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评估成分安全性的进展。

Advances in assessing ingredient safety.

作者信息

Dourson Michael L, York Raymond G

机构信息

Toxicology Excellence for Risk Assessment (TERA), 2300 Montana Avenue, Suite 409, Cincinnati, OH 45211, USA.

R G York & Associates LLC, Cincinnati, OH, USA.

出版信息

Regul Toxicol Pharmacol. 2016 Aug;79 Suppl 2:S112-8. doi: 10.1016/j.yrtph.2016.07.008. Epub 2016 Jul 15.

Abstract

The safety of food ingredients will be assessed in the 21st century by mixture of traditional methods, such as the "safe" dose concept, which is thought to be an accurate but imprecise estimation of dose below the population threshold for adverse effect, and contemporary methods, such as the Benchmark Dose (BMD), Chemical Specific Adjustment Factors (CSAF), physiologically-based pharmacokinetic models, and biologically-informed dose response modeling. New research on the horizon related to toxicology 21 may also improve these risk assessment methods, or suggest new ones. These traditional, contemporary and new methods and research will be briefly described.

摘要

21世纪将通过传统方法与当代方法相结合来评估食品成分的安全性。传统方法如“安全”剂量概念,该概念被认为是对低于人群不良反应阈值剂量的一种准确但不精确的估计;当代方法如基准剂量(BMD)、化学物质特定调整因子(CSAF)、基于生理学的药代动力学模型以及生物信息剂量反应模型。与毒理学21相关的新研究也可能改进这些风险评估方法,或提出新的方法。将简要介绍这些传统、当代和新的方法及研究。

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