Quan Shi, Michael G Penman, Juan-Carlos Carrillo, An R Van Rompay, Lenny Kamelia, Martijn Rooseboom, Hua Shen, Sophie Jia, Yuan Tian, Jamie Dunn, Fabienne Hubert, Peter J Boogaard
{"title":"高碳烯烃对汉代 Wistar 大鼠的亚慢性毒性。","authors":"Quan Shi, Michael G Penman, Juan-Carlos Carrillo, An R Van Rompay, Lenny Kamelia, Martijn Rooseboom, Hua Shen, Sophie Jia, Yuan Tian, Jamie Dunn, Fabienne Hubert, Peter J Boogaard","doi":"10.1186/s40360-024-00786-y","DOIUrl":null,"url":null,"abstract":"<p><p>Higher olefins (HO) are a category of unsaturated hydrocarbons widely used in industry applications to make products essential for daily human life. Establishing safe exposure limits requires a solid data matrix that facilitates understanding of their toxicological profile. This in turn allows for data to be read across to other members of the category, which are structurally similar and have predictable physico-chemical properties. Five independent subchronic oral toxicity studies were conducted in Wistar rats with Oct-1-ene, Nonene, branched, Octadec-1-ene, Octadecene and hydrocarbon C12-30, olefin-rich, ethylene polymn. by product, at doses ranging from 20 to 1000 mg/kg bw. These HO were selected considering gut absorption, carbon chain length, double-bond position and carbon backbone structural variations. Generally, limited and non-adverse toxicity effects were observed at the end of the treatment for short carbon chain HO. For instance, alpha 2u-globulin nephropathy in the male rats and liver hypertrophy. No clear trend in systemic toxicity was linked to the double-bond position. Key factors for hazard assessment include absorption, carbon chain length, and branching, with Nonene, branched, identified as the worst-case substance. Taken together, the no observed adverse effect level (NOAEL) of each HO in these subchronic studies was set at the highest dose tested.</p>","PeriodicalId":9023,"journal":{"name":"BMC Pharmacology & Toxicology","volume":null,"pages":null},"PeriodicalIF":2.8000,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11380337/pdf/","citationCount":"0","resultStr":"{\"title\":\"The subchronic toxicity of higher olefins in Han Wistar rats.\",\"authors\":\"Quan Shi, Michael G Penman, Juan-Carlos Carrillo, An R Van Rompay, Lenny Kamelia, Martijn Rooseboom, Hua Shen, Sophie Jia, Yuan Tian, Jamie Dunn, Fabienne Hubert, Peter J Boogaard\",\"doi\":\"10.1186/s40360-024-00786-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Higher olefins (HO) are a category of unsaturated hydrocarbons widely used in industry applications to make products essential for daily human life. Establishing safe exposure limits requires a solid data matrix that facilitates understanding of their toxicological profile. This in turn allows for data to be read across to other members of the category, which are structurally similar and have predictable physico-chemical properties. Five independent subchronic oral toxicity studies were conducted in Wistar rats with Oct-1-ene, Nonene, branched, Octadec-1-ene, Octadecene and hydrocarbon C12-30, olefin-rich, ethylene polymn. by product, at doses ranging from 20 to 1000 mg/kg bw. These HO were selected considering gut absorption, carbon chain length, double-bond position and carbon backbone structural variations. Generally, limited and non-adverse toxicity effects were observed at the end of the treatment for short carbon chain HO. For instance, alpha 2u-globulin nephropathy in the male rats and liver hypertrophy. No clear trend in systemic toxicity was linked to the double-bond position. Key factors for hazard assessment include absorption, carbon chain length, and branching, with Nonene, branched, identified as the worst-case substance. Taken together, the no observed adverse effect level (NOAEL) of each HO in these subchronic studies was set at the highest dose tested.</p>\",\"PeriodicalId\":9023,\"journal\":{\"name\":\"BMC Pharmacology & Toxicology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2024-09-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11380337/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BMC Pharmacology & Toxicology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1186/s40360-024-00786-y\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Pharmacology & Toxicology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s40360-024-00786-y","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
摘要
高碳烯烃(HO)是一类不饱和碳氢化合物,广泛应用于工业领域,制造人类日常生活中不可或缺的产品。确定安全接触限值需要一个可靠的数据矩阵,以帮助了解其毒理学特征。这反过来又可以将数据解读为该类别的其他成员,因为这些成员结构相似,具有可预测的物理化学特性。对 Wistar 大鼠进行了五项独立的亚慢性口服毒性研究,研究对象包括辛-1-烯、壬烯、支链、十八-1-烯、十八烯和碳氢化合物 C12-30、富含烯烃的乙烯多聚物副产品,研究剂量为 20 至 1000 毫克/千克体重。选择这些 HO 时考虑了肠道吸收、碳链长度、双键位置和碳骨架结构变化。一般来说,短碳链 HO 在治疗结束时会出现有限的非不良毒性反应。例如,雄性大鼠的α-2u-球蛋白肾病和肝脏肥大。全身毒性的明显趋势与双键位置无关。危害评估的关键因素包括吸收、碳链长度和支链,支链壬烯被确定为最严重的物质。总之,在这些亚慢性研究中,每种 HO 的无观测不良效应水平 (NOAEL) 都设定为测试的最高剂量。
The subchronic toxicity of higher olefins in Han Wistar rats.
Higher olefins (HO) are a category of unsaturated hydrocarbons widely used in industry applications to make products essential for daily human life. Establishing safe exposure limits requires a solid data matrix that facilitates understanding of their toxicological profile. This in turn allows for data to be read across to other members of the category, which are structurally similar and have predictable physico-chemical properties. Five independent subchronic oral toxicity studies were conducted in Wistar rats with Oct-1-ene, Nonene, branched, Octadec-1-ene, Octadecene and hydrocarbon C12-30, olefin-rich, ethylene polymn. by product, at doses ranging from 20 to 1000 mg/kg bw. These HO were selected considering gut absorption, carbon chain length, double-bond position and carbon backbone structural variations. Generally, limited and non-adverse toxicity effects were observed at the end of the treatment for short carbon chain HO. For instance, alpha 2u-globulin nephropathy in the male rats and liver hypertrophy. No clear trend in systemic toxicity was linked to the double-bond position. Key factors for hazard assessment include absorption, carbon chain length, and branching, with Nonene, branched, identified as the worst-case substance. Taken together, the no observed adverse effect level (NOAEL) of each HO in these subchronic studies was set at the highest dose tested.
期刊介绍:
BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.