Development and Validation of Stability Indicating RP-HPLC Method for Estimation of Ceftaroline Fosamil in Bulk and Its Parenteral Dosage Forms

Table 3

Validation parameters.

Parameters	Ceftaroline fosamil
Retention time (min)	3.533
Peak asymmetric factor	1.02
Number of theoretical plates	6803
% RSD of peak area	0.98
Linearity range (µg/mL)	40–120
LOD (µg/mL)	1.64
LOQ (µg/mL)	4.85
Accuracy (%)	98.76–99.98
Precision (% RSD)
Intraday precision (𝑛=3)	0.45–0.98
Interday precision (𝑛=3)	0.65–1.25