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Simultaneous detection of Homovanillic acid (HVA) and Vanillyl mandelic acid (VMA) in urine sample by HPLC method
Simultaneous detection of Homovanillic acid (HVA) and Vanillyl mandelic acid (VMA) in urine sample by HPLC method
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Simultaneous detection of Homovanillic acid (HVA) and Vanillyl mandelic acid (VMA) in urine sample by HPLC method
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Simultaneous detection of Homovanillic acid (HVA) and Vanillyl mandelic acid (VMA) in urine sample by HPLC method
Simultaneous detection of Homovanillic acid (HVA) and Vanillyl mandelic acid (VMA) in urine sample by HPLC method

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Simultaneous detection of Homovanillic acid (HVA) and Vanillyl mandelic acid (VMA) in urine sample by HPLC method
Simultaneous detection of Homovanillic acid (HVA) and Vanillyl mandelic acid (VMA) in urine sample by HPLC method
Journal Article

Simultaneous detection of Homovanillic acid (HVA) and Vanillyl mandelic acid (VMA) in urine sample by HPLC method

2022
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Overview
Objective: The research was carried out to develop a validated analytical method for assessing the biogenic amines metabolites Vanillyl mandelic acid (VMA) and Homovanillic acid (HVA) simultaneously in biological fluids by High performance liquid chromatography- Photodiode Array (HPLC-PDA). Method: An HPLC technique was developed and validated for the measurement of VMA and HVA in artificial urine samples. The chromatographic separation was achieved on a Kromasil C8, 5µm (125 X 4.6 mm) column at 250C with combination of mobile phase of acetonitrile: 0.1 % o-phosphoric acid (30:70 v/v), flow rate of 0.9 mL/min using an Shimadzu HPLC system with LC Solutions liquid chromatography software. Different mobile phases were used on a trial and error basis to separate these two metabolites. Validation of ICH parameters in terms of linearity, accuracy, repeatability, precision, and robustness of methodology was performed. Result: The separation of vanillyl mandelic acid and homovanillic acid was achieved using a highresolution HPLC technique. The linearity range for VMA and HVA was selected from 10 µg/mL to 60 µg/mL, and were found to be linear, with coefficients of determination (r2) of 0.996 and 0.990 for both metabolites, respectively. The detection limits for VMA and HVA were 1.96 µg/mL and 1.31 µg/mL, respectively, with quantification limits of 5.96 µg/mL and 3.97 µg/mL. For repeatability, precision, and robustness parameters, the results demonstrated a low percent RSD value. Conclusion: A validated HPLC-PDA approach was developed for quantifying Vanillyl mandelic acid and Homovanillic acid in urine samples.