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
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
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.