Development and Validation of a Novel RP-HPLC Method for Estimation of Losartan Potassium in Dissolution Samples of Immediate and Sustained Release Tablets

<table class="table-group" id="tab7"><tr><td><table class="table"><tr><td class="thead-hr" colspan="4"><hr/></td></tr><tr class="thead"><td align="left">Parameter</td><td align="center">Low</td><td align="center">Nominal</td><td align="center">High</td></tr><tr><td class="thead-hr" colspan="4"><hr/></td></tr><tr><td align="left">Wavelength (nm)</td><td align="center">223</td><td align="center">225</td><td align="center">227</td></tr><tr><td align="left">Flow rate (mL/min)</td><td align="center">0.8</td><td align="center">1.0</td><td align="center">1.2</td></tr><tr><td align="left">Temperature (°C)</td><td align="center">20</td><td align="center">25</td><td align="center">30</td></tr><tr class="table-tr"><td colspan="4"><hr class="tbody-hr"/></td></tr></table></td></tr></table>

Chromatography Research International

tab7

Table 7

Table 7: Development and Validation of a Novel RP-HPLC Method for Estimation of Losartan Potassium in Dissolution Samples of Immediate and Sustained Release Tablets 

Table 7 | Development and Validation of a Novel RP-HPLC Method for Estimation of Losartan Potassium in Dissolution Samples of Immediate and Sustained Release Tablets 