Abstract

Exposure of a drug to UV irradiation could affect its physicochemical properties. Hence, photostability testing is essential for topically administered drugs. Tazarotene, a receptor-selective, third-generation retinoid, is commonly used to treat acne vulgaris and psoriasis. In the present study, an in-depth analysis of the photostability of tazarotene in ethanolic solution in the presence of zinc oxide and/or titanium dioxide as well as benzophenone-type UV filters was performed. Eleven presumed products were derived from the photocatalytic degradation of tazarotene using ultra-performance liquid chromatography–tandem mass spectrometry, and transformation pathways were proposed. The degradation process mainly affected the 4,4-dimethyl-3,4-dihydro-2H-thiopyran moiety. The fragments most susceptible to oxidation were the methyl groups and the sulfur atom. Moreover, in the presence of sulisobenzone, under UV irradiation, tazarotene was subjected to a degradation process, which resulted in two photodecomposition products. In silico studies performed by OSIRIS Property Explorer demonstrated that five of the degradation products could be harmful in terms of the reproductive effects, which are associated with 3,4-dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide, while one of them demonstrated potential irritant activity. The cytotoxic properties of the degradation products of tazarotene were assessed by MTT assay on a panel of human adherent cancer cells. Time- and concentration-dependent growth inhibition was evidenced in ovary (A2780) and breast (MDA-MB-231) cancer cell lines. The potential implication of the outcomes of the present research requires further studies mainly concerning the photostability of tazarotene in the topical formulations.

Highlights

  • Tazarotene (ethyl 6-[2-(4,4-dimethyl-2,3-dihydrothiochromen-6-yl)ethynyl]pyridine-3-carboxylate) is a third-generation topical retinoid, which is applied to the skin

  • This study revealed the impact of the presence of UV absorbers on the photostability of tazarotene in ethanol solution under UV irradiation

  • The photodecomposition of tazarotene in the presence of TiO2, ZnO, and sulisobenzone was observed under the applied experimental conditions

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Summary

Introduction

Tazarotene (ethyl 6-[2-(4,4-dimethyl-2,3-dihydrothiochromen-6-yl)ethynyl]pyridine-3-carboxylate) is a third-generation topical retinoid, which is applied to the skin. A better understanding of the potential interactions between different substances applied simultaneously to the skin, e.g. UV absorbers and active pharmaceutical ingredients, is essential for ensuring the safe and effective administration of drug products [14]. The behavior of these substances is not predictable from independent photostability testing [15,16]. The present study aimed to assess the impact of selected UV absorbers extensively used in sunscreens and cosmetics on the photostability of tazarotene in ethanol solutions under UV irradiation. The overarching goal of the conducted in vitro tests was to determine the Pharmaceutics 2020, 12, 899 plausible structures of the photoproducts formed under experimental conditions and to evaluate their cytotoxicity

Reagents
Reagent Solutions Preparation
Photostability Assessments
Investigated Solutions
Cell Lines and Cell Growth Inhibitory Assay
In Silico Toxicity Prediction
Ultra-Performance Liquid Chromatography–Tandem Mass Spectrometry Analysis
Results and Discussion
Conclusions

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