Literature DB >> 12191714

Development and validation of an LC assay for sumatriptan succinate residues on surfaces in the manufacture of pharmaceuticals.

María J Nozal1, José L Bernal, L Toribio, María T Martín, Francisco J Diez.   

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 degrees 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.

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Year:  2002        PMID: 12191714     DOI: 10.1016/s0731-7085(02)00336-9

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  3 in total

1.  Cleaning level acceptance criteria and HPLC-DAD method validation for the determination of Nabumetone residues on manufacturing equipment using swab sampling.

Authors:  Nitin Dubey; Nidhi Dubey; Mayank Mandhanya; Dinesh Kumar Jain
Journal:  J Pharm Anal       Date:  2012-04-25

2.  Development and Validation of Liquid Chromatography-Tandem Mass Spectrometry Method for Simple Analysis of Sumatriptan and its Application in Bioequivalence Study.

Authors:  Wisut Wichitnithad; Siriwan Nantaphol; Petploy Vicheantawatchai; Thanyaporn Kiatkumjorn; Wachirasak Wangkangwan; Pornchai Rojsitthisak
Journal:  Pharmaceuticals (Basel)       Date:  2020-01-24

3.  Development and validation of a UPLC method for the determination of duloxetine hydrochloride residues on pharmaceutical manufacturing equipment surfaces.

Authors:  Navneet Kumar; D Sangeetha; P Balakrishna
Journal:  Pharm Methods       Date:  2011-07
  3 in total

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