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基于多血卟啉或5-氨基乙酰丙酸的光动力疗法后的肿瘤血管关闭

Tumor vascular shutdown following photodynamic therapy based on polyhematoporphyrin or 5-aminolevulinic Acid.

作者信息

Roberts D, Cairnduff F, Driver I, Dixon B, Brown S

机构信息

COOKRIDGE HOSP,DEPT CLIN ONCOL,LEEDS LS16 6QB,W YORKSHIRE,ENGLAND. COOKRIDGE HOSP,DEPT MED PHYS,LEEDS LS16 6QB,W YORKSHIRE,ENGLAND. UNIV LEEDS,DEPT BIOCHEM & MOLEC BIOL,LEEDS LS2 9JT,W YORKSHIRE,ENGLAND.

出版信息

Int J Oncol. 1994 Oct;5(4):763-8. doi: 10.3892/ijo.5.4.763.

DOI:10.3892/ijo.5.4.763
PMID:21559639
Abstract

The effects of photodynamic therapy (PDT) based on polyhaematoporphyrin (PHP) or 5-aminolaevulinic acid (ALA) on the tumour vascular perfusion (TVP) of a rat fibrosarcoma were examined using an (RbCl)-Rb-86 extraction technique. Both forms of therapy induced large and highly significant reductions in TVP, countering the previous suggestion that ALA-PDT has no vascular effects. Ultrasensitive digital imaging fluorescence microscopy indicated that ALA-induced PpIX was distributed relatively evenly throughout the tumour. Use of Hoechst 33342 as a vascular marker revealed that PpIX was also present in cells lining the tumour microvascular spaces, contrary to previous findings.

摘要

采用(RbCl)-Rb-86提取技术,研究了基于多血卟啉(PHP)或5-氨基酮戊酸(ALA)的光动力疗法(PDT)对大鼠纤维肉瘤肿瘤血管灌注(TVP)的影响。两种治疗方式均导致TVP大幅且极显著降低,这与之前认为ALA-PDT无血管效应的观点相悖。超灵敏数字成像荧光显微镜检查表明,ALA诱导产生的原卟啉IX(PpIX)在肿瘤中分布相对均匀。使用Hoechst 33342作为血管标记物显示,与之前的研究结果相反,PpIX也存在于肿瘤微血管空间的内皮细胞中。

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In vivo evaluation of battery-operated light-emitting diode-based photodynamic therapy efficacy using tumor volume and biomarker expression as endpoints.以肿瘤体积和生物标志物表达为终点,对基于电池供电发光二极管的光动力疗法疗效进行体内评估。
J Biomed Opt. 2015 Apr;20(4):048003. doi: 10.1117/1.JBO.20.4.048003.
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