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Determination of genotoxic impurities of aromatic aldehydes in pharmaceutical preparations by high performance liquid chromatography after derivatization with N-Cyclohexyl-4-hydrazino-1,8-naphthalenediimide.
Xu, Zenghui; Reheman, Abudurexiti; Lu, Zhihao; Yu, Shuiqiang; Sun, Zhiwei; You, Jinmao.
Affiliation
  • Xu Z; Key Laboratory of Life-Organic Analysis of Shandong Province, Qufu Normal University, Qufu 273165, China.
  • Reheman A; Key Laboratory of Life-Organic Analysis of Shandong Province, Qufu Normal University, Qufu 273165, China.
  • Lu Z; Key Laboratory of Life-Organic Analysis of Shandong Province, Qufu Normal University, Qufu 273165, China.
  • Yu S; Key Laboratory of Life-Organic Analysis of Shandong Province, Qufu Normal University, Qufu 273165, China.
  • Sun Z; Key Laboratory of Life-Organic Analysis of Shandong Province, Qufu Normal University, Qufu 273165, China. Electronic address: zhiweisun@qfnu.edu.cn.
  • You J; College of Chemistry and Chemical Engineering, Shaoxing University, Shaoxing 312000, China. Electronic address: jmyou6304@163.com.
J Chromatogr A ; 1722: 464866, 2024 May 10.
Article in En | MEDLINE | ID: mdl-38581976
ABSTRACT
The detection of aromatic aldehydes, considered potential genotoxic impurities, holds significant importance during drug development and production. Current analytical methods necessitate complex pre-treatment processes and exhibit insufficient specificity and sensitivity. This study presents the utilization of naphthalenediimide as a pre-column derivatisation reagent to detect aromatic aldehyde impurities in pharmaceuticals via high-performance liquid chromatography (HPLC). We screened a series of derivatisation reagents through density functional theory (DFT) and investigated the phenomenon of photoinduced electron transfer (PET) for both the derivatisation reagents and the resulting products. Optimal experimental conditions for derivatisation were achieved at 40 °C for 60 min. This approach has been successfully applied to detect residual aromatic aldehyde genotoxic impurities in various pharmaceutical preparations, including 4-Nitrobenzaldehyde, 2-Nitrobenzaldehyde, 1,4-Benzodioxane-6-aldehyde, and 5-Hydroxymethylfurfural. The pre-column derivatisation method significantly enhanced detection sensitivity and reduced the limit of detection (LOD), which ranged from 0.002 to 0.008 µg/ml for the analytes, with relative standard deviations < 3 %. The correlation coefficient (R2) >0.998 demonstrated high quality. In chloramphenicol eye drops, the concentration of 4-Nitrobenzaldehyde was measured to be 8.6 µg/mL below the specified concentration, with recoveries ranging from 90.0 % to 119.2 %. In comparison to existing methods, our work simplifies the pretreatment process, enhances the sensitivity and specificity of the analysis, and offers comprehensive insights into impurity detection in pharmaceutical preparations.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Drug Contamination / Aldehydes / Limit of Detection / Imides / Naphthalenes Language: En Journal: J Chromatogr A Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Drug Contamination / Aldehydes / Limit of Detection / Imides / Naphthalenes Language: En Journal: J Chromatogr A Year: 2024 Document type: Article Affiliation country: