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在 REACH 下,应用人体生物监测(HBM)技术对化学暴露的健康风险进行特征描述。

Application of human biomonitoring (HBM) of chemical exposure in the characterisation of health risks under REACH.

机构信息

Shell International BV, Shell Health, PO Box 162, 2501 AN The Hague, The Netherlands.

出版信息

Int J Hyg Environ Health. 2012 Feb;215(2):238-41. doi: 10.1016/j.ijheh.2011.09.009. Epub 2011 Dec 15.

Abstract

REACH requires health risk management for workers and the general population and introduced the concept of Derived No-Effect Level (DNEL). DNELs must be derived for all substances that are classified as hazardous. In analogy to other health-risk based guidance values, such as reference doses (RfDs) and tolerable daily intakes (TDIs), risk to health is considered negligible if the actual exposure is less than the DNEL. Exposure assessment is relatively simple for occupational situations but more complex for the general public, in which exposure may occur via multiple pathways, routes, and media. For such complex or partially defined exposure scenarios, human biomonitoring (HBM) gives a snapshot of the internal or absorbed dose of a chemical and is often the most reliable exposure assessment methodology. For human risk management, HBM data can be interpreted using the recently developed concept of Biomonitoring Equivalents (BEs). Basically, a BE translates an established reference value into a biomarker concentration using toxicokinetic data. If the results of an exposure assessment using HBM indicate that the levels measured are below the DNEL-based BE (BE(DNEL)), it would indicate that the combined exposure via all potential exposure routes is unlikely to pose a risk to human health and that health risk management measures might not be needed. Hence, BEs do not challenge existing risk assessments but rather build upon them to help risk management, the ultimate goal of any risk assessment. A challenge in implementing this approach forms the limited availability of toxicokinetic information for many substances. However, methodologies such as generic physiologically based toxicokinetic models, which allow estimation of biomarker concentrations based on physicochemical properties, are being developed for less data-rich chemicals. Acceptance of the use of BE by regulatory authorities will allow initial screening of population exposure to chemicals to identify those chemicals requiring more detailed risk and exposure assessment, assisting in priority setting and ultimately leading to improved product stewardship and risk management.

摘要

REACH 要求对工人和普通民众进行健康风险管理,并引入了衍生无作用水平 (DNEL) 的概念。对于所有被归类为危险的物质,都必须推导出 DNEL。如果实际暴露量低于 DNEL,则认为对健康的风险可以忽略不计。对于职业情况,暴露评估相对简单,但对于普通公众来说,暴露可能通过多种途径、路线和介质发生,因此更为复杂。对于这种复杂或部分定义的暴露情况,人体生物监测 (HBM) 可以提供化学物质内部或吸收剂量的快照,通常是最可靠的暴露评估方法。对于人类风险管理,可以使用最近开发的生物监测等效物 (BE) 概念来解释 HBM 数据。基本上,BE 使用毒代动力学数据将既定的参考值转换为生物标志物浓度。如果使用 HBM 进行暴露评估的结果表明测量水平低于基于 DNEL 的 BE(BE(DNEL)),则表明通过所有潜在暴露途径的综合暴露不太可能对人类健康构成风险,并且可能不需要健康风险管理措施。因此,BE 并没有挑战现有的风险评估,而是在其基础上构建,以帮助风险管理,这是任何风险评估的最终目标。在实施这种方法时面临的一个挑战是许多物质的毒代动力学信息有限。然而,正在开发通用生理毒代动力学模型等方法,这些方法可以根据物理化学性质来估计生物标志物浓度,从而用于数据较少的化学物质。监管机构接受使用 BE 将允许对人群接触化学物质进行初步筛选,以确定需要更详细的风险和暴露评估的化学物质,从而有助于确定优先事项,并最终导致更好的产品管理和风险管理。

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