Katsuyuki, Matsubara Takao, Shintani Ken, Wakabayashi Toru, Matsumine Akihiko, Uchida Atsumasa

机构信息

Department of Orthopedic Surgery, Mie University Faculty of Medicine, Tsu, Japan.

出版信息

Oncology. 2006;70(6):465-73. doi: 10.1159/000098874. Epub 2007 Jan 19.

Abstract

Various imaging methods have been employed for the extracorporeal detection of malignant tumors in the human body, such as scintigraphy and PET; however, none is sufficiently accurate and all are also very expensive. To resolve these issues, we attempted to develop a new imaging technique of photodynamic diagnosis (PDD) with acridine orange (AO). AO has the ability to rapidly and specifically accumulate in malignant tumors and emit brilliant green fluorescence after blue light excitation. In this study, we investigated the feasibility of PDD utilizing the fluorovisualization effect of AO, for the extracorporeal detection of mouse osteosarcoma inoculated into the soft tissues. At 2 h after intravenous administration of 0.1, 0.2, 0.5, 1.0, 2.0 and 5.0 mg/kg AO, the tumor and the surrounding normal tissues were illuminated by blue light. The visual fluorescence contrast and ratio (X) of the difference in fluorescence intensity between the tumor and the surrounding normal tissues were evaluated using a high-resolution digital camera equipped with an absorption filter. In addition, the fluorescence contrast was also detected sequentially at 0.5, 1, 2, 3, 6 and 12 h after intravenous administration of AO at 1.0 mg/kg. The results revealed that the optimal condition for clear detection of the tumor was evaluation 2 h after intravenous injection of AO at 0.1 mg/kg, because it provided the best visual contrast on the digital images, and the fluorescence intensity as well as the value of X were higher as compared to the values under other conditions of dose and timing. Based on the results of an acute toxicity study of AO, the estimated LD50 of this substance following intravenous administration was 27.30 mg/kg. In conclusion, we believe that PDD using AO administered intravenously may be feasible for the detection of human musculoskeletal sarcomas in the soft tissues at extremities, and this technique might be a less invasive, less expensive, quicker and more accurate imaging modality than other previously reported imaging methods for this purpose.

摘要

已经采用了各种成像方法用于人体恶性肿瘤的体外检测,如闪烁扫描和正电子发射断层扫描(PET);然而,没有一种方法足够准确,而且所有方法都非常昂贵。为了解决这些问题,我们尝试开发一种使用吖啶橙(AO)的光动力诊断(PDD)新成像技术。AO能够快速且特异性地在恶性肿瘤中积聚,并在蓝光激发后发出明亮的绿色荧光。在本研究中,我们研究了利用AO的荧光可视化效应进行PDD用于体外检测接种到软组织中的小鼠骨肉瘤的可行性。静脉注射0.1、0.2、0.5、1.0、2.0和5.0mg/kg AO后2小时,用蓝光照射肿瘤和周围正常组织。使用配备吸收滤光片的高分辨率数码相机评估肿瘤与周围正常组织之间荧光强度差异的视觉荧光对比度和比率(X)。此外,在静脉注射1.0mg/kg AO后的0.5、1、2、3、6和12小时依次检测荧光对比度。结果显示,静脉注射0.1mg/kg AO后2小时进行评估是清晰检测肿瘤的最佳条件,因为它在数字图像上提供了最佳视觉对比度,并且与其他剂量和时间条件下的值相比,荧光强度以及X值更高。基于AO的急性毒性研究结果,该物质静脉注射后的估计半数致死量(LD50)为27.30mg/kg。总之,我们认为静脉注射AO进行PDD对于检测四肢软组织中的人类肌肉骨骼肉瘤可能是可行的,并且该技术可能是一种比其他先前报道的用于此目的的成像方法侵入性更小、成本更低、更快且更准确的成像方式。

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