Effect of vehicle on the in vitro penetration and metabolism of genistein and daidzein in ex vivo skin explants and the Phenion full-thickness skin model.

IF 2.7 4区 医学 Q3 TOXICOLOGY Journal of Applied Toxicology Pub Date : 2024-08-27 DOI:10.1002/jat.4693
Camille Géniès, Corinne Jeanjean, Abdulkarim Najjar, Andreas Schepky, Daniela Lange, Jochen Kühnl, Eric Fabian, Anne Zifle, Helene Duplan, Nicola J Hewitt, Carine Jacques
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Abstract

In a read-across assessment of the safety of genistein and daidzein in cosmetic products, additional information was required to account for differences in their systemic exposure after topical application in a typical body lotion formulation. Therefore, we measured the penetration and metabolism of two doses (3 and 30 nmoles/cm2) of genistein and daidzein applied in ethanol and in a body formulation to fresh pig skin, fresh and frozen human skin, and PhenionFT models. Both chemicals readily penetrated all skin models when applied in ethanol. The same sulfate and glucuronide metabolites were formed in fresh pig skin, fresh human skin, and PhenionFT models, which also all demonstrated that (a) these pathways could be saturated between 3 and 30 nmoles/cm2 and (b) the extent of metabolism of daidzein was lower than genistein. Although the relative amounts of radiolabeled chemical in human skin and medium compartments were altered by freezing, their overall bioavailability was not affected. The greatest impact on the bioavailability and distribution of both chemicals was observed when they were applied in the formulation. Most of the dose applied in the formulation was retained on the skin surface, especially at 30 nmoles/cm2 (60%-90%), resulting in much lower amounts in the medium and/or skin. In conclusion, all four skin models demonstrated first-pass metabolism of genistein and daidzein and a marked alteration in their disposition by applying them in a body lotion formulation. This supports the use of fresh pig skin and PhenionFT models as alternatives to human skin for investigating skin metabolism and formulation effects for these two chemicals. The results were used to develop the dermal module of a PBPK model and dose setting for organ-on-chip experiments. They could also be used to refine internal exposure estimates in regulatory safety assessments.

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载体对染料木素和染料木素在体外皮肤外植体和菲尼克斯全厚皮肤模型中的体外渗透和代谢的影响。
在对化妆品中的染料木素和大豆异黄酮的安全性进行交叉评估时,需要提供更多信息,以说明在典型的身体乳液配方中局部施用这两种物质后全身暴露量的差异。因此,我们测量了两种剂量(3 和 30 nmoles/cm2)的染料木素和大豆异黄酮在乙醇中的渗透和代谢情况,以及在新鲜猪皮肤、新鲜和冷冻人类皮肤以及 PhenionFT 模型中的体用配方中的渗透和代谢情况。在乙醇中使用时,这两种化学物质很容易渗透到所有皮肤模型中。在新鲜猪皮、新鲜人皮和 PhenionFT 模型中形成了相同的硫酸盐和葡萄糖醛酸代谢物,这也都表明:(a) 这些途径的饱和度在 3 至 30 nmoles/cm2 之间;(b) 麦冬苷的代谢程度低于染料木素。虽然人体皮肤和培养基中放射性标记化学物质的相对含量会因冷冻而发生变化,但其总体生物利用度并未受到影响。在制剂中使用这两种化学物质时,对其生物利用率和分布的影响最大。制剂中施用的大部分剂量都保留在皮肤表面,尤其是在 30 nmoles/cm2 的剂量下(60%-90%),因此在培养基和/或皮肤中的剂量要低得多。总之,所有四种皮肤模型都表明,通过在身体乳液配方中使用染料木素和染料木苷,染料木素和染料木苷会发生首过代谢,并明显改变其处置方式。这支持使用新鲜猪皮和 PhenionFT 模型替代人体皮肤来研究这两种化学物质的皮肤代谢和配方效应。研究结果被用于开发 PBPK 模型的皮肤模块和芯片上器官实验的剂量设定。这些结果还可用于完善监管安全评估中的内部暴露估计值。
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来源期刊
CiteScore
7.00
自引率
6.10%
发文量
145
审稿时长
1 months
期刊介绍: Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.
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