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使用苝醌对鸡胚绒毛尿囊膜模型进行光动力诱导的血管损伤。

Photodynamic-induced vascular damage of the chick chorioallantoic membrane model using perylenequinones.

作者信息

Chin William, Lau Weber, Lay Saw Lay, Wei Kho Kiang, Olivo Malini

机构信息

Department of Urology, Singapore General Hospital, Singapore.

出版信息

Int J Oncol. 2004 Oct;25(4):887-91.

Abstract

The chorioallantoic membrane (CAM) assay is a widely used bioassay in early in vivo cancer research. The CAM allows non-invasive study of in vivo microvasculature and blood circulation. This report describes the first topical application investigation of photodynamic response in the CAM model using Hypericin (HY) and Hypocrellin B (HB) that belongs to the perylenequinone family. Briefly, cultivated carcinoma of the human bladder cell line (MGH), were inoculated on the CAM of fertilized eggs of embryo age (EA) 9. Tumor growth was evaluated by digital stereomicroscopy. Photodynamic therapy (PDT) was performed following topical application of the photosensitizers. We were able to demonstrate that these perylenequinones localized selectively in the xenografted bladder tumor and in the vasculature of the CAM. Photodynamic treatments were performed using a custom-made non-laser light source coupled into a flexible fiber bundle to selectively excite the photosensitizers in order to induce photodamage to the tumor and vasculature. The vascular damage induced was quantitatively measured following topical application of the photosensitizers. Both photosensitizers exhibited very similar degrees of photodamage to the CAM. The CAM model offers an exciting avenue for the study of PDT induced effect on the vasculature. Our preliminary results support that the CAM model could potentially serve as a customized model to study photodynamic therapy effects of various photosensitizers on specific tumor models.

摘要

绒毛尿囊膜(CAM)试验是早期体内癌症研究中广泛使用的生物测定法。CAM允许对体内微血管系统和血液循环进行非侵入性研究。本报告描述了首次在CAM模型中使用属于苝醌家族的金丝桃素(HY)和竹红菌素B(HB)进行光动力反应的局部应用研究。简要地说,将培养的人膀胱癌细胞系(MGH)接种到胚胎龄(EA)为9的受精卵的CAM上。通过数字立体显微镜评估肿瘤生长。在局部应用光敏剂后进行光动力疗法(PDT)。我们能够证明这些苝醌选择性地定位于异种移植的膀胱肿瘤和CAM的脉管系统中。使用定制的非激光光源耦合到柔性纤维束中进行光动力治疗,以选择性地激发光敏剂,从而对肿瘤和脉管系统造成光损伤。在局部应用光敏剂后,对诱导的血管损伤进行定量测量。两种光敏剂对CAM均表现出非常相似程度的光损伤。CAM模型为研究PDT对脉管系统的诱导作用提供了一条令人兴奋的途径。我们的初步结果支持CAM模型有可能作为一个定制模型,用于研究各种光敏剂对特定肿瘤模型的光动力治疗效果。

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