Cleaning level acceptance criteria and a high pressure liquid chromatography procedure for the assay of Meclizine Hydrochloride residue in swabs collected from pharmaceutical manufacturing equipment surfaces

Citation
T. Mirza et al., Cleaning level acceptance criteria and a high pressure liquid chromatography procedure for the assay of Meclizine Hydrochloride residue in swabs collected from pharmaceutical manufacturing equipment surfaces, J PHARM B, 19(5), 1999, pp. 747-756
Citations number
17
Categorie Soggetti
Chemistry & Analysis
Journal title
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
ISSN journal
07317085 → ACNP
Volume
19
Issue
5
Year of publication
1999
Pages
747 - 756
Database
ISI
SICI code
0731-7085(199904)19:5<747:CLACAA>2.0.ZU;2-4
Abstract
A method using pharmacologically based and visual limit of detection criter ia to determine the acceptable residue level for Meclizine Hydrochloride (M H) on pharmaceutical manufacturing equipment surfaces after cleaning is des cribed. A formula was used in order to determine the pharmacologically safe cleaning level for MH. This level was termed as specific residual cleaning Level (SRCL) and calculated to be 50 mu g 100 cm(-2). The visual limit of detection (VLOD) was determined by spiking different levels of MH on stainl ess steel plates and having the plates examined by a group of observers. Th e lowest level that could be visually detected by the majority of the obser vers, 62.5 mu g 100 cm(-2), was considered as the VLOD for MH. The lower of the SRCL and VLOD values, i.e. 50 mu g 100 cm(-2),was therefore chosen as the cleaning acceptance criterion. A sensitive reversed-phase HPLC method w as developed and validated for the assay of MH in swabs used to test equipm ent surfaces. Using this method, the mean recoveries of MH from spiked swab s and '180-Grit' stainless steel plates were 87.0 and 89.5% with relative s tandard deviations (RSD) of +/- 3.3 and +/- 2.4%, respectively. The method was successfully applied to the assay of actual swab samples collected from the equipment surfaces. The stability of MH on stainless steel plates, on cleaning swabs and in the extraction solution was investigated. (C) 1998 El sevier Science B.V. All rights reserved.