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Nitrosamine Impurities Application Guide - Confidently Detect and Quantify Mutagenic Impurities in APIs and Drug Products

Příručky, Prezentace | 2020 | Agilent TechnologiesInstrumentace
GC/MSD, GC/MS/MS, HeadSpace, GC/SQ, GC/QQQ, LC/TOF, LC/HRMS, LC/MS, LC/MS/MS, LC/QQQ
Zaměření
Farmaceutická analýza
Výrobce
Agilent Technologies
Klíčová slova
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nitrosamine, nitrosaminenmpa, nmpandipa, ndipandpa, ndpanmba, nmbaneipa, neipandba, ndbandea, ndeandma, ndmaimpurities, impuritiesquantifier, quantifierqualifier, qualifierresponses, responsesconcentration, concentrationdrug
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ndma, ndmandea, ndeanmba, nmbaneipa, neipandba, ndbandipa, ndipandpa, ndpanmpa, nmpametformin, metforminnitrosamines, nitrosaminesdrug, drugppm, ppmloq, loqlosartan, losartanarea
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nitrosamine, nitrosaminenmpa, nmpandipa, ndipandpa, ndpandba, ndbaneipa, neipandea, ndeanmba, nmbandma, ndmaresponses, responsesimpurities, impuritiesmetformin, metformindrug, drugeight, eightconcentration
Simultaneous quantitation of nine nitrosamines using a highly sensitive and LC-HRAM mass spectrometry method in multiple drug products
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nitrosamine, nitrosamineimpurities, impuritiesprm, prmndma, ndmanmba, nmbanmea, nmeasim, simnmpa, nmpaimpurity, impuritynine, ninenitroso, nitrosorecovery, recoveryneipa, neipandipa, ndipandpa
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