Analysis of impurity profiling of arbekacin sulfate by ion-pair liquid chromatography coupled with pulsed electrochemical detection and online ion suppressor-ion trap-time off light mass spectrometry.


Journal

Journal of pharmaceutical and biomedical analysis
ISSN: 1873-264X
Titre abrégé: J Pharm Biomed Anal
Pays: England
ID NLM: 8309336

Informations de publication

Date de publication:
30 Nov 2022
Historique:
received: 22 05 2022
revised: 23 08 2022
accepted: 14 09 2022
pubmed: 3 10 2022
medline: 14 10 2022
entrez: 2 10 2022
Statut: ppublish

Résumé

Ion-pair liquid chromatography with pulsed electrochemical detection (LC-PED) was established for the analysis of impurities in arbekacin (ABK) sulfate. APursuit pentafluorophenylpropyl (PFP) column was used as stationary phase. This novel method showed greater separation and sensitivity ability. In a representative ABK sample, 24 impurity peaks were detected in LC-PED, where of only 9 were monitored by a post-column derivatization method prescribed by the Japanese Pharmacopoeia (JP). For identification of the chemical structures of the impurities detected by LC-PED, LC-Mass Spectrometry (MS) was used. Two challenges had to be overcome in this work. The first was the transfer of the MS incompatible mobile phase to an MS compatibleone while maintaining the elution order of the peaks in the chromatograms. Previously reported approaches such as two-dimensional (2D)LC were hardly applicable in this case due to the lack of ultraviolet (UV) absorbing chromophores in ABK and its impurities. The sodium hydroxide solution was replaced by aqueous ammonia to adjust the pH of the mobile phase used in LC-PED. The other challenge encountered was the ion suppression effect caused by trifluoroacetic acid (TFA) and pentafluoroproponic acid (PFPA) in the mobile phase. Some strategies such as "TFA-fixed" and its modifications were tried, but they were inconvenient and severe contamination of the MS was observed. A cationself-regenerating suppressor (CSRS), which was originally designed for increasing analyte conductivityof ammonia and amines analysis in ion chromatography (IC), was coupled between the LC and Ion Trap-Time of Flight (IT-TOF)-MS and almost all TFA and PFPA in the mobile phase were removed. The limit of detection (LOD) of ABK in this integrated system improved significantly to 20 ng/mL. The chemical structures of the 28 impurities were elucidated and 15 impurities were reported for the first time.

Identifiants

pubmed: 36183632
pii: S0731-7085(22)00482-4
doi: 10.1016/j.jpba.2022.115061
pii:
doi:

Substances chimiques

Amines 0
Sulfates 0
Dibekacin 45ZFO9E525
Sodium Hydroxide 55X04QC32I
Ammonia 7664-41-7
Trifluoroacetic Acid E5R8Z4G708
arbekacin G7V6SLI20L

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

115061

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Zhouzhou Chen (Z)

School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China; NMPA Key Laboratory for Impurity Profile of Chemical Drugs, Nanjing 210019, China.

Xiaoyue Zhu (X)

NMPA Key Laboratory for Impurity Profile of Chemical Drugs, Nanjing 210019, China; Jiangsu Institute for Food and Drug Control, Nanjing 210019, China.

Yue Geng (Y)

NMPA Key Laboratory for Impurity Profile of Chemical Drugs, Nanjing 210019, China; Jiangsu Institute for Food and Drug Control, Nanjing 210019, China; Nanjing Normal University, College of Food and Pharmaceutical Engineering, Nanjing 210023, China.

Jun Dai (J)

Inner Mongolia Puyin Pharmaceutical Co. Ltd, Chifeng 024000, China.

Sheng Tang (S)

School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang 212003, China.

Erwin Adams (E)

Department of Pharmaceutical and Pharmacological Sciences, Pharmaceutical Analysis, KU Leuven, Herestraat 49, O&N2, PB 923, B-3000 Leuven, Belgium.

Daijie Chen (D)

School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China. Electronic address: hccb001@163.com.

Yaozuo Yuan (Y)

NMPA Key Laboratory for Impurity Profile of Chemical Drugs, Nanjing 210019, China; Jiangsu Institute for Food and Drug Control, Nanjing 210019, China; Nanjing Normal University, College of Food and Pharmaceutical Engineering, Nanjing 210023, China. Electronic address: yyzyz7256@163.com.

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Classifications MeSH