• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

皮肤接触对人体双酚 A 内暴露的贡献。

The contribution of dermal exposure to the internal exposure of bisphenol A in man.

机构信息

Federal Institute for Risk Assessment, Berlin, Germany.

出版信息

Toxicol Lett. 2011 Jul 28;204(2-3):190-8. doi: 10.1016/j.toxlet.2011.04.032. Epub 2011 May 5.

DOI:10.1016/j.toxlet.2011.04.032
PMID:21571050
Abstract

New findings on Bisphenol A (BPA) contents in thermal printing papers, and receipts, in g/kg concentrations and on its dermal uptake (up to 60%) prompted us to assess the risk arising from dermal exposure. Using physiologically based toxicokinetic modelling, we simulated concentrations in blood, in liver and kidney, the target organs exhibiting the lowest no observed adverse effect levels (NOAEL). By comparing organ concentrations at the dose level of the NOAEL divided by a safety factor of 100 (liver: 50μg/kg/day; kidney: 500μg/kg/day), with concentrations arising from the dermal dose of 0.97μg/kg/day (worst case assumption by Biedermann et al., 2010) this dermal exposure can be assumed safe. Additionally, based on the model simulations the high blood concentrations, reported earlier in the literature, are highly improbable because the related exposure levels are orders of magnitude higher than the currently estimated aggregate exposure levels.

摘要

新发现热敏打印纸和收据中双酚 A(BPA)的含量以 g/kg 浓度计,以及其经皮吸收率(高达 60%),这促使我们评估经皮暴露所带来的风险。我们使用基于生理学的毒代动力学模型模拟了血液、肝脏和肾脏中的浓度,这些器官表现出最低的无观察到不良效应水平(NOAEL)。通过比较 NOAEL 剂量水平除以 100 安全系数(肝脏:50μg/kg/天;肾脏:500μg/kg/天)下的器官浓度与 0.97μg/kg/天的经皮剂量(Biedermann 等人,2010 年的最坏情况假设)产生的浓度,可假定这种经皮暴露是安全的。此外,基于模型模拟,文献中先前报道的高血液浓度极不可能,因为相关暴露水平比目前估计的总暴露水平高出几个数量级。

相似文献

1
The contribution of dermal exposure to the internal exposure of bisphenol A in man.皮肤接触对人体双酚 A 内暴露的贡献。
Toxicol Lett. 2011 Jul 28;204(2-3):190-8. doi: 10.1016/j.toxlet.2011.04.032. Epub 2011 May 5.
2
Derivation of a bisphenol A oral reference dose (RfD) and drinking-water equivalent concentration.双酚A口服参考剂量(RfD)及饮水等效浓度的推导
J Toxicol Environ Health B Crit Rev. 2008 Feb;11(2):69-146. doi: 10.1080/10937400701724303.
3
Commentary: dermal penetration of bisphenol A--consequences for risk assessment.评论:双酚 A 的皮肤渗透——对风险评估的影响。
Toxicol Lett. 2013 Feb 27;217(2):159-61. doi: 10.1016/j.toxlet.2012.12.009. Epub 2012 Dec 20.
4
Application of physiologically-based toxicokinetic modelling in oral-to-dermal extrapolation of threshold doses of cosmetic ingredients.生理毒代动力学模型在化妆品成分经口-皮渗透阈剂量外推中的应用。
Toxicol Lett. 2014 Jun 16;227(3):189-202. doi: 10.1016/j.toxlet.2014.03.013. Epub 2014 Apr 13.
5
Case study: Is bisphenol S safer than bisphenol A in thermal papers?案例研究:热敏纸中双酚 S 是否比双酚 A 更安全?
Arch Toxicol. 2019 Jul;93(7):1835-1852. doi: 10.1007/s00204-019-02474-x. Epub 2019 May 20.
6
Physiologically based toxicokinetic modelling as a tool to assess target organ toxicity in route-to-route extrapolation--the case of coumarin.基于生理学的毒代动力学模型作为评估不同暴露途径间靶器官毒性的工具——以香豆素为例。
Toxicol Lett. 2011 Apr 25;202(2):100-10. doi: 10.1016/j.toxlet.2011.01.022. Epub 2011 Feb 1.
7
Widespread occurrence of bisphenol A in paper and paper products: implications for human exposure.双酚 A 广泛存在于纸张和纸制品中:对人类暴露的影响。
Environ Sci Technol. 2011 Nov 1;45(21):9372-9. doi: 10.1021/es202507f. Epub 2011 Oct 5.
8
Development of physiologically based toxicokinetic models for improving the human indoor exposure assessment to water contaminants: trichloroethylene and trihalomethanes.用于改进人体对水中污染物(三氯乙烯和三卤甲烷)室内暴露评估的基于生理的毒代动力学模型的开发。
J Toxicol Environ Health A. 2006 Dec;69(23):2095-136. doi: 10.1080/15287390600631789.
9
Toxicokinetics of bisphenol A in pregnant DA/Han rats after single i.v. application.单次静脉注射后双酚A在怀孕的DA/Han大鼠体内的毒代动力学
Arch Toxicol. 2006 Oct;80(10):647-55. doi: 10.1007/s00204-006-0097-x. Epub 2006 Apr 8.
10
High levels of bisphenol A in paper currencies from several countries, and implications for dermal exposure.来自多个国家的纸币中存在高水平的双酚 A,及其对皮肤接触的影响。
Environ Sci Technol. 2011 Aug 15;45(16):6761-8. doi: 10.1021/es200977t. Epub 2011 Jul 21.

引用本文的文献

1
The cuticle plays an important role against toxicity to bisphenol A and bisphenol S.角质层在抵抗双酚A和双酚S的毒性方面发挥着重要作用。
Toxicol Rep. 2023 Mar 2;10:341-347. doi: 10.1016/j.toxrep.2023.02.013. eCollection 2023.
2
The Role of "Physiologically Based Pharmacokinetic Model (PBPK)" New Approach Methodology (NAM) in Pharmaceuticals and Environmental Chemical Risk Assessment.“生理药代动力学模型 (PBPK)”新方法学 (NAM) 在药品和环境化学风险评估中的作用。
Int J Environ Res Public Health. 2023 Feb 16;20(4):3473. doi: 10.3390/ijerph20043473.
3
An insight into bisphenol A, food exposure and its adverse effects on health: A review.
双酚A、食物暴露及其对健康的不良影响洞察:综述
Front Nutr. 2022 Nov 3;9:1047827. doi: 10.3389/fnut.2022.1047827. eCollection 2022.
4
Application of Physiologically Based Pharmacokinetic Modeling in Preclinical Studies: A Feasible Strategy to Practice the Principles of 3Rs.基于生理药代动力学模型在临床前研究中的应用:践行3R原则的可行策略
Front Pharmacol. 2022 May 12;13:895556. doi: 10.3389/fphar.2022.895556. eCollection 2022.
5
Pregnancy-specific physiologically-based toxicokinetic models for bisphenol A and bisphenol S.用于双酚 A 和双酚 S 的妊娠特异性生理毒代动力学模型。
Environ Int. 2021 Feb;147:106301. doi: 10.1016/j.envint.2020.106301. Epub 2020 Dec 22.
6
Evaluation of the effects of hair colouring products on the oxidative status in rats.染发产品对大鼠氧化状态影响的评估。
Postepy Dermatol Alergol. 2020 Oct;37(5):766-770. doi: 10.5114/ada.2020.100486. Epub 2020 Nov 7.
7
Neuro-toxic and Reproductive Effects of BPA.双酚 A 的神经毒性和生殖毒性。
Curr Neuropharmacol. 2019;17(12):1109-1132. doi: 10.2174/1570159X17666190726112101.
8
Physiologically Based Pharmacokinetic (PBPK) Modeling of the Bisphenols BPA, BPS, BPF, and BPAF with New Experimental Metabolic Parameters: Comparing the Pharmacokinetic Behavior of BPA with Its Substitutes.基于生理学的双酚 A(BPA)、双酚 S(BPS)、双酚 F(BPF)和双酚 AF(BPAF)代谢新参数的药代动力学模型:比较 BPA 与其替代品的药代动力学行为。
Environ Health Perspect. 2018 Jul 10;126(7):077002. doi: 10.1289/EHP2739. eCollection 2018 Jul.
9
Developmental Neurotoxic Effects of Percutaneous Drug Delivery: Behavior and Neurochemical Studies in C57BL/6 Mice.经皮给药的发育神经毒性作用:C57BL/6小鼠的行为和神经化学研究
PLoS One. 2016 Sep 8;11(9):e0162570. doi: 10.1371/journal.pone.0162570. eCollection 2016.
10
Recent advances in simultaneous analysis of bisphenol A and its conjugates in human matrices: Exposure biomarker perspectives.人体基质中双酚A及其共轭物同步分析的最新进展:暴露生物标志物视角
Sci Total Environ. 2016 Dec 1;572:770-781. doi: 10.1016/j.scitotenv.2016.07.062. Epub 2016 Aug 30.