Development and Validation of RP-HPLC Method for Quantitative Estimation of Vinpocetine in Pure and Pharmaceutical Dosage Forms

<table class="table-group" id="tab1"><tr><td><table class="table"><tr><td class="thead-hr" colspan="2"><hr/></td></tr><tr class="thead"><td align="left">Parameter</td><td align="center">Value (Mean ±  %RSD)*</td></tr><tr><td class="thead-hr" colspan="2"><hr/></td></tr><tr><td align="left">Peak area</td><td align="center">3457550 ± 0.096</td></tr><tr><td align="left">Tailing factor</td><td align="center">1.109 ± 0.378</td></tr><tr><td align="left">Theoretical plate</td><td align="center">2945.667 ± 0.099</td></tr><tr><td align="left">Retention time</td><td align="center">10.581 ± 0.083</td></tr><tr class="table-tr"><td colspan="2"><hr class="tbody-hr"/></td></tr></table></td></tr><tr class="table-fn"><td>
                  *Mean and % Relative Standard Deviation of six replicates.<br/></td></tr></table>

Chromatographic characteristics of system suitability solution.

Chromatography Research International

tab1

Table 1

Table 1: Development and Validation of RP-HPLC Method for Quantitative Estimation of Vinpocetine in Pure and Pharmaceutical Dosage Forms 