Quantitative Method For The Determination Of Phenyl Hydrazine, A Potential Genotoxic Impurity Of Ondansetron Hydrochloride Using Tandem Mass Spectrometry
{"title":"Quantitative Method For The Determination Of Phenyl Hydrazine, A Potential Genotoxic Impurity Of Ondansetron Hydrochloride Using Tandem Mass Spectrometry","authors":"Palnati Narmada Kotapati Nalini, G. Vaidyanathan","doi":"10.46624/ajptr.2020.v10.i5.003","DOIUrl":null,"url":null,"abstract":"To estimate the level of Phenylhydrazine, a potential genotoxic impurity in Ondansetron Hydrochloride API, a new simple, sensitive and accurate method was developed using Liquid Chromatographic Mass Spectrometry (LC-MS/MS). The chromatographic separation was achieved on Inert Sustain Swift C18, 5μ (150 x 4.6) mm column with gradient programme and elution was monitored by mass spectrometer in Multiple Reaction Monitoring mode using electrospray ionization. The LOD and LOQ values found to be 5 ppm and 15 ppm for the impurity with respect to the test concentration 2 mg/ml. The method was linear (r>0.99), precise (RSD<2%), accurate and well within acceptable ICH limits.","PeriodicalId":7701,"journal":{"name":"American Journal of PharmTech Research","volume":"7 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of PharmTech Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46624/ajptr.2020.v10.i5.003","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
To estimate the level of Phenylhydrazine, a potential genotoxic impurity in Ondansetron Hydrochloride API, a new simple, sensitive and accurate method was developed using Liquid Chromatographic Mass Spectrometry (LC-MS/MS). The chromatographic separation was achieved on Inert Sustain Swift C18, 5μ (150 x 4.6) mm column with gradient programme and elution was monitored by mass spectrometer in Multiple Reaction Monitoring mode using electrospray ionization. The LOD and LOQ values found to be 5 ppm and 15 ppm for the impurity with respect to the test concentration 2 mg/ml. The method was linear (r>0.99), precise (RSD<2%), accurate and well within acceptable ICH limits.
为测定盐酸昂丹司琼原料药中潜在遗传毒性杂质苯肼的含量,建立了一种简便、灵敏、准确的液相色谱-质谱(LC-MS/MS)方法。色谱柱为Inert Sustain Swift C18,色谱柱为5μ (150 x 4.6) mm,采用梯度程序,质谱联用,电喷雾电离,多重反应监测模式。相对于测试浓度2mg /ml,杂质的LOD和LOQ值分别为5ppm和15ppm。该方法线性(r>0.99),精密度(RSD<2%),准确度在可接受的ICH范围内。