Rounds D E, Jacques S, Shelden C H, Shaller C A, Olson R S
Neurosurgery. 1982 Oct;11(4):500-5.
The successful application of phototherapy to subcutaneous tumors has suggested that a similar procedure should be developed for treating gliomas. As a result, attempts are being made to determine a set of conditions that would optimize the destruction of tumor cells while minimizing injury to surrounding brain tissue. To initiate this task, we developed a novel assay method to assess the amount of phototoxicity induced in normal brain by light exposure of mice treated with hematoporphyrin derivative (HPD). The application of this procedure demonstrated that a sufficient amount of HPD was retained in brain tissue, even 72 hours after injection, to cause severe cerebral damage in light-treated mice.
光疗法在皮下肿瘤治疗中的成功应用表明,应该开发一种类似的方法来治疗神经胶质瘤。因此,人们正在尝试确定一组条件,以在使对周围脑组织的损伤最小化的同时,优化肿瘤细胞的破坏。为了启动这项任务,我们开发了一种新的检测方法,以评估用血卟啉衍生物(HPD)处理的小鼠经光照后在正常大脑中诱导的光毒性量。该方法的应用表明,即使在注射后72小时,脑组织中仍保留有足够量的HPD,可在光照处理的小鼠中引起严重的脑损伤。