A novel stability indicating RP-HPLC method development and validation for estimation of Phenylephrine hydrochloride and Bromhexine hydrochloride in their tablet dosage form.
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چکیده
منابع مشابه
Development and Validation of Rp-hplc Method for Estimation of Atemoxetine Hydrochloride in Tablet Dosage Form
A RP-HPLC method was developed for the estimation of Atomoxetine Hydrochloride in tablet formulation, which is novel to the market. Chromatographic separation of the drug was achieved on a ENABLE C-18 G, 5μm, column (250 × 4.6 mm) using a mobile phase, Methanol: Ammonium phosphate buffer pH-3 (80:20 V/V) at a flow rate of 1ml/min. The drug eluted was monitored at 227 nm. The retention time was ...
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The objective of the present work was to develop a stability-indicating RP-HPLC method for duloxetine hydrochloride (DUL) in the presence of its degradation products generated from forced decomposition studies. The drug substance was found to be susceptible to stress conditions of acid hydrolysis. The drug was found to be stable to dry heat, photodegradation, oxidation and basic condition attem...
متن کاملRP-HPLC method development for the estimation of Levocetirizine and Phenylephrine hydrochloride in combined dosage form
A rapid, accurate RP Levocetirizine and phenylephrine separation was achieved on column Luna 5u C18 (20mm X 4mm) using mobile phase of methanol: Pot. Dihydrogen Phosphate Buffer (pH 6.0), (70:30) .The UV detection was performed at 251nm with flow rate of 1.0 mL Phenylephrine hydrochloride was found to be 8.42 min and 2.70 min with mean recovery 100.64 & 100.40% respectively. The proposed method...
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A new simple, fast accurate and reproducible reverse phase high performance liquid chromatographic method has been developed and validated for simultaneous estimation of Metformin Hydrochloride and Glimepiride from tablet dosage form. The method was developed using Waters HPLC system on C18 column (Spherisorb ODS 2: 250mm x 4.6 μm) using a mixture of 25mM Phosphoric Acid pH 3.0 (with KOH) and A...
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Objectives: To perform stability indicating analytical method development and validation of Lafutidine in tablet dosage form by reverse phase HPLC method. Materials and Methods: The method was developed employing isocratic RP-HPLC and validated for assay of Lafutidine in tablet dosage form. The method employs the use of a UV detector. Results: The developed assay method was found to be accurate...
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ژورنال
عنوان ژورنال: Journal of Current Pharma Research
سال: 2016
ISSN: 2230-7834,2230-7842
DOI: 10.33786/jcpr.2016.v06i03.004