Development and validation of UPLC method for simultaneous quantification of carvedilol and ivabradine in the presence of degradation products using DoE concept-Reference-Cited by-同舟云学术

Development and validation of UPLC method for simultaneous quantification of carvedilol and ivabradine in the presence of degradation products using DoE concept

Published:2018-02-07 Issue:3 Volume:41 Page:143-153
ISSN:1082-6076
Container-title:Journal of Liquid Chromatography & Related Technologies
language:en
Short-container-title:Journal of Liquid Chromatography & Related Technologies

Author:

Nadella Nukendra Prasad¹²,Ratnakaram Venkata Nadh³,Srinivasu N.¹

Affiliation:

1. Department of Science and Humanities, VFSTR, Vignan’s University, Guntur, Andhra Pradesh, India

2. AET Laboratories Pvt. Ltd, Kazipally Industrial Area, Hyderabad, Telangana, India

3. Department of Chemistry, GITAM University, Bengaluru, Karnataka, India

Publisher

Informa UK Limited

Subject

Clinical Biochemistry,Pharmaceutical Science,Biochemistry,Analytical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10826076.2018.1427595

Reference25 articles.

1. https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/020297s029lbl.pdf (accessed October 10, 2017)

2. www.ema.europa.eu/docs/en_GB/document_library/… /WC500221259.pdf, European medicines agency assessment report of Ivabradine, procedure number EMEA/H/C/004217/0000.

3. National center for biotechnology information. PubChem Compound Database; CID = 86643432. https://pubchem.ncbi.nih.gov/compound/86643432 (accessed October 22,2017).

4. http://www.tlcstandards.com/ProdDetail.aspx?ID=I-3030&name=IVABRADINE (accessed October 28, 2017)

5. Carvedilol Ph. Eur. monograph, European Pharmacopoeia.

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