Development and Validation of RP-HPLC Method for Azilsartan Medoxomil Potassium Quantitation in Human Plasma by Solid Phase Extraction Procedure

<table>HPLC-PDA chromatograms of blank plasma sample and LLOQ (1.0 <i>μ</i>g/mL) standard (a); chromatogram of extracted blank plasma (b); Chromatogram of extracted LLOQ sample spiked with 1.0 <i>μ</i>g/mL of calibration standard.</table>

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Figure 2: Development and Validation of RP-HPLC Method for Azilsartan Medoxomil Potassium Quantitation in Human Plasma by Solid Phase Extraction Procedure 

Figure 2 | Development and Validation of RP-HPLC Method for Azilsartan Medoxomil Potassium Quantitation in Human Plasma by Solid Phase Extraction Procedure 