Development and Validation of Rp-Hplc Method for the Simultaneous Estimation of 8 Relative Substances in Milrinone Api

Author:

Pang Yujiang,Shi Xiaoyan,Li Zhengzhao,Pan Zengyu,Liu Kai,Zhu Xianyong,Feng Zhong

Publisher

Elsevier BV

Reference29 articles.

1. Characterization, quantification and a multi-computational in silico toxicity assessment of impurity (feruloyl methane) in synthetic curcumin using RP-HPLC-UV technique;R S Nunavath;Journal of pharmaceutical and biomedical analysis,2023

2. HPLC separation, synthesis, isolation and characterization of process related and degradation impurities in larotaxel including method development and validation;K Yao;Journal of pharmaceutical and biomedical analysis,2023

3. Development of HPLC-CAD method for simultaneous quantification of nine related substances in ursodeoxycholic acid and identification of two unknown impurities by HPLC-Q-TOF-MS;Y Huang;Journal of pharmaceutical and biomedical analysis,2023

4. Development and validation of a stability-indicating RP-HPLC method for the determination of fifteen impurities in rivaroxaban;W Rao;Journal of pharmaceutical and biomedical analysis,2023

5. The Mortality Benefit of Milrinone as a Continuous Outpatient Intravenous Inotrope Therapy in Advanced Heart Failure: A Systemic Review and Meta-Analysis;Del Rio-Pertuz;International journal of heart failure,2023

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