Laser flash photolysis studies of the UVA sunscreen Mexoryl® SX

被引:8
作者
Cantrell, A [1 ]
McGarvey, DJ [1 ]
Mulroy, L [1 ]
Truscott, TG [1 ]
机构
[1] Univ Keele, Sch Chem & Phys, Keele ST5 5BG, Staffs, England
关键词
D O I
10.1111/j.1751-1097.1999.tb08138.x
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
The results of a nanosecond laser hash photolysis investigation of the WA sunscreen Mexoryl* SX in various solvent environments and within a commercial sunscreen formulation are reported, To the best of our knowledge this is the first laser hash photolysis study of a commercial suncare formulation, In each of these environments kinetic UV-visible absorption measurements following nanosecond 355 nn laser excitation reveals a short-lived species with a solvent-dependent absorption maximum around 470-500 nm and a solvent-dependent lifetime of similar to 50-120 ns, This transient absorption is attributed to the triplet state of Mexoryl(R) SX on the basis that it is quenched by molecular oxygen leading to the formation of singlet oxygen in acetonitrile, The singlet oxygen quantum yield (Phi(Delta)), determined by comparative time-resolved near-infrared luminescence measurements and extrapolated to the limit of complete triplet state quenching, is estimated as 0.09 +/- 0.03 in acetonitrile. In aqueous solution the shorter triplet state lifetime combined with lower ambient oxygen concentrations precludes significant triplet state quenching, For the commercial sunscreen formulation there was no observable difference in the measured triplet lifetime between samples exposed to oxygen or argon, suggesting that the singlet oxygen quantum yield in such environments is likely to be orders of magnitude lower than that measured in acetonitrile.
引用
收藏
页码:292 / 297
页数:6
相关论文
共 12 条
[1]   A UVA filter (4-tert-butyl-4'-methoxydibenzoylmethane): Photoprotection reflects photophysical properties [J].
Andrae, I ;
Bringhen, A ;
Bohm, F ;
Gonzenbach, H ;
Hill, T ;
Mulroy, L ;
Truscott, TG .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1997, 37 (1-2) :147-150
[2]   STUDY OF THE PHOTOCHEMICAL BEHAVIOR OF SUNSCREENS - BENZYLIDENE CAMPHOR AND DERIVATIVES [J].
BECK, I ;
DEFLANDRE, A ;
LANG, G ;
ARNAUD, R ;
LEMAIRE, J .
INTERNATIONAL JOURNAL OF COSMETIC SCIENCE, 1981, 3 (03) :139-152
[3]   PHOTOSTABILITY ASSESSMENT OF SUNSCREENS - BENZYLIDENE CAMPHOR AND DIBENZOYLMETHANE DERIVATIVES [J].
DEFLANDRE, A ;
LANG, G .
INTERNATIONAL JOURNAL OF COSMETIC SCIENCE, 1988, 10 (02) :53-62
[4]  
Deflandre A., 1988, COSMET TOILETRIES, V103, P69
[5]  
Gasparro FP, 1998, PHOTOCHEM PHOTOBIOL, V68, P243, DOI 10.1111/j.1751-1097.1998.tb09677.x
[6]   A STUDY OF THE PHOTOCHEMICAL PROPERTIES OF SOME CINNAMATE SUNSCREENS BY STEADY-STATE AND LASER FLASH-PHOTOLYSIS [J].
MORLIERE, P ;
AVICE, O ;
MELO, TSE ;
DUBERTRET, L ;
GIRAUD, M ;
SANTUS, R .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1982, 36 (04) :395-399
[7]  
Murov S. L., 1993, HDB PHOTOCHEMISTRY
[8]   Mexoryl® SX:: A broad absorption UVA filter protects human skin from the effects of repeated suberythemal doses of UVA [J].
Seite, S ;
Moyal, D ;
Richard, S ;
de Rigal, J ;
Leveque, JL ;
Hourseau, C ;
Fourtanier, A .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1998, 44 (01) :69-76
[9]   Investigation of carotenoid radical cations and triplet states by laser flash photolysis and time-resolved resonance Raman spectroscopy: Observation of competitive energy and electron transfer [J].
Tinkler, JH ;
Tavender, SM ;
Parker, AW ;
McGarvey, DJ ;
Mulroy, L ;
Truscott, TG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (07) :1756-1761
[10]   EXCITED TRIPLET-STATE INTERACTIONS WITH MOLECULAR-OXYGEN - INFLUENCE OF CHARGE-TRANSFER ON THE BIMOLECULAR QUENCHING RATE CONSTANTS AND THE YIELDS OF SINGLET OXYGEN (O-2(ASTERISK),(1)DELTA(G)) FOR SUBSTITUTED NAPHTHALENES IN VARIOUS SOLVENTS [J].
WILKINSON, F ;
MCGARVEY, DJ ;
OLEA, AF .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (14) :3762-3769