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

被引:0
|
作者
Delbono, Vittoria [1 ]
Larch, Christopher P. P. [1 ]
Newlands, Katrina Carol [1 ]
Rhydderch, Shona [2 ]
Baddeley, Thomas Craven [1 ,2 ]
Storey, John Mervyn David [1 ,2 ]
机构
[1] Univ Aberdeen, Sch Nat & Comp Sci, Dept Chem, Aberdeen AB24 3UE, Scotland
[2] TauRx Therapeut Ltd, 395 King St, Aberdeen AB24 5RP, Scotland
关键词
AGGREGATION INHIBITOR THERAPY; CARBONYL-COMPOUNDS; FLUOROMETRIC-DETERMINATION; PHARMACEUTICAL EXCIPIENTS; HPLC; ALDEHYDES; 2,4-DINITROPHENYLHYDRAZINE; DERIVATIZATION; AIR; QUANTIFICATION;
D O I
10.1155/2022/9171836
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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.
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页数:10
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