首页|5种β受体拮抗剂类药物中的N-亚硝基类杂质的含量研究

5种β受体拮抗剂类药物中的N-亚硝基类杂质的含量研究

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目的 测定普萘洛尔、美托洛尔、阿替洛尔、艾司洛尔、比索洛尔原料药/制剂中N-亚硝基类杂质含量,明确其含量的关注阈值。方法 采用超高效液相色谱-四极杆/静电场轨道阱高分辨质谱技术。以ACE Excel 3 C18-AR为色谱柱,以含0。01 mol/L乙酸铵的0。2%甲酸溶液-甲醇为流动相进行梯度洗脱,流速为0。60 mL/min,柱温为40℃,进样量为5 μL;以可加热的电喷雾离子源为离子源,以全扫描-选择离子监测模式进行正离子扫描。采用该法对10家企业生产的15批β受体拮抗剂类药物原料药/制剂中N-亚硝基类杂质含量进行测定,并采用Discovery Studio软件对待测杂质进行毒性预测和关注阈值估算。结果 5种β受体拮抗剂类药物中,N-亚硝基普萘洛尔、N-亚硝基美托洛尔、N-亚硝基阿替洛尔、N-亚硝基艾司洛尔、N-亚硝基比索洛尔检测质量浓度的线性范围分别为1。01~503。38、1。02~508。38、0。97~483。63、1。11~554。27、1。05~523。92 ng/mL(r>0。999),定量限分别为1。04、0。25、0。05、0。55、1。05 ng/mL,检测限分别为0。52、0。08、0。02、0。17、0。52 ng/mL,精密度、重复性、加样回收率、稳定性、耐用性试验的RSD均小于7。5%(n=6或n=5)。15批样品中,除1批样品外,其余批次均检出了N-亚硝基普萘洛尔(1。07~8。91 ng/mg)、N-亚硝基美托洛尔(1。43~3。37 ng/mg)、N-亚硝基阿替洛尔(1。33 ng/mg)、N-亚硝基艾司洛尔(0。19 ng/mg)、N-亚硝基比索洛尔(1。27 ng/mg)。经预测,上述5种杂质有不同程度的生育毒性、致突变性、致癌性,关注阈值分别为1。0、0。4、4。3、0。2、46。7 ng/mg。结论 所建方法简单快捷、灵敏度高、专属性强,估算的关注阈值明确,可用于多种β受体拮抗剂类药物中N-亚硝基类杂质的含量控制。
Content study of N-nitroso impurities in 5 types of β-blockers
OBJECTIVE To determine the contents of N-nitroso impurities in raw materials/formulations of propranolol,metoprolol,atenolol,esmolol and bisoprolol,and clarify the attention threshold.METHODS Ultra-high performance liquid chromatography-quadrupole/electrostatic field orbitrap high-resolution mass spectrometry(UPLC-Q/Orbitrap HRMS)was adopted.An ACE Excel 3 C18-AR column was used for the separation and a mixture of 0.2%formic acid solution with 0.01 mol/L ammonium acetate and methanol was employed as the mobile phase by gradient elution,at a flow rate of 0.60 mL/min.The column temperature was set at 40℃,and the sample size was 5 μL.The heated electrospray ionization source was employed in the positive full mass spectra-selected ion monitoring mode.The contents of N-nitroso impurities in raw materials/formulations of 15 batches of β-blockers from 10 manufacturers were determined by this method.Discovery Studio software was applied to predict the toxicity of the impurities and estimate the attention threshold.RESULTS Among 5 kinds of β-blockers,the linear ranges of N-nitroso propranolol,N-nitroso metoprolol,N-nitroso atenolol,N-nitroso esmolol and N-nitroso bisoprolol were 1.01-503.38,1.02-508.38,0.97-483.63,1.11-554.27 and 1.05-523.92 ng/mL,respectively(r>0.999).The limits of quantitation were 1.04,0.25,0.05,0.55 and 1.05 ng/mL,and the limits of detection were 0.52,0.08,0.02,0.17 and 0.52 ng/mL,respectively.RSDs of precision,reproducibility,recovery,stability and durability tests were all lower than 7.5%(n=6 or n=5).Among the 15 batches of samples,except for 1 batch,N-nitroso propranolol(1.07-8.91 ng/mg),N-nitroso metoprolol(1.43-3.37 ng/mg),N-nitroso atenolol(1.33 ng/mg),N-nitroso esmolol(0.19 ng/mg)and N-nitroso bisoprolol(1.27 ng/mg)were detected in all other batches.According to predictions,the above 5 impurities had varying degrees of reproductive toxicity,mutagenicity and carcinogenicity,with attention thresholds of 1.0,0.4,4.3,0.2 and 46.7 ng/mg,respectively.CONCLUSIONS The established method is simple,rapid,sensitive and specific,the estimated attention thresholds are clear,which can be used for the control of N-nitroso impurities in variousβ-blockers.

β-blockersN-nitroso impuritiesUPLC-Q/Orbitrap HRMSgene toxicityattention thresholds

田珩、杨仪雪、戴聪、刘亚雄、严全鸿

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广东省药品检验所/国家药品监督管理局药用辅料质量控制与评价重点实验室,广州 510180

β受体拮抗剂类药物 N-亚硝基类杂质 超高效液相色谱-四极杆/静电场轨道阱高分辨质谱技术 基因毒性 关注阈值

广东省医学科学技术研究项目

B2023406

2024

中国药房
中国医院协会,中国药房杂志社

中国药房

CSTPCD北大核心
影响因子:0.956
ISSN:1001-0408
年,卷(期):2024.35(8)
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