Liquid Chromatographic Method for the Quantification of Antipsychotic Agent Iloperidone in Pharmaceutical Formulation

<table class="table-group" id="tab2"><tr><td><table class="table"><tr><td class="thead-hr" colspan="2"><hr/></td></tr><tr class="thead"><td align="left">System suitability parameters</td><td align="center">ILO</td></tr><tr><td class="thead-hr" colspan="2"><hr/></td></tr><tr><td align="left">Retention time (min)</td><td align="center">11.6</td></tr><tr><td align="left">Theoretical plates/meter</td><td align="center">5353.92</td></tr><tr><td align="left">Asymmetric factor</td><td align="center">1.06</td></tr><tr class="table-tr"><td colspan="2"><hr class="tbody-hr"/></td></tr></table></td></tr></table>

System suitability test parameters for the proposed method.

International Scholarly Research Notices

tab2

Table 2

Table 2: Liquid Chromatographic Method for the Quantification of Antipsychotic Agent Iloperidone in Pharmaceutical Formulation 