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中国医药导刊 ›› 2025, Vol. 27 ›› Issue (9): 950-953.

• 检验检测 • 上一篇    下一篇

碳酸钙D3制剂标准中维生素D3含量测定方法的改进

朱晓月, 张喆, 孙毅, 安京烨, 郑洁, 吴兆伟*   

  1. 北京市药品检验研究院(北京市疫苗检验中心),国家药品监督管理局仿制药研究与评价重点实验室,
    中药成分分析与生物评价北京市重点实验室,北京 102206
  • 收稿日期:2025-02-13 修回日期:2025-05-27 接受日期:2025-11-12 出版日期:2025-09-28 发布日期:2025-11-18

Improvement of Determination Method about Vitamin D3 Assay in Standards for Calcium Carbonate and Vitamin D3 Preparations

ZHU Xiaoyue, ZHANG Zhe, SUN Yi, AN Jingye, ZHENG Jie, WU Zhaowei*   

  1. Beijing Institute for Drug Control Beijing Center for Vaccine Control), NMPA Key Laboratory for Research and Evaluation of
    Generic Drugs Beijing Key Laboratory of Analysis and Evaluation on Chinese Medicine Beijing 102206, China
  • Received:2025-02-13 Revised:2025-05-27 Accepted:2025-11-12 Online:2025-09-28 Published:2025-11-18

摘要:

目的:解决现行碳酸钙D3制剂国家药品标准中维生素D3的两份含量测定样品结果不平行的问题,建立准确、可靠的维生素D3测定方法,为碳酸钙D3制剂的质量控制提供技术支撑。方法:取制剂细粉,加入75%二甲基亚砜水溶液20 mL 45 ℃振摇提取15 min,放冷,精密加入稀释溶剂15 mL,密塞,振摇萃取90 min3000 r·min-1离心10 min,取上清液。结果:维生素D3平均回收率(n=9)为99.18%RSDn=9)为1.01%,共测定11批碳酸钙D3制剂,平行两份样品标准偏差均小于1.1%。结论:采用现行方法,维生素D375%二甲基亚砜水溶中超声降解,导致样品测定结果偏差大,采用振摇提取的方式制备碳酸钙D3制剂样品,方法准确可靠。建议将现行标准方法修改为“加入75%二甲基亚砜水溶液约20 mL,摇匀,45 ℃振摇提取15 min,放冷”。

 

关键词: 维生素D3, 碳酸钙D3制剂, 含量测定, 方法改进, 国家药品标准

Abstract:

Objective: To solve the problem that determination results of two vitamin D3 assay samples are unparallel by current national drug standards for calcium carbonate and vitamin D3 preparations. To establish the accurate and reliable assay method about vitamin D3. To support the quality control of calcium carbonate and vitamin D3 preparations.Methods: Add 20 mL of 75% dimethyl sulfoxide to the powder of the preparation and shake at 45 ℃ for 15 min then take it cool. Add 15 mL of diluted solvent to 75% dimethyl sulfoxide layer and stopper it then shake it for 90 min. Centrifuge it at 3 000 r·min-1 for 10 min and withdraw the diluted solvent layer.Results: The average recovery of vitamin D3 n=9 was 99.12% RSD n=9 was 1.03%. 11 batches of calcium carbonate and vitamin D3 preparations were determined. The standard deviation of the two parallel samples was less than1.1%.Conclusion: Vitamin D3 is degrading by current national drug standards when ultrasonic extraction in 75% dimethyl sulfoxide. That brings the larger RSD of sample determination results. The method is accurate and reliable about shaking the samples of calcium carbonate and vitamin D3 preparations. The suggestion is to amend the method in current standards as add 20 mL of 75% dimethyl sulfoxide to the powder of the preparation and shake at 45 ℃ for 15 min then take it cool.


Key words: Vitamin D3 , Calcium carbonate and Vitamin D3 , Preparations assay , Improvement , National drug standards

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