Solvent effects on sunscreen active ingredients using Raman spectroscopy

Journal of Raman Spectroscopy

Volumn 34, Issue 10, 2003, Pages 743-750

  Beyere, L ^a   Yarasi, S ^a   Loppnow, G R ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

Author keywords

Applications; Intensity; Solvent effects; Sunscreens

Indexed keywords

HYDROGEN; HYDROGEN BONDS; POLARIZATION; RAMAN SCATTERING; SUN HOODS;

ABSORPTION MAXIMA; ACTIVE INGREDIENTS; INTENSITY; POLARIZABILITIES; RAMAN MODES; SHIFT-AND; SOLVENT EFFECTS; UV ABSORPTION; WAVE NUMBERS; WAVENUMBER SHIFTS;

SOLVENTS;

4 AMINOBENZOIC ACID DERIVATIVE; 4 METHOXYCINNAMIC ACID 2 ETHYLHEXYL ESTER; ACETONE; ACETONITRILE; BENZENE; DICHLOROMETHANE; DIOXANE; ETHER; HEXANE; METHANOL; N,N DIMETHYLFORMAMIDE; OCTYL N,N DIMETHYL 4 AMINOBENZOIC ACID; OXYBENZONE; SALICYLIC ACID OCTYL ESTER; SOLVENT; SUNSCREEN; TETRAHYDROFURAN; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; HYDROGEN BOND; LIGHT ABSORPTION; POLARIZATION; RAMAN SPECTROMETRY; SOLUTE; SOLVENT EFFECT; ULTRAVIOLET RADIATION;

EID: 0242354968     PISSN: 03770486     EISSN: None     Source Type: Journal    
DOI: 10.1002/jrs.1042     Document Type: Article

References (29)

1. Mitchell DL. In CRC Handbook of Organic Photochemistry and Photobiology, Horspool WH, Song P-S (eds). CRC Press: New York, 1995; 1326-1331.
2. Hidaka H, Horikoshi S. J. Photochem. Photobiol. A: Chem. 1997; 111: 205.
3. Allen JM, Engenolf S, Allen SK. Biochem. Biophys. Res. Commun. 1995; 212: 1145.
4. Allen JM, Gossett CJ, Allen SK. Chem. Res. Toxicol. 1996; 9: 605.
5. Schauder S, Ippen H. Contact Dermatitis 1997; 37: 221.
6. Gasparro FP, Mitchnick M, Nash JF. Photochem. Photobiol. 1998; 68: 243.
7. Shaath NA. In Sunscreens: Development, Evaluation, and Regulatory Aspects, Lowe NJ, Shaath NA (eds). Marcel Dekker: New York, 1990; 211.
8. Martincigh BS, Aleen JM, Allen SK. In Sunscreen Photobiology, Gasparro FP (ed.). Landes Press: Georgetown, TX, 1997; 11-45.
9. Riegelman S, Penna RP. J. Soc. Cosmet. Chem. 1960; 11: 280.
10. Agrapidis-Paloympis LE, Nash RA. J. Soc. Cosmet. Chem. 1987; 38: 209.
11. Kolling OW. J. Phys. Chem. 1996; 100: 16 087.
12. Nyquist RA. Appl. Spectrosc. 1990; 44: 433.
13. Nyquist RA. Appl. Spectrosc. 1992; 46: 306.
14. Nyquist RA. Appl. Spectrosc. 1991; 45: 92.
15. Picquart M, Lefevre T, Lacrampe G. Appl. Spectrosc. 1995; 49: 1268.
16. Fawcett WR, Kloss AA. J. Phys. Chem. 1996; 100: 2019.
17. Yamaguchi T, Kimura Y, Hirota N. J. Phys. Chem. A 1997; 101: 9050.
18. Mitambo MM, Loppnow GR. Chem. Phys. Lett. 1996; 261: 691.
19. Beyere LH. MSc Dissertation, University of Alberta, 2000.
20. Schallreuter KU, Wood JM, Farwell DW, Moore J, Edwards HGM. J. Invest. Dermatol. 1996; 106: 583.
21. Hester E, Forster M. J. Chem. Soc, Faraday Trans. 2 1981; 77: 1535.
22. Gasparro FP, Battista J. Photochem. Photobiol. 1987; 45: 49S.
23. Weast R (ed.). Handbook of Chemistry and Physics. CRC Press: Boca Raton, FL, 1977; C81-C548.
24. Riddle FL Jr, Fowkes FM. J. Am. Chem. Soc. 1990; 112: 3259.
25. Gutmann V. The Donor-Acceptor Approach to Molecular Interactions. Plenum Press: New York, 1978; 17.
26. Kamlet MJ, Abboud J-LM, Taft RW. J. Am. Chem. Soc. 1977; 99: 6027.
27. Kamlet MJ, Abboud J-LM, Abraham MH, Taft RW. J. Org. Chem. 1983; 48: 2877.
28. Heyde ME, Gill D, Kilponen RG, Rimai L. J. Am. Chem. Soc. 1971; 93: 6776.
29. Kosower EM, Huppert D. Annu. Rev. Phys. Chem. 1986; 37: 127.