标准研讨

盐酸二甲双胍缓释片中N-亚硝基二甲胺测定方法的优化

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  • 1.广东省科学院测试分析研究所(中国广州分析测试中心) 广东省化学测量与应急检测技术重点实验室广东省中药质量安全工程技术研究中心,广州 510070;
    2.广东赛康制药厂有限公司,惠州 516820
第一作者 Tel:(020)88321850;E-mail:liang_ziyang@qq.com
* Tel:(020)88320139;E-mail:luohuitai@qq.com

修回日期: 2024-04-09

  网络出版日期: 2024-08-07

Optimization of determination of N-nitrosodimethylamine in metformin hydrochloride sustained-release tablets

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  • 1. Institute of Analysis, Guangdong Academy of Sciences(China National Analytical Center, Guangzhou), Guangdong Provincial Key Laboratory of Chemical Measurement and Emergency Test Technology, Guangdong Provincial Engineering Research Center for Quality and Safety of Traditional Chinese Medicine, Guangzhou 510070, China;
    2. Guangdong Sinocorp Pharmaceutical Co., Ltd., Huizhou 516820, China

Revised date: 2024-04-09

  Online published: 2024-08-07

摘要

目的: 建立一种稳定且可靠的气相色谱-串联质谱法测定盐酸二甲双胍缓释片中N-亚硝基二甲胺(NDMA),同时通过考察异丙醇和硫代甘油2个添加剂对供试品溶液稳定性的影响,确定了最优的提取条件。方法: 采用聚乙二醇为固定相的AB-InoWax毛细管柱(30 m×0.25 mm×0.25 μm),利用电子轰击电离源(EI),在多反应监测(MRM)模式下检测,分别以外标法和内标法定量。结果: 添加硫代甘油可显著改善供试品溶液稳定性,NDMA在0.25~50 ng·mL-1浓度范围内有良好的线性(r>0.999),方法检测限为0.1 ng·g-1,方法定量限为0.2 ng·g-1,分别在内标法和外标法计算下,平均加标回收率(n=9)均为97.3%和94.9%,精密度、重复性、稳定性及耐用性的RSD均小于8%。对90批次的盐酸二甲双胍缓释片进行检测,结果均小于国家药品监督管理局以及FDA规定的可接受限度的30%之内。结论: 本文建立的方法灵敏度高,专属性强,结果准确且稳定性好,适用于盐酸二甲双胍缓释片中NDMA的定量分析,可为有关产品的质量安全提供技术支撑。

本文引用格式

梁梓洋, 罗辉泰, 张秋炎, 梁维维, 梁梓豪, 周熙, 吴惠勤, 黄芳, 黄飞云, 罗向东 . 盐酸二甲双胍缓释片中N-亚硝基二甲胺测定方法的优化[J]. 药物分析杂志, 2024 , 44(6) : 1089 -1096 . DOI: 10.16155/j.0254-1793.2024.06.21

Abstract

Objective: To establish a stable and reliable gas chromatography-tandem mass spectrometry method for the determination of N-nitrosodimethylamine (NDMA) in metformin hydrochloride sustained-release tablets, and to optimize extraction conditions by investigating the effects of isopropyl alcohol and thioglycerin on the stability of the tested solution. Methods: Separation was achieved on AB-InoWax capillary column (30 m×0.25 mm×0.25 μm) with polyethylene glycol as the stationary phase. Electron ion(EI) source and multiple reaction monitoring (MRM) mode were used. Quantitative determination was performed by both external standard and internal standard. Results: The addition of thioglycerin could significantly improve the stability of the test solution. NDMA showed good linearity within the concentration range of 0.25-50 ng·mL-1(r>0.999). The detection limit of the method was 0.1 ng·g-1 and the quantification limit of the method was 0.2 ng·g-1. The average recoveries (n=9) were 97.3% and 94.9% while using external standard and internal standard, respectively. Precision, repeatability and stability were good with RSD less than 8%. Ninety batches of metformin hydrochloride sustained release tablets were tested. NDMA content in all detected samples were all less than 30% of the acceptable limit set by the National Medical Products Administration and FDA. Conclusions: This method shows satisfactory sensibility, specificity, accuracy, stability and durability, which is suitable for quantitative analysis of NDMA in metformin hydrochloride sustained-release tablets, providing technical support for the quality and safety of related products.

参考文献

[1] LIU DQ, SUN M, KORD AS. Recent advances in trace analysis of pharmaceutical genotoxic impurities[J]. J Pharm Biomedical Anal, 2010, 51(5): 999
[2] WHITE CM. Understanding and preventing (N-nitrosodimethylamine) NDMA contamination of medications[J]. Annals Pharmacotherapy, 2019, 54(6): 611
[3] 国家药品监督管理局. 世界卫生组织国际癌症研究机构致癌物清单[EB/OL]. https://www.nmpa.gov.cn/xxgk/mtbd/20171030163101383.html
National Medical Products Administration. List of Classifications by Cancer Site[EB/OL]. https://www.nmpa.gov.cn/xxgk/mtbd/20171030163101383.html
[4] Control of Nitrosamine Impurities in Human Drugs[S]. 2021
[5] MILLS AL, ALEXANDERM. N-nitrosamine formation by cultures of several microorganisms[J]. Appl Environ Microb, 1976, 31(6): 892
[6] BUNKAN AJC, HETZLER J, MIKOVINY T, et al. The reactions of N-methylformamide and N,N-dimethylformamide with oh and their photo-oxidation under atmospheric conditions: Experimental and theoretical studies[J]. Phys Chem Chem Phys, 2015, 17(10): 7046
[7] FDA. FDA Requests Removal of All Ranitidine Products (zantac) from the Market[EB/OL]. https://www.fda.gov/news-events/press-announcements/fda-requests-removal-all-ranitidine-products-zantac-market
[8] 张玉英. 盐酸二甲双胍片的含量测定[J]. 化学世界, 2003, 44(6): 300
ZHANG YY. Determination of metformin tablets by HPLC[J]. Chemical World, 2003, 44(6):300
[9] FDA. FDA Alerts Patients and Health Care Professionals to Nitrosamine Impurity Findings in Certain Metformin Extended-Release Products[EB/OL]. https://www.fda.gov/news-events/press-announcements/fda-alerts-patients-and-health-care-professionals-nitrosamine-impurity-findings-certain-metformin
[10] 吴兆伟, 杜凯, 王琳, 等. GC-MS法测定缬沙坦中的N-亚硝基二甲胺[J]. 中国新药杂志, 2019, 28(20):2478
WU ZW, DU K, WANG L, et al. Determination of the contents of N-nitrosodimethylamine in valsartan by GC-MS[J]. Chin J New Drug, 2019, 28(20):2478
[11] LIU J, XIE B, MAI B, et al. Development of a sensitive and stable GC-MS/MS method for simultaneous determination of four N-nitrosamine genotoxic impurities in sartan substances[J]. J Anal Sci Technol, 2021, 12(1): 3
[12] WICHITNITHAD W, SUDTANON O, SRISUNAK P, et al. Development of a sensitive headspace gas chromatography-mass spectrometry method for the simultaneous determination of nitrosamines in losartan active pharmaceutical ingredients[J]. ACS Omega, 2021, 6(16): 11048
[13] ALSHEHRI YM, ALGHAMDI TS, ALDAWSARI FS. HS-SPME-GC-MS as an alternative method for NDMA analysis in ranitidine products[J]. J Pharm Biomed Anal, 2020, 191: 113582
[14] CHANG SH, HO HY, CHANG CC, et al. Evaluation and optimization of a HS-SPME-assisted GC-MS/MS method for monitoring nitrosamine impurities in diverse pharmaceuticals[J]. J Pharm Biomed Anal, 2022, 221: 115003
[15] SOLANKI R, PATEL C, PATEL R, et al. UHPLC-APCI-TQ-MS analytical method to quantify nitrosamine impurities in the commercial formulation of metformin and glipizide[J]. J Liq Chromatogr R T, 2022: 1
[16] YANG J, MARZAN TA, YE W, et al. A cautionary tale: quantitative LC-HEMS analytical procedures for the analysis of n-nitrosodimethylamine in metformin[J]. AAPS J, 2020, 22(4): 89
[17] KIM H, SUNG D, YU H, et al. Comparison of EI-GC-MS/MS, APCI-LC-MS/MS, and ESI-LC-MS/MS for the simultaneous analysis of nine nitrosamines eluted from synthetic resins into artificial saliva and health risk assessment[J]. Toxics, 2021, 9(10): 230
[18] 景援朝, 王海燕, 孙涛, 等. 基于气相色谱-串联质谱法测定盐酸二甲双胍制剂中基因毒性杂质N-二甲基亚硝胺的质量评价研究[J]. 药物分析杂志, 2022, 42(12):2122
JING YC, WANG HY, SUN T, et al. Quality evaluation of N-ntrosadimethylamine(NDMA) in metformin hydrochloride preparation by gas chromatography tandem mass spectrometry[J]. Chin J Pharm Anal, 2022, 42(12):2122
[19] FRITZSCHE M, BLOM G, KEITEL J, et al. NDMA analytics in metformin products: Comparison of methods and pitfalls[J]. Eur J Pharm Sci, 2022, 168: 106026
[20] EP 11.0[S]. 2023
[21] LIAO X, SHEN L, JIANG Z, et al. NDMA formation during ozonation of metformin: Roles of ozone and hydroxyl radicals[J]. Sci Total Environ, 2021, 796: 149010
[22] JIREŠ J, KALÁŠEK S, GIBALA P, et al. Insight into the formation of N-nitrosodimethylamine in metformin products[J]. J Pharm Biomed Anal, 2021, 195: 113877
[23] BADRAN I, MANASRAH AD, NASSAR NASHAAT N. A combined experimental and density functional theory study of metformin oxy-cracking for pharmaceutical wastewater treatment[J]. RSC Adv, 2019, 9(24): 13403
[24] 叶晓霞, 葛雨琦, 乐健, 等. 缓释制剂辅料导致盐酸二甲双胍降解产生N-亚硝基二甲胺的影响因素研究[J]. 药物分析杂志, 2021, 41(2): 239
YE XX, GE YQ, LE J, et al. Study on influencing factors of metformin hydrochloride’s degradation to N-nitrosodimethylamine inducd by sustained-release excipients[J]. Chin J Pharm Anal, 2021, 41(2):239
[25] HAO G, HU R, WANG X, et al. N-nitrosodimethylamine formation in metformin hydrochloride sustained-release tablets: Effects of metformin and hypromellose used in drug product formulation[J]. J Pharm Biomed Anal, 2023, 222: 115066
[26] NARANG AS, DESAI D, BADAWY S. Impact of excipient interactions on solid dosage form stability[J]. Pharm Res Dordr, 2012, 29(10): 2660
[27] WU Y, LEVONS J, NARANG AS, et al. Reactive impurities in excipients: Profiling, identification and mitigation of drug-excipient incompatibility[J]. AAPS Pharm Sci Tech, 2011, 12(4): 1248
[28] 戴慧旺, 陈建新, 苗笑增, 等. 醇类对UV-Fenton体系羟基自由基淬灭效率的影响[J]. 中国环境科学, 2018, 38(1): 202
DAI HW, CHEN JX, MIAO XZ, et al. Effect of alcohols on scavenging efficiencies to hydroxyl radical in UV-Fenton system[J]. China Environ Sci, 2018, 38(1):202
[29] WANG L, LI B, DIONYSIOU DD, et al. Overlooked formation of H2O2 during the hydroxyl radical-scavenging process when using alcohols as scavengers[J]. Environ Sci Technol, 2022, 56(6): 3386
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