Development and Validation of an HPLC Method for the Analysis of Saxagliptin in Bulk Powder
DEVELOPMENT AND VALIDATION OF STABILITY INDICATING RP-HPLC METHOD FOR SAXAGLIPTIN AND METFORMIN IN TABLET DOSAGE FORM
... 4. Development and Validation of HPLC method: Present study was conducted to obtain a new, affordable, cost-effective and convenient method for HPLC determination of ...
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Development and Validation of an HPLC Method for the Analysis of Saxagliptin in Bulk Powder
... proposed method was found to be simple, precise, accurate, rapid and specific for determination of Saxagliptin from pure and its dosage ...for method development is very simple to prepare and ...
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DEVELOPMENT AND VALIDATION RP HPLC METHOD FOR SAXAGLIPTIN MONOHYDRATE IN BULK AND PHARMACEUTICAL DOSAGE FORM
... ( HPLC Grade) saxagliptin monohydrat drug was procured from Glenmark Generics ...no HPLC 3000 Series, detector UV-3000-M Column C1 8 ( Grace) ...
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Development and validation of an HPLC method for analysis of etoricoxib in human plasma
... The above mentioned bioanalytical method was used in bioequivalence study of etoricoxib. The study was approved by the ethics committee of Jadavpur University, Kolkata, India. It was an open, randomized crossover ...
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A Study of New Method Development, Validation and Forced Degradation for Simultaneous Analysis of Dapagliflozin and Saxagliptin in Pharmaceutical Dosage Form by HPLC Method
... (RP-HPLC) method has been developed for simultaneous quantification of Dapagliflozin (DGFZ) and Saxagliptin (SGPT) in combined dosage ...developed method has been validated with respect to ...
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DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR QUANTITATIVE ANALYSIS OF ETRAVIRINE IN PURE AND PHARMACEUTICAL FORMULATIONS
... the method was determined by standard addition ...addition method was performed at 50%, 100% and 150% level of 100 ...proposed method. This indicates that the proposed method was ...the ...
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STABILITY INDICATING RP HPLC METHOD AND ITS VALIDATION FOR ANALYSIS OF METFORMIN HYDROCHLORIDE & SAXAGLIPTIN IN BULK AND PHARMACEUTICAL DOSAGE FORM
... the method was studied by recovery ...for Saxagliptin and Metformin hydrochloride ranged from ...the method was determined from one lot of combined dosage ...developed method experimental ...
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Development and Validation of A UV Spectroscopic Method for Analysis of Paracetamol in Bulk Powder and Tablet
... The working standard solutions for the drug having concentration 2 to 24µg/ml were prepared with phosphate buffer 6.8 from the stock solution. The linearity was determined by plotting standard calibration curves for the ...
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A RP-HPLC METHOD DEVELOPMENT AND VALIDATION FOR THE ESTIMATION OF DIHYDRALAZINE IN BULK AND PHARMACEUTICAL DOSAGE FORMS
... the method, two parameters (temperature, composition of mobile phase) from the optimized chromatographic conditions were ...Statistical analysis showed no significant difference between results obtained ...
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DEVELOPMENT AND VALIDATION OF REVERSE-PHASE HPLC METHOD FOR ESTIMATION OF KETOCONAZOLE IN BULK DRUG
... the method was investigated by serially diluting the working standard to give a concentration range of 1-50 µm/ml and 20 µl from this was ...The method was validated for linearity, precision, accuracy, ...
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DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR THE SIMULTANEOUS ESTIMATION OF DOXOFYLINE AND SERTRALINE IN PURE BULK AND PHARMACEUTICAL DOSAGE FORMS
... RP- HPLC method for the analysis of sertraline and doxofyline and developed method will be validated for parameters like accuracy, linearity, precision, specificity, robustness, and system ...
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METHOD DEVELOPMENT AND VALIDATION FOR THE ANALYSIS OF PENCICLOVIR AND RELATED IMPURITY IN BULK AND PHARMACEUTICAL DOSAGE FORMS BY RP HPLC
... developed method was validated according to ICH guide ...Statistical analysis revealed that the proposed method was found to be highly sensitive, precise, accurate, robust and ...the analysis ...
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DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR DIAZEPAM AND IMIPRAMINE IN BULK & PHARMACEUTICAL FORMULATIONS
... and were purchased from Merck and CDH respectively. Potassium dihydrogen phosphate was purchased from Rankem. The suspension formulation (Parfil, Perron Pharmaceuticals, Karampura, New Delhi, India) containing 125 mg of ...
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DEVELOPMENT AND VALIDATION OF A METHOD FOR SIMULTANEOUS DETERMINATION OF DAPAGLIFLOZIN AND SAXAGLIPTIN IN A FORMULATION BY RP UPLC
... robust method for the analysis of Saxagliptin and Dapagliflozin was developed and its applicability as a method for analyzing stability was ...The method was found to be specific, ...
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Development and Validation of Rp – Hplc Method for the Simultaneous Determination of Hydrochlorothiazide, Amlodipine Besylate and Telmisartan in Bulk and Pharmaceutical Formulation
... considered for monitoring the drugs at 333nm (Figure 2). Solutions of each substance in the mobile phase were also injected directly for HPLC analysis and the responses (peak area) were recorded at 333nm. ...
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RP-HPLC METHOD DEVELOPMENT AND VALIDATION OF BALSALAZIDE IN BULK AND CAPSULE DOSAGE FORM
... RP-HPLC method was validated as per ICH guidelines and can be applied for the determination of Balsalazide in bulk and capsule dosage ...The method was found to be system suitability, ...
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DEVELOPMENT AND VALIDATION OF A NEW RP-HPLC METHOD FOR THE DETERMINATION OF DACLATASVIR DIHYDROCHLORIDE IN BULK AND PHARMACEUTICAL DOSAGE FORMS
... The present research work has been carried out by using 50% of acetonitrile and tri-ethylamine buffer (pH 5.00), for buffer preparation only need about 2.4 mL tri-ethylamine and less percentage organic solvent used would ...
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DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR THE ESTIMATION OF PROCESS RELATED IMPURITIES FROM NIMODIPINE BULK AND FORMULATION
... in bulk and formulations was synthesized, characterized and the RP-HPLC method was developed according to ICH Q2B guidelines for quantitation of impurity in bulk and ...
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DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR THE SIMULTANEOUS ESTIMATION OF NEBIVOLOL AND VALSARTAN IN PURE BULK AND PHARMACEUTICAL DOSAGE FORM
... UV-Visible, HPLC, HPTLC, Volta metric methods reported for the estimation nebivolol and valsartan pharmaceutical dosage ...RP-HPLC method for the analysis of nebivolol and valsartan and ...
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DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR THE ESTIMATION OF ROSUVASTATIN CALCIUM IN BULK AND TABLET DOSAGE FORM
... RP-HPLC method was developed for the determination of Rosuvastatin in pure and pharmaceutical ...formulations. Method was carried on Symmetry C18 column (100 X ...proposed method obeyed ...
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