Literature DB >> 11459315

Validation of a liquid chromatographic method for the determination of ranitidine hydrochloride residues on surfaces in the manufacture of pharmaceuticals.

M J Nozal1, J L Bernal, L Toribio, M T Martín, F J Diez.   

Abstract

A liquid chromatographic method for determination of the residues of ranitidine hydrochloride on various surfaces employed in drug manufacture is described. Cotton swabs, moistened with a methanol-water (1:1, v/v) mixture were used to remove any residues of drugs from glass, vinyl, and stainless steel surfaces, and gave recoveries of 85%, 78% and 90%, respectively. Residues were determined by high-performance liquid chromatography on a C18 column at 25 degrees C with methanol-ammonium acetate (40:60 v/v) pH 6.7 as the mobile phase and detection at 320 nm. The method was validated over a concentration range of 20-10 000 ng/ml and had a detection limit of 2 ng/ml.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11459315     DOI: 10.1016/s0021-9673(01)00803-2

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  1 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
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.