Quality by Design (QbD): A Practical Experimental Design Approach by Blocking and Varying Certain Factors of a Stability-Indicating HPLC Method for Simultaneous Determination of Omeprazole and Ketoprofen-Reference-Cited by-同舟云学术

Quality by Design (QbD): A Practical Experimental Design Approach by Blocking and Varying Certain Factors of a Stability-Indicating HPLC Method for Simultaneous Determination of Omeprazole and Ketoprofen

Published:2014-08-22 Issue:6 Volume:38 Page:677-686
ISSN:1082-6076
Container-title:Journal of Liquid Chromatography & Related Technologies
language:en
Short-container-title:Journal of Liquid Chromatography & Related Technologies

Author:

Garg Lovleen Kumar¹²,Sait Shakil S.³,Krishnamurthy T.¹,Kumar C. H. R. Phani¹

Affiliation:

1. Analytical Research and Development, Integrated Product Development, Dr. Reddy's Laboratories Ltd., Bachupally, Hyderabad, India

2. Department of Chemistry, Jawaharlal Nehru Technological University, Hyderabad, India

3. Analytical Research Department, Piramal Enterprises Ltd., Mumbai, India

Funder

The authors would like to thank Dr. Reddy's Laboratories Ltd., IPDO, Bachupally, Hyderabad, India for supporting this work. The IPM department has given this manuscript the internal publication number PUB00322-14.

Publisher

Informa UK Limited

Subject

Clinical Biochemistry,Pharmaceutical Science,Biochemistry,Analytical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10826076.2014.951766

Reference34 articles.

1. U.S. Department of Health and Human Services Food and Drug Administration. Pharmaceutical Quality for the 21st Century: A Risk-Based Approach. May 2007. http://www.fda.gov/oc/cgmp/report0507.html (accessed).

2. Simultaneous HPLC determination of ketoprofen and its degradation products in the presence of preservatives in pharmaceuticals

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