Wednesday , 13 December 2017

Tag Archives: RP-HPLC Method

Stability Indicating Method Development and Validation for Oflaxacin and Metronidazole in Bulk and Dosage Form Using RP-HPLC

Sanju Srinivas1, T. Mounika2 1Associate Professor Department of Pharmacy, Ganga Pharmacy College, Nizamabad, Telangana 2Department of Pharmaceutical Analysis, Ganga Pharmacy College, Nizamabad, Telangana ABSTRACT A new method was established for simultaneous estimation of Ofloxacin and Metronidazole by RP-HPLC method. The chromatographic conditions were  successfully  developed  for  the separation  of Ofloxacin  and  Metronidazole  by  using  Agilent  C18  5µ m  (4.6*250mm) column, ... Read More »

Development of Validated Stability Indicating Assay Method by RP-HPLC for Simultaneous Estimation of Azilsartan Medoximil and Chlorthalidone in Their Bulk and Combination Form

S. Priyanka Yadav*1, P. Sowjanya2, Dr. Gampa Vijaya Kumar3 1,2KGR Institute of Technology and Management, Rampally, Kesara, Rangareddy, Telangana, India, 3Professor and Head, Department of Pharmacy, KGR Institute of Technology and Management, Rampally, Kesara, Rangareddy, Telangana, India ABSTRACT Method was established for simultaneous estimation of Azilsartan medoxomil and Chlorthalidone by RP-HPLC method.  The chromatographic conditions were successfully developed for the ... Read More »

Method Development and Validation of Voglibose in pure and Pharmaceutical Dosage form by RP-HPLC

Jogu Anitha*, P. Sunitha, Vijaya Kuchana Department of Pharmaceutical Analysis, Teegala Krishna Reddy College of Pharmacy, Meerpet, Hyderbad. A B S T R A C T The chromatographic conditions were successfully developed for the separation of Voglibose by Deveosil ODS-HG-5 C18 (250×4.6mm, 5cm) column. Flow rate was 1ml/min, mobile phase ratio was 70:30% v/v Acetonitrile : Buffer, UV detection at ... Read More »

Comparative Study for the Analysis of Cefixime trihydrate and its Degraded Products by Two RP-HPLC methods, one its Official and the other Developed Validated Method

Elsadig H. Kh. Adam*1 and Abdalfatah M.Bashir2 1,2Department of Pharmaceutical Chemistry, College of Pharmacy, Prince Sattam bin Abdulaziz University, Riyadh, Al-kharj 11942, Saudi Arabia A B S T R A C T The aim of the present work was aimed to carry out comparative study between method (1) [official method (BP, 2017)] and method (2) [developed validated analytical method (Adam et ... Read More »

A New Validated Stability indicating RP-HPLC Method for the Quantitative Analysis of Phentermine Hydrochloride in Tablet Dosage Form

K.V. Lalitha*1, R. Kiranjyothi2 1Department of Pharmaceutical Analysis, Raghavendra Institute of Pharmaceutical Education and Research, Ananthapuramu – 515001, Andhra Pradesh, India. 2Department of Pharmaceutical Analysis, JNTUA – Oil Technological Research Institute, Ananthapuramu – 515001, Andhra Pradesh, India. A B S T R A C T A novel stability indicating RP-HPLC method was developed for the estimation of Phentermine hydrochloride in ... Read More »

Validated RP-HPLC Method Development for the Simultaneous Estimation of Lisinopril and Hydrochlorthiazide in Bulk and Pharmaceutical Dosage Form

Amarnath Mundra*, Harshini.S, Sireesha. D, Akifulhaque, Vasudha.B Department of Pharmaceutical Analysis and Quality assurance, Anurag group of institutions (Formerly Lalitha college of pharmacy), Hyderabad. A B S T R A C T A simple and cost effective RP-HPLC method is described for the determination of lisinopril and Hydrochlorothiazide in pure form and in pharmaceutical formulations. The drug was highly soluble ... Read More »

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