Kryczyk-Poprawa Agata, Zupkó István, Bérdi Péter, Żmudzki Paweł, Popiół Justyna, Muszyńska Bożena, Opoka Włodzimierz
Department of Inorganic and Analytical Chemistry, Jagiellonian University Medical College, 30-688 Kraków, Poland.
Department of Pharmacodynamics and Biopharmacy, University of Szeged, 6720 Szeged, Hungary.
Pharmaceutics. 2020 Sep 22;12(9):899. doi: 10.3390/pharmaceutics12090899.
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-2-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. 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-2-1-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.
药物暴露于紫外线照射下可能会影响其物理化学性质。因此,光稳定性测试对于局部给药的药物至关重要。他扎罗汀是一种受体选择性的第三代维甲酸,常用于治疗寻常痤疮和银屑病。在本研究中,对他扎罗汀在乙醇溶液中,在存在氧化锌和/或二氧化钛以及二苯甲酮类紫外线滤过剂的情况下的光稳定性进行了深入分析。使用超高效液相色谱-串联质谱法从他扎罗汀的光催化降解中获得了11种推测产物,并提出了转化途径。降解过程主要影响4,4-二甲基-3,4-二氢-2-硫代吡喃部分。最易被氧化的片段是甲基和硫原子。此外,在存在舒利苯酮的情况下,在紫外线照射下,他扎罗汀会发生降解过程,产生两种光分解产物。OSIRIS Property Explorer进行的研究表明,其中五种降解产物在生殖效应方面可能有害,这与3,4-二氢-6-甲基-2H-1-苯并噻喃1,1-二氧化物有关,而其中一种表现出潜在的刺激活性。通过MTT法在一组人贴壁癌细胞上评估了他扎罗汀降解产物的细胞毒性。在卵巢(A2780)和乳腺(MDA-MB-231)癌细胞系中证实了时间和浓度依赖性的生长抑制。本研究结果的潜在影响需要进一步研究,主要涉及他扎罗汀在局部制剂中的光稳定性。