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Battu, Prasanna Reddy
- Development and Validation of RP-HPLC for the Rabeprazole sodium in Pharmaceutical Formulations and Human Plasma
Abstract Views :175 |
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Authors
Affiliations
1 Dept. Quality Control and Analytical R and D, Smilax Laboratories Limited, Jeedimetla, Hyderabad-500055, A.P, IN
2 Department of Entomology and Plant Pathology, Auburn University, US
1 Dept. Quality Control and Analytical R and D, Smilax Laboratories Limited, Jeedimetla, Hyderabad-500055, A.P, IN
2 Department of Entomology and Plant Pathology, Auburn University, US
Source
Asian Journal of Research in Chemistry, Vol 2, No 1 (2009), Pagination: 49-51Abstract
A simple, selective, accurate high Performance Liquid Chromatographic (HPLC) method was developed and validated for the analysis of Rebeprazole sodium. Chromatographic separation achieved isocratically on a C18 column [Use Inertsil C18, 5 μ, 150 mm×4.6 mm] utilizing a mobile phase of acetonitrile/phosphate buffer (70:30, v/v, pH 7.0) at a flow rate of 0.8 ml/min with UV detection at 228 nm. The retention time of Rabeprazole sodium was 2.44 min. The method is accurate (99.15-101.85%), precise (intra-day variation 0.13-1.56% and inter-day variation 0.30-1.60%) and linear within range 0.1-30 μg/ml (R2=0.999) concentration and was successfully used in monitoring left over drug. The detection limit of Rabeprazole sodium at a signal-to-noise ratio of 3 was 1.80 ng/ml in human plasma while quantification limit in human serum was 5.60 ng/ml. The proposed method is applicable to routine analysis of Rabeprazole sodium in pharmaceutical formulations as well as in human plasma samples.Keywords
Rabeprazole Sodium, RP-HPLC, Validation, Human Blood Samples, Pharmaceutical Dosage Forms.- RP-HPLC Method for Simultaneous Estimation of Paracetamol and Ibuprofen in Tablets
Abstract Views :176 |
PDF Views:0
Authors
Affiliations
1 Dept. Quality Control and Analytical R and D, Smilax Laboratories Limited, Jeedimetla, Hyderabad-500055, A.P, IN
2 Department of Entomology and Plant Pathology, Auburn University, US
1 Dept. Quality Control and Analytical R and D, Smilax Laboratories Limited, Jeedimetla, Hyderabad-500055, A.P, IN
2 Department of Entomology and Plant Pathology, Auburn University, US
Source
Asian Journal of Research in Chemistry, Vol 2, No 1 (2009), Pagination: 70-72Abstract
A simple, selective, accurate high Performance Liquid Chromatographic (HPLC) method was developed and validated for the analysis of Paracetamol and Ibuprofen. Chromatographic separation achieved isocratically on a C18 column [Use Inertsil C18, 5 μ, 150 mm×4.6 mm] utilizing a mobile phase of acetonitrile/phosphate buffer (60:40, v/v, pH 7.0) at a flow rate of 0.8 ml/min with UV detection at 260 nm. Aceclofenac was used as an internal standard. The retention time of ibuprofen, paracetamol and aceclofenac was 2.48, 4.45 and 6.34 min respectively. The developed method was validated in terms of accuracy, precision, linearity, limit of detection, limit of quantitation. This study aimed at developing and validating an HPLC method, being simple, accurate and selective, and the proposed method can be used for the estimation of these drugs in combined dosage forms.Keywords
Paracetamol, Ibuprofen, RP-HPLC, Validation.- Isolation of Secondary Metabolites from Pseudomonas fluorescens and its Characterization
Abstract Views :220 |
PDF Views:0
Authors
Affiliations
1 Dept. Quality Control and Analytical R and D, Smilax Laboratories Limited, Jeedimetla, Hyderabad-500055, A.P, IN
2 Department of Entomology and Plant Pathology, Auburn University, US
1 Dept. Quality Control and Analytical R and D, Smilax Laboratories Limited, Jeedimetla, Hyderabad-500055, A.P, IN
2 Department of Entomology and Plant Pathology, Auburn University, US