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NDMA in macrolides : GC-MS/MS method for its detection and study of its formation
ID Golob, Nejc (Author), ID Grahek, Rok (Author), ID Roškar, Robert (Author)

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Abstract
N-nitrosodimethylamine (NDMA) is the most commonly found N-nitrosamine in pharmaceutical drug substances (DSs) and drug products. This paper investigates the potential of macrolide antibiotics, containing dimethylamino group, as precursors for NDMA formation in pharmaceuticals. A direct injection GC–MS/MS method was qualified for the quantification of NDMA in various macrolide DSs and film-coated tablets, and the use of pyrrolidine as a scavenger was further emphasized. As an alternative method, GC–MS/MS method with solid phase microextraction was tested, which proved to be unsuitable due to the limited water solubility of macrolides. However, its applicability was confirmed for the analysis of NDMA in water-soluble DSs, such as metformin. The observations regarding the solubility can be applied to a wide range of drug products and analytical methods for the accurate determination of nitrosamines. Various macrolide DSs showed significant levels of NDMA, confirming macrolides as NDMA precursors. In macrolide film-coated tablets, NDMA traces of up to about 70 ppb and 165 ppb were found in azithromycin and spiramycin, respectively, greatly exceeding the acceptable intake limit for NDMA. These findings confirmed the potential of macrolides for NDMA formation which was further enhanced in spiramycin that contains two dimethylamino groups. Furthermore, it has been shown that a stable DS form can successfully prevent NDMA formation, as observed with azithromycin dihydrate. The NDMA content in macrolides can also increase significantly during storage as shown in an accelerated stability study, which together with the levels above the AI limits highlights the need for greater attention and consideration.

Language:English
Keywords:N-nitrosodimethylamine, NDMA, macrolide antibiotics, film-coated tablets, GC–MS/MS, direct injection, solid phase microextraction, stability study
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:FFA - Faculty of Pharmacy
Publication status:Published
Publication version:Version of Record
Year:2025
Number of pages:10 str.
Numbering:Vol. 211, art. 107135
PID:20.500.12556/RUL-169466 This link opens in a new window
UDC:615.45
ISSN on article:0928-0987
DOI:10.1016/j.ejps.2025.107135 This link opens in a new window
COBISS.SI-ID:237580803 This link opens in a new window
Publication date in RUL:29.05.2025
Views:337
Downloads:114
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Record is a part of a journal

Title:European journal of pharmaceutical sciences
Shortened title:Eur. j. pharm. sci.
Publisher:Elsevier
ISSN:0928-0987
COBISS.SI-ID:17553413 This link opens in a new window

Licences

License:CC BY-NC 4.0, Creative Commons Attribution-NonCommercial 4.0 International
Link:http://creativecommons.org/licenses/by-nc/4.0/
Description:A creative commons license that bans commercial use, but the users don’t have to license their derivative works on the same terms.

Secondary language

Language:Slovenian
Keywords:N-nitrozodimetilamin, NDMA, makrolidni antibiotiki, filmsko obložene tablete, GC–MS/MS, neposredno injiciranje, trdnofazna mikroekstrakcija, stabilnostne študije, farmacevtske oblike

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