Complexation Constants Research Articles

Complexation of Trivalent Lanthanides with Hexaalkyl Nitrilotriacetamides into Methylimidazolium-Based Ionic Liquids: Spectroscopic, Electrochemical, Calorimetric, and Theoretical Insights.

Exothermic, spontaneous inner-sphere complexation of trivalent lanthanides with N,N,N',N',N″,N″-hexaalkyl-substituted nitrilotriacetamides (HRNTAs) into 1-hexyl-3-methylimidazolium-bis(trifluoromethylsulfonyl)imide (C6mim NTf2) is reported with a predominant presence of ML and ML2 complexes having complexation constants, β1Eu 3.10 ± 0.02 ,β1Nd 2.67 ± 0.03 and β2Eu 5.22 ± 0.04, β2Nd 4.95 ± 0.02, respectively, for the n-butyl-substituted HRNTA (HBNTA); while those for the n-hexyl derivative (HHNTA) are β1Eu 4.27 ± 0.03, β1Nd 3.71 ± 0.03 and β2Eu 7.70 ± 0.03, β2Nd 7.18 ± 0.04, respectively. HHNTA shows better complexing ability; whereas the stronger complexation of the Nd3+ over Eu3+ is attributed to the lanthanide contraction. Furthermore, the nature of the ionic liquid also influences the extent of complexation with the trend: C4mim NTf2 > C6mim NTf2 > C8mim NTf2, which follows the order of their dielectric constants. Judd-Ofelt parameters were calculated from photoluminescence data to get an idea about the symmetry of the Eu3+ complexes. Electrochemical investigations give diffusion coefficient values of 1.17 × 10-7 and 8.26 × 10-8 cm2/s for the Eu3+ complexes of HBNTA and HHNTA, respectively. Changes in the spectral characteristics and peak positions are evidenced in the FTIR spectra on the complexation of Eu3+ with the HRNTA ligands in C6mim NTf2. Structure optimization for the complexes was performed by DFT computations.

Perturbational Analysis of Magnetic Force Theorem for Magnetic Exchange Interactions in Molecules and Solids.

There have been increasing efforts to compute magnetic exchange coupling constants for transition metal complexes and magnetic insulators using the magnetic force theorem and Green's function-based linear response methods. These were originally conceived for magnetic metals, yet it has not been clear how these methods fare conceptually with the conventional models based on electron-correlation interactions among so-called magnetic orbitals. We present a spinor-based theoretical analysis pertinent to the magnetic force theorem and linear response theory using Brillouin-Wigner perturbation method and Green's function perturbation method, and we shed light on the conceptual nature of the Lichtenstein formula in its applications for calculations of the total energy and magnetic exchange coupling constants for both molecules and solids. Derivation of the magnetic force theorem in this perturbational analysis identifies the first-order energy correction terms, which are considered as the ferromagnetic component for the magnetic exchange interactions of transition metal compounds but are not included in the Lichtenstein formula. Detailed perturbational analysis of the energy components involved in the magnetic force theorem identifies the energy components that are missing in the Lichtenstein formula but are critical in the Anderson's model for transition metal complexes and magnetic insulators where magnetic orbitals can overlap.

Parallel (competitive) reactions of micelle formation and cyclodextrin–surfactant inclusion complex formation in aqueous solution: A consequence of the Gibbs–Duhem equation—invariance of the mass action law and the possibility of determining the equilibrium constant of the inclusion complex

The Gibbs–Duhem equation results in the independence between the standard Gibbs free energy of micelle formation and the standard Gibbs free energy of monocomponent surfactant’s and cyclodextrin’s (CD’s) inclusion complex formation in aqueous solution. The experimental data show that the surfactant’s critical micellar concentration increases in the presence of CD. At a constant temperature, the standard Gibbs free energy of micelle formation remains constant, irrespective of the presence of parallel competitive processes such as inclusion complex formation. This indicates that the critical micellar concentration remains unchanged at the corresponding concentration scale. As a result, the equilibrium constant for surfactant–CD inclusion complex formation can be determined by changing the critical micellar concentration in the presence and absence of CD. A graphical method for determining the equilibrium constant of the inclusion complex is also presented. An analytical approach for analyzing the influence of the formation of the inclusion complex with CD on the formation of the binary mixed micellar pseudophase is presented. Suppose that different values exist for the equilibrium constants of the formation of the inclusion complex for two surfactants from their binary mixture. In this case, there is a change in the initial mole fraction from the initial mixture of surfactants, which should be considered when applying the regular solution theory protocol when determining the parameters of a binary mixed micelle in the presence of CD.

Binding studies of ruthenium complexes with antithyroid drug

Medicinal substances are essential to our daily existence. A prudent approach to metal complexation with already available medications may result in more stylish, intelligent, and effective drug compositions. Thus, the binding of [Ru(NN)3]2+ (NN = 2,2ˈ-bipyridine, 1,10-phenanthroline) with the antithyroid medication thyronorm has been studied in the current attempt. The use of absorption and emission spectrum techniques allowed researchers to examine the complexes' interactions with antithyroid medications. Studies of absorption and emission spectra show that the complex and medication interact through coordinated ligand hydrophobic and hydrogen bonding interactions.Analysis has also been done on the binding of the antithyroid medication Thyronorm to ruthenium complexes. The Benesi-Hildebrand plot was used to determine the binding constants of the drug complexes. Current research indicates that the Thyronorm pill has good affinity with [Ru(phen)3]2+complex.

COMPLEXATION OF THE CURCUMIN BY THE CAFEIN IN ETHANOL BY MEANS OF UV – VIS SPETROPHOTOMETER

Why this miraculous and amphiphilic compound, curcumin, which has a very extraordinary therapeutic potential (because can react with many targets in the organism), has a weak bioavailability in the organism and is metabolized in compoumds having very weak activity or inactive compounds? How to improve substantially its bioavailability and therefore its absorption in the organism in order to allow its incorporation in making of pharmaceuticals regardless of its nanoparticles of which the obtention is furthermore hardworking? It seems indicated to search the response in the kinetic and thermodynamic behavior of this compound or in its co – administration with the other compounds (more soluble in water) in vitro in order to understand how to increase its absorption in vivo. So our objective is to make better our understanding of the absorption of natural curcuminoids in the organism without resorting to their chemical transformation in nanoparticles that is additionally hardworking. In this paper, curcumin was examined in the presence of cafein in ethanol with the aim to deepen the knowledge of the interaction between them. The study has revealed the presence of two complexes A6B4 and AB9 (A = curcumin, B = cafein), evidenced by the Job’s method (continuous variations method) whose complexation constants have been calculated and the value of K_(A_6 B_4 ) (1.12 1032) is higher than the value of K_(〖AB〗_9 ) (2.7 10-10) suggesting the great stability of A_6 B_4 .

Temperature Changes in Luminescence of Mixed Complexes of Terbium and Samarium with Organic Ligands Based on 2,2-bipyridyldicarboxamides

Solutions in acetonitrile of three mixed complexes of rare earth elements (terbium and samarium) with organic ligands with various pyridine substituents were studied in this work. The ratios of ligands and metals in the resulting complexes were determined, and the stability constants of samarium complexes were calculated using the spectrophotometric titration method. Measurements of absorption, emission and excitation spectra of luminescence, luminescence kinetics of solutions of mixed complexes of rare earth elements with an excess of metal relative to the ligand were carried out at various temperatures in the range 298–328 K. An increase of luminescence intensity of a samarium ion in complex upon heating has been discovered for the first time. The dependences of the luminescence quantum yield and lifetime of mixed complexes on temperature were obtained. A thermometric parameter — the ratio of the integral luminescence intensities of samarium and terbium ions — was proposed, and the temperature sensitivity coefficient of this parameter was determined for different complexes.

Influence of Sodium Lauryl Sulfate Anionic Micelles on the Complex Equilibria of Divalent Metal Ions with Isoleucine Amino Acid

The main objective of the present investigation is the formation analysis of metal-ligand complexes of isoleucine with divalent calcium, magnesium and zinc metal ions in various concentrations of sodium dodecyl sulphate (0.0, 0.5, 1.0, 1.5, 2.0 and 2.5 percent w/v). To look into the impact of the concentration of negatively charged micelles, the parameters were changed and the possible chemical species of isoleucine that interact with the metal ions, are being studied. The experiment was performed using pH meter at 303 K using NaCl to keep ionic strength stable at 0.16 mol dm-3 in the presence of anionic surfactant sodium dodecyl sulphate (SDS). The determination of the correction factor was conducted via the computer program SCPHD. The computational software MINIQUAD75 is utilized to determine the stability constants of ligand-metal complexes through the analysis of titration data. Based on statistical features such as skewness, 2, kurtosis and crystallographic R-factor, the best fit to the complicated speciation was selected. The metal ions Ca (II), Mg (II) and Zn (II) formed complexes ML, ML2 and ML2H2 for Ca (II), Mg(II) and ML, ML2 and ML2H for Zn (II) through the complexation of isoleucine. In order to validate the accuracy of the final established model, deliberate defects were introduced into the relevant components.

Synthesis of Ferrocenyl Chalcone-Containing Aminourea Schiff Bases and Their Detection on Tryptophan.

In this paper, 1-phenyl-3-ferrocenylenone aminourea Schiff bases were synthesized by a novel method. A multifunctional molecular probe (Probe A) of 1-phenyl-3-ferrocenylenone, carbon-based solid acid, aminourea, and anhydrous ethanol was synthesized by adding them to a vessel at elevated temperatures and refluxing for the synthesis of a multifunctional molecular probe (Probe A) of 1-phenyl-3-ferrocenylenone aminourea Schiff base, and it was found that it recognizes tryptophan (Trp) in solution, and that the catalyst can be reused more than five times after recycling. This method is characterised by low cost, high efficiency, green environment and no waste acid. Fluorescence and UV spectra show that probe A specifically recognizes tryptophan (Trp) without interference by other amino acids or pH and time does not affect it within 45min. The lowest limit of detection for Trp was 1.307 × 10- 4 mol/L for probe A. The binding ratios of probe A to Trp were measured to be 1:1 by Job's plotting method, respectively. The complexation constant of probe A with Trp was found to be 2.733 × 107 L/mol according to the Benesi-Hildebrand equation. The bonding mechanism was explored through IR spectroscopy and ¹H NMR titration.

Regulatory effects of cyclodextrins on light-responsive phase transition behaviors of poly(N-isopropylacrylamide-co-N-(4-phenylazophenyl)methylacrylamide)

The physicochemical properties of light-responsive polymers have attracted widespread attention due to their ability to be precisely and conveniently modulated by light without additives or contact. Here, we report a thermo/light dual-responsive polymer, PNMA, synthesized through the free radical copolymerization of azobenzene derivative (mAzo) and N-isopropylacrylamide (NIPAM) monomers. By switching between 365 nm UV light and 450 nm visible light, the E/Z photoisomerization of the light-responsive mAzo can be reversibly controlled, and thereby adjusting the conformational changes of the PNMA polymer chain. Significantly, the stretching and contraction conformations of PNMA polymer chains can be manipulated by incorporating different types of cyclodextrins. A comprehensive comparative study was conducted to determine the light-controlled binding and dissociation processes between the azobenzene units and CDs (α-CD, β-CD and γ-CD), the influences of CDs on the photoisomerization kinetics and complexation constants of azobenzene with CDs, as well as the effect of CDs on the light-responsive phase transition behaviors of PNMA. Our results highlight the superior advantage of α-CD in constructing light-responsive systems with significant changes in hydrophilicity. Notably, by tuning the concentration of α-CD and the proportion of mAzo in PNMA, the range of light-induced thermosensitive response is significantly expanded. This study is the first to present a comparative study on the effects of three CDs on the thermo/light dual-responsive properties of polymer systems based on PNIPAM and azobenzene, providing new ideas for CD selection in the design and construction of advanced light-responsive materials based on light-responsive guest-host dissociation or hydrophilic changes of azobenzene/CD complexes.

A new three-dimensional modeling of fluorescence excitation-emission measurements to explore the interaction of hydroxychloroquine and DNA, and to quantify their binding constant

A new three-dimensional chemometric approach was introduced to explore the interaction of hydroxychloroquine (HCQ)-calf thymus deoxyribonucleic acid (DNA) and quantify binding constant using fluorescence excitation and emission measurements. The fluorescence excitation-emission spectra were recorded after gradual titration of HCQ with DNA. Then, the excitation and emission curves and relative concentrations of the drug and drug-DNA complex were quantitatively estimated using a three-dimensional model called Parallel Factor Analysis (PARAFAC) to a cubic fluorescence data array. The interaction of HCQ and DNA was predicted by applying newly modified Stern-Volmer equations to the relationship between the actual DNA concentration, and the HCQ concentration in the relative concentration profile of the PARAFAC model. In the PARAFAC application, the binding constants of the HCQ-DNA complex at 288, 298, and 310 K were found as 6.78 × 103, 5.07 × 103, and 3.74 × 103 L mol−1, respectively. From the temperature studies, the thermodynamic parameters (ΔS0= 3.528 J mol−1 K−1, ΔH0= −20.099 kJ mol−1 and ΔG0=-21.11, −21.12, and −21.19 kJ mol−1 at 288, 298, and 310 K, respectively) were calculated. The drug-DNA interaction is spontaneous due to negative ΔG0 values. The positive ΔS0 and negative ΔH0 values revealed the major role of the electrostatic force on the binding of HCQ to DNA. Assay results obtained from the proposed three-way modeling were compared to those provided by the traditional spectrofluorimetric method.

Evaluation of Stability constant of Binary complex of Tannic Acid with Fe(II) in Aqueous Solution: Potentiometric Study

In this study, the protonation equilibria of the tannic acid was determined and used for determining the stability constants of the binary complexes formed with iron (II) ions in the aqueous medium under the experimental conditions by potentiometric method using Irving and Rossotti equation, where Stability constant was 3.205 for Fe(II)–tannic acid complex, while Fe(II) was formed complexes with tannic acid of various stoichiometries, which in the 1:1 molar ratio at pH = 11.24. Furthermore, the ionic strength and the influence of temperature on the stability of the complexes is investigated, where stability constant in presence 0.1 M NaCl (ionic strength) of binary iron-Tan complex equal 3.254, and at different temperatures were log K1= 3.156 at 298.15 K, log K1 = 3.205 at 310.15 K, and log K1 = 3.256 at 313.15 K.

Metal-Fluoride Complex Stability Constant in Acid Solution as an Indicator to Identify the Corrosion Behavior of Metal Cations on Titanium

The Ti was immersed in 0.058 mol/L NaF containing 1.68 mol/L H2SO4 solution with different metal cations (Ca2+, Cu2+, Fe2+, Mg2+, Mn2+, Ni2+, Zn2+, Al3+, and Fe3+) for 7 d to identify the role of metal cations on corrosion behavior of titanium. To elucidate the role of metal cations on the corrosion behavior of Ti in acid solution, the standard electrode potential, E0, hardness of metal cations, X, and metal-fluoride complex stability constant, Kn, were chosen as the potential indicator. It is found that the mass loss fraction obtained from the immersion tests as a function of the metal-fluoride complex stability constant, Kn, has the highest correlation coefficient (0.92). The metal cations (Al3+ and Fe3+) with higher stability constant of the metal-fluoride complex in acid solution, (Kn > 3.27), show corrosion inhibition effect on Ti in acid solution. The Kn could be a suitable indicator to understand the role of metal cations on the Ti corrosion mechanism.

Stability of metal ion complexes with the synthetic phytosiderophore proline-2'-deoxymugineic acid.

Adequate micronutrient concentrations in crops are essential for human health and agricultural productivity. However, 30% of plants growing on cultivated soils worldwide are deficient in iron (Fe). Because of low micronutrient bioavailability, graminaceous plants have evolved to exude small molecules, called phytosiderophores, into the soil environment, which strongly complex and promote uptake of trace elements. The development of a synthetic phytosiderophore, proline-2'-deoxymugeneic acid (PDMA), has been shown to promote Fe uptake in rice plants; however, its binding capabilities with other metals, which may impact the ability to promote the uptake of Fe and other trace nutrient metals commonly found in soils, remain unknown. We conducted spectrophotometric titrations to determine the stability constants (logK) of PDMA complexes with Mn(II), Co(II), Cu(II), Ni(II), and Zn(II). We determined that PDMA complex stability constants correlated with: (1) the hydrolysis constants of metal ions (logKOH) in complexes; (2) the ionic potential of complexed metals; and (3) the corresponding complex stability constants of other mugineic acid type phytosiderophores, as well as the trishydroxamate microbial siderophore DFOB. These correlations demonstrate the potential, and limitations, on our ability to predict the stability of phytosiderophore complexes with metal ions with different physicochemical properties and with potentially different coordination structures.

Influence of Sodium Dodecyl Sulfate Anionic Micelles on The Complex Equilibria of Divalent Metal Ions with L-Leucine Amino Acid

The main objectives of the present investigation are the formation analysis of metal-ligand complexes of L-Leucine with divalent calcium, magnesium, and zinc metal ions in various concentrations of sodium dodecyl sulphate (0.0, 0.5, 1.0, 1.5, 2.0, and 2.5 percent w/v). To also look into the impact of the concentration of negatively charged micelles, the parameters that were changed, and the possible chemical species of L-Leucine that interact with the metal ions that were being studied. The experiment was performed using pH meter at 303 K using NaCl to keep your ionic strength stable of 0.16mol dm-3 in the presence of anionic surfactant, sodium dodecyl sulphate (SDS). The determination of the correction factor was conducted via the computer program SCPHD. The computational software MINIQUAD75 is utilized to determine the stability constants of ligand-metal complexes through the analysis of titration data. Based on statistical features such as skewness, 2, kurtosis, and crystallographic R-factor, the best fit to the complicated speciation was selected. The metal ions Ca (II), Mg (II), and Zn (II) formed complexes ML, ML2, and ML2H2 for Ca (II), and ML, ML2, and ML2H for Mg (II) and Zn (II) through the complexation of L-Leucine. In order to validate the accuracy of the final established model, deliberate defects were introduced into the relevant components.

Spectroscopic and solution properties characterization of quaternary ammonium ion containing polycations complexed with fluorescent rhodamine sulfonic acid dyes

Based on the growing range of applications for polycations in research and commercial materials, a continuing need exists to advance the fundamental knowledge and understanding of this class of materials. Spectroscopic and solution properties characterizations of noncovalently labeled, fluorescent Alexa Fluor® dye complexes of two commercial polycations, poly(2-(trimethylamino) ethyl methacrylate) monocation and poly[bis[2-chloroethyl] ether-alt-1,3-bis[3-(dimethylamino) propyl] urea] dication are reported to help address this need. A variety of fluorescence spectroscopic methods are used with a special emphasis on fluorescence correlation spectroscopy (FCS) which is applied to characterize the Stokes radius (RS) and equilibrium dissociation constants (Kd) of dye-polycation complexes at nanomolar dye concentrations. Resulting RS values indicate dye binding to individual polycation chains. Measured Kd values in the sub-micromolar range are consistent with strong dye binding. Increasing solution ionic strength with sodium chloride addition inhibits dye binding and decreases the RS of dye-polycation complexes due to size collapse of polycation chains. The complexes differ in their solution stability to ionic strength changes suggesting that both electrostatic and hydrophobic binding interactions influence dye binding. This study establishes the viability of noncovalent dye-polycation complexation in concert with FCS characterization as a general approach for investigating the properties of quaternary ammonium ion containing polycations in aqueous solution.

Lattice Realization of Complex Conformal Field Theories: Two-Dimensional Potts Model with Q>4 States.

The two-dimensional Q-state Potts model with real couplings has a first-order transition for Q>4. We study a loop-model realization in which Q is a continuous parameter. This model allows for the collision of a critical and a tricritical fixed point at Q=4, which then emerge as complex conformally invariant theories at Q>4, or even complex Q, for suitable complex coupling constants. All critical exponents can be obtained as analytic continuation of known exact results for Q≤4. We verify this scenario in detail for Q=5 using transfer-matrix computations.

Integrated experiments and numerical simulations for chromium (VI) surface complexation in natural unconsolidated sediments

This study focuses on the adsorption and transport of Cr (VI) on natural sediments from Qiqihar, China. Through batch and column experiments, we assessed the adsorption capacities influenced by factors such as contact time, initial concentration, pH, ionic strength, solid-to-solution ratio, coexisting ions in groundwater, sediment characteristics and flow rate. The adsorption kinetics of Cr (VI) follow the pseudo-first-order model well, while the isotherms of all three sediments are accurately represented by the Freundlich model. The adsorption edges reveal a strong pH dependence in Cr (VI) adsorption: the stronger the acidity, the more favorable it is for adsorption. The adsorption capacity decreases with an increasing solid-to-solution ratio, stabilizing at higher ratios. Coexisting ions in groundwater reduce Cr (VI) adsorption in loam under neutral pH. Additionally, Fourier transform infrared spectroscopy (FTIR) results indicate that the hydroxyl group is the primary reactive functional group in all three sediments. X-ray photoelectron spectroscopy (XPS) results further show partial adsorbed Cr (VI) was reduced to Cr (III) by organic matters. However, surface complexation reactions dominate the removal of Cr (VI). On the base above, we introduced a surface complexation model, optimizing equilibrium complexation constants by fitting adsorption edges. Subsequently, reactive transport models incorporating both surface complexation and reduction processes for Cr (VI) were established to simulate column experiments. As the flow rate decreases, the adsorption capacity and the amount of reduction reaction for Cr (VI) increase, while the reduction rate decreases. Specifically, the reduction for Cr (VI) was found to be more significant in loam compared to sand, correlating with the organic matter content. The results emphasize the existence of surface complexation reactions and the role of organic matters in electron transfer. Our study provides significant information for understanding Cr (VI) adsorption and transport behavior in natural aquifer sediments.

Gold in sulfide fluids revisited

Gold solubility was measured at temperatures of 350, 400, 450, and 490 °C and pressures of 500 and 1000 bar in an ’oxidized sulfide’ system, as a function of pHT (2 – 10) and sulfur concentration (m(Stotal) = 0.03 – 1.2 [mol·(kg H2O)-1]). In this system, sulfur primarily exists as H2S, H2SO3, H2SO4, their dissociation products, and radical species such as S2- and S3-. The complexes Au(HS)2-, Au2S22-, AuHS(aq), AuHS(H2S)3(aq), and AuOH(aq) were identified as the primary gold species in the experimental fluids, varying with pH and m(Stotal). The solubility constants for Au(HS)2-, a critical (hydro)sulfide complex, align excellently with literature for ’reduced sulfide’ fluids, where sulfur predominantly exists in the 2- oxidation state. New experimental data from the ’oxidized sulfide’ system were regressed along with reliable literature data from ’reduced sulfide’ systems to calculate standard thermodynamic properties and parameters of the Helgeson-Kirkham-Flowers (HKF) model. The solubility constants for charged complexes, Au(HS)2- and Au2S22-, increase sharply with temperature, whereas those for neutral species, AuHS(aq) and AuHS(H2S)3(aq), show a pronounced peak near 300 °C. These (hydro)sulfide complexes account for gold solubility ranging from a few tens of ppb to a few tens of ppm in natural sulfide fluids, depending on the fluid pH. Thermodynamic calculations also indicate that, in addition to (hydro)sulfide species and the hydroxide complex, AuCl2- significantly contributes to Au mobility in high-temperature acidic chloride fluids. Based on new experimental data and prior studies using solubility and X-ray absorption spectroscopy methods, other gold complexes including mixed Au-HS-Cl, Au-HS-S3- species, and complexes with alkali metal cations, are deemed redundant. Above 250 °C, the influence of chloride salts on gold solubility can be accurately modeled using a simple extended Debye-Hückel equation with the term bγ·I = 0. The Setchenov coefficient bn = 0 suffices for calculating the activity coefficients of neutral species. This streamlined thermodynamic model aligns closely with earlier experimental work by Terry Seward and his team, effectively describing the state of Au in all types of natural fluids where Au exists in the 1+ oxidation state, under any set of P-T-f(O2)-f(S2)-compositional parameters.

Poly-Eriochrome Black T Decorated with Nickel Hydroxide Nanoparticles Modified Electrode for the Electrochemical Detection of Streptomycin and Probing its Interaction with Double-stranded DNA

We present a simple platform of poly-eriochrome Black T decorated with nickel hydroxide nanoparticles (Ni(OH)2NPs/PEBT) for the electrocatalytic oxidation of streptomycin (STRP) and probing its interaction with double-stranded DNA (ds-DNA). The electropolymerized eriochrome Black T modified glassy carbon electrode (GCE) was used to stabilize and synthesize Ni(OH)2NPs. The oxidation of STRP on Ni(OH)2NPs/PEBT/GCE mainly proceeded as a surface mechanism with the contribution of a diffusion-controlled process. A significant catalytic oxidation current of STRP was measured from an alkaline medium. It showed a dependence on the STRP concentrations in the range of 0.1 to 1.0 mM with a detection limit of 0.04 mM. The sensor has shown good recovery (85.3% to 90.2%, with RSD range of 1.27 to 8.83%) for the detection of STRP in diluted human serum. The interaction of STRP with ds-DNA was investigated from phosphate buffer pH 7.4 (0.2 M) using different electrode modifications (PEBT/GCE, and Ni(OH)2NPs/PEBT) in addition to bare GCE using voltammetric and impedance techniques. The binding constant of the STRP-DNA complex was calculated. Under the studied conditions, the interaction of ds-DNA with STRP in solution or on the surface of PEBT/GCE demonstrates their binding in intercalative and electrostatic modes.

Metal Complexes in Biology and Medicine: The System Cadmium (II)/ Iron (II)/ Zinc (II)- α- Aminobutyric Acid

Metal ions play an important role in biological systems. The importance of metal ions to essential functions of living systems and for wellbeing of living organisms is well known. Complexation reactions of α– aminobutyric acid with cadmium (II), iron (II) and zinc (II) have been studied in solution phase using paper ionophoretic technique. The present method is based upon the migration of a spot of metal ion on a paper strip at different pH values of background electrolyte containing 0.01M α -aminobutyric acid. A graph of pH against mobility was used to obtained information in the binary complexes and to calculate its stability constants. The logarithm stability constants of ML and ML2 complexes of α -aminobutyric acid were found to be (4.01 ± 0.02; 2.72 ± 0.01), (3.73 ± 0.03; 2.65 ± 0.09), (4.45 ± 0.02; 2.80 ± 0.03) for cadmium (II), iron (II) and zinc (II) complexes, respectively at ionic strength 0.1 molL-1 and a temperature of 35º C. Metal based drugs bioactivity can be increase by metal chelation, which in turn increase their absorbance and stability. Metal complexes can offer their action such as anti-inflammatory, anti-diabetic, antimicrobial, anticancer and ant thyroid compounds.