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Chromatography Research International
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Chromatography Research International
/
2016
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Article
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Tab 5
/
Research Article
Validated Stability Indicating Chromatographic Method for the Simultaneous Estimation of Camylofin with NSAID Drugs and a New Approach of Method Transfer from Classical HPLC to a Modern UPLC Instrument
Table 5
System suitability results.
System suitability parameter
% RSD
(NMT
2.0)
Validation parameters
Drugs
CMF
DCF
Solution stability
0.24
0.86
Specificity
0.32
1.05
Limit of quantification
0.38
0.15
Linearity
0.77
0.23
Method precision
0.61
0.53
Intermediate precision
0.41
1.10
Accuracy
0.12
0.10
Robustness
0.53
0.17
Relative standard deviation.
Not more than.