Development and validation of UV spectrophotometric method for estimation of Lafutidine in bulk and pharmaceutical dosage form

International Journal of Drug Development and Research

Volumn 4, Issue 1, 2012, Pages 325-329

  Parekh Ravishkumar, R ^a   Patel Pinkal, H ^a   Patel Chinmay, D ^a   Patel Krupali, S ^a   Patel Hardik, N ^a  

^a GUJARAT TECHNOLOGICAL UNIVERSITY   (India)

Author keywords

0.1 N HCl; Anti Ulcer; Lafutidine; Quantitative determination; UV

Indexed keywords

LAFUTIDINE;

ACCURACY; ARTICLE; CORRELATION COEFFICIENT; COST EFFECTIVENESS ANALYSIS; DRUG DETERMINATION; DRUG DOSAGE FORM; DRUG FORMULATION; LIMIT OF DETECTION; LIMIT OF QUANTITATION; LINEAR SYSTEM; QUALITY CONTROL; REPRODUCIBILITY; SENSITIVITY ANALYSIS; ULTRAVIOLET SPECTROPHOTOMETRY; VALIDATION STUDY;

EID: 84861322461     PISSN: None     EISSN: 09759344     Source Type: Journal    
DOI: None     Document Type: Article

References (8)

1. Indian Pharmacopoeia, Govt. of India, Ministry of Health & Family Welfare, Indian Pharmacopoeial commission; Ghaziabad, 2007.
2. ICH-Guidelines Q2(R1), Validation of Analytical Procedures: Text and Methodology. (2005).
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6. Lili wu et. al, "Determination of lafutidine in human plasma by high-performance liquid chromatography electrospray ionization mass spectrometry, application to bioequivalence study", Journal of Mass Spectrometry, Vol 40, Issue 12, December 2005, pp 1637-1643.
7. Zhwng Heng et. al, "Determination of lafutidine in human plasma by HPLC-MS", The Chinese journal of Clinical Pharmacology, Issue 01, 2008.
8. Xiuhong Sun et. al, "A single LC-tandem mass spectrometry method for the simultaneous determination of four H2 antagonists in human plasma", Journal of chromatography, Issue 31, December 2009, pp 3953-3959.