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1 2008

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Validation of an HPLC method for analysis of nifedipine residues on stainless-steel surfaces in the manufacture of pharmaceuticals

Milenović D. M., Lazić M. L., Veljković V. B., Todorović Z. B.

Acta Chromatographica

2008

Vol. 20, no. 2

183-194

A simple, sensitive, and convenient HPLC method has been developed, validated, and applied to analysis of nifedipine residues on the stainless-steel surfaces of equipment used in drug manufacture. Cotton swabs moistened with methanol were used to remove residues of the drug from the surfaces; recoveries were 82.26, 86.88, and 88.95% for 25, 125, and 250 µg per swab. The precision of the results, as relative standard deviation (RSD), was <5%. The method was validated over the concentration range 3-50 µg mL-1. Small quantities of residues of the drug and its main impurities were determined by HPLC on an ODS column with methanol-water-phosphate buffer (pH 3; 0.05 M)-sodium heptanesulfonate 65:35:3:0.13 (v/v/v/w) as mobile phase at a flow rate of 0.8 mL min-1. Detection was at 235 nm.