Research Article
Validated RP-HPLC Method for the Determination of Buspirone in Pharmaceutical Formulations
Table 2
System suitability and validation parameters.
| Parameters | Results |
| Theoretical plates | 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 |
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