Targeted screening and profiling of massive components of colistimethate sodium by two-dimensional-liquid chromatography-mass spectrometry based on self-constructed compound database.
10.1016/j.jpha.2024.101072
- Author:
Xuan LI
1
;
Minwen HUANG
1
;
Yue-Mei ZHAO
1
;
Wenxin LIU
1
;
Nan HU
2
;
Jie ZHOU
3
;
Zi-Yi WANG
4
;
Sheng TANG
5
;
Jian-Bin PAN
6
;
Hian Kee LEE
5
;
Yao-Zuo YUAN
1
;
Taijun HANG
4
;
Hai-Wei SHI
1
;
Hongyuan CHEN
6
Author Information
1. Jiangsu Institute for Food and Drug Control, Nanjing, 210019, China.
2. Agilent Technologies Inc., Beijing, 100102, China.
3. Jiangsu Zhengda Tianqing Pharmaceutical Group Co., Ltd., Lianyungang, Jiangsu, 222006, China.
4. School of Pharmacy, China Pharmaceutical University, Nanjing, 211112, China.
5. School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang, Jiangsu, 212003, China.
6. School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210046, China.
- Publication Type:Journal Article
- Keywords:
2D-LC-MS;
Colistimethate sodium;
Component deduction;
Database;
Profiling;
Targeted screening
- From:
Journal of Pharmaceutical Analysis
2025;15(2):101072-101072
- CountryChina
- Language:English
-
Abstract:
In-depth study of the components of polymyxins is the key to controlling the quality of this class of antibiotics. Similarities and variations of components present significant analytical challenges. A two-dimensional (2D) liquid chromatography-mass spectrometr (LC-MS) method was established for screening and comprehensive profiling of compositions of the antibiotic colistimethate sodium (CMS). A high concentration of phosphate buffer mobile phase was used in the first-dimensional LC system to get the components well separated. For efficient and high-accuracy screening of CMS, a targeted method based on a self-constructed high resolution (HR) mass spectrum database of CMS components was established. The database was built based on the commercial MassHunter Personal Compound Database and Library (PCDL) software and its accuracy of the compound matching result was verified with six known components before being applied to genuine sample screening. On this basis, the unknown peaks in the CMS chromatograms were deduced and assigned. The molecular formula, group composition, and origins of a total of 99 compounds, of which the combined area percentage accounted for more than 95% of CMS components, were deduced by this 2D-LC-MS method combined with the MassHunter PCDL. This profiling method was highly efficient and could distinguish hundreds of components within 3 h, providing reliable results for quality control of this kind of complex drugs.
