Validated RP-HPLC Method for the Determination of Buspirone in Pharmaceutical Formulations

Table 2

System suitability and validation parameters.

Parameters	Results
Theoretical plates (𝑁)	5378.36
Retention time (min)	7.057
Asymmetric factor	1.09
LOD (ng/mL)	20
LOQ (ng/mL)	65
Accuracy (%)	98.52
R.S.D. (%)	1.352