癌变·畸变·突变 ›› 2025, Vol. 37 ›› Issue (6): 483-488.doi: 10.3969/j.issn.1004-616x.2025.06.010

• 检测研究 • 上一篇    

1,4-丁二醇二缩水甘油醚标准物质的研究

刘璟1,2, 郭采妮1,3, 张玉龙1,4, 付步芳1   

  1. 1. 中国食品药品检定研究院, 北京 102629;
    2. 爱美客技术发展股份有限公司, 北京 102299;
    3. 中国药科大学药学院, 江苏 南京 211198;
    4. 中国药科大学工学院, 江苏 南京 211198
  • 收稿日期:2025-05-10 修回日期:2025-06-15 发布日期:2025-12-06
  • 通讯作者: 付步芳,E-mail:fubufang@nifdc.org.cn
  • 作者简介:刘璟,E-mail:liujingkxx@163.com。

Usefulness of 1,4-butanediol diglycidyl ether as a reference material

LIU Jing1,2, GUO Caini1,3, ZHANG Yulong1,4, FU Bufang1   

  1. 1. National Institutes for Food and Drug Control, Beijing 102629;
    2. IMEIK Technology Development Co., Ltd., Beijing 102299;
    3. College of Pharmacy, China Pharmaceutical University, Nanjing 211198;
    4. College of Engineering, China Pharmaceutical University, Nanjing 211198, Jiangsu, China
  • Received:2025-05-10 Revised:2025-06-15 Published:2025-12-06

摘要: 目的:以市售1,4-丁二醇二缩水甘油醚(BDDE)为原料研制用于医疗产品检测的BDDE标准物质。方法:采用气相色谱质谱联用技术、红外光谱技术、核磁共振氢谱及碳谱技术对原材料进行筛选和考核,采用质量平衡法对BDDE原料的纯度进行检查,对有机成分中BDDE含量采用气相色谱面积归一化法进行纯度检查。纯度定值也使用质量平衡法,其中对有机成分中BDDE含量采用气相色谱1%自身对照法。同时对BDDE标准物质的均匀性和稳定性进行了考察,并进行不确定度评定。此外,本实验室选择气相色谱仪、气相色谱质谱联用仪、液相色谱质谱联用仪3种分析仪器,丙酮、水和乙酸乙酯3种溶剂,1%自身对照法、面积归一化法、外标曲线法3种定量方法对BDDE标准物质进行了纯度测定。结果:所研制的BDDE标准物质纯度为(98.14±0.21)%,定值结果准确;均匀性考察采用单因素方差分析进行评估,F=1.137<F0.05(14,30),P>0.05,认为在95%的置信区间内,待测标准物质是均匀的。短期稳定性试验结果表明BDDE标准物质在室温及-18~-22 ℃环境中保存14 d是稳定的;长期稳定性试验结果表明截至目前保存6个月是稳定的。此外,不同仪器、溶剂及方法对测量结果无明显影响,同时验证了BDDE溶液的定值结果准确。结论:所研制的BDDE标准物质定值准确、不确定度小、均匀性和稳定性良好,适宜作为医疗产品检测用标准物质。

关键词: 1,4-丁二醇二缩水甘油醚, 标准物质, 医疗器械, 气相色谱

Abstract: OBJECTIVE:To prepare 1,4-butanediol diglycidyl ether (BDDE) as a reference material for the detection of medical products. METHODS:Raw materials were screened and evaluated by gas chromatography-mass spectrometry,infrared spectroscopy,nuclear magnetic resonance spectroscopy and carbon spectroscopy. Its purity was checked by the mass balance method,and its content in organic components was checked by the gas chromatography area normalization method. The purity was also determined by the mass balance method,and the content by the gas chromatography 1% self-control method. Its uniformity and stability were investigated,and uncertainty was evaluated. In addition,the purity of BDDE was determined using three analytical instruments:gas chromatograph,gas chromatograph-mass spectrometer and liquid chromatograph-mass spectrometer;three solvents:acetone,water and ethyl acetate;and three quantitative methods:1% self-control method,area normalization method and external standard curve method. RESULTS:The purity of the acquired BDDE reference material was (98.14±0.21)%,and the accurate value of the fixed value was stable. The homogeneity was evaluated by one-way analysis of variance,F=1.137<F0.05(14,30),P>0.05,and it was considered that the standard substance to be tested was uniform within the 95% confidence interval. The short-term stability test results showed that it was stable at room temperature and at -18~-22 ℃ for 14 days,and the long-term stability was stable for 6 months. In addition,different instruments,solvents and methods had no significant effect on the measurement results,and the accuracy of the fixed value results of BDDE solution was verified. CONCLUSION:The acquired BDDE reference material showed accurate value,low uncertainty,good uniformity and stability,and can poteenteially be used for detection of medical products.

Key words: 1,4-butanediol diglycidyl ether, standard material, medical devices, gas chromatography

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