RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF ATORVASTATIN CALCIUM, LOSARTAN POTASSIUM, ATENOLOL, AND ASPIRIN FROM TABLET DOSAGE FORM AND PLASMA

REFERENCES

• Erk , N. Simultaneous Determination of Irbesartan and Hydrochlorothiazide in Human Plasma by Liquid Chromatography . J. Chromatogr. B 2003 , 784 , 195 – 201 .
   PubMed Web of Science ®Google Scholar
• Moffat , A. C. ; Osselton , M. D. ; Widdop , B. Clarke's Analysis of Drugs and Poisons in Pharmaceuticals; Body Fluids and Postmortem Material. , 3rd ed. , 653, 654, 651, 1190 . London : Pharmaceutical Press , 2004 .
   Google Scholar
• Rao , L. ; Rajeswari , K. R. ; Sankar , G. G. Spectrophotometric Method for Simultaneous Estimation of Atorvastatin and Amlodipine in Tablet Dosage Form . Res. J. Pharm. Biol. Chem. Sci. 2010 , 1 ( 2 ), 66 .
   Google Scholar
• Saravanamuthukumar , M. ; Palanivelu , M. ; Anandarajagopal , K. ; Sridharan , D. Simultaneous Estimation and Validation of Atorvastatin Calcium and Ubidecarenone (Coenzyme Q10) in Combined Tablet Dosage Form by RPHPLC Method . Int. J. Pharm. Pharm. Sci. 2010 , 2 ( 2 ), 36 – 38 .
   Google Scholar
• Joseph , L. ; George , M. ; Venkata Ranga Rao , B. Simultaneous Estimation of Atorvastatin and Ramipril by RP-HPLC and Spectroscopy . Pakistan J. Pharm. Sci. 2008 , 21 ( 3 ), 282 – 284 .
   PubMed Web of Science ®Google Scholar
• Novakova , L. ; Satinsky , D. ; Solich , P. HPLC Methods for the Determination of Simvastatin and Atorvastatin . Trends Anal. Chem. 2008 , 27 ( 4 ), 352 – 367 .
   Web of Science ®Google Scholar
• Chaudhary , B. G. ; Patel , N. M. ; Shah , P. B. Stability Indicating RP-HPLC Method for Simultaneous Determination of Atorvastatin and Amlodipine from their Combination Drug Products . Chem. Pharm. Bull. 2007 , 55 ( 2 ), 241 – 246 .
   PubMed Web of Science ®Google Scholar
• Mohammadi , A. ; Rezanour , N. ; Dogaheh , M. A. ; Bidkorbeh , F. G. ; Hashemb , M. ; Walker , R. B. A stability-indicating High Performance Liquid Chromatographic (HPLC) Assay for the Simultaneous Determination of Atorvastatin and Amlodipine in Commercial Tablets . J. Chromatogr. B 2007 , 846 , 215 – 221 .
   PubMed Web of Science ®Google Scholar
• Patel , G. F. ; Vekariya , N. R. ; Dholakiya , R. B. Estimation of Aspirin and Atorvastatin Calcium in Combined Dosage Form using Derivative Spectrophotometric Method . Int. J. Pharm. Res. 2010 , 2 ( 1 ), 62 – 66 .
   Google Scholar
• Jamshidi , A. ; Nateghi , A. R. HPTLC Determination of Atorvastatin in Plasma. Chromatographia 2007 , 65 , 11 – 12 .
   Google Scholar
• Gholamreza , B. ; Bahareh , M. Determination of Atorvastatin in Human Serum by Reversed-Phase High-Performance Liquid Chromatography with UV Detection . J. Chromatogr. B 2005 , 826 , 41 – 45 .
   PubMed Web of Science ®Google Scholar
• Ismail , R. R. ; Ganesh , M. ; Jagadeeswaran , M. ; Srinivasan , K. ; Valarmathi , J. ; Sivakumar , T. RP-HPLC Method for the Simultaneous Determination of Aspirin, Atorvastatin and Pioglitazone in Capsuled form . Asian J. Res. Chem. 2008 , 1 ( 1 ), 974 – 4169 .
   Google Scholar
• Gandhimathi , M. ; Ravi , T. K. ; Abraham , A. ; Thomas , R. Simultaneous Determination of Aspirin and Isosorbide 5-Mononitrate in Formulation by Reversed Phase High Pressure Liquid Chromatography . J. Pharm. Biomed. Anal. 2003 , 32 , 1145 – 1148 .
   PubMed Web of Science ®Google Scholar
• Shrivastava , P. K. ; Basniwal , P. K. ; Jain , D. ; Shrivastava , S. K. Concurrent Estimation of Clopidogrel Bisulphate and Aspirin in Tablets by Validated RP-HPLC Method . Indian J. Pharm. Sci. 2008 , 70 ( 5 ), 667 – 669 .
   PubMedGoogle Scholar
• Yamamoto , E. ; Takakuwa , S. ; Kato , T. ; Asakawa , N. Sensitive Determination of Aspirin and Its Metabolites in Plasma by LC-UV using Online Solid Phase Extraction with Methyl Cellulose Immobilized Anion–Exchange Restricted Access Media . J. Chromatogr. B 2007 , 846 ( 1–2 ), 132 – 138 .
   PubMed Web of Science ®Google Scholar
• Walter , L. J. ; Biggs , D. F. ; Coutts , R. T. Simultaneous GLC Estimation of Salicylic Acid and Aspirin in Plasma . J. Pharm. Sci. 1974 , 63 ( 11 ), 1754 – 1758 .
   PubMed Web of Science ®Google Scholar
• Cesar , J. ; Ronei , L. A. ; Poppi , J. Simultaneous Determination of Acetylsalicylic Acid, Paracetamol and Caffeine using Solid-Phase Molecular Fluorescence and Parallel Factor Analysis. Anal. Chim. Acta 2009, 642, 212–216.
   PubMed Web of Science ®Google Scholar
• Cagigal , E. ; Gonzalez , L. ; Alonso , R. M. ; Jimenez , R. M. Experimental Design Methodologies to Optimise the Spectrofluorimetric Determination of Losartan and Valsartan in Human Urine . Talanta 2001 , 54 , 1121 – 1133 .
   PubMed Web of Science ®Google Scholar
• Brunetto , M. R. ; Contrerasa , Y. ; Clavijo , S. ; Torresa , D. ; Delgadoa , T. ; Delgadoa , Y. ; Ovalles , F. ; Ayala , C. ; Gallignania , M. ; Gallignania , J. M. ; Martin , V. C. Determination of Losartan, Telmisartan, and Valsartan by Direct Injection of Human Urine into a Column-Switching Liquid Chromatographic System with Fluorescence Detection . J. Pharm. Biomed. Anal. 2009 , 50 , 194 – 199 .
   PubMed Web of Science ®Google Scholar
• Sathe , S. R. ; Bari , S. B. Simultaneous Analysis of Losartan Potassium, Atenolol and Hydrochlorothiazide in Bulk and in Tablets by High-Performance Thin-layer Chromatography with UV Absorption Densitometry . Acta Chromatogr. 2007 , 19 , 270 – 278 .
   Web of Science ®Google Scholar
• Durga Rao , D. ; Satyanarayana , N. V. ; Sait , S. S. ; Reddy , Y. R. ; Mukkanti , K. Simultaneous Determination of Losartan Potassium, Atenolol and Hydrochlorothiazide in Pharmaceutical Preparations by Stability-Indicating UPLC . Chromatographia 2009 , 70 ( 3–4 ), 647 .
   Web of Science ®Google Scholar
• Lamprecht , G. ; Kraushofer , T. ; Stoschitzky , K. ; Lidner , W. Enantioselective Analaysis of (R)- and (S)-Atenolol in Urine Samples by High-Performance Liquid Chromatography Column Switching Set-up . J. Chromatogr. B 2000 , 21 , 219 – 226 .
   Google Scholar
• Wilding , I. R. ; Dobson , C. L. ; Davis , S. S. ; Chauhan , S. ; Sparrow , R. A. The Effect of Illeal Brake Activators on the Oral Bio-availability of Atenolol in Man . Int. J. Pharm. 2002 , 248 ( 1–2 ), 61 – 70 .
   PubMedGoogle Scholar
• Barman , R. ; Islam , M. A. ; Ahmed , M. ; Wahed , M. I. I. ; Islam , R. ; Khan , A. ; Hossain , M. B. ; Rahman , B. M. Simultaneous High-Performance Liquid Chromatographic Determination of Atenolol and Amlodipine in Pharmaceutical Dosage Form . Pakistan J. Pharm. Sci. 2007 , 20 ( 4 ), 274 – 279 .
   PubMed Web of Science ®Google Scholar
• Laud , A. J. ; Pednekar , S. ; Vaidya , V. V. ; Joshi , S. S. ; Parekh , S. A. Simultaneous Estimation of Anti-Hypertensive Drugs and a Vitamin A in a Pharmaceutical Formulation . Anal. Chem. 2009 , 8 ( 4 ).
   Google Scholar
• Kumar , P. ; Shukla , S. ; Ganure , A. L. ; Subudhi , B. B. Development and Validation of a Novel Isocratic RP-HPLC Method for Simultaneous Determination of Atenolol and Aspirin in Fixed Dose Combinations . Der Pharm. Chim. 2011 , 3 ( 2 ), 13 – 21 .
   Google Scholar
• Kirtawade , R. R. ; Salve , P. L. ; Kulkarni , A. S. ; Dhabale , P. N. RP-HPLC Method for Simultaneous Estimation of Losartan Potassium and Atenolol in Tablet Formulation . Int. J. Pharm. Sci. 2010 , 1 ( 2 ), 50 – 57 .
   Google Scholar
• International Conference on Harmonization (ICH) . Stability Testing of New Drug Substances and Products (Q1AR2) ; Geneva : IFPMA , 2003 .
   Google Scholar
• Center for Drug Evaluation and Research (CDER) . Reviewer Guidance: Validation of Chromatographic Methods , November 1994 , Division of Communications Management CDER , FDA , Rockville , MD .
   Google Scholar
• Snyder , L. R. ; Kirkland , J. J. ; Glajch , J. L. Practical Method Development. , 2nd ed. ; Hoboken : John Wiley and Sons, Inc. , 1997 , p 653 .
   Google Scholar
• Alpert , A. J. ; Shukla , A. K. Precipitation of Large, High-Abundance Proteins from Serum with Organic Solvents. ABRF 2003 (2/03; Denver): Poster# P111-W, 2003.
   Google Scholar
• U.S. Department of Health and Human Services Food and Drug Administration (USFDA). Guidance for Industry: Bio-analytical Method Validation. Rockville: Center for Drug Evaluation and Research, USFDA, May 2001.
   Google Scholar
• Pal , P. K. ; Ganesan , M. Bioavailability and Bioequivalence in Pharmaceutical Technology. , 1st ed. ; CBS Publishers and Distributors : New Delhi , 1999 , pp 1 – 145 .
   Google Scholar