国产药用气雾剂辅料1,1,1,2-四氟乙烷的吸入毒理安全性评价

    Evaluation of the Inhalation Safety of Domestic Pharmaceutical Metered-dose Inhalers Accessories Hydrofluoroalkane-134a

    • 摘要:
      目的  对国产药用气雾剂辅料1,1,1,2-四氟乙烷(hydrofluoroalkane-134a,HFA-134a)进行吸入毒理安全性评价。
      方法 对国内2个主要生产厂家的药用吸入气雾剂HFA-134a样品进行大鼠21 d重复吸入亚慢性毒性试验和Hartley豚鼠主动全身过敏试验。
      结果 2个厂家的HFA-134a剂量分别为(2 140±58)g·m–3和(2 129±59)g·m–3时,21 d重复吸入(每天2 h),出现统计学差异的指标有:血液学部分指标(中性粒细胞数、嗜碱性粒细胞、嗜碱性粒细胞比率、单核细胞比率、红细胞容积、血小板计数)、血液生化学部分指标(白蛋白、总胆红素、氯离子、钾离子)、尿液检测部分指标(亚硝酸盐、白细胞、尿胆原、蛋白和胆红素)、部分脏器器官的脏器湿重值和脏器系数值(肾脏、胸腺、心脏、垂体、肺脏)。未见豚鼠全身致敏反应。
      结论 国产药用气雾剂辅料HFA-134a在相当于临床最大用量的250倍下连续染毒21 d,对大鼠部分脏器和血尿生化指标有一定的毒性作用,但在临床正常应用中是否吸入安全还需进一步进行安全性评价研究。

       

      Abstract:
      OBJECTIVE  To evaluate the inhalation safety of domestic pharmaceutical metered-dose inhalers accessories hydrofluoroalkane(HFA)-134a.
      METHODS  The 21 d repeat dose inhalation toxicity study and Hartley guinea pig active systemic anaphylaxis for samples from two major domestic manufacturers were tested.
      RESULTS  SD rats were exposed nose-only separately to the samples from two major domestic manufacturers at the concentration of (2 140±58)g·m–3 and (2 129±59)g·m–3 respectively for 21 consecutive days(2 h each day), there were statistically significant differences in the following indicators: some indicators of hematology such as neutrophil count, basophil, basophil ratio, monocyte ratio, hematocrit and platelet count, some indicators of blood biochemistry such as albumin content, total bilirubin content, chloride ion and potassium ion, some indicators of urine such as nitrite, leukocytes, urobilinogen, protein and bilirubin, organ weight and coefficients of kidney, thymus, heart, pituitary and lung. No systemic sensitization reaction were observed in guinea pigs.
      CONCLUSION  The domestic pharmaceutical HFA-134a have certain toxic effects on some organs, blood and urine biochemical indicators of SD rats exposed to 250 times of the clinical maximum dose for continuously 21 d, however, further research is need to access whether inhalation is safe in normal clinical dose.

       

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