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HFA - 134a(1,1,1,2 - 四氟乙烷);吸入后在啮齿动物中无致癌性。

HFA-134a (1,1,1,2-tetrafluoroethane); lack of oncogenicity in rodents after inhalation.

作者信息

Alexander D J, Libretto S E, Chevalier H J, Imamura T, Pappritz G, Wilson J

机构信息

Medicines Safety Evaluation Division, Glaxo Research and Development Ltd., Ware, Hertfordshire, UK.

出版信息

Hum Exp Toxicol. 1995 Sep;14(9):706-14. doi: 10.1177/096032719501400902.

Abstract
  1. Groups of 60 male and 60 female B6C3F1 mice or HanIbm Wistar rats were exposed to HFA-134a using snout-only inhalation exposure techniques for periods of one hour daily for at least 104 weeks. HFA-134a was delivered directly from cylinders at vapour concentrations of 2500, 15,000 and 75,000ppm for mice and from metered-dose inhalers at vapour concentrations of 2500, 10,000 and 50,000ppm for rats. 2. Intended dosages were achieved. 3. Evidence of absorption was found at each dose level and was dose related. 4. Neither species suffered treatment related effects on survival, clinical signs, body weights, haematology nor on the type, incidence, site or severity of gross lesions. 5. There was no effect of treatment on the type, incidence, site or severity of neoplasms in mice or rats. 6. There were no non-neoplastic findings related to treatment in mice. 7. HFA-134a was considered not to be oncogenic and to provide a safe alternative to chlorofluorocarbons for use in pharmaceutical metered-dose inhalers.
摘要
  1. 将60只雄性和60只雌性B6C3F1小鼠或HanIbm Wistar大鼠分为一组,采用仅经口鼻吸入暴露技术,每天暴露于HFA - 134a中1小时,持续至少104周。对于小鼠,HFA - 134a直接从气瓶中输送,蒸汽浓度分别为2500、15000和75000ppm;对于大鼠,HFA - 134a从定量吸入器中输送,蒸汽浓度分别为2500、10000和50000ppm。2. 达到了预期剂量。3. 在每个剂量水平均发现了吸收证据,且与剂量相关。4. 两种动物在生存、临床症状、体重、血液学以及大体病变的类型、发生率、部位或严重程度方面均未出现与治疗相关的影响。5. 治疗对小鼠或大鼠肿瘤的类型、发生率、部位或严重程度没有影响。6. 在小鼠中未发现与治疗相关的非肿瘤性结果。7. HFA - 134a被认为不具有致癌性,是用于制药定量吸入器的氯氟烃的安全替代品。

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