Derivative-Based Non-Target Identification of DNA-Reactive Impurities with Fragment Ion Filtering

DNA direct reactive impurities (DDRIs) can react with nucleophilic sites of DNA, leading to mutations. The control strategies outlined in International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) M7 are based on the known compound structure of DDRIs. Non-target screening of DDRIs in drugs is still challenging due to the diversity of the species and the poor stability. In this study, a derivatization reagent including a reactive group and report group was designed to screen DDRIs. Based on the electrophilic theory of chemical carcinogenesis, an amine reagent was used as a reactive group to interact with DDRIs. Two derivatization reagents, p-methoxyaniline and p-methoxybenzoyl-β-alaninamide, were employed, each containing different chromatographic modification groups to mitigate matrix effects. The derivatization products were analyzed by ultra-high-performance liquid chromatography coupled to high-resolution mass spectrometry (UPLC-HRMS). Non-target screening for DDRIs was achieved by product ions filtering of the report group.

Authors

Institutions

Publication Details

Journal
Molecules
Published
2025-10-04
DOI
https://doi.org/10.3390/molecules30193981
Primary Topic
DNA and Nucleic Acid Chemistry
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Derivative-Based Non-Target Identification of DNA-Reactive Impurities with Fragment Ion Filtering

Baojian Hang, Yiran Zhang, Liping Gong, Dongmei Zhang et al.
Molecules
DNA and Nucleic Acid Chemistry
article

Derivative-Based Non-Target Identification of DNA-Reactive Impurities with Fragment Ion Filtering

Baojian Hang, Yiran Zhang, Liping Gong, Dongmei Zhang, Pengfei You, Feng Shi
article en

Abstract

DNA direct reactive impurities (DDRIs) can react with nucleophilic sites of DNA, leading to mutations. The control strategies outlined in International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) M7 are based on the known compound structure of DDRIs. Non-target screening of DDRIs in drugs is still challenging due to the diversity of the species and the poor stability. In this study, a derivatization reagent including a reactive group and report group was designed to screen DDRIs. Based on the electrophilic theory of chemical carcinogenesis, an amine reagent was used as a reactive group to interact with DDRIs. Two derivatization reagents, p-methoxyaniline and p-methoxybenzoyl-β-alaninamide, were employed, each containing different chromatographic modification groups to mitigate matrix effects. The derivatization products were analyzed by ultra-high-performance liquid chromatography coupled to high-resolution mass spectrometry (UPLC-HRMS). Non-target screening for DDRIs was achieved by product ions filtering of the report group.

MoleculesVol. 30(19)
Johns Hopkins University (US), National Medical Products Administration (CN), Shandong Institute of Food and Drug Inspection (CN), Jinan Institute of Quantum Technology (CN)
Openalex Percentile: Top 75%
DNA and Nucleic Acid Chemistry
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Derivative-Based Non-Target Identification of DNA-Reactive Impurities with Fragment Ion Filtering — Baojian Hang, Yiran Zhang, et al. · Molecules (2025) | TGRS Research Map | TGRS