Buffer concentration dramatically affects the stability of S-nitrosothiols in aqueous solutions.
Buffer concentration
Density functional theory
Nitric oxide donor
S-nitroso-N-Acetylpenicillamine
S-nitrosoglutathione
S-nitrosothiol stability
Journal
Nitric oxide : biology and chemistry
ISSN: 1089-8611
Titre abrégé: Nitric Oxide
Pays: United States
ID NLM: 9709307
Informations de publication
Date de publication:
01 01 2022
01 01 2022
Historique:
received:
12
09
2021
revised:
19
11
2021
accepted:
25
11
2021
pubmed:
2
12
2021
medline:
22
2
2022
entrez:
1
12
2021
Statut:
ppublish
Résumé
S-nitrosothiols (RSNOs) are an important group of nitric oxide (NO)-donating compounds with low toxicity and wide biomedical applications. In this paper, we, for the first time, demonstrate that the concentration of buffer remarkably affects the stability of RSNOs including naturally occurring S-nitrosoglutathione (GSNO) and synthetic S-nitroso-N-acetylpenicillamine (SNAP). For a solution with a high concentration of GSNO (e.g., 50 mM) and an initial near-neutral pH, the optimal buffer concentration is close to the GSNO concentration under our experimental conditions. A lower buffer concentration does not have adequate buffer capacity to resist the pH drop caused by GSNO decomposition. The decreased solution pH further accelerates GSNO decomposition because GSNO is most stable at near-neutral pH according to our density functional theory (DFT) calculations. A higher-than-optimal buffer concentration also reduces the GSNO stability because buffer ingredients including phosphate, Tris base, and HEPES consume NO/N
Identifiants
pubmed: 34848361
pii: S1089-8603(21)00122-1
doi: 10.1016/j.niox.2021.11.002
pii:
doi:
Substances chimiques
Buffers
0
Nitrogen Oxides
0
S-Nitrosothiols
0
Solutions
0
Water
059QF0KO0R
nitrogen trioxide
16E0524PXI
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
59-65Informations de copyright
Copyright © 2021 Elsevier Inc. All rights reserved.