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Development of a sensitive and stable GC-MS/MS method for simultaneous determination of four N-nitrosamine genotoxic impurities in sartan substances


Recently, N-nitrosamines have been unexpectedly found in generic sartan products. Herein, we developed a sensitive and stable GC-MS/MS method with multiple reactions monitoring mode for the simultaneous determination of four N-nitrosamines in sartan substances, namely, N-nitrosodimethylamine, N-nitrosodiethylamine, N-nitrosodibutylamine, and N-nitrosodiisopropylamine. The conditions of gas chromatography and mass spectrometry were optimized. The method was validated according to the International Council for Harmonization guidelines in terms of sensitivity, linearity, accuracy, precision, specificity, and stability. The limits of detection of N-nitrosamines in sartan substances ranged from 0.002 to 0.150 ppm, and the corresponding limits of quantification were in the range of 0.008-0.500 ppm, which met the sensitivity requirements for the limits set by the Food and Drug Administration of the United States. The internal standard curve of four N-nitrosamines showed good linearity of regression coefficients over 0.99. The recoveries of N-nitrosamines in selected sartan drugs ranged from 87.68 to 123.76%. The intraday and interday relative standard deviation values were less than 9.15%. Therefore, this proposed method exhibited good sensitivity and precision, high accuracy, and fast analysis speed, which provide a reliable method for quality control of N-nitrosamines in sartan products.


In the manufacturing processes of active pharmaceutical ingredients (APIs), impurities are generated from a variety of sources, such as starting materials, intermediates, reagents, solvents, catalysts, and by-products. As a kind of special impurities, genotoxic impurities (GTIs) could induce genetic mutations, cause chromosomal breakage and rearrangements, and increase the risk of cancer even under a low concentration condition (Szekely et al. 2015; Benigni and Bossa 2011). Therefore, the European Medicines Agency and Food and Drug Administration (FDA) of the USA have established a threshold of toxicological concern for GTIs, namely, 1.5 μg·day−1 for long-term treatments and higher limits for shorter durations in the clinic (Raman et al. 2011). In a view of the low concentration level, the development of a sensitive, high-efficient, and robust analytical methodology for detecting potential GTIs in APIs has been a great challenge for the pharmaceutical industry in recent years (Teasdale and Elder 2014).

Sartan substances are one of the most frequently prescribed antihypertensive drugs and have been widely applied in the treatment of cardiovascular diseases all over the world (Muszalska et al. 2014). In the production process of sartan products, organic solvents containing amide groups might form secondary amines in acidic solution at high temperature, and then react with nitrous acid, thereby leading to the formation of N-nitrosamines (Scherf-Clavel et al. 2019). Since this reaction probably occurred in syntheses of various sartan substances, many kinds of N-nitrosamines might be found in the sartan products.

N-Nitrosamine GTIs have been recognized as a kind of potent carcinogens. They showed mutagenic activities in Ames test with Salmonella typhimurium and triggered the carcinogenic effect in rats, mice, hamsters, guinea pigs, and rabbits (Wagner et al. 2012; Santos et al. 2014; Buist et al. 2015; Ravnum et al. 2014). Since the valsartan and losartan products produced by several pharmaceutical companies were proven to contain potential contamination with carcinogenic nitrosamine impurities, namely, N-nitrosodimethylamine (NDMA), N-nitrosodiethylamine (NDEA), and N-nitroso-N-methyl-4-aminobutyric acid (NMBA) (Fig. 1), FDA has recalled them since July 2018 (Parr and Joseph 2019).

Fig. 1

Molecular structures of four N-nitrosamines and sartan substances in this study

Recently, GC and LC tandem mass spectrometry have been widely used in the detection of N-nitrosamines in water (Chen et al. 2017; Ngongang et al. 2015), food (Herrmann et al. 2014; Scheeren et al. 2015), and personal care products (Miralles et al. 2019). Pre-treatment methods, for example, solid-phase extraction (Sieira et al. 2020; Luo et al. 2016; McDonald et al. 2012), liquid extraction (Hong et al. 2017), and simultaneous distillation extraction (Zhu et al. 2019) have been commonly used to extract N-nitrosamines from matrix before analysis. However, the determination of N-nitrosamines in APIs through LC-MS/MS and/or GC-MS/MS is not well understood till now. Sörgel group (Sörgel et al. 2019) developed a highly sensitive HPLC-APCI-MS/MS method for quantitation of NDMA and NDEA in sartan substances. In their work, the limits of quantification (LOQs) and detection (LODs) for NDMA and NDEA were 0.26 ppb and 0.13 ppb, respectively, and the recoveries were in the range of 94.2-102.3%. Schmidtsdorff et al. (Schmidtsdorff and Schmidt 2019) developed a supercritical fluid chromatography-MS/MS method to determine eight N-nitrosamines in sartan drugs, including NDMA, NDEA, and NDBA, in which the running time was less than 20 min and the LODs for eight N-nitrosamines were in the range of 0.02-0.46 ppm. FDA has established the interim acceptable daily intake limits for N-nitrosamines in sartan substances (Table 1) (US FDA, 2019a, d), and applied GC-MS/MS through utilizing liquid injection and headspace (US FDA, 2019b), RapidFire-MS/MS (US FDA, 2019c), and HPLC-HRMS (US FDA, 2019e) for quantitation of the N-nitrosamines in sartan substances.

Table 1 Interim limits for NDMA and NDEA in sartan substances set by FDA

It was very necessary for complex matrices of food, water, and personal care products to take extraction and purification steps during the analysis. However, these were not suitable for rapid and high-throughput analysis in the pharmaceutical industry. Herein, we have developed a simple, sensitive, accurate, and reproducible GC-MS/MS method by direct injection for the detection of four N-nitrosamines in four sartan substances, namely, candesartan cilexetil, olmesartan medoxomi, irbesartan, and valsartan (Fig. 1). The obtained LODs and LOQs met the sensitivity requirements set by FDA. Then, this developed method was validated according to the International Council for Harmonization (ICH) guidelines in terms of sensitivity, linearity, accuracy, precision, specificity, and stability.

Materials and methods

Chemicals and materials

Four kinds of sartan drugs, namely, candesartan cilexetil, olmesartan medoxomi, irbesartan, and valsartan were friendly provided by a local pharmaceutical company (Zhuhai, China). NDMA (purity ≥ 99.3%) and NDBA (purity ≥ 99.9%) standards were purchased from Tokyo Chemical Industry (Shanghai) Co. Ltd. (Shanghai, China). NDEA (purity ≥ 99.0%) was bought from Adamas Reagent Ltd. (Shanghai, China). NDIPA (purity ≥ 99.0%) was obtained from Beijing Manhage Biotechnology Co. Ltd. (Beijing, China). NDMA-d6 (purity ≥ 99.5%) was bought from Cato Research Chemicals Inc. (Guangzhou, China). HPLC-grade methanol, acetonitrile, ethyl acetate, acetone were purchased from LabScience Inc. (Pittsburg, USA).

Instrumentation and optimized GC-MS/MS conditions

Analyses of N-nitrosamines were performed on an Agilent 7890B gas chromatography-tandem mass spectrometry with the Agilent 7693A auto sampler system. Agilent VF-Wax ultra-inert capillary column (30 m × 0.25 mm i.d., 1.0 μm) was used as the analytical column in this work. MS/MS detection was carried out on a Waters Xevo TQ-GC triple quadrupole mass spectrometer with electron ionization (EI) ion source. The GC oven program utilized an initial oven temperature of 40 °C, held for 0.5 min, raised firstly at 20 °C·min−1 to 200 °C, then to 240 °C at 40 °C/min, finally held for 3 min. The total run time was 12.5 min. Helium as the carrier gas was set at a flow of 1.0 mL/min. Both the interface temperature and injection temperature were set to be 250 °C. The injection volume was 1 μL in the splitless mode.

The MS was operated in EI mode at 70 eV with a quadrupole temperature of 150 °C. The temperature of the ion source was set at 200 °C. The delay time of the solvent was 5 min. Multiple reactions monitoring (MRM) mode was selected as the data acquisition for the quantitative determination of four kinds of N-nitrosamine GTIs. The precursor ions and product ions of four N-nitrosamine GTIs, as well as the optimized collision energy (CE) were summarized in Table 2.

Table 2 Multiple reactions monitoring (MRM) transitions and optimized collision energy for four N-nitrosamine GTIs and the internal standard (NDMA-d6)

Preparation of standard and sample solutions

The standard stock solutions of NDMA-d6, NDMA, NDEA, NDBA, and NDIPA with each concentration of 1 mg·mL−1 were prepared by dissolving accurately weighed reference standards in methanol, respectively, and stored at 4 °C. For NDMA and NDIPA, a series of standard working solutions at the concentrations of 3, 6, 15, 24, 30, 36, 45, and 60 ng·mL−1 in methanol were obtained from a stock solution through the serial dilution method. The concentrations of series standard working solution for NEDA were 0.8, 1.6, 4.0, 6.4, 8.0, 9.6, 12, and 16 ng·mL−1, respectively. In addition, the concentrations of the working solution for NDBA were 6, 15, 24, 30, 36, 45, and 60 ng·mL−1, respectively.

In this work, the concentration of NDMA-d6 (the internal standard) was fixed to be 50 ng·mL−1. Candesartan cilexetil and olmesartan medoxomi were dissolved in methanol at a concentration of 10 mg·mL−1. Valsartan was also dissolved in methanol at a concentration of 100 mg·mL−1. Sample preparation for irbesartan was described as follows. Firstly, 1.0 g of irbesartan was accurately weighed into a 10-mL volumetric flask and 10 mL of NDMA-d6 solution was added. Then, after sonicated for 30 min, the mixture was placed in a centrifuge tube and vortexed for 1 min, and then centrifuged at 2500 rpm for 10 min. Finally, the supernatant was filtered with a 0.22 μm nylon syringe filter into a vial for chromatographic injection.

Method validation

The quantification method of four N-nitrosamines through GC-MS/MS with MRM mode was validated through the following parameters, such as system suitability, specificity, sensitivity, linearity, LOD, LOQ, accuracy, precision, and solution stability. The LODs were defined as 3 times the signal-to-noise (S/N) ratio, and the corresponding LOQs were S/N = 10. The matrix effect (ME) value was calculated according to the following equation (Chawla et al. 2017):

$$ \mathrm{ME}\%=\frac{Slope\ of\ matrix\ matched\ curve- slope\ of\ solvent\ curve}{Slope\ of\ solvent\ curve}\times 100 $$

Accuracy of this proposed method was evaluated by the recovery assays at three spiked levels in the blank sartan samples. Moreover, precision was estimated by interday and intraday relative standard deviations (RSDs) of six samples spiked at one concentration over 3 continuous days.

Results and discussion

Method development

Optimization of the sample solvent

Methanol, CH2Cl2, ethyl acetate, and acetone were used for the solubility study of four APIs, and the results were summarized in Supplementary Information Table S1. The solubility of valsartan, irbesartan, and olmesartan medoxomi in methanol was much higher than that in the other three solvents. For valsartan, it was up to 600 mg·mL−1. Candesartan cilexetil showed the best solubility in CH2Cl2 among four organic solvents. Taking into consideration of the trace level nature of N-nitrosamine GTIs in the selected APIs, good solubility of the sartan in the selected solvent would helpfully meet the requirements for the safety control of N-nitrosamines. Therefore, methanol was selected to dissolve the sartan drugs in the following work.

Investigation of mass spectrometric method

The trace detection method for GTIs is a very crucial part in the analysis of pharmaceuticals. Herein, the LODs and LOQs for N-nitrosamines were used to evaluate the difference of single ion monitoring (SIM) mode and MRM mode in triple quadrupole mass spectrometer. As summarized in Supplementary Information Table S2, the LODs and LOQs for four kinds of N-nitrosamines in SIM mode ranged from 10-50 ng·mL−1 and 25-150 ng·mL−1, respectively. Through using MRM mode, the LODs and LOQs remarkably decreased to 0.2-1.5 ng·mL−1 and 0.8-5.0 ng·mL−1, respectively. Clearly, the MRM mode for the quantification of N-nitrosamines was more highly sensitive than the SIM mode. The latter mode is difficult to meet the sensitivity requirements for the interim limits (Table 1). Therefore, MRM mode was selected as the MS method in the following quantification of four N-nitrosamine GTIs in sartan substances.

Matrix effect

In the GC system, the matrix effect (ME) might be caused through masking silanol active sites in the injection liner and GC column (Rimayi et al. 2015). Herein, the ME was investigated through comparing the slope between the standard solvent curve and the matrix-matched standard curve. Matrix effect can be negligible in the quantification when the value is less than 15% (Chawla et al. 2017). In Table 3, the signal enhancements for NDEA in candesartan cilexetil and valsartan, NDIPA in olmesartan medoxomi, and NDBA in valsartan were observed, and the ME values were in the range of 20.47-56.41%, indicating that the matrix effect could not be negligible. In addition, no significant suppression or enhancement differences for the others were observed. Therefore, in order to obtain accurate result, calibration of N-nitrosamines in sartan substances has been performed through internal matrix-matched standards in the recovery assay.

Table 3 Comparison of the calibration curves and calculation of matrix effect (ME) for N-nitrosamines in solvent and in sartan matrices

Method validation

The proposed determination method for four N-nitrosamine GTIs has been validated according to the (ICH) guidelines.


To demonstrate the specificity of the proposed method, methanol, the sartan matrices, and the mixture solution of four N-nitrosamine standards were subjected to the GC-MS/MS analysis. In Fig. 2, no interference peaks in the solvent and the sartan matrices were observed at the retention times of four N-nitrosamines, indicating that this method for the determination of four N-nitrosamines in sartan substances showed good specificity.

Fig. 2

GC chromatograms of methanol, four sartan substances, and the mixed standard solution of four N-nitrosamines

Linearity and sensitivity

Linearity, LODs, and LOQs results were summarized in Table 4. The chromatographic peak area ratio (N-nitrosamines/NDMA-d6, y) were plotted against standard concentrations of N-nitrosamines (x), and the standard curves were in the form of y = Ax + B, in which A and B represented as the slope and the intercept, respectively. Eight standard concentrations were evaluated to verify the linearity of the analysis method. The linearity for four N-nitrosamines was established in the tested concentration range. The linear regression coefficients of determination (R2) for four N-nitrosamines were over 0.99 in the corresponding concentration range, which meant a good linearity and suitable for quantitative analysis.

Table 4 Calibration curves, LODs, and LOQs for four N-nitrosamines

Then, the sensitivity of the method was assessed according to the LODs and LOQs, respectively. In Table 5, the LODs for NDMA, NDEA, NDIPA, and NDBA in methanol were determined to be 1.2, 0.2, 0.4, and 1.5 ng·mL−1, respectively, which relative to four sartan substances were in the range of 0.002-0.150 ppm. The LOQs for NDMA, NDEA, NDIPA, and NDBA in methanol were 3.0, 0.8, 1.0, and 5.0 ng·mL−1, respectively, which relative to four sartan substances were in the range of 0.008-0.500 ppm. These low LODs and LOQs values for this GC-MS/MS method were satisfactory and adequate for the detection of N-nitrosamines in sartan samples.

Table 5 Precision assay results of four N-nitrosamines in sartan substances.


Method accuracy was determined by using six replicate samples for each sartan substance. The recoveries of four N-nitrosamines were measured to assess the performance of the proposed GC-MS/MS method by spiking the blank samples with three different concentrations of which were 50%, 100%, and 150% of the limits, respectively. According to the daily exposure and the TD50 value, the limits of NDMA and NDEA in sartan set by FDA were validated in accuracy assays. Considering the toxicity of NDIPA and NDBA has been less than NDMA and the risk for occurrence would be lower than NDMA, the concentration limits for NDIPA and NDBA validated in accuracy assays were set to be the same with NDMA in this study. The results exhibited that the recoveries for NDMA, NDEA, NDIPA, and NDBA in four sartan substances ranged from 87.68 to 123.76% (Supplementary Information Table S3). Since the acceptance criteria for recovery was refined to be in the range of 70-130% according to the ultra-trace level nature of the analysis, the recoveries for four N-nitrosamines in this work can meet that criteria.


Method precision was evaluated by both intraday and interday precisions. The intraday precision was measured by comparing the standard deviation of the recovery percentages of the spiked samples ran during the same day. The interday precision was determined by analyzing the spiked samples for three distinct days. As summarized in Table 5, this GC-MS/MS method exhibited satisfactory mean recovery values (75.07-116.44%) and precision, in which the RSD values for the intraday and interday precision were in the range of 1.45-6.38% and 2.88-9.15%, respectively.

Stabilities of four N-nitrosamines in methanol

Solution stabilities of four N-nitrosamines in methanol solutions were evaluated by preparing 30 ng·mL−1 standard solutions and analyzing them every 4 or 12 h against a freshly prepared standard. All the solutions were kept in the dark place at 25 °C. The results are summarized in Supplementary Information Table S4. Clearly, the percentage recoveries of these stock solutions were in the range of 97.51-105.04%, and the difference between recoveries at 0 h and 24 h were not more than 10%, which indicated that these stock solutions were stable for at least 24 h.

Applications in sartan samples

This GC-MS/MS analytical method was used to determine four N-nitrosamine GTIs in Chinese commercial sartan products, and no N-nitrosamines were found in four batches of sartan substances (Supplementary Information Table S5).


As a result, a sensitive and simple GC-MS/MS method with MRM mode was developed for the determination of NDMA, NDEA, NDIPA, and NDBA in sartan substances. This GC-MS/MS method presented satisfactory selectivity and sensitivity. The analysis time was less than 13 min. More importantly, the LODs and LOQs of four N-nitrosamines were in the range of 0.002-0.150 ppm and 0.008-0.500 ppm, respectively, which was proved to be suitable for sensitive quantification of four N-nitrosamines in sartan products.

Availability of data and materials

All data generated or analyzed during this study are included in this published article and its supplementary information files.



Atmospheric pressure chemical ionization


Active pharmaceutical ingredients


Food and Drug Administration


Genotoxic impurity


International Council for Harmonization


Limit of detection


Limit of quantification


Matrix effect


Multiple reactions monitoring






N-nitrosodiisopropyl amine




Relative standard deviation


Single ion monitoring


Signal to noise


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This work was supported by the National Natural Science Foundation of China under Grant number 21571070 and Natural Science Foundation of Guangdong Province under Grant number 2018A030313193.

Author information




ZWG designed this study and gave constructive advices of the project and the manuscript. XB performed the material preparation. The GC-MS/MS analysis work was performed by MBL, HRJ, and ZZF. GD did pre-treatment of sartan samples. CQ performed the data analysis of the obtained results. LJ finished the draft of the manuscript. FJ revised the manuscript. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Jun Fan or Weiguang Zhang.

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Supplementary Information

Additional file 1: Table S1.

Solubility results of sartan substances in four organic solvents. Table S2. LODs and LOQs for four N-nitrosamines through using different MS method. Table S3. Recovery assay results of N-nitrosamines in four sartan matrices through the proposed GC-MS/MS method. Table S4. Recovery results for stability assays of N-nitrosamines in methanol. Table S5. Results of N-nitrosamines in four batches of commercial sartan substances.

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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 Anal Sci Technol 12, 3 (2021).

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  • Sartan substances
  • N-nitrosamine genotoxic impurity
  • GC-MS/MS
  • Multiple reactions monitoring
  • Quantitative determination