Novel Method of Analysis for the Determination of Residual Formaldehyde by High-Performance Liquid Chromatography

Author:

Delbono Vittoria1ORCID,Larch Christopher P.1ORCID,Newlands Katrina Carol1ORCID,Rhydderch Shona2ORCID,Baddeley Thomas Craven12ORCID,Storey John Mervyn David12ORCID

Affiliation:

1. Department of Chemistry, School of Natural and Computing Sciences, University of Aberdeen, Aberdeen AB24 3UE, UK

2. TauRx Therapeutics Ltd, 395 King Street, Aberdeen AB24 5RP, UK

Abstract

Formaldehyde is commonly used as an alkylating agent in the pharmaceutical industry. Consequently, its residual level in drug substances and/or their intermediates needs to be accurately quantified. Formaldehyde is a small, volatile molecule with a weak chromophore (the carbonyl group), and its direct analysis by GC-FID and HPLC-UV is difficult. For these reasons, the majority of papers found in the literature are based upon a derivatisation process (most commonly using the desensitised explosive 2,4-dinitrophenylhydrazine) prior to the analysis of formaldehyde. A novel high-performance liquid chromatography (HPLC) method with UV detection for its quantification in a pharmaceutical is described in this paper. The method proposed herein is based upon a derivatisation reaction between formaldehyde and 4-methylbenzenesulfonohydrazide (MBSH) before analysis by HPLC-UV. Selectivity, linearity, limit of quantification, accuracy, repeatability, intermediate precision, and solution stability were successfully assessed as per ICH guideline Q2(R1), and the method has also been validated in a good manufacturing practice (GMP) laboratory in the UK.

Funder

TauRx Therapeutics Ltd

Publisher

Hindawi Limited

Subject

Analytical Chemistry

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