4.3 Article

Increased stability of S-nitrosothiol solutions via pH modulations

Journal

FREE RADICAL RESEARCH
Volume 46, Issue 2, Pages 214-225

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.3109/10715762.2011.647692

Keywords

S-nitrosothiols; GSNO; pH; decomposition; polymer matrices; UV spectroscopy; ESR spectroscopy

Funding

  1. GVOP KMA [0124]
  2. TAMOP [4 2 2-08/1/KMR-2008-0004]
  3. TET ARG and SIN
  4. Baross G program
  5. Irinyi program
  6. Bolyai Fellowship
  7. veges Fellowship

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S-nitrosothiol (RSNO) solutions represent a valuable source of nitric oxide and could be used as topical vasodilators, but their fast decomposition rate poses a serious obstacle to their potentially widespread therapeutic use. Our aim was to characterize and quantify the effect of pH on S-nitrosothiol formation and decomposition in simple aqueous solutions of S-nitrosoglutathione (GSNO), S-nitroso-N-acetylcysteine (SNAC) and S-nitroso-3-mercaptopropionic acid (SN3MPA). Furthermore, we investigated the effect of storage pH on the stability of GSNO incorporated in poly(ethylene glycol)/ poly(vinyl alcohol) matrices. S-nitrosothiol concentrations were measured spectrophotometrically and laser Doppler scanning method was used to assess dermal blood flow. GSH and NAC solutions reached a complete transformation to nitrosothiols when synthesized using acidic NaNO2 solution. The initial concentration of all investigated RSNOs decreased more slowly with pH adjusted to mildly basic values (8.4-8.8) for the storage period. Polymer gels of PVA/PEG compositions at mildly basic storage pH further reduced the decomposition rate succeeding to contain 46.8% of the initial GSNO concentration for 25 days. This amount of topically administered GSNO was still capable of increasing the dermal blood flow over 200% in human subjects.

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