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Table 4 Robustness of the proposed HPLC method

From: Simultaneous determination of newly developed antiviral agents in pharmaceutical formulations by HPLC-DAD

Parameter

PAR

DAS

RIT

OMB

RSD % of peak areas

k ± SD

RSD % of peak areas

k ± SD

RSD % of peak areas

k ± SD

RSD % of peak areas

k ± SD

Percentage of acetonitrile in the mobile phase [64, 65 and 66 ml]

0.290

0.48 ± 0.007

0.177

2.08 ± 0.005

0.446

2.81 ± 0.001

0.335

6.11 ± 0.002

pH of the aqueous phase [6.9, 7 and 7.1]

0.363

0.53 ± 0.011

0.178

2.03 ± 0.010

0.413

2.73 ± 0.001

0.471

5.85 ± 0.003

Flow rate [0.9, 1, and 1.1 ml/min]

0.239

0.53 ± 0.005

0.182

2.12 ± 0.005

0.32

2.87 ± 0.000

0.579

6.25 ± 0.003

Injection volume [15, 20, 25 µl]

0.255

0.53 ± 0.024

0.141

1.97 ± 0.026

0.80

2.68 ± 0.01

0.314

5.66 ± 0.007

Detection wavelength [253, 254 and 255 nm]

0.403

0.55 ± 0.007

0.089

1.99 ± 0.003

0.394

2.69 ± 0.001

0.580

5.75 ± 0.002

  1. All results are average of three determinations