›› 2016, Vol. 43 ›› Issue (1): 256-260.doi: 10.16431/j.cnki.1671-7236.2016.01.037

• 疾病防治 • 上一篇    下一篇

伊维菌素微乳无菌检查方法学的研究

邢守叶1,2, 周绪正1, 李冰1, 牛建荣1, 魏小娟1, 张继瑜1   

  1. 1. 中国农业科学院兰州畜牧与兽药研究所, 农业部兽用药物创制重点实验室, 兰州 730070;
    2. 甘肃农业大学动物医学院, 兰州 730050
  • 收稿日期:2015-05-09 出版日期:2016-01-20 发布日期:2016-01-23
  • 通讯作者: 张继瑜 E-mail:infzjy@sina.com
  • 作者简介:邢守叶(1988-),女,山东济南人,硕士,研究方向:兽医药理学与毒理学,E-mail:xingshouye1988@163.com
  • 基金资助:
    国家现代农业肉牛牦牛产业技术体系建设专项资金(CARS-38);重点牧区生产生态生活保障技术集成与示范(2012BAD13BOO)

Study on Sterility Test Method of Ivermectin Microemulsion

XING Shou-ye1,2, ZHOU Xu-zheng1, LI Bing1, NIU Jian-rong1, WEI Xiao-juan1, ZHANG Ji-yu1   

  1. 1. Key Laboratory of New Animal Drug Discovery, Ministry of Agriculture, Lanzhou Institute of Husbandry and Pharmaceutical Sciences, Chinese Academy of Agricultural Sciences, Lanzhou 730070, China;
    2. College of Veterinary Medicine, Gansu Agricultural University, Lanzhou 730050, China
  • Received:2015-05-09 Online:2016-01-20 Published:2016-01-23

摘要: 本试验旨在对伊维菌素微乳制剂进行无菌检查方法学验证和无菌检查试验,确认本试验所用的方法适用于该制剂的无菌检查。按《中国兽药典》2005版一部(附录118)所载"无菌检查法"项下进行试验,通过对阳性对照菌、不同量冲洗液等条件的选择,采用薄膜过滤法对10瓶供试品(每种试验菌的样品量)进行检测,建立了无菌检查方法。经方法验证,用400mL 0.1%蛋白胨水溶液冲洗后,含供试品容器中的7个阳性菌试验组与阳性菌对照组相比均生长良好,说明供试品的该检验量在该检验条件下无抑菌作用或其抑菌作用可以忽略不计,可以用该方法进行供试品的无菌检查。对3批供试品进行无菌检查,阳性对照菌均在24h内生长良好,阴性对照均澄清,无菌生长,3批供试品均澄清,无菌生长,无菌检查试验结果符合规定。

关键词: 伊维菌素微乳制剂; 无菌检查; 薄膜过滤法; 方法验证

Abstract: The assay was aimed to study the sterility test and validation test of ivermectin microemulsion preparation and establish a sterility test method for ivermectin microemulsion preparation.The test method was carried out according to the method in volumeⅠ, Chinese Veterinary Pharmacopoeia Edition 2005.By choosing positive control bacteria and defining washing volumes in sterility test, the membrane-filter method was used to test the quantity of 10 bottles of test samples, and the sterility test was established.The result of method validation test showed that the test and all of positive control bacteria and microorganism growth after each filter being washed with 400 mL 0.1% peptone solution.It illustrated that the samples had no antimicrobial activity under the sample quantity and test condition.This method was available for sterility test of ivermectin microemulsion preparation.Using this method to test three lots test samples, the results showed that the positive control bacteria grew well within 24 h.The negative control bacteria and three lots test samples were sterile.It indicated that sterility test results met the requirements.

Key words: ivermectin microemulsion preparation; sterility test; membrane-filter method; method validation test

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