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[光敏剂Ⅱ在人永生化食管上皮细胞系SHEE及其恶性转化细胞系SHEEC中的吸收与消除]

[Absorption and elimination of photofrin-II in human immortalization esophageal epithelial cell line SHEE and its malignant transformation cell line SHEEC].

作者信息

Gao She-Gan, Wang Li-Dong, Feng Xiao-Shan, Qu Zhi-Feng, Shan Tan-You, Xie Xuan-Hu

机构信息

Henan Key Laboratory for Esophageal Cancer, Laboratory for Cancer Research, Basic Medical College, Zhengzhou University, Zhengzhou, Henan, 450052, P. R. China.

出版信息

Ai Zheng. 2009 Dec;28(12):1248-54. doi: 10.5732/cjc.008.10585.

DOI:10.5732/cjc.008.10585
PMID:19958617
Abstract

BACKGROUND AND OBJECTIVE

The mechanism of tumor tissues selectively uptake the photosensitizer in photodynamic therapy (PDT) is still unclear. This study was to investigate the affinity of tumor cells to the photosensitizer photofrin-II.

METHODS

Ultraviolet spectrophotometer was applied to measure the absorption spectra of various cell culture media. The fluorescence spectrum of photofrin-II was determined by spectrofluorometer. The absorption and elimination condition of photofrin-II were detected in immortalized human esophageal epithelial cell line SHEE and its malignant transformation cell line SHEEC.

RESULTS

The maximum excitation wavelength of fluorescence for photofrin-II was (395.0+/-0.5) nm, and the maximum emission wavelength of that was (634.1+/-0.5) nm. The laser at the wavelength of 630 nm used in this experiment could permeate various types of cell culture media. There was no significant difference in the absorption and elimination of photofrin-II between SHEE and SHEEC at the same concentration and time. The absorption of photofrin-II in SHEE and SHEEC increased with the increase in photofrin-II concentration and duration, and reached the platform at the concentration of 30 microg/mL and a time point of 150 min, respectively. The photofrin-II contents of SHEE and SHEEC showed a slight change after 15-30 min, and diminished rapidly after 30 min.

CONCLUSION

High photosensitizer concentration in tumor tissues may be not correlated with the affinity of tumor cells.

摘要

背景与目的

在光动力疗法(PDT)中,肿瘤组织选择性摄取光敏剂的机制仍不清楚。本研究旨在探讨肿瘤细胞对光敏剂卟啉钠-II的亲和力。

方法

采用紫外分光光度计测量各种细胞培养基的吸收光谱。用荧光分光光度计测定卟啉钠-II的荧光光谱。检测永生化人食管上皮细胞系SHEE及其恶性转化细胞系SHEEC中卟啉钠-II的吸收和消除情况。

结果

卟啉钠-II的最大荧光激发波长为(395.0±0.5)nm,最大发射波长为(634.1±0.5)nm。本实验中使用的波长为630nm的激光可穿透各种类型的细胞培养基。在相同浓度和时间下,SHEE和SHEEC对卟啉钠-II的吸收和消除无显著差异。SHEE和SHEEC中卟啉钠-II的吸收随卟啉钠-II浓度和作用时间的增加而增加,分别在浓度为30μg/mL和时间点为150min时达到平台期。SHEE和SHEEC的卟啉钠-II含量在15 - 30min后略有变化,30min后迅速下降。

结论

肿瘤组织中高浓度的光敏剂可能与肿瘤细胞的亲和力无关。

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