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Development and validation of an LC assay for sumatriptan succinate residues on surfaces in the manufacture of pharmaceuticals
- Source :
- Journal of pharmaceutical and biomedical analysis. 30(2)
- Publication Year :
- 2002
-
Abstract
- A high performance liquid chromatographic (HPLC) method for the assay of sumatriptan succinate residues in swabs collected from manufacturing equipment surfaces was developed and validated in order to control a cleaning procedure. The swabbing procedure using two cotton swabs moistened with water was validated applying a wipe-test and a HPLC method developed to determine low quantities of the drug. The HPLC method involves a C18 column at 25 °C, a mixture of ammonium phosphate monobasic (0.05 M)–acetonitrile (84:16, v/v) as a mobile phase and UV detection at 228 nm. Using the proposed method, the average recoveries obtained are of 88.5% for vinyl, 94.2% for glass and 95.2% for stainless steel plates with RSD of 5.5 (n=36), 2.3 (n=36), 2.2% (n=36), respectively. The method was successfully applied to the assay of real swab samples collected from the equipment surfaces.
- Subjects :
- Residue (complex analysis)
Chromatography
Chemistry
Ammonium phosphate
Sumatriptan
Monobasic acid
Clinical Biochemistry
Pharmaceutical Science
Reversed-phase chromatography
Cleaning validation
High-performance liquid chromatography
Analytical Chemistry
chemistry.chemical_compound
Sumatriptan Succinate
Drug Discovery
Steel plates
Technology, Pharmaceutical
Spectroscopy
Chromatography, High Pressure Liquid
Subjects
Details
- ISSN :
- 07317085
- Volume :
- 30
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Journal of pharmaceutical and biomedical analysis
- Accession number :
- edsair.doi.dedup.....855973150086f4bb4f12f90274efeb0a