Pepakayala Sriram, Ratnakaram Venkata Nadh, Zunjarrao Yuvaraj, Lohia Yogesh Kumar
Analytical Research and Development, IOL Chemicals and Pharmaceuticals Ltd, Barnala, Punjab, 148101, India.
Industrial Chemical Product Development and Analysis Centre, Department of Chemistry, GITAM School of Science, GITAM Deemed to be University - Bengaluru Campus, Bengaluru, Karnataka, 561203, India.
BMC Chem. 2025 May 20;19(1):135. doi: 10.1186/s13065-025-01503-4.
The International Agency for Research on Cancer categorized nitrosamines as potential or probable human carcinogens. Hence, nitrosamine impurities should be controlled to minimize the cancer risk. Sustainable Development Goal 9 (SDG9: Industry, Innovation, and Infrastructure), Target 9.4 was realized by developing a simple and straightforward LC-APCI-MS/MS method for simultaneous determination of potential nitrosamines: N-nitroso dimethylamine, N-nitroso di isopropyl amine, N-nitroso isopropyl ethylamine and N-nitroso methyl aminopyridine (NDMA, NDIPA, NIPEA and NMAP) in Sitagliptin Phosphate Monohydrate API (STG-API), an antidiabetic medication for type-2 diabetes and validated as per ICH (Q2 R2) guidelines. As a part of SDG9 (Industry, Innovation, and Infrastructure), Target 9.4, greater adoption of clean and environmentally sound technologies is possible by using the current analytical method in view of (a) less consumption of solvents as it has a lower run time of 18 min (b) at-line sample collection (c) simple sample preparation (d) sample preparation process that does not require derivatization or sample extraction. The optimized LC method conditions are an Agilent Poroshell EC C18 column, a flow rate of 0.6 mL/min, an injection volume of 40 µL, a column oven temperature set at 50 °C, and a sample cooler temperature set at 6 °C. A gradient method was adopted using a mixture of mobile phases (Solvent A: 0.1% formic acid in water and Solvent B: a mixture of 50% Methanol and 50% Acetonitrile). The response was obtained with Multiple Reaction Monitoring (MRM) in APCI mode. The current method can quantify NDMA, NIPEA, NDIPA, and NMAP to a lower level of 74.19 ng/g, 19.62 ng/g, 20.36 ng/g, and 13.65 ng/g, respectively, which is less than 10% of the specified limits. Good linearity in the range of Limit of Quantitation (LOQ) to 150% of the specification limit was observed, with correlation coefficients higher than 0.996. The recoveries were over the range between 90.23 and 103.36%. Assessed the method's eco-friendliness by greenness tools like the Modified Green Analytical Procedure Index (MoGAPI), ComplexMoGAPI, Analytical GREEnness (AGREE), and Analytical Eco-Scale, and found it to be eco-friendly.
国际癌症研究机构将亚硝胺归类为潜在或可能的人类致癌物。因此,应控制亚硝胺杂质,以将癌症风险降至最低。通过开发一种简单直接的液相色谱-大气压化学电离串联质谱法(LC-APCI-MS/MS),用于同时测定磷酸西他列汀一水合物原料药(STG-API,一种用于2型糖尿病的抗糖尿病药物)中的潜在亚硝胺:N-亚硝基二甲胺、N-亚硝基二异丙胺、N-亚硝基异丙基乙胺和N-亚硝基甲基氨基吡啶(NDMA、NDIPA、NIPEA和NMAP),实现了可持续发展目标9(SDG9:产业、创新和基础设施)的具体目标9.4,并按照国际人用药品注册技术协调会(ICH)(Q2 R2)指南进行了验证。作为SDG9(产业、创新和基础设施)具体目标9.4的一部分,鉴于(a)溶剂消耗较少,因为其运行时间较短,为18分钟;(b)在线样品采集;(c)简单的样品制备;(d)样品制备过程不需要衍生化或样品萃取,使用当前的分析方法有可能更多地采用清洁和环境友好型技术。优化后的液相色谱方法条件为:安捷伦Poroshell EC C18色谱柱,流速0.6 mL/min,进样体积40 μL,柱温箱温度设定为50℃,样品冷却器温度设定为6℃。采用梯度方法,使用流动相混合物(溶剂A:0.1%甲酸水溶液和溶剂B:50%甲醇与50%乙腈的混合物)。在大气压化学电离模式下通过多反应监测(MRM)获得响应。当前方法可分别将NDMA、NIPEA、NDIPA和NMAP定量至74.19 ng/g、19.62 ng/g和13.65 ng/g的较低水平,均低于规定限度的10%。在定量限(LOQ)至规定限度150%的范围内观察到良好的线性,相关系数高于0.996。回收率在90.23%至103.36%之间。使用改良绿色分析程序指数(MoGAPI)、综合MoGAPI、分析绿色度(AGREE)和分析生态尺度等绿色工具评估了该方法的生态友好性,发现其具有生态友好性。