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Laser picosecond microspectrofluorometry of haematoporphyrin in cells and liposomes
The results of a laser picosecond microspectrofluorometric study of the spectral and kinetic characteristics of haematoporphyrin (Hp) fluorescence at various sites in cultured SPEV cells and phosphatidylcholine liposomes are presented. The computer-controlled detection system is based on the single-...
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Published in: | Journal of photochemistry and photobiology. B, Biology Biology, 1991-08, Vol.10 (3), p.239-248 |
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container_end_page | 248 |
container_issue | 3 |
container_start_page | 239 |
container_title | Journal of photochemistry and photobiology. B, Biology |
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creator | Chernyaeva, E.B. Vardanyan, A.G. Koroteev, N.I. Kamalov, V.F. Lobanov, O.V. Mironov, A.F. Rumyanzeva, V.D. |
description | The results of a laser picosecond microspectrofluorometric study of the spectral and kinetic characteristics of haematoporphyrin (Hp) fluorescence at various sites in cultured SPEV cells and phosphatidylcholine liposomes are presented. The computer-controlled detection system is based on the single-photon counting method with picosecond time resolution. In aqueous medium, the Hp fluorescence spectrum is characterized by two bands at 615 and 675 nm. In living cells and liposomes, Hp fluorescence is red shifted to 630 and 690 nm. In addition a new band at 665 nm is detected. The dependence of this band on the incubation time and Hp concentration was investigated. The fluorescence decay kinetics of Hp in a culture medium, liposome and a cell nuclear membrane were measured. Possible Hp aggregate formation in the lipid bilayer and its implications are discussed. |
doi_str_mv | 10.1016/1011-1344(91)85005-2 |
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The computer-controlled detection system is based on the single-photon counting method with picosecond time resolution. In aqueous medium, the Hp fluorescence spectrum is characterized by two bands at 615 and 675 nm. In living cells and liposomes, Hp fluorescence is red shifted to 630 and 690 nm. In addition a new band at 665 nm is detected. The dependence of this band on the incubation time and Hp concentration was investigated. The fluorescence decay kinetics of Hp in a culture medium, liposome and a cell nuclear membrane were measured. Possible Hp aggregate formation in the lipid bilayer and its implications are discussed.</description><identifier>ISSN: 1011-1344</identifier><identifier>EISSN: 1873-2682</identifier><identifier>DOI: 10.1016/1011-1344(91)85005-2</identifier><identifier>PMID: 1779278</identifier><identifier>CODEN: JPPBEG</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>Animals ; Biological and medical sciences ; Cell Line ; Fundamental and applied biological sciences. Psychology ; Hematoporphyrins - chemistry ; Kinetics ; Lasers ; Liposomes ; Porphyrins ; Spectrometry, Fluorescence - instrumentation ; Spectrometry, Fluorescence - methods ; Swine ; Time Factors ; time-resolved fluorescence microscopy ; Tissues, organs and organisms biophysics</subject><ispartof>Journal of photochemistry and photobiology. 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B, Biology</title><addtitle>J Photochem Photobiol B</addtitle><description>The results of a laser picosecond microspectrofluorometric study of the spectral and kinetic characteristics of haematoporphyrin (Hp) fluorescence at various sites in cultured SPEV cells and phosphatidylcholine liposomes are presented. The computer-controlled detection system is based on the single-photon counting method with picosecond time resolution. In aqueous medium, the Hp fluorescence spectrum is characterized by two bands at 615 and 675 nm. In living cells and liposomes, Hp fluorescence is red shifted to 630 and 690 nm. In addition a new band at 665 nm is detected. The dependence of this band on the incubation time and Hp concentration was investigated. The fluorescence decay kinetics of Hp in a culture medium, liposome and a cell nuclear membrane were measured. Possible Hp aggregate formation in the lipid bilayer and its implications are discussed.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>Fundamental and applied biological sciences. 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subjects | Animals Biological and medical sciences Cell Line Fundamental and applied biological sciences. Psychology Hematoporphyrins - chemistry Kinetics Lasers Liposomes Porphyrins Spectrometry, Fluorescence - instrumentation Spectrometry, Fluorescence - methods Swine Time Factors time-resolved fluorescence microscopy Tissues, organs and organisms biophysics |
title | Laser picosecond microspectrofluorometry of haematoporphyrin in cells and liposomes |
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