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Solriamfetol impurities: Synthesis, characterization, and analytical method (UPLC-UV) validation.

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第一作者： Nafisah,Al-Rifai

第一单位： Pharmaceutical and Chemical Engineering Department, School of Medical Sciences, German Jordanian University, Amman, Jordan.

作者： Nafisah,Al-Rifai ^[1] ; Anas,Alshishani ^[2] ; Fouad,Darras ^[3] ; Ola,Taha ^[3] ; Shereen,Abu-Jalloud ^[3] ; Lena,Shaghlil ^[4] ; Yousef,Al-Ebini ^[5]

作者单位： Pharmaceutical and Chemical Engineering Department, School of Medical Sciences, German Jordanian University, Amman, Jordan. ^[1] Faculty of Pharmacy, Zarqa University, Zarqa, Jordan.;Research and Development Department, Resonance Research Lab, Amman, Jordan. ^[2] Research and Development Department, Resonance Research Lab, Amman, Jordan. ^[3] Faculty of Pharmacy, Zarqa University, Zarqa, Jordan. ^[4] Department of Pharmaceutics, College of Pharmacy, King Khalid University, Abha, Saudi Arabia. ^[5]

关键词 Impurity analysis Impurity synthesis Method validation Solriamfetol UPLC

DOI 10.1016/j.jpha.2023.02.012

PMID 37181290

发布时间 2023-05-16

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Journal of pharmaceutical analysis

2023年13卷4期

403-411页

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Journal of pharmaceutical analysis

2023年13卷4期

403-411页

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Solriamfetol impurities: Synthesis, characterization, and analytical method (UPLC-UV) validation.

Journal of pharmaceutical analysis

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Solriamfetol impurities: Synthesis, characterization, and analytical method (UPLC-UV) validation.

Journal of pharmaceutical analysis

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