Literature DB >> 15022248

Comparative study of the phototoxicity of two chrolin type photosensitizers, ATX-S10(Na) and verteporfin, on vascular endothelial and retinal pigment epithelial cells.

Yufang Huang1, Akira Obana, Yuko Gohto, Susumu Nakajima.   

Abstract

BACKGROUND AND OBJECTIVES: To compare the phototoxicity in photodynamic therapy (PDT) of ATX-S10(Na) and Verteporfin on human microvascular endothelial cells (HMVEC), vascular endothelial cells of monkey choroid and retina (CRVEC), and human retinal pigment epithelial cells (HRPE). STUDY DESIGN/
MATERIALS AND METHODS: PDT was performed in two different ways. In short dye-exposure PDT, HMVEC and CRVEC were exposed to each photosensitizer for 5 minutes followed by laser irradiation of 670 nm wavelength for ATX-S10(Na) or 689 nm for Verteporfin without washing out the photosensitizer in the medium. In long dye-exposure PDT, the cells were exposed to photosensitizers for times ranging from 5 minutes to 2 hours, washed out the photosensitizers, followed by laser irradiation in a fresh medium. PDT was performed on HRPE with PDT doses that resulted in damaging 90% of the HMVEC (ED(90)). Phototoxicity was determined by MTS Assay 1 day after PDT.
RESULTS: The degree of phototoxicity depended on the dye concentration, laser dose, and dye exposure time. In short dye-exposure PDT on HMVEC with a laser dose of 50 J/cm(2), the ED(90) was 6.3 microg/ml of ATX-S10(Na) and 0.04 microg/ml of Verteporfin, while in long dye-exposure PDT the ED(90) was 50.0 microg/ml of ATX-S10(Na) and 0.04 microg/ml of Verteporfin when the medium was supplemented with 5% fetal calf serum. The phototoxic rate on HMVEC was higher when the medium contained 5% as contrasted with 10% of serum. In short dye-exposure PDT, the ED(90) of CRVEC was 100 microg/ml of ATX-S10(Na) and an irradiance of 100 J/cm(2), and 0.08 microg/ml of Verteporfin and an irradiance of 100 J/cm(2) when the medium was supplemented with 10% serum. With some doses of short dye-exposure PDT, the ATX-S10(Na) achieved higher phototoxic rates on HMVEC and CRVEC than on the HRPE. However, long dye-exposure PDT with ATX-S10(Na) and short and long dye-exposure PDT with Vereteporfin failed to obtain higher phototoxic rates on HMVEC and CRVEC than on HRPE.
CONCLUSIONS: Verteporfin had a higher phototoxicity than ATX-S10(Na) on HMVEC and CRVEC. The CRVEC resisted more than HMVEC following PDT with both photosensitizers. In short dye-exposure PDT, ATX-S10(Na) had a more selective phototoxicity on HMVEC and CRVEC than on HRPE. Copyright 2004 Wiley-Liss, Inc.

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Year:  2004        PMID: 15022248     DOI: 10.1002/lsm.10251

Source DB:  PubMed          Journal:  Lasers Surg Med        ISSN: 0196-8092            Impact factor:   4.025


  4 in total

1.  The study of the characteristic of photocytotoxicity under high peak power pulsed irradiation with ATX-S10Na(II) in vitro.

Authors:  Sayaka Ohmori; Kensuke Masuda; Masatake Yoshida; Tsunenori Arai; Susumu Nakajima
Journal:  Lasers Med Sci       Date:  2005-07-09       Impact factor: 3.161

Review 2.  Verteporfin: a review of its use in the management of subfoveal choroidal neovascularisation.

Authors:  Caroline Fenton; Caroline M Perry
Journal:  Drugs Aging       Date:  2006       Impact factor: 3.923

3.  Novel transdermal photodynamic therapy using ATX-S10.Na(II) induces apoptosis of synovial fibroblasts and ameliorates collagen antibody-induced arthritis in mice.

Authors:  S Miyazawa; K Nishida; T Komiyama; Y Nakae; K Takeda; M Yorimitsu; A Kitamura; T Kunisada; A Ohtsuka; H Inoue
Journal:  Rheumatol Int       Date:  2005-10-12       Impact factor: 2.631

4.  Understanding and improving assays for cytotoxicity of nanoparticles: what really matters?

Authors:  Hagar I Labouta; Christopher Sarsons; Jacob Kennard; M Juliana Gomez-Garcia; Kenrick Villar; Hyungbok Lee; David T Cramb; Kristina D Rinker
Journal:  RSC Adv       Date:  2018-06-22       Impact factor: 4.036

  4 in total

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