Formation of cyclobutane thymine dimers by tiaprofenic acid and its photoproducts: approach to the photosensitizer triplet state energy limit value-Reference-Cited by-同舟云学术

Formation of cyclobutane thymine dimers by tiaprofenic acid and its photoproducts: approach to the photosensitizer triplet state energy limit value

Published:2015 Issue:84 Volume:5 Page:68595-68600
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Michaud Sandra¹²³⁴⁵,Bordeau Guillaume¹²³⁴⁵,Sartor Valérie¹²³⁴⁵,Bourdelande Jose Luis⁶⁷⁸⁹,Hernando Jordi⁶⁷⁸⁹,Guirado Gonzalo⁶⁷⁸⁹,Chouini-Lalanne Nadia¹²³⁴⁵

Affiliation:

1. Laboratoire des Interactions Moléculaires et Réactivité Chimique et Photochimique (IMRCP)

2. UMR 5623

3. Université Paul Sabatier

4. 31062 Toulouse Cedex

5. France

6. Departement de Quimica

7. Universitat Autonoma de Barcelona

8. Barcelona

9. Spain

Abstract

Tiaprofenic acid family photosensitizes cyclobutane thymine dimer formation allowing to approach the lower limit threshold of a photosensitizer triplet state energy to excite the triplet state of thymine in DNA.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA11869G

Reference36 articles.

1. Ultraviolet radiation-mediated damage to cellular DNA

2. Toxic effects of ultraviolet radiation on the skin

3. DNA, sunlight and skin cancer

4. Cyclobutane pyrimidine dimers are predominant DNA lesions in whole human skin exposed to UVA radiation

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