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1.
Photochem Photobiol ; 97(2): 360-371, 2021 03.
Article in English | MEDLINE | ID: mdl-33107602

ABSTRACT

The use of sunscreen has become an indispensable daily routine since UV radiation is a critical environmental stress factors for human skin. This study focused on the design, synthesis, thermal/chemical stability and efficacy/safety evaluations of a new heterocyclic derivative, namely LQFM184, as a photoprotective agent. The compound showed stability when submitted under oxidative and high-temperature conditions. It also revealed an absorption at 260-340 nm (UVA/UVB), with a main band at 298 nm and a shoulder close to 334 nm. LQFM184 showed capacity to interact with other existing UV filters, promoting an increase in the sun protection factor. In relation to acute toxicity, its estimated LD50 was >300-2000 mg kg-1 , probably with a low potential of inducing acute oral systemic toxicity hazard. In addition, our data showed that this compound did not have eye irritation, skin sensitization or phototoxicity potentials. Taken together, these findings make LQFM184 a promising ingredient to be used, alone or in association with other UV filters, in cosmetic products such as sunscreens with a broad spectrum of protection.


Subject(s)
Sunscreening Agents/chemistry , Ultraviolet Rays , 3T3 Cells , Animals , Cattle , Cosmetics/chemistry , Humans , Mice , Mice, Inbred BALB C , Spectrum Analysis/methods , Sunscreening Agents/pharmacology , Sunscreening Agents/toxicity , U937 Cells
2.
J Photochem Photobiol B ; 161: 50-8, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27208746

ABSTRACT

The new heterocyclic derivative LQFM048 (3) (2,4,6-tris ((E)-ethyl 2-cyano-3-(4-hydroxy-3-methoxyphenyl)acrylate)-1,3,5-triazine) was originally designed through the molecular hybridization strategy from Uvinul® T 150 (1) and (E)-ethyl 2-cyano-3-(4hydroxy-3-methoxyphenyl)acrylate (2) sunscreens, using green chemistry approach. This compound was obtained in global yields (80%) and showed an interesting redox potential. In addition, it is thermally stable up to temperatures around 250°C. It was observed that LQFM048 (3) showed a low degradation after 150min of sunlight exposure at 39°C, whereas the extreme radiation conditions induced a considerable photodegradation of the LQFM048 (3), especially when irradiated by VIS and VIS+UVA. During the determination of sun protection factor, LQFM048 (3) showed interesting results, specially as in association with other photoprotective compounds and commercial sunscreen. Additionally, the compound (3) did not promote cytotoxicity for 3T3 fibroblasts. Moreover, it was not able to trigger acute oral systemic toxicity in mice, being classified as a compound with low acute toxicity hazard (2.000mg/kg>LD50<5.000mg/kg). Therefore, this compound synthesized using green chemistry approach is promising showing potential to development of a new sunscreen product with advantage of presenting redox potential, indicating antioxidant properties.


Subject(s)
Apoptosis/drug effects , Heterocyclic Compounds/pharmacology , Sunscreening Agents/pharmacology , Triazines/pharmacology , 3T3 Cells , Animals , Antioxidants/chemistry , Antioxidants/pharmacology , Antioxidants/toxicity , Cell Line , Cell Survival/drug effects , Electrochemical Techniques , Heterocyclic Compounds/chemical synthesis , Heterocyclic Compounds/chemistry , Male , Mice , Molecular Conformation , Photolysis/radiation effects , Sun Protection Factor , Sunscreening Agents/chemical synthesis , Sunscreening Agents/chemistry , Thermogravimetry , Triazines/chemical synthesis , Triazines/chemistry , Ultraviolet Rays
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