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光动力治疗剂量学理论:敏化剂光破坏的后果

The theory of photodynamic therapy dosimetry: consequences of photo-destruction of sensitizer.

作者信息

Potter W R, Mang T S, Dougherty T J

出版信息

Photochem Photobiol. 1987 Jul;46(1):97-101. doi: 10.1111/j.1751-1097.1987.tb04741.x.

Abstract

Photodynamic dose is defined as the area under the curve of sensitizer level plotted as a function of light dose. This is a photochemical definition of dose. We will show that this definition is useful in predicting photobiological response. The photodestruction of sensitizer during photodynamic therapy is shown to result in an upper limit on the photodynamic dose which can be delivered by an unlimited light dose. This limit results in the opportunity to make total photodynamic dose uniform to considerable depths (one to two centimeters). The existence of thresholds for permanent tissue damage allows protection of normal tissue from the large light doses required to achieve this limiting dose deep in the tissue. Higher sensitizer levels in the tumor permit tumor destruction while the normal tissues are protected. A clinical trial to determine the proper level of injected dose necessary for these results is required. This theory of photodynamic therapy (PDT) dosimetry is tested in the DBA-SMT experimental mouse tumor system. Combinations of drug and light which are not reciprocal but are nearly equal by this theory are shown to give equivalent tumor control at seven days post treatment. Reciprocal combinations of drug and light fail to give equivalent results when they ae selected using the theory to choose a combination where reciprocity should fail.

摘要

光动力剂量定义为以光剂量为函数绘制的敏化剂水平曲线下的面积。这是剂量的光化学定义。我们将证明这个定义在预测光生物学反应方面是有用的。光动力疗法期间敏化剂的光破坏表明,对于无限光剂量所能输送的光动力剂量存在一个上限。这个限制使得在相当深度(一到两厘米)实现总光动力剂量均匀成为可能。永久性组织损伤阈值的存在使得正常组织能够免受在组织深处达到此极限剂量所需的大光剂量的影响。肿瘤中较高的敏化剂水平允许破坏肿瘤,同时保护正常组织。需要进行一项临床试验来确定实现这些结果所需的适当注射剂量水平。这种光动力疗法(PDT)剂量测定理论在DBA - SMT实验小鼠肿瘤系统中进行了测试。通过该理论显示,药物和光的组合不是相互的,但几乎相等,在治疗后七天能产生等效的肿瘤控制效果。当使用该理论选择药物和光的相互组合应无效的组合时,它们未能产生等效结果。

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