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采用在线内管固相微萃取-液相色谱-串联质谱法同时分析二甲双胍片中致癌性 N-亚硝胺杂质。

Simultaneous analysis of carcinogenic N-nitrosamine impurities in metformin tablets using on-line in-tube solid-phase microextraction coupled with liquid chromatography-tandem mass spectrometry.

机构信息

School of Pharmacy, Shujitsu University, Nishigawara, Okayama 703-8516, Japan.

School of Pharmacy, Shujitsu University, Nishigawara, Okayama 703-8516, Japan.

出版信息

J Chromatogr A. 2023 Nov 8;1710:464416. doi: 10.1016/j.chroma.2023.464416. Epub 2023 Sep 30.

Abstract

Contamination of active pharmaceutical ingredients (APIs) and pharmaceutical preparations with carcinogenic N-nitrosamines has led to recalls of these products and supply shortages to patients. The present study describes the development of a highly sensitive method for simultaneous analysis of seven N-nitrosamines using on-line in-tube solid-phase microextraction (IT-SPME) coupled with liquid chromatography-tandem mass spectrometry (LC-MS/MS) to determine their actual contamination in metformin tablets. Using a Carboxen 1006 PLOT capillary as the extraction device for IT-SPME, these compounds were efficiently extracted and concentrated 6‒24-fold by subjecting 40 µL of sample to 25 repeated draw/eject cycles at a rate of 0.2 mL/min. The seven N-nitrosamines were separated within 11 min by gradient elution with 0.1 % formic acid solution and acetonitrile as the mobile phase using a CAPCELL PAK C18 MGII column and detected by multiple reaction monitoring in positive ion mode. The calibration curve showed linearity in the range 0.2‒50 ng/mL and detection limits (S/N = 3) in the range 3‒112 pg/mL. The intra-day and inter-day precisions were less than 5.5 % and 7.0 % (n = 6), respectively, with accuracies ranging from 93‒117 %. Following ultrasonic extraction with water, centrifugation and filtration of the supernatant liquid through a membrane filter, the N-nitrosamine impurities in metformin tablets could be analyzed by IT-SPME/LC‒MS/MS. Their limits of quantification (S/N = 10) were 0.1‒5.1 pg/mg API and recoveries ranged from 87‒102 %. Analysis of eight metformin tablets from eight manufacturers showed that 5.8‒7.5 pg/mg N-nitrosodimethylamine were present in three tablets, with no other N-nitrosamines detected in any of the eight tablets. This method may be useful in testing for N-nitrosamine impurities in pharmaceutical preparations.

摘要

活性药物成分 (API) 和药物制剂受到致癌性 N-亚硝胺的污染,导致这些产品的召回和患者的供应短缺。本研究描述了一种使用在线管内固相微萃取 (IT-SPME) 与液相色谱-串联质谱 (LC-MS/MS) 同时分析七种 N-亚硝胺的高灵敏度方法,用于确定二甲双胍片中实际的污染情况。使用 Carboxen 1006 PLOT 毛细管作为 IT-SPME 的萃取装置,通过在 0.2 mL/min 的速率下对 40 µL 样品进行 25 次重复的抽取/推出循环,这些化合物被有效地提取和浓缩了 6-24 倍。七种 N-亚硝胺在 11 分钟内通过梯度洗脱,以 0.1%甲酸溶液和乙腈作为流动相,使用 CAPCELL PAK C18 MGII 柱进行分离,并以正离子模式进行多反应监测进行检测。校准曲线在 0.2-50 ng/mL 范围内呈线性,检测限 (S/N=3) 在 3-112 pg/mL 范围内。日内和日间精密度分别小于 5.5%和 7.0%(n=6),准确度范围为 93-117%。通过水超声提取、离心和通过膜过滤器过滤上清液后,可通过 IT-SPME/LC-MS/MS 分析二甲双胍片中的 N-亚硝胺杂质。它们的定量限 (S/N=10) 为 0.1-5.1 pg/mg API,回收率范围为 87-102%。对来自八个制造商的八种二甲双胍片进行分析表明,三种片剂中存在 5.8-7.5 pg/mg 的 N-亚硝二甲胺,而在八个片剂中的任何一个片剂中均未检测到其他 N-亚硝胺。该方法可用于检测药物制剂中的 N-亚硝胺杂质。

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