SEPARATION AND ESTIMATION OF PROCESS RELATED IMPURITIES AND DEGRADATION PRODUCTS OF LEVETIRACETAM IN SOLID PHARMACEUTICAL FORMULATION USING ION-PAIR CHROMATOGRAPHY-Reference-Cited by-同舟云学术

SEPARATION AND ESTIMATION OF PROCESS RELATED IMPURITIES AND DEGRADATION PRODUCTS OF LEVETIRACETAM IN SOLID PHARMACEUTICAL FORMULATION USING ION-PAIR CHROMATOGRAPHY

Published:2013-05 Issue:13 Volume:36 Page:1835-1848
ISSN:1082-6076
Container-title:Journal of Liquid Chromatography & Related Technologies
language:en
Short-container-title:Journal of Liquid Chromatography & Related Technologies

Author:

Kumar Navneet¹²,Sangeetha D.²

Affiliation:

1. a Dr. Reddy's Laboratories Ltd., IPDO, Bachupally , Hyderabad , A.P , India

2. b Department of Chemistry , S.A.S., V.I.T. University , Vellore , Tamilnadu , India

Publisher

Informa UK Limited

Subject

Clinical Biochemistry,Pharmaceutical Science,Biochemistry,Analytical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10826076.2012.704606

Reference17 articles.

1. U.S. Food and Drug Administration. Drug Approval Package Keppra (Levetiracetam) Tablets NDA 21035, 1999. http://www.accessdata.fda.gov/drugsatfda_docs/nda/99/21035_Keppra.cfm (Accessed March 2011)

2. Validation of a high-performance thin-layer chromatographic method with densitometric detection for quantitative analysis of two anticonvulsants in tablets

3. Microemulsion electrokinetic chromatography applied for separation of levetiracetam from other antiepileptic drugs in polypharmacy

4. Analysis of the antiepileptic drug keppra by capillary electrophoresis

5. Determination of levetiracetam in human plasma with minimal sample pretreatment

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