Bioanalytical method development and validation of memantine in human plasma by high performance liquid chromatography with tandem mass spectrometry: Application to bioequivalence study

Journal of Analytical Methods in Chemistry

Volumn 1, Issue 1, 2012, Pages

  Konda, Ravi Kumar ^a,b   Challa, B R ^c   Chandu, Babu Rao ^d   Chandrasekhar, Kothapalli B ^b  

^a HINDU COLLEGE OF PHARMACY   (India)

^b JAWAHARLAL NEHRU TECHNOLOGICAL UNIVERSITY   (India)

^c Nirmala College of Pharmacy   (India)

^d Donbosco college of Pharmacy   (India)

Author keywords

[No Author keywords available]

Indexed keywords

MEMANTINE;

ACCURACY; AREA UNDER THE CURVE; ARTICLE; BIOEQUIVALENCE; CALIBRATION; DRUG DETERMINATION; DRUG ELIMINATION; DRUG HALF LIFE; DRUG SELECTIVITY; DRUG STABILITY; FOOD AND DRUG ADMINISTRATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HUMAN EXPERIMENT; HUMAN TISSUE; LIMIT OF QUANTITATION; MALE; MAXIMUM PLASMA CONCENTRATION; NORMAL HUMAN; PRIORITY JOURNAL; QUALITY CONTROL; SENSITIVITY AND SPECIFICITY; TANDEM MASS SPECTROMETRY; TIME TO MAXIMUM PLASMA CONCENTRATION; VALIDATION PROCESS;

EID: 84865037789     PISSN: 20908865     EISSN: 20908873     Source Type: Journal    
DOI: 10.1155/2012/101249     Document Type: Article

References (12)

1. Liu M.-Y., Meng S.-N., Wu H.-Z., Wang S., Wei M.-J., Pharmacokinetics of single-dose and multiple-dose memantine in healthy chinese volunteers using an analytic method of liquid chromatography-tandem mass spectrometry Clinical Therapeutics 2008 30 4 641 653 (Pubitemid 351680492)
2. Almeida A. A., Campos D. R., Bernasconi G., Calafatti S., Barros F. A. P., Eberlin M. N., Meurer E. C., Paris E. G., Pedrazzoli J., Determination of memantine in human plasma by liquid chromatography-electrospray tandem mass spectrometry: application to a bioequivalence study Journal of Chromatography B 2007 848 2 311 316 (Pubitemid 46453301)
3. Pan R.-N., Chian T.-Y., Kuo B. P.-C., Pao L.-H., Determination of memantine in human plasma by LC-MS-MS: application to a pharmacokinetic study Chromatographia 2009 70 5-6 783 788
4. Koeberle M. J., Hughes P. M., Wilson C. G., Skellern G. G., Development of a liquid chromatography-mass spectrometric method for measuring the binding of memantine to different melanins Journal of Chromatography B 2003 787 2 313 322 (Pubitemid 36316011)
5. Suckow R. F., Zhang M. F., Collins E. D., Fischman M. W., Cooper T. B., Sensitive and selective liquid chromatographic assay of memantine in plasma with fluorescence detection after pre-column derivatization Journal of Chromatography B 1999 729 1-2 217 224 (Pubitemid 29264126)
6. Shuangjin C., Fang F., Han L., Ming M., New method for high-performance liquid chromatographic determination of amantadine and its analogues in rat plasma Journal of Pharmaceutical and Biomedical Analysis 2007 44 5 1100 1105 (Pubitemid 47239293)
7. Higashi Y., Nakamura S., Matsumura H., Fujii Y., Simultaneous liquid chromatographic assay of amantadine and its four related compounds in phosphate-buffered saline using 4-fluoro-7-nitro-2,1,3-benzoxadiazole as a fluorescent derivatization reagent Biomedical Chromatography 2006 20 5 423 428
8. Duh T. H., Wu H. L., Pan C. W., Kou H. S., Fluorimetric liquid chromatographic analysis of amantadine in urine and pharmaceutical formulation Journal of Chromatography A 2005 1088 1-2 175 181
9. Leis H. J., Fauler G., Windischhofer W., Quantitative analysis of memantine in human plasma by gas chromatography/negative ion chemical ionization/mass spectrometry Journal of Mass Spectrometry 2002 37 5 477 480 (Pubitemid 34578389)
10. Yeh H. H., Yang Y. H., Chen S. H., Simultaneous determination of memantine and amantadine in human plasma as fluorescein derivatives by micellar electrokinetic chromatography with laser-induced fluorescence detection and its clinical application Electrophoresis 2010 31 11 1903 1911
11. Guidance for industry Food-effect bio availability and fed bio equivalence studies,. U.S. Department of health and human services food and drug administration centre for drug evaluation and research (CDER), December 2002
12. Guidance for industry bio availability and fed bio equivalence Studies for Orally Administered Drug Products-General considerations,. U.S. Department of health and human services food and drug administration centre for drug evaluation and research (CDER), March 2003