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注射苯卟啉衍生物的大鼠恶性及正常组织中的激光诱导荧光

Laser-induced fluorescence in malignant and normal tissue of rats injected with benzoporphyrin derivative.

作者信息

Andersson-Engels S, Ankerst J, Johansson J, Svanberg K, Svanberg S

机构信息

Department of Physics, Lund Institute of Technology, Sweden.

出版信息

Photochem Photobiol. 1993 Jun;57(6):978-83. doi: 10.1111/j.1751-1097.1993.tb02958.x.

DOI:10.1111/j.1751-1097.1993.tb02958.x
PMID:8367537
Abstract

Laser-induced fluorescence was used to characterize the localization of intravenously administered benzoporphyrin derivative-monoacid (BPD-MA) 3 h postinjection in different rat tissue types, including an induced experimental malignant tumor. A comparison of the fluorescence properties and demarcation potential between the newer sensitizer BPD-MA and four other substances, hematoporphyrin (HP), polyhematoporphyrin ester (PHE), tetrasulfonated phthalocyanine (TSPc) and the commercially available Photofrin earlier investigated, is included. The fluorescence light was induced with a nitrogen laser, emitting at 337 nm. The fluorescence spectrum in the region 380-750 nm was analyzed by a polychromator equipped with a diode array detector. The demarcation potential between tumor and surrounding tissue in terms of fluorescence signal for the tumor model used was 2:1 for BPD-MA. In comparison with the other drugs, HP shows about the same demarcation potential, whereas Photofrin and PHE exhibit about 3 times better and TSPc about 1.5 times better demarcation. By also employing the endogenous tissue fluorescence signature the contrast was enhanced by a factor of about 2 for each of the five drugs.

摘要

采用激光诱导荧光技术,对静脉注射苯卟啉衍生物单酸(BPD-MA)3小时后在不同大鼠组织类型(包括诱导实验性恶性肿瘤)中的定位进行了表征。文中还比较了新型敏化剂BPD-MA与其他四种物质(血卟啉(HP)、聚血卟啉酯(PHE)、四磺酸酞菁(TSPc)以及之前研究过的市售光卟啉)之间的荧光特性和分界潜力。用发射波长为337nm的氮激光诱导荧光。用配备二极管阵列探测器的多色仪分析380 - 750nm区域的荧光光谱。对于所使用的肿瘤模型,BPD-MA的肿瘤与周围组织之间基于荧光信号的分界潜力为2:1。与其他药物相比,HP的分界潜力大致相同,而光卟啉和PHE的分界效果约好3倍,TSPc的分界效果约好1.5倍。通过利用组织内源性荧光特征,这五种药物的对比度均提高了约2倍。

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