Laboratory of Celullar Toxicology and Pharmacology - FarmaTec, Faculty of Pharmacy, Federal University of Goiás, Goiânia, GO, Brazil.
Laboratory of Pharmaceutical Technology - FarmaTec, Faculty of Pharmacy, Federal University of Goiás, Goiânia, GO, Brazil.
Toxicol In Vitro. 2017 Dec;45(Pt 3):397-408. doi: 10.1016/j.tiv.2017.04.002. Epub 2017 Apr 4.
In the context of developing a new natural product-based cosmetic, the in vitro efficacy and safety evaluations of a complex botanical mixture based on Eugenia dysenterica leaf hydroalcoholic extract (EDE) (2.5-1000μg/mL) were carried out. Chromatographic analysis demonstrated the presence of the tannin (ellagic acid) and flavonoids (quercetin and gallic acid) which characterize the EDE as a polyphenol-rich mixture. Using HFF-1 fibroblasts, it was shown that EDE promoted cell regeneration after UVA exposure. It also led to the inhibition of the collagenase, elastase and tyrosinase enzymes, which are involved in skin-related disorders. In terms of toxicological evaluation, the EDE was classified as non-phototoxic through the 3T3 Neutral Red Uptake Phototoxicity Test (OECD N° 432, 2004) and non-eye irritant by Bovine Corneal Opacity and Permeability (OECD N° 437, 2013) assay, in conjunction with corneal histomorphometric analysis. Furthermore, the EDE has no skin sensitization potential as demonstrated by a two-out-of-three prediction model [protein-binding/haptenization (OECD N° 442C, 2015), keratinocyte and dendritic cell activations]. In addition, it was shown that the EDE seems to be non-genotoxic through the cytokinesis-block micronucleus assay (OECD N° 487, 2014) using HepG2 cells. When considered together, these findings support the use of EDE botanical mixture in cosmetic/pharmaceutical products.
在开发一种新的天然产物基础的化妆品的背景下,对基于 Eugenia dysenterica 叶水醇提取物(EDE)(2.5-1000μg/mL)的复杂植物混合物的体外功效和安全性进行了评估。色谱分析表明存在单宁(鞣花酸)和类黄酮(槲皮素和没食子酸),这使 EDE 成为富含多酚的混合物。使用 HFF-1 成纤维细胞,表明 EDE 促进了 UVA 暴露后的细胞再生。它还导致胶原酶、弹性蛋白酶和酪氨酸酶的抑制,这些酶参与皮肤相关疾病。在毒理学评价方面,EDE 通过 3T3 中性红摄取光毒性试验(OECD N° 432,2004)被归类为非光毒性,并且通过牛角膜混浊和通透性(OECD N° 437,2013)试验与角膜组织形态计量学分析结合,被归类为非眼部刺激性。此外,EDE 没有皮肤致敏潜力,这是由一个三分之二预测模型[蛋白结合/半抗原化(OECD N° 442C,2015)、角质形成细胞和树突状细胞激活]证明的。此外,通过 HepG2 细胞的细胞有丝分裂阻断微核试验(OECD N° 487,2014)表明,EDE 似乎是非遗传毒性的。综合这些发现,支持将 EDE 植物混合物用于化妆品/制药产品。