The Nonclinical Assessment of Trans-1,3,3,3-tetrafluoropropene (HFO-1234ze (E)), a Near Zero Global Warming Potential Propellant for Use in Metered Dose Inhalation Products.

IF 1.2 4区 医学 Q4 PHARMACOLOGY & PHARMACY
International Journal of Toxicology Pub Date : 2024-01-01 Epub Date: 2023-10-20 DOI:10.1177/10915818231206025
Paul S Giffen, Joanne D Kilgour, Matthew Jacobsen, Karen Thacker, Ann A Holmberg
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引用次数: 0

Abstract

HFO-1234ze (E) is proposed as a near zero global warming propellant for use in metered dose inhaled (MDI) products. This paper describes the non-clinical safety assessment in mice, rats, and dogs and supplements previously reported data (genetic toxicology, short-term toxicology, and reproductive toxicology). In all species, HFO-1234ze (E) was only detectable in blood for a short period after dosing with no evidence of accumulation. HFO-1234ze (E) was without any toxicological effects at very high doses in subchronic (13-week mouse) and chronic (39-week dog) studies. Chronic (26-week) administration to rats at very high doses was associated with an exacerbation of rodent progressive cardiomyopathy, a well-documented background finding in rodents. In a 2-generation study, extremely high doses were associated with the early euthanasia of some lactating female rats. This finding was considered to be significantly influenced by a state of negative energy balance, reflecting the specific vulnerability of rats during lactation. These findings are considered to not pose a risk to humans with typical MDI use given they occurred at doses which far exceed those expected in patients. Overall, the nonclinical safety data for HFO-1234ze (E) support its further development as an MDI propellant.

反-1,3,3,3-四氟丙烯(HFO-1234ze(E))的非临床评估,这是一种用于计量剂量吸入产品的近零全球变暖潜能推进剂。
HFO-1234ze(E)被提议作为一种近零全球变暖推进剂,用于计量剂量吸入(MDI)产品。本文描述了小鼠、大鼠和狗的非临床安全性评估,并补充了先前报道的数据(遗传毒理学、短期毒理学和生殖毒理学)。在所有物种中,HFO-1234ze(E)仅在给药后的短时间内在血液中检测到,没有积累的证据。在亚慢性(13周小鼠)和慢性(39周狗)研究中,HFO-1234ze(E)在非常高的剂量下没有任何毒理学影响。大鼠长期(26周)高剂量给药与啮齿类动物进行性心肌病的恶化有关,这是啮齿类动物的一个有充分记录的背景发现。在一项两代研究中,极高剂量与一些哺乳期雌性大鼠的早期安乐死有关。这一发现被认为受到负能量平衡状态的显著影响,反映了大鼠在哺乳期的特殊脆弱性。这些发现被认为不会对典型MDI使用的人类构成风险,因为它们的剂量远远超过了患者的预期。总体而言,HFO-1234ze(E)的非临床安全性数据支持其作为MDI推进剂的进一步发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.40
自引率
4.50%
发文量
53
审稿时长
4.5 months
期刊介绍: The International Journal of Toxicology publishes timely, peer-reviewed papers on current topics important to toxicologists. Six bi-monthly issues cover a wide range of topics, including contemporary issues in toxicology, safety assessments, novel approaches to toxicological testing, mechanisms of toxicity, biomarkers, and risk assessment. The Journal also publishes invited reviews on contemporary topics, and features articles based on symposia. In addition, supplemental issues are routinely published on various special topics, including three supplements devoted to contributions from the Cosmetic Review Expert Panel.
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