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Development and Validation of RP-HPLC Method for the Estimation of L-Methyl Folate and Tofisopam in combined Formulation
The non-methylated form, folic acid (vitamin B9), is a synthetic folate form and must undergo enzymatic reduction to become biologically active by methylenetetrahydrofolate reductase (MTHFR)1-3. Knowledge of its molecular weight, polarity, ionic character, pKa values, absorption wavelength, compound...
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Published in: | Asian Journal of Research in Chemistry 2021, Vol.14 (1), p.1-9 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | The non-methylated form, folic acid (vitamin B9), is a synthetic folate form and must undergo enzymatic reduction to become biologically active by methylenetetrahydrofolate reductase (MTHFR)1-3. Knowledge of its molecular weight, polarity, ionic character, pKa values, absorption wavelength, compound purity and solubility must be understood in order to create a new HPLC process for any drug.8,9 for the estimation of Lmethylfolate and Tofisopam in pharmaceutical dosage form, The objective of this research was to develop and validate a process of HPLC that was sensitive, accurate, precise and specific. Chromatographic Terms: Using Isocratic elution and Acetonitrile, chromatographic analysis was carried out: 0.1 percent PH modified to 2.5 with OPA (50:50 by volume) as a mobile phase and filtered through 0.45p membrane filter paper. Validating: The aim of the optimized chromatographic separation was to achieve a resolution above 1.5 between all components, the tailing factor is less than 2.0, and the plate count will be more than 2000 w.r. to the stationary, mobile phase compositions, and flow rate, volume of sample, wavelength and temperature detection. |
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ISSN: | 0974-4169 0974-4150 |
DOI: | 10.5958/0974-4150.2021.00005.5 |