• 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

评估人造纤维毒性和致癌性的方法:1991年11月11日至13日在北卡罗来纳州达勒姆举办的研讨会总结

Approaches to evaluating the toxicity and carcinogenicity of man-made fibers: summary of a workshop held November 11-13, 1991, Durham, North Carolina.

作者信息

McClellan R O, Miller F J, Hesterberg T W, Warheit D B, Bunn W B, Kane A B, Lippmann M, Mast R W, McConnell E E, Reinhardt C F

机构信息

Chemical Industry Institute of Toxicology, Research Triangle Park, North Carolina 27709.

出版信息

Regul Toxicol Pharmacol. 1992 Dec;16(3):321-64. doi: 10.1016/0273-2300(92)90011-w.

DOI:10.1016/0273-2300(92)90011-w
PMID:1293648
Abstract

The Workshop on Approaches to Evaluating the Toxicity and Carcinogenicity of Man-Made Fibers (MMF) was held in Durham, North Carolina, on November 11-13, 1991. The goal of the workshop was to reach a consensus, or to determine the extent to which a consensus existed, in two areas. Participants were asked to identify scientifically sound approaches for evaluating the toxicity and carcinogenicity of man-made fibers based on today's science and to determine research appropriate for study during the next 5 years that can provide an improved scientific basis for future revisions of approaches used to evaluate man-made fiber toxicity and carcinogenicity. During the first day, a series of "state of knowledge" presentations were made to provide all participants with a common data base from which to interact and discuss scientific issues. The workshop participants were assigned to one of four discussion groups, which met separately in three half-day sessions following the first day of presentations. All groups discussed the same topics: exposure assessment, hazard identification, and dose-response information needed to integrate to characterize risk in the first session; approaches to obtaining the needed information in the second session; and recommended approaches and guidelines for evaluating the toxicity and carcinogenicity of MMF and research needs in the third session. The workshop participants reconvened as a whole after each discussion session, and one member from each group reported the group's conclusions. A closure period was also included at the end of the workshop for review and discussion of items that had been considered during the workshop. The primary conclusions reached were the following: -All fiber types capable of depositing in the thorax are not alike in their pathogenic potential. -Only fiber samples with dimensions similar to those to which humans can inhale should be tested. -A complete characterization (i.e., dimensions, fiber number, mass, and aerodynamic diameter) of the fiber aerosol and retained dose is essential. -Appropriate aerosol generation methods must be used for inhalation studies in order to preserve fiber lengths. -A tiered approach to toxicity evaluation is recommended that includes: 1. In vitro screening for durability, surface properties, cytotoxicity, and similar properties, etc; 2. Short-term inhalation or other in vivo studies; 3. That chronic inhalation studies are the "gold standard" (i.e., provide most appropriate data for risk characterization). -The rat is the most appropriate species for inhalation studies. -In chronic inhalation studies, animals should be retained to at least 20% survival after 2-year exposure. -Serial lung burden analyses are an essential component of inhalation studies and are essential for understanding exposure-dose-response relationships. -Studies oriented to understanding mechanisms of toxicity and carcinogenicity are important adjuncts to traditional toxicity studies. -Histopathological analyses of tissues of the respiratory tract represent primary endpoints for evaluating effects of inhaled fibers. Major effects include pulmonary fibrosis, lung tumors, and mesotheliomas. Experimental tissues should be archived for future studies; wherever possible, handling and preservation of tissues should be done in a way that maximizes their future use in mechanistic studies. -Potential human exposures throughout the entire life-cycle of the fiber must be considered and fibrous material for toxicologic studies prepared accordingly. -Intracavity studies are inappropriate for risk characterization but can play a useful screening role in assessing fiber toxicity.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

“人造纤维(MMF)毒性和致癌性评估方法研讨会”于1991年11月11日至13日在北卡罗来纳州达勒姆市举行。该研讨会的目标是在两个领域达成共识,或确定已达成共识的程度。要求参会者基于当今科学,确定评估人造纤维毒性和致癌性的科学合理方法,并确定未来5年适合开展的研究,以便为未来修订人造纤维毒性和致癌性评估方法提供更完善的科学依据。在第一天,进行了一系列“知识现状”报告,为所有参会者提供一个共同的数据库,以便相互交流和讨论科学问题。研讨会参会者被分成四个讨论小组之一,在第一天报告之后,分三个半天会议分别进行讨论。所有小组讨论相同的主题:在第一场会议中讨论整合以表征风险所需的暴露评估、危害识别和剂量反应信息;在第二场会议中讨论获取所需信息的方法;在第三场会议中讨论评估MMF毒性和致癌性的推荐方法和指南以及研究需求。每次讨论会议后,研讨会参会者全体重新集合,每组一名成员汇报小组结论。在研讨会结束时还安排了一个总结期,用于回顾和讨论研讨会期间审议的事项。得出的主要结论如下:

  • 所有能够沉积在胸部的纤维类型,其致病潜力并不相同。

  • 仅应测试尺寸与人可吸入尺寸相似的纤维样本。

  • 对纤维气溶胶和留存剂量进行完整表征(即尺寸、纤维数量、质量和空气动力学直径)至关重要。

  • 吸入研究必须使用合适的气溶胶生成方法以保持纤维长度。

  • 建议采用分层毒性评估方法,包括:1. 进行体外耐久性、表面特性、细胞毒性等类似特性的筛选;2. 进行短期吸入或其他体内研究;3. 慢性吸入研究是“金标准”(即提供最适合风险表征的数据)。

  • 大鼠是吸入研究最合适的物种。

  • 在慢性吸入研究中,动物在2年暴露后应留存至至少20%存活。

  • 连续肺负荷分析是吸入研究的重要组成部分,对于理解暴露-剂量-反应关系至关重要。

  • 旨在理解毒性和致癌机制的研究是传统毒性研究的重要辅助。

  • 呼吸道组织的组织病理学分析是评估吸入纤维效应的主要终点。主要影响包括肺纤维化、肺癌和间皮瘤。实验组织应存档以备未来研究;只要可能,组织的处理和保存方式应使其在未来机制研究中的用途最大化。

  • 必须考虑纤维整个生命周期内潜在的人体暴露,并据此制备用于毒理学研究的纤维材料。

  • 腔内研究不适用于风险表征,但在评估纤维毒性方面可发挥有用的筛选作用。(摘要截选至400词)

相似文献

1
Approaches to evaluating the toxicity and carcinogenicity of man-made fibers: summary of a workshop held November 11-13, 1991, Durham, North Carolina.评估人造纤维毒性和致癌性的方法:1991年11月11日至13日在北卡罗来纳州达勒姆举办的研讨会总结
Regul Toxicol Pharmacol. 1992 Dec;16(3):321-64. doi: 10.1016/0273-2300(92)90011-w.
2
Chronic inhalation toxicity and carcinogenicity testing of respirable fibrous particles. Workshop report.
Regul Toxicol Pharmacol. 1996 Dec;24(3):202-12. doi: 10.1006/rtph.1996.0128.
3
Chronic inhalation toxicity and carcinogenicity study on potassium octatitanate fibers (TISMO) in rats.大鼠八钛酸钾纤维(TISMO)的慢性吸入毒性和致癌性研究
Inhal Toxicol. 2004 May;16(5):291-310. doi: 10.1080/08958370490428391.
4
Determinants of the pathogenicity of man-made vitreous fibers (MMVF).人造玻璃纤维(MMVF)致病性的决定因素。
Int Arch Occup Environ Health. 2000 Jun;73 Suppl:S60-8. doi: 10.1007/pl00014628.
5
Synthetic vitreous fibers: a review of toxicology research and its impact on hazard classification.合成玻璃纤维:毒理学研究综述及其对危害分类的影响
Crit Rev Toxicol. 2001 Jan;31(1):1-53. doi: 10.1080/20014091111668.
6
Toxicology and carcinogenesis studies of indium phosphide (CAS No. 22398-90-7) in F344/N rats and B6C3F1 mice (inhalation studies).磷化铟(CAS编号:22398-90-7)对F344/N大鼠和B6C3F1小鼠的毒理学和致癌性研究(吸入研究)
Natl Toxicol Program Tech Rep Ser. 2001 Jul(499):7-340.
7
Significance of durability of mineral fibers for their toxicity and carcinogenic potency in the abdominal cavity of rats in comparison with the low sensitivity of inhalation studies.与吸入研究的低敏感性相比,矿物纤维在大鼠腹腔中的毒性和致癌潜力的持久性的意义。
Environ Health Perspect. 1994 Oct;102 Suppl 5(Suppl 5):145-50. doi: 10.1289/ehp.94102s5145.
8
Studies on the inhalation toxicology of two fiberglasses and amosite asbestos in the Syrian golden hamster. Part II. Results of chronic exposure.两种玻璃纤维和铁石棉在叙利亚金黄地鼠体内的吸入毒理学研究。第二部分。慢性暴露结果。
Inhal Toxicol. 1999 Sep;11(9):785-835. doi: 10.1080/089583799196754.
9
NTP Toxicology and Carcinogenesis Studies of Talc (CAS No. 14807-96-6)(Non-Asbestiform) in F344/N Rats and B6C3F1 Mice (Inhalation Studies).滑石(CAS编号:14807-96-6)(非石棉状)在F344/N大鼠和B6C3F1小鼠中的NTP毒理学和致癌性研究(吸入研究)
Natl Toxicol Program Tech Rep Ser. 1993 Sep;421:1-287.
10
Testing strategies to establish the safety of nanomaterials: conclusions of an ECETOC workshop.用于确定纳米材料安全性的测试策略:欧洲生态毒理学与化学品毒性中心研讨会结论
Inhal Toxicol. 2007 Jun;19(8):631-43. doi: 10.1080/08958370701353080.

引用本文的文献

1
Health risk of chrysotile revisited.重新探讨温石棉的健康风险。
Crit Rev Toxicol. 2013 Feb;43(2):154-83. doi: 10.3109/10408444.2012.756454.
2
Pulmonary endpoints (lung carcinomas and asbestosis) following inhalation exposure to asbestos.吸入石棉后肺部终点(肺癌和石棉肺)。
J Toxicol Environ Health B Crit Rev. 2011;14(1-4):76-121. doi: 10.1080/10937404.2011.556047.
3
Clearance of man made mineral fibres from the lungs of sheep.绵羊肺中人造矿物纤维的清除
Occup Environ Med. 1999 Oct;56(10):684-90. doi: 10.1136/oem.56.10.684.
4
Approaches to characterizing human health risks of exposure to fibers.评估纤维接触对人类健康风险的方法。
Environ Health Perspect. 1997 Sep;105 Suppl 5(Suppl 5):1329-36. doi: 10.1289/ehp.97105s51329.
5
Susceptibility of p53-deficient mice to induction of mesothelioma by crocidolite asbestos fibers.p53基因缺陷小鼠对青石棉纤维诱发间皮瘤的易感性。
Environ Health Perspect. 1997 Sep;105 Suppl 5(Suppl 5):1069-72. doi: 10.1289/ehp.97105s51069.
6
Fibrogenic effect of wollastonite compared with asbestos dust and dusts containing quartz.硅灰石与石棉粉尘及含石英粉尘相比的致纤维化作用。
Occup Environ Med. 1994 May;51(5):343-6. doi: 10.1136/oem.51.5.343.
7
Lung retention of cerium in humans.铈在人体肺部的潴留情况。
Occup Environ Med. 1994 Mar;51(3):195-9. doi: 10.1136/oem.51.3.195.
8
The occupational physician's point of view: the model of man-made vitreous fibers.职业医生的观点:人造玻璃纤维模型
Environ Health Perspect. 1994 Oct;102 Suppl 5(Suppl 5):31-6. doi: 10.1289/ehp.94102s531.
9
Role of biopersistence in the pathogenicity of man-made fibers and methods for evaluating biopersistence: a summary of two round-table discussions.生物持久性在人造纤维致病性中的作用及生物持久性评估方法:两次圆桌讨论综述
Environ Health Perspect. 1994 Oct;102 Suppl 5(Suppl 5):277-83. doi: 10.1289/ehp.94102s5277.
10
Significance of durability of mineral fibers for their toxicity and carcinogenic potency in the abdominal cavity of rats in comparison with the low sensitivity of inhalation studies.与吸入研究的低敏感性相比,矿物纤维在大鼠腹腔中的毒性和致癌潜力的持久性的意义。
Environ Health Perspect. 1994 Oct;102 Suppl 5(Suppl 5):145-50. doi: 10.1289/ehp.94102s5145.