Transcription of HPLC method development for the simultaneous …
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*Correspondence: S. Alt n z. Hacettepe University, Faculty of Pharmacy, Department of Analytical Chemistry. 06100 - Ankara- TURKEY. E-mail: Journal of Pharmaceutical Sciencesvol. 46, n. 4, , 2010 HPLC method development for the simultaneous analysis of amlodipine and valsartan in combined dosage forms and in vitro dissolution studiesMustafa elebier1, Mustafa Sinan Kaynak2,3, Sacide Alt n z1,*, Selma Sahin21 Department of Analytical Chemistry, Faculty of Pharmacy, Hacettepe University, Ankara, Turkey, 2 Department of Pharmaceutical Technology, Faculty of Pharmacy, Hacettepe University, Ankara, Turkey, 3 Department of Pharmaceutical Technology, Faculty of Pharmacy, In n University, Malatya, TurkeyA simple, rapid and reproducible HPLC method was developed for the simultaneous determination of amlodipine and valsartan in their combined dosage forms, and for drug dissolution studies. A C18 column (ODS 2, 10 m, 200 x mm) and a mobile phase of phosphate buffer (pH , mol L-1):acetonitrile: methanol (46:44:10 v/v/v) mixture were used for separation and quantification.
HPLC method development for the simultaneous analysis of amlodipine and valsartan 763 Array Detector (Waters, USA). A C18 column (Waters Spherisorp (PSS832514) ODS 2, 10 µm, 200 x 4.6 mm;
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COMPARISON OF DISSOLUTION PROFILES:, Dissolution, Comparison, Comparison of dissolution profile of extended, Comparison of US Pharmacopeia Simulated, Guideline for Bioequivalence, Guideline on quality of oral modified release, Friability and improve tablet performance, Friability and improve tablet performance during