Experimental study on phototoxicity and the photosensitization potential of ketoprofen, suprofen, tiaprofenic acid and benzophenone and the photocross-reactivity in guinea pigs
- PMID: 12147041
- DOI: 10.1034/j.1600-0781.2002.180205.x
Experimental study on phototoxicity and the photosensitization potential of ketoprofen, suprofen, tiaprofenic acid and benzophenone and the photocross-reactivity in guinea pigs
Abstract
Background: Ketoprofen, suprofen and tiaprofenic acid are arylpropionic anti-inflammatories. Their chemical structures share the same elements as the benzoyl radical and the tiophene ring. We experienced nine cases of ketoprofen photoallergy, seven cases of suprofen photoallergy and three cases of tiaprofenic photoallergy.
Purpose: To find the key structure of photosensitivity and photocross-reactivity to ketoprofen, suprofen and tiaprofenic acid.
Methods: : Three animals were tested for phototoxicity and six animals for the photosensitization potentials of ketoprofen, suprofen, tiaprofenic acid and benzophenone, and the photocross-reactivity of the above chemicals. Test substances were applied symmetrically on both sides of the animals' backs. The animals were irradiated with 180 mJ/cm2 UVB ((1/2) MED) and 10 J/cm2 UVA on the left side. The reactions were read on days 2, 3 and 4. The photosensitization potentials of ketoprofen, suprofen, tiaprofenic acid and benzophenone were determined using the Adjuvant-Strip method. Six animals were assigned to each test group and to a control group.
Results: Ketoprofen, suprofen, tiaprofenic acid and propionic acid showed negative reactions with the phototoxic test. Benzophenone showed phototoxic reactions to 40% acetone (ac.), 20% ac. and 10% ac. Therefore, we used 5% aq. benzophenone with the photosensitization test. Ketoprofen was the strongest photosensitizer (6/6) and showed photocross-reactivities to suprofen (2/6), tiaprofenic acid (3/6) and benzophenone (6/6). Suprofen was a strong photosensitizer (4/6) and showed photocross-reactivities to ketoprofen (1/4) and tiaprofenic acid (2/4), but not to benzophenone. Tiaprofenic acid was also a photosensitizer (2/6) but showed a photocross-reactivity only to benzophenone (2/2). Benzophenone was also the strongest photosensitizer (6/6), but did not photocross-react to the above three chemicals.
Conclusion: From the test results, it appears that benzoyl radical is the key structure for photosensitivity and the photocross-reactivity of ketoprofen, suprofen and tiaprofenic acid. The whole structure of benzophenone was needed to induce photosensitization of benzophenone. The animals that were photosensitized from the entire structure of benzophenone did not photocross-react to ketoprofen, suprofen or tiaprofenic acid.
Similar articles
-
Photocontact dermatitis from ketoprofen and tiaprofenic acid: cross-reactivity study in 12 consecutive patients.Contact Dermatitis. 1998 May;38(5):245-52. doi: 10.1111/j.1600-0536.1998.tb05737.x. Contact Dermatitis. 1998. PMID: 9667440
-
[Photoaggravated contact allergy and contact photoallergy caused by ketoprofen: 19 cases].Ann Dermatol Venereol. 2001 Oct;128(10 Pt 1):1020-4. Ann Dermatol Venereol. 2001. PMID: 11907961 French.
-
Prolonged photosensitivity following contact photoallergy to ketoprofen.Dermatology. 2000;201(2):171-4. doi: 10.1159/000018466. Dermatology. 2000. PMID: 11053926
-
4 cases of photocontact dermatitis due to ketoprofen.Contact Dermatitis. 2000 Jul;43(1):16-9. doi: 10.1034/j.1600-0536.2000.043001016.x. Contact Dermatitis. 2000. PMID: 10902583 Review.
-
Photosensitizing drugs containing the benzophenone chromophore.J Photochem Photobiol B. 1998 Apr;43(1):1-26. doi: 10.1016/s1011-1344(98)00062-1. J Photochem Photobiol B. 1998. PMID: 9639910 Review.
Cited by
-
Ketoprofen-induced photoallergic dermatitis.Indian J Med Res. 2016 Dec;144(6):803-806. doi: 10.4103/ijmr.IJMR_626_16. Indian J Med Res. 2016. PMID: 28474616 Free PMC article. Review.
-
Ibuprofen and ketoprofen potentiate UVA-induced cell death by a photosensitization process.Sci Rep. 2017 Aug 21;7(1):8885. doi: 10.1038/s41598-017-09406-8. Sci Rep. 2017. PMID: 28827702 Free PMC article.
-
Ketoprofen-loaded polymer carriers in bigel formulation: an approach to enhancing drug photostability in topical application forms.Int J Nanomedicine. 2017 Aug 26;12:6221-6238. doi: 10.2147/IJN.S140934. eCollection 2017. Int J Nanomedicine. 2017. PMID: 28894363 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources