The [Ru(Hedta)NO] 0,1- system: Structure, chemical reactivity and biological assays

The [Ru II(Hedta)NO +] complex is a diamagnetic species crystallizing in a distorted octahedral geometry, with the Ru-N(O) length 1.756(4) Å and the RuNO angle 172.3(4)°. The complex contains one protonated carboxylate (pK a = 2.7 ± 0.1). The [Ru II(Hedta)NO +] complex undergoes a nitrosyl-centered...

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Autores principales: Zanichelli, P.G., Miotto, A.M., Estrela, H.F.G., Soares, F.R., Grassi-Kassisse, D.M., Spadari-Bratfisch, R.C., Castellano, E.E., Roncaroli, F., Parise, A.R., Olabe, J.A., De Brito, A.R.M.S., Franco, D.W.
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spelling todo:paper_01620134_v98_n11_p1921_Zanichelli2023-10-03T15:01:30Z The [Ru(Hedta)NO] 0,1- system: Structure, chemical reactivity and biological assays Zanichelli, P.G. Miotto, A.M. Estrela, H.F.G. Soares, F.R. Grassi-Kassisse, D.M. Spadari-Bratfisch, R.C. Castellano, E.E. Roncaroli, F. Parise, A.R. Olabe, J.A. De Brito, A.R.M.S. Franco, D.W. Nitrosyl reactivity NO-donors Nucleophilic reactivity Ruthenium nitrosyl Vasodilator activity carboxylic acid hydroxide metal nitric oxide nitroprusside sodium ruthenium derivative addition reaction animal experiment article bioaccumulation bioassay chemical reaction controlled study crystallization death drug effect drug structure electricity electrochemistry electron endothelium geometry injection kidney liver male nonhuman parameter plasma proton transport rat reaction analysis reduction sample structure analysis time toxicity urine vascular ring vasodilatation Animals Crystallography, X-Ray Edetic Acid Electrochemistry Male Mice Models, Molecular Molecular Conformation Nitric Oxide Ruthenium Tissue Distribution Xenox The [Ru II(Hedta)NO +] complex is a diamagnetic species crystallizing in a distorted octahedral geometry, with the Ru-N(O) length 1.756(4) Å and the RuNO angle 172.3(4)°. The complex contains one protonated carboxylate (pK a = 2.7 ± 0.1). The [Ru II(Hedta)NO +] complex undergoes a nitrosyl-centered one-electron reduction (chemical or electrochemical), with E NO+/NO = -0.31 V vs SCE (I = 0.2 M, pH 1), yielding [Ru II(Hedta)NO] -, which aquates slowly: k -NO = 2.1 ± 0.4 × 10 -3 s -1 (pH 1.0, I = 0.2 M, CF 3COOH/NaCF 3COO, 25°C). At pHs > 12, the predominant species, [Ru II(edta)NO] -, reacts according to [Ru II(edta) NO] - + 2OH - ⇒ [Ru II(edta)NO 2] 3-, with K eq = 1.0 ± 0.4 × 10 3 M -2 (I = 1.0 M, NaCl; T = 25.0 ± 0.1°C). The rate-law is first order in each of the reactants for most reaction conditions, with k OH - = 4.35 ± 0.02 M -1 s -1 (25.0°C), assignable mechanistically to the elementary step comprising the attack of one OH - on [Ru II(edta)NO] -, with subsequent fast deprotonation of the [Ru II(edta) NO 2H] 2- intermediate. The activation parameters were ΔH # = 60 ± 1 kJ/mol, ΔS # = -31 ± 3 J/K mol, consistent with a nucleophilic addition process between likely charged ions. In the toxicity up-and-down tests performed with Swiss mice, no death was observed in all the doses administered (3-9.08 × 10 -5 mol/kg). The biodistribution tests performed with Wistar male rats showed metal in the liver, kidney, urine and plasma. Eight hours after the injection no metal was detected in the samples. The vasodilator effect of [Ru II(edta)NO] - was studied in aortic rings without endothelium, and was compared with sodium nitroprusside (SNP). The times of maximal effects of [Ru II(edta)NO] - and SNP were 2 h and 12 min, respectively, suggesting that [Ru II(edta)NO] - releases NO slowly to the medium in comparison with SNP. © 2004 Elsevier Inc. All rights reserved. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_01620134_v98_n11_p1921_Zanichelli
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Nitrosyl reactivity
NO-donors
Nucleophilic reactivity
Ruthenium nitrosyl
Vasodilator activity
carboxylic acid
hydroxide
metal
nitric oxide
nitroprusside sodium
ruthenium derivative
addition reaction
animal experiment
article
bioaccumulation
bioassay
chemical reaction
controlled study
crystallization
death
drug effect
drug structure
electricity
electrochemistry
electron
endothelium
geometry
injection
kidney
liver
male
nonhuman
parameter
plasma
proton transport
rat
reaction analysis
reduction
sample
structure analysis
time
toxicity
urine
vascular ring
vasodilatation
Animals
Crystallography, X-Ray
Edetic Acid
Electrochemistry
Male
Mice
Models, Molecular
Molecular Conformation
Nitric Oxide
Ruthenium
Tissue Distribution
Xenox
spellingShingle Nitrosyl reactivity
NO-donors
Nucleophilic reactivity
Ruthenium nitrosyl
Vasodilator activity
carboxylic acid
hydroxide
metal
nitric oxide
nitroprusside sodium
ruthenium derivative
addition reaction
animal experiment
article
bioaccumulation
bioassay
chemical reaction
controlled study
crystallization
death
drug effect
drug structure
electricity
electrochemistry
electron
endothelium
geometry
injection
kidney
liver
male
nonhuman
parameter
plasma
proton transport
rat
reaction analysis
reduction
sample
structure analysis
time
toxicity
urine
vascular ring
vasodilatation
Animals
Crystallography, X-Ray
Edetic Acid
Electrochemistry
Male
Mice
Models, Molecular
Molecular Conformation
Nitric Oxide
Ruthenium
Tissue Distribution
Xenox
Zanichelli, P.G.
Miotto, A.M.
Estrela, H.F.G.
Soares, F.R.
Grassi-Kassisse, D.M.
Spadari-Bratfisch, R.C.
Castellano, E.E.
Roncaroli, F.
Parise, A.R.
Olabe, J.A.
De Brito, A.R.M.S.
Franco, D.W.
The [Ru(Hedta)NO] 0,1- system: Structure, chemical reactivity and biological assays
topic_facet Nitrosyl reactivity
NO-donors
Nucleophilic reactivity
Ruthenium nitrosyl
Vasodilator activity
carboxylic acid
hydroxide
metal
nitric oxide
nitroprusside sodium
ruthenium derivative
addition reaction
animal experiment
article
bioaccumulation
bioassay
chemical reaction
controlled study
crystallization
death
drug effect
drug structure
electricity
electrochemistry
electron
endothelium
geometry
injection
kidney
liver
male
nonhuman
parameter
plasma
proton transport
rat
reaction analysis
reduction
sample
structure analysis
time
toxicity
urine
vascular ring
vasodilatation
Animals
Crystallography, X-Ray
Edetic Acid
Electrochemistry
Male
Mice
Models, Molecular
Molecular Conformation
Nitric Oxide
Ruthenium
Tissue Distribution
Xenox
description The [Ru II(Hedta)NO +] complex is a diamagnetic species crystallizing in a distorted octahedral geometry, with the Ru-N(O) length 1.756(4) Å and the RuNO angle 172.3(4)°. The complex contains one protonated carboxylate (pK a = 2.7 ± 0.1). The [Ru II(Hedta)NO +] complex undergoes a nitrosyl-centered one-electron reduction (chemical or electrochemical), with E NO+/NO = -0.31 V vs SCE (I = 0.2 M, pH 1), yielding [Ru II(Hedta)NO] -, which aquates slowly: k -NO = 2.1 ± 0.4 × 10 -3 s -1 (pH 1.0, I = 0.2 M, CF 3COOH/NaCF 3COO, 25°C). At pHs > 12, the predominant species, [Ru II(edta)NO] -, reacts according to [Ru II(edta) NO] - + 2OH - ⇒ [Ru II(edta)NO 2] 3-, with K eq = 1.0 ± 0.4 × 10 3 M -2 (I = 1.0 M, NaCl; T = 25.0 ± 0.1°C). The rate-law is first order in each of the reactants for most reaction conditions, with k OH - = 4.35 ± 0.02 M -1 s -1 (25.0°C), assignable mechanistically to the elementary step comprising the attack of one OH - on [Ru II(edta)NO] -, with subsequent fast deprotonation of the [Ru II(edta) NO 2H] 2- intermediate. The activation parameters were ΔH # = 60 ± 1 kJ/mol, ΔS # = -31 ± 3 J/K mol, consistent with a nucleophilic addition process between likely charged ions. In the toxicity up-and-down tests performed with Swiss mice, no death was observed in all the doses administered (3-9.08 × 10 -5 mol/kg). The biodistribution tests performed with Wistar male rats showed metal in the liver, kidney, urine and plasma. Eight hours after the injection no metal was detected in the samples. The vasodilator effect of [Ru II(edta)NO] - was studied in aortic rings without endothelium, and was compared with sodium nitroprusside (SNP). The times of maximal effects of [Ru II(edta)NO] - and SNP were 2 h and 12 min, respectively, suggesting that [Ru II(edta)NO] - releases NO slowly to the medium in comparison with SNP. © 2004 Elsevier Inc. All rights reserved.
format JOUR
author Zanichelli, P.G.
Miotto, A.M.
Estrela, H.F.G.
Soares, F.R.
Grassi-Kassisse, D.M.
Spadari-Bratfisch, R.C.
Castellano, E.E.
Roncaroli, F.
Parise, A.R.
Olabe, J.A.
De Brito, A.R.M.S.
Franco, D.W.
author_facet Zanichelli, P.G.
Miotto, A.M.
Estrela, H.F.G.
Soares, F.R.
Grassi-Kassisse, D.M.
Spadari-Bratfisch, R.C.
Castellano, E.E.
Roncaroli, F.
Parise, A.R.
Olabe, J.A.
De Brito, A.R.M.S.
Franco, D.W.
author_sort Zanichelli, P.G.
title The [Ru(Hedta)NO] 0,1- system: Structure, chemical reactivity and biological assays
title_short The [Ru(Hedta)NO] 0,1- system: Structure, chemical reactivity and biological assays
title_full The [Ru(Hedta)NO] 0,1- system: Structure, chemical reactivity and biological assays
title_fullStr The [Ru(Hedta)NO] 0,1- system: Structure, chemical reactivity and biological assays
title_full_unstemmed The [Ru(Hedta)NO] 0,1- system: Structure, chemical reactivity and biological assays
title_sort [ru(hedta)no] 0,1- system: structure, chemical reactivity and biological assays
url http://hdl.handle.net/20.500.12110/paper_01620134_v98_n11_p1921_Zanichelli
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