Novel synthetic UV screen compounds inspired in mycosporine-like amino acids (MAAs): Antioxidant capacity, photoprotective properties and toxicity

IF 3.9 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Félix L. Figueroa , Pablo Castro-Varela , Julia Vega , Raúl Losantos , Beatriz Peñín , Leonardo López-Cóndor , María Jesús Pacheco , Sofía Latorre Redoli , Manuel Marí-Beffa , Roberto Abdala-Díaz , Diego Sampedro
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Abstract

The combination of environmental stress on the ozone layer, climate change and a greater sun exposure due to outdoor habits has led to an increase in skin cancer cases and other health issues related with UV radiation. Researchers are searching for new alternative UV filters that could protect our skin from the deleterious effects of UV radiation while also presenting low toxicity and biodegradable character (unlike the UV filters currently available in the market). In this work, two compounds inspired in the natural oxo-mycosporine-like amino acids (MAAs) have been synthesized and their antioxidant and photoprotective properties, as well as their in vitro and in vivo toxicity effects were evaluated. Both compounds featured a strong UV-B absorption together with a high antioxidant capacity, close to 50 μmol TE g−1 DW in the ABTS assay. Compound 1 presented an absorption peak at 285–300 nm, whereas compound 2 showed a wider band with a peak around 295–305 nm and two shoulders at 318 and 342 nm. The addition of 5 % of compound 2 to galenic formulas increased the photoprotection, reaching SPF values of 4. Both compounds were stable under UV radiation exposure. Regarding toxicity, the synthetic compounds did not show cytotoxic activity against healthy human cell lines or significant toxicity over zebrafish embryos. Compound 1 showed a complete lack of toxicity over zebrafish, although compound 2 showed slight, not-significant effects on viability, hatching, pericardial stability or body axis formation over 5 mg mL−1. Moreover, compound 1 presented relatively antitumoral activities against HCT-116 cells (selective index:1.49). The relevant antioxidant and photoprotective ability together with the great advantage provided by the reduced toxicity to health cells or zebrafish embryos, make these compounds promising candidates to be exploited as functional ingredients with specific applications in the biotechnological or pharma sector.
从类菌体氨基酸(MAAs)中获得灵感的新型合成紫外线筛选化合物:抗氧化能力、光保护特性和毒性。
环境对臭氧层造成的压力、气候变化以及户外习惯导致的更多阳光照射,导致皮肤癌病例和其他与紫外线辐射有关的健康问题增加。研究人员正在寻找新的紫外线过滤器替代品,以保护我们的皮肤免受紫外线辐射的有害影响,同时还具有低毒性和可生物降解的特点(与目前市场上销售的紫外线过滤器不同)。在这项工作中,受天然氧代霉菌素样氨基酸(MAAs)的启发,合成了两种化合物,并对它们的抗氧化和光保护特性,以及体外和体内毒性效应进行了评估。这两种化合物都具有很强的紫外线-B 吸收能力和很高的抗氧化能力,在 ABTS 试验中接近 50 μmol TE g-1 DW。化合物 1 在 285-300 纳米波长处有一个吸收峰,而化合物 2 的吸收带更宽,在 295-305 纳米波长处有一个吸收峰,在 318 和 342 纳米波长处有两个吸收肩。在 galenic 配方中添加 5% 的化合物 2 可以提高光防护能力,达到 SPF 值 4。在毒性方面,合成化合物没有显示出对健康人体细胞系的细胞毒性,也没有显示出对斑马鱼胚胎的显著毒性。化合物 1 对斑马鱼完全没有毒性,但化合物 2 对斑马鱼的存活率、孵化率、心包稳定性或体轴形成有轻微影响,但影响不显著(5 毫克/毫升-1)。此外,化合物 1 对 HCT-116 细胞具有较强的抗肿瘤活性(选择性指数:1.49)。相关的抗氧化和光保护能力,以及对健康细胞或斑马鱼胚胎的毒性降低所带来的巨大优势,使这些化合物有望成为生物技术或制药领域具有特殊用途的功能成分。
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来源期刊
CiteScore
12.10
自引率
1.90%
发文量
161
审稿时长
37 days
期刊介绍: The Journal of Photochemistry and Photobiology B: Biology provides a forum for the publication of papers relating to the various aspects of photobiology, as well as a means for communication in this multidisciplinary field. The scope includes: - Bioluminescence - Chronobiology - DNA repair - Environmental photobiology - Nanotechnology in photobiology - Photocarcinogenesis - Photochemistry of biomolecules - Photodynamic therapy - Photomedicine - Photomorphogenesis - Photomovement - Photoreception - Photosensitization - Photosynthesis - Phototechnology - Spectroscopy of biological systems - UV and visible radiation effects and vision.
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