Method development and validation study for quantitative determination of nifedipine and related substances by ultra-high-performance liquid chromatography-Reference-Cited by-同舟云学术

Method development and validation study for quantitative determination of nifedipine and related substances by ultra-high-performance liquid chromatography

Published:2014-07-03 Issue:2 Volume:29 Page:233-239
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomed. Chromatogr.

Author:

Galan-Rodriguez Cristobal¹,González-Álvarez Jaime²,Valls-Remolí Màrius¹

Affiliation:

1. Moehs Ibérica, Research and Development Department; Polígono Industrial Cova-Solera C.P. 08191; Rubí Barcelona

2. Moehs Cántabra, Quality Control Department; Polígono Industrial Requejada S/N, C.P. 39312; Polanco Santander

Publisher

Wiley

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,General Medicine,Biochemistry,Analytical Chemistry

Reference33 articles.

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3. Evaluation of ultra performance liquid chromatography. Part I. Possibilities and limitations;Villiers;Journal of Chromatography A,2006

4. Reversed-phase liquid chromatographic separation of complex samples by optimizing temperature and gradient time: I. Peak capacity limitations;Dolan;Journal of Chromatography A,1999

5. European Pharmacopoeia 2009

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