Quantitative time-resolved fluorescence spectrum of the cortical sarcoma and the adjacent normal tissue.

Quantitative time-resolved fluorescence spectrum of the cortical sarcoma and the adjacent normal tissue. Research Abstract Details 

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Quantitative time-resolved fluorescence spectrum of the cortical sarcoma and the adjacent normal tissue. Abstract Text:

Yuezhi Li,Mingzhao Li,Tao Xu,Yuezhi Li,Mingzhao Li,Tao Xu,

The difference in time-resolved fluorescence spectrum between the cortical sarcoma and the adjacent normal tissue was studied in both experimental and theoretical ways. The Clinical data were obtained in vivo using a time-resolved fluorescence spectrometer employing a single fiber-optic probe for excitation and detection. Tissue was modeled as s-180 sarcoma tumor surrounded with normal muscle and was mediated by the Palladium-porphyrin photosensitizer (Pd-TCPP). The emitted fluorescence was considered as arising from the tumor tissue or the normal muscle, due to the presence of the photosensitizer. A computational code which could simulating time-resolved fluorescence emission was presented and applied to comparing fluorescence decay of photosensitizer in different stages of tumor growth. In this code the different stages of the tumor was modeled through changing the time tau, the delay of the fluorescence photon emission and z (max), the thickness of the tumor. It was found in the in vivo experiment that the fluorescence from tumor tissue decayed more quickly than from the adjacent normal muscle. For the ten rats in the first experiment day, the mean decay constant of tumor T (s) and normal tissue T (n) were 554 and 526 mus, respectively. And T (s) increased with the tumor growth, from 554 mus in the first day to 634 mus in the eighth day while T (s) kept steady. It was believed that the more adequate oxygen supplied by the normal tissue can more effectively quench the fluorescence and in the normal tissue the photosensitizer lifetime is smaller. As a result the simulated time-resolved fluorescence spectrum of normal tissue showed more quickly decay. And the thickness of the tumor can also delay the fluorescence decay. Both the experimental and simulated results indicated that the germination of the tumor would increase the decay constant of the time-resolved fluorescence spectrum. So decay constant of the tumor tissue spectrum should be larger than that of adjacent normal tissue for the reason of hypoxia and overgrouth. This fact could be of use in the tumor diagnoses.

Quantitative time-resolved fluorescence spectrum of the cortical sarcoma and the adjacent normal tissue. Publishing Authors By Initials

Y Li,M Li,T Xu,Y Li,M Li,T Xu,

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Quantitative time-resolved fluorescence spectrum of the cortical sarcoma and the adjacent normal tissue. Journal Published:

PUBLICATION TYPE: Journal Article

Journal: Journal of fluorescence

VOLUME: 17

Page Numbers: 643-8

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ISSN: 1053-0509

DAY: 23

MONTH: 06

YEAR: 2006

Quantitative time-resolved fluorescence spectrum of the cortical sarcoma and the adjacent normal tissue. Information

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LANGUAGE: eng

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Grant and Affiliation Information for Quantitative time-resolved fluorescence spectrum of the cortical sarcoma and the adjacent normal tissue.

AFFILIATION: Department of Engineering, Shenzhen University, Shenzhen, P.R. China.

Country: United States

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MEDLINETA: J Fluoresc

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