Literature DB >> 27208624

A simple and sensitive method to analyze genotoxic impurity hydrazine in pharmaceutical materials.

Jenny Wang1, Samuel Yang1, Kelly Zhang2.   

Abstract

Hydrazine (N2H4) is a known genotoxic impurity that typically needs to be controlled down to low ppm level in pharmaceutical development. Hydrazine, however, is a challenging molecule to analyze using conventional analytical techniques due to its physical and chemical properties (e.g. lack of chromophore, absence of any carbon atom, low molecular weight, high polarity and volatility). Additionally, analysis in pharmaceutical samples commonly encounters significant interference from matrix components that greatly overshadow the response of hydrazine. This work describes a simple, accurate and sensitive reversed-phase liquid chromatography-UV derivatization method for determination of trace amount hydrazine in pharmaceutical materials featuring three prominent strategies to address the problems associated with hydrazine analysis. First, the derivatization reaction attaches chromophores to hydrazine, which greatly increases its sensitivity by UV-vis detection. Secondly, the derivatization reaction generates a lambda max that is well-shifted away from the absorption wavelengths of pharmaceutical matrix interferences. Thirdly, from a separation standpoint, the derivatization further removes matrix interference effects through chromatography by achieving higher resolution of the derivative product from the active pharmaceutical ingredient (API) and its related impurities for accurate quantitation for trace level of genotoxic impurities (GTIs). 2-Hydroxy-1-Naphthalaldehyde (HNA) was chosen as the derivatizing reagent, and the resulting hydrazone product has a maximum UV absorbance at wavelength of 406/424nm which is in the visible range. Since most drug substance and impurities have UV absorbance ranging from 190 to 380nm, interference from the matrix was minimized and the appropriate selectivity was obtained, the detection limit is 0.25ppm (0.25μg/g API). This method was validated and applied as a generic method to determine hydrazine for pharmaceutical process control and drug material release.
Copyright © 2016 The Author(s). Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  2-Hydroxy-1-Naphthaldehyde; Derivatization; Genotoxic impurity (GTI); HPLC; Hydrazine; Matrix interference; Trace analysis

Mesh:

Substances:

Year:  2016        PMID: 27208624     DOI: 10.1016/j.jpba.2016.04.038

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  1 in total

1.  A new HPLC-UV derivatization approach for the determination of potential genotoxic benzyl halides in drug substances.

Authors:  Shunli Ji; Hongbin Gao; Xingya Xia; Feng Zheng
Journal:  RSC Adv       Date:  2019-08-16       Impact factor: 3.361

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.