Simultaneous Estimation of Atorvastatin Calcium, Ramipril and Aspirin in Capsule Dosage Form by RP-LC
Autor: | Natvarlal J. Patel, Hiral J. Panchal, I. S Rathod, Bhanubhai N Suhagia, Bhavesh H. Patel |
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Rok vydání: | 2008 |
Předmět: |
Detection limit
Chromatography Chemistry Organic Chemistry Clinical Biochemistry chemistry.chemical_element Reversed-phase chromatography Capsule Dosage Form Calcium Biochemistry High-performance liquid chromatography Dosage form Analytical Chemistry medicine Antipyretic Quantitative analysis (chemistry) medicine.drug |
Zdroj: | Chromatographia. 69:91-95 |
ISSN: | 1612-1112 0009-5893 |
DOI: | 10.1365/s10337-008-0831-z |
Popis: | A simple, sensitive, precise and accurate reversed phase liquid chromatographic method has been developed for the simultaneous estimation of atorvastatin (AT) calcium, ramipril (RA) and aspirin (AS) from capsule dosage form. The method was developed using a Phenomenex Luna C18 (250 mm, 4.6 mm i.d., 5 µm) column with a mobile phase consisting of 0.1%, orthophosphoric acid buffer:acetonitrile:methanol (45:50:5 v/v/v), pH 3.3, at a flow rate of 1 mL min−1. Detection was carried out with ultra-violet detection at 210 nm. The retention times were about 12.19, 2.35, and 3.95 min for AT calcium, RA and AS, respectively. The developed method was validated for linearity, accuracy, precision, limit of detection, limit of quantitation and robustness. The linearity ranges were 1–6 µg mL−1 for AT calcium, 0.5–3 µg mL−1 for RA and 7.5–45 µg mL−1 for AS with mean recoveries of 100.59 ± 0.68, 100.62 ± 0.83 and 100.49 ± 0.73% for AT calcium, RA and AS, respectively. Limit of detection obtained were 29.85 ng mL−1 for AT calcium, 4.71 ng mL−1 for RA and 85.13 ng mL−1 for AS. Impurity of salicylic acid was found in capsule dosage form at the retention time of about 4.84 min. The proposed method can be used for the estimation of these drugs in combined dosage forms. |
Databáze: | OpenAIRE |
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