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2009 |
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Transaction on Civil Engineering |
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Transaction on Mechanical Engineering |
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Transactions on Chemistry and Chemical Engineering |
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Transaction on Computer Science & Engineering and Electrical Engineering |
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Transaction on Industrial Engineering |
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Transaction on Nanotechnology |
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Volume 16, Issue 2, 2009
Transactions on Chemistry and Chemical Engineering
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Spectroscopic and Thermodynamic
Studies of Interaction Between Dopamine
and Cobalt(III) Schi-Base Complexe
D.M. Boghaei (Professor)
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In this paper, the interactions of cobalt(III) tetradentate Schi-base complexes, [Co(3-
MeO-salophen)]ClO4, (1), [Co(5-NO2-salophen)]ClO4, (2), and [Co(5-Br-salophen)]ClO4, (3), with
dopamine, an important neurotransmitter, have been investigated. The formation and kinetic constants for
complex formation of [Co(3-MeO-salophen)]ClO4, (1), with dopamine were determined spectrophotometrically
in H2O/EtOH solution (4:1) at 30 C by using the Benesi-Hildbrand and Guggenheim equations,
respectively. The stoichiometry has been found to be 1:1. The rate and equilibrium constants for the
coordination of dopamine to [Co(3-MeO-salophen)]ClO4 were found to be 0.0053 min1 and 1600 dm3
mol1, respectively.
Keywords: Cobalt(III) Schi-base complexesDopamineBenesi-Hildbrand equation |
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DFT Study of the Interaction
of Thymine with Cu+ and Zn2+
A. Fattahi (PhD.)
M. Shakorian Fard Jahromi [MSc.]
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Interaction of the DNA thymine base with Cu+ and Zn2+ was studied to explore: a) The
metal binding energy (MIA) of thymine with Cu+ and Zn2+ and b) The possible correlation between
charge transfer and MIAs. The gas-phase Cu+ and Zn2+ anities of thymine, as well as the Mulliken
charges, on the complexed metal cations were both determined at the same computational level, including
the density functional level and employing the hybrid B3LYP exchange correlation potential in connection
with the 6-311++G (dp) basis set. All the molecular complexes were obtained by interaction between the
most stable tautomer of thymine and two transition mono and divalent (Cu+, Zn2+) metal ions. To probe
all possible binding sites, these two cations were placed around the thymine nucleobase and optimized. For
both Cu+ and Zn2+, the complexes of thymine with O4 are the most stable structure. For complexes of
thymine with mono cations (Li+, Na+, K+ and Cu+) and dications (Mg2+, Ca2+ and Zn2+), the results
indicate a linear correlation between the transferred charge and metal binding energy. The results also
indicate that the amount of charge transfer and bonding strength are the highest for the transion metal
ions Cu+ and Zn2+, respectively.
Keywords: Divalent cations |
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An Improved Procedure for the Enrichment
of Plasma F2-Isoprostanes Prior to
Final Determination by GC-MS/NICI
J. Nourooz-Zadeh (Professor)
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One of the most popular approaches to quantify oxidative injury is to measure lipid
peroxidation products and, in particular, F2-isoprostanes (F2-IPs). F2-IPs is a group of prostaglandin
F2-like compounds derived from the non-enzymatic oxidation of arachidonic acid. Of these, the
15-F2t-isoprostane (8-iso-PGF2) has received considerable attention, because it possesses adverse
biological activities. Previous Gas Chromatographic-Mass Spectrometric (GC-MS) methods for measuring
plasma F2-IPs from this laboratory involved two chromatography steps on C18 and NH2-cartridges.
Problems may, however, arise with chromatography on C18 cartridges, as it can be time-consuming
and losses may occur depending upon the pH and eciency of the sample loading. Therefore, it was
decided that the C18 chromatography step be replaced with a single lipid partitioning step and the
NH2-chromatography be simplied. In 70 plasma samples from healthy individuals, total (sum of free and
esteried) 15-F2t-isoprostane concentrations ranged from 0.5 to 3.13 nM. This assay meets all predened
method performances in terms of specicity and sensitivity. The improved method is suitable for the
analysis of samples from larger clinical trials investigating the role of oxidant injury under conditions
associated with oxidative stress.
One of the most popular approaches to quantify oxidative injury is to measure lipid
peroxidation products and, in particular, F2-isoprostanes (F2-IPs). F2-IPs is a group of prostaglandin
F2-like compounds derived from the non-enzymatic oxidation of arachidonic acid. Of these, the
15-F2t-isoprostane (8-iso-PGF2) has received considerable attention, because it possesses adverse
biological activities. Previous Gas Chromatographic-Mass Spectrometric (GC-MS) methods for measuring
plasma F2-IPs from this laboratory involved two chromatography steps on C18 and NH2-cartridges.
Problems may, however, arise with chromatography on C18 cartridges, as it can be time-consuming
and losses may occur depending upon the pH and eciency of the sample loading. Therefore, it was
decided that the C18 chromatography step be replaced with a single lipid partitioning step and the
NH2-chromatography be simplied. In 70 plasma samples from healthy individuals, total (sum of free and
esteried) 15-F2t-isoprostane concentrations ranged from 0.5 to 3.13 nM. This assay meets all predened
method performances in terms of specicity and sensitivity. The improved method is suitable for the
analysis of samples from larger clinical trials investigating the role of oxidant injury under conditions
associated with oxidative stress.
Keywords: F2-isoprostanesLipid peroxidationOxidative stressGas chromatography-mass spectrometry. |
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