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Does the red shift in UV–Vis spectra really provide a sensing option for detection of N-nitrosamines using metalloporphyrins?
ID Trampuž, Marko (Author), ID Žnidarič, Mateja (Author), ID Gallou, Fabrice (Author), ID Časar, Zdenko (Author)

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Abstract
N-nitrosamines are widespread cancerogenic compounds in human environment, including water, tobacco products, food, and medicinal products. Their presence in pharmaceuticals has recently led to several recalls of important medicines from the market, and strict controls and tight limits of N-nitrosamines are now required. Analytical determination of N-nitrosamines is expensive, laborious, and time-inefficient making development of simpler and faster techniques for their detection crucial. Several reports published in the previous decade have demonstrated that cobalt porphyrin-based chemosensors selectively bind N-nitrosamines, which produces a red shift of characteristic Soret band in UV−Vis spectra. In this study, a thorough re-evaluation of metalloporphyrin/N-nitrosamine adducts was performed using various characterization methods. Herein, we demonstrate that while N-nitrosamines can interact directly with cobalt-based porphyrin complexes, the red shift in UV−Vis spectra is not selectively assured and might also result from the interaction between impurities in N-nitrosamines and porphyrin skeleton or interaction of other functional groups within the N-nitrosamine structure and the metal ion within the porphyrin. We show that pyridine nitrogen is the interacting atom in tobacco-specific N-nitrosamines (TSNAs), as pyridine itself is an active ligand and not the N-nitrosamine moiety. When using Co(II) porphyrins as chemosensors, acidic and basic impurities in dialkyl N-nitrosamines (e.g., formic acid, dimethylamine) are also UV−Vis spectra red shift-producing species. Treatment of these N-nitrosamines with K$_2$CO$_3$ prevents the observed UV−Vis phenomena. These results imply that cobalt-based metalloporphyrins cannot be considered as selective chemosensors for UV−Vis detection of N-nitrosamine moiety-containing species. Therefore, special caution in interpretation of UV−Vis red shift for chemical sensors is suggested.

Language:English
Keywords:N-nitrosamines, metalloporphyrins, UV-Vis spectra, cobalt, impurities, metals, pyrroles, sensors
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:FFA - Faculty of Pharmacy
Publication status:Published
Publication version:Version of Record
Year:2023
Number of pages:Str. 1154-1167
Numbering:Vol. 8, iss. 1
PID:20.500.12556/RUL-144319 This link opens in a new window
UDC:615.1
ISSN on article:2470-1343
DOI:10.1021/acsomega.2c06615 This link opens in a new window
COBISS.SI-ID:137131523 This link opens in a new window
Publication date in RUL:14.02.2023
Views:576
Downloads:108
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Record is a part of a journal

Title:ACS omega
Shortened title:ACS omega
Publisher:American Chemical Society
ISSN:2470-1343
COBISS.SI-ID:525873945 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Projects

Funder:Other - Other funder or multiple funders
Funding programme:Lek Pharmaceuticals d.d., a Sandoz company, Novartis Genesis Labs project, Cohort Three

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