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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
(
Avtor
),
ID
Žnidarič, Mateja
(
Avtor
),
ID
Gallou, Fabrice
(
Avtor
),
ID
Časar, Zdenko
(
Avtor
)
PDF - Predstavitvena datoteka,
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MD5: 9282CBF358C7451B4F2212CAD9978199
URL - Izvorni URL, za dostop obiščite
https://pubs.acs.org/doi/10.1021/acsomega.2c06615
Galerija slik
Izvleček
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.
Jezik:
Angleški jezik
Ključne besede:
N-nitrosamines
,
metalloporphyrins
,
UV-Vis spectra
,
cobalt
,
impurities
,
metals
,
pyrroles
,
sensors
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
FFA - Fakulteta za farmacijo
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2023
Št. strani:
Str. 1154-1167
Številčenje:
Vol. 8, iss. 1
PID:
20.500.12556/RUL-144319
UDK:
615.1
ISSN pri članku:
2470-1343
DOI:
10.1021/acsomega.2c06615
COBISS.SI-ID:
137131523
Datum objave v RUL:
14.02.2023
Število ogledov:
574
Število prenosov:
108
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
ACS omega
Skrajšan naslov:
ACS omega
Založnik:
American Chemical Society
ISSN:
2470-1343
COBISS.SI-ID:
525873945
Licence
Licenca:
CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:
To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Projekti
Financer:
Drugi - Drug financer ali več financerjev
Program financ.:
Lek Pharmaceuticals d.d., a Sandoz company, Novartis Genesis Labs project, Cohort Three
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