Calculation of singlet oxygen dose from photosensitizer fluorescence and photobleaching during mTHPC photodynamic therapy of MLL cells

被引:119
作者
Dysart, JS
Singh, G
Patterson, MS
机构
[1] Juravinski Canc Ctr, Hamilton, ON L8V 5C2, Canada
[2] McMaster Univ, Dept Pathol & Mol Med, Hamilton, ON, Canada
[3] McMaster Univ, Dept Med Phys & Appl Radiat Sci, Hamilton, ON, Canada
关键词
D O I
10.1562/2004-07-23-RA-244.1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Predicting the therapeutic outcome of photodynamic therapy (PDT) requires knowledge of the amount of cytoxic species generated. An implicit approach to assessing PDT efficacy has been proposed where changes in photosensitizer (PS) fluorescence during treatment are used to predict treatment outcome. To investigate this, in vitro experiments were performed in which Mat-LyLu cells were incubated in meta-tetra(hydroxyphenyl)chlorin (mTHPC) and then irradiated with 652 nm light. PS concentration, fluence rate and oxygenation were independently controlled and monitored during the treatment. Fluorescence of mTHPC was monitored during treatment and, at selected fluence levels, cell viability was determined using a colony-formation assay. Singlet oxygen dose was calculated using four different models and was compared with cell survival. For the dose metric based on singlet oxygen-mediated PS photobleaching, a universal relationship between cell survival and singlet oxygen dose was found for all treatment parameters. Analysis of the concentration dependence of bleaching suggests that the lifetime of singlet oxygen within the cell is 0.05-0.25 mus. Generation of about 9 X 10(8) molecules of singlet oxygen per cell reduces the surviving fraction by 1/e.
引用
收藏
页码:196 / 205
页数:10
相关论文
共 56 条
  • [1] [Anonymous], 1986, LASERS SURG MED, DOI DOI 10.1117/12.937328
  • [2] QUENCHING OF SINGLET OXYGEN BY BIOMOLECULES FROM L1210 LEUKEMIA-CELLS
    BAKER, A
    KANOFSKY, JR
    [J]. PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1992, 55 (04) : 523 - 528
  • [3] Boere IA, 2003, PHOTOCHEM PHOTOBIOL, V78, P271, DOI 10.1562/0031-8655(2003)078<0271:MISDAP>2.0.CO
  • [4] 2
  • [5] Photophysical properties of 5,10,15,20-tetrakis(m-hydroxyphenyl)porphyrin-(m-THPP), 5,10,15,20-tetrakis(m-hydroxyphenyl)chlorin (m-THPC) and 5,10,15,20-tetrakis(m-hydroxyphenyl)bacteriochlorin (m-THPBC):: a comparative study
    Bonnett, R
    Charlesworth, P
    Djelal, BD
    Foley, S
    McGarvey, DJ
    Truscott, TG
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1999, (02): : 325 - 328
  • [6] A comparative study of the cellular uptake, localization and phototoxicity of meta-tetra(hydroxyphenyl) chlorin encapsulated in surface-modified submicronic oil/water carriers in HT29 tumor cells
    Bourdon, O
    Mosqueira, V
    Legrand, P
    Blais, J
    [J]. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 2000, 55 (2-3) : 164 - 171
  • [7] Braichotte DR, 1996, LASER SURG MED, V19, P340, DOI 10.1002/(SICI)1096-9101(1996)19:3<340::AID-LSM10>3.0.CO
  • [8] 2-8
  • [9] OXYGEN DEPENDENCY OF TUMOR-CELL KILLING INVITRO BY LIGHT-ACTIVATED PHOTOFRIN-II
    CHAPMAN, JD
    STOBBE, CC
    ARNFIELD, MR
    SANTUS, R
    LEE, J
    MCPHEE, MS
    [J]. RADIATION RESEARCH, 1991, 126 (01) : 73 - 79
  • [10] Correlation of in vivo photosensitizer fluorescence and photodynamic-therapy-induced depth of necrosis in a murine tumor model
    Cheung, R
    Solonenko, M
    Busch, TM
    Del Piero, F
    Putt, ME
    Hahn, SM
    Yodh, AG
    [J]. JOURNAL OF BIOMEDICAL OPTICS, 2003, 8 (02) : 248 - 252