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一种用于未来卵巢癌治疗的新型光敏剂(13(2)-羟基-细菌脱镁叶绿酸-a甲酯)的特性研究(一项实验性研究)

Characterization of a new photosensitizer (13(2)-hydroxy- bacteriopheophorbide-a methylester) for future treatment of ovarian carcinoma (an experimental study).

作者信息

Ismail M S

机构信息

Department of Obstetrics and Gynecology, King Fahd University Hospital, King Faisel University, Al Khobar, KSA.

出版信息

Gulf J Oncolog. 2008 Jan(3):54-7.

PMID:20084798
Abstract

UNLABELLED

The photosensitizer 132-hydroxy bacteriopheophorbide-a methyl ester (13(2) OH- BPME) is characterized by a high absorption coefficient at the far red wavelength 750 nm and a good singlet oxygen quantum yield.

METHODS & RESULTS: The pharmacokinetics of 132-OH- BPME were studied in ovarian carcinoma on mice after i.v. administration of 7.8 micromole/kg body weight at different incubation intervals. The accumulated dye was chemically extracted from selected tissues and the concentrations were measured by absorption spectroscopy. The parenchymatous organs (liver, spleen and kidney) showed maximum 13(2)- OH- BPME concentrations after 2 hours incubation (liver, spleen), and 4 hours post injection (kidney). A high uptake was detected in the lung with maximum concentration at 2 hours. The malignant tissue accumulated high 13(2)- OH- BPME concentrations between 2-12 hours post injection with peaking at 8 hours. The 13(2)- OH- BPME concentrations in muscle tissue, representing the normal tumour surroundings, and in the skin were very low.

CONCLUSION

The results of our study suggest that PDT using 13(2)-OH-BPME could be effective at 8h post injection, where the tumour 13(2)- OH-BPME uptake is maximum and the muscle and skin uptake will be minimum.

摘要

未标记

光敏剂13(2)-羟基脱镁叶绿酸-a甲酯(13(2)OH-BPME)的特征在于在远红波长750nm处具有高吸收系数和良好的单线态氧量子产率。

方法与结果

在以7.8微摩尔/千克体重静脉注射后,于不同孵育间隔对小鼠卵巢癌模型研究13(2)-OH-BPME的药代动力学。从选定组织中化学提取累积的染料,并通过吸收光谱法测量浓度。实质器官(肝脏、脾脏和肾脏)在孵育2小时后(肝脏、脾脏)以及注射后4小时(肾脏)显示出最高的13(2)-OH-BPME浓度。在肺中检测到高摄取,在2小时时浓度最高。恶性组织在注射后2至12小时内累积高浓度的13(2)-OH-BPME,在8小时达到峰值。代表正常肿瘤周围组织的肌肉组织和皮肤中的13(2)-OH-BPME浓度非常低。

结论

我们的研究结果表明,使用13(2)-OH-BPME的光动力疗法在注射后8小时可能有效,此时肿瘤对13(2)-OH-BPME的摄取最大,而肌肉和皮肤的摄取最小。

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