Study of the impurity profile and characteristic fragmentation of Δ 3 ‐isomers in cephapirin sodium using dual liquid chromatography coupled with ion trap/time‐of‐flight mass spectrometry

Author:

Ren Xiaojuan1ORCID,Zhou Jinjin1,Hu Feifeng2,Wang Jian13

Affiliation:

1. Zhejiang University of Technology Hangzhou 310014 China

2. Zhejiang Drug Inspection Center Hangzhou 310013 China

3. Key Laboratory for Core Technology of Generic Drug Evaluation National Medical Product Administration Zhejiang Institute for Food and Drug Control Hangzhou 310052 China

Funder

National Major Science and Technology Projects of China

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference16 articles.

1. European Pharmacopoeia 9.0.European Directorate for the Quality of Medicines & Health Care. France;2016.

2. The United States Pharmacopoeia USP 40‐NF35.The United States Pharmacopeial Convention: Washington.

3. Study on the synthesis of cephapirin sodium;Huang JL;Chinese J Antibiotics,2012

4. Relationship between in vitro susceptibility test results and treatment outcomes for gram-positive mastitis pathogens following treatment with cephapirin sodium

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