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Electrochemical Study of Interaction between Anticancer Drugs and DNA
Author: DongYanMin
Tutor: ZhouChangLi
School: Jinan University
Course: Chemical Engineering and Technology , Analytical Chemistry
Keywords: Anti-cancer drugs DNA Electrochemical methods Interaction
CLC: R96
Type: Master's thesis
Year: 2010
Downloads: 69
Quote: 0
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Abstract
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This article electrochemical method the anticancer drugs Magnolol, methotrexate, aminoglutethimide, leucovorin electrochemical behavior of its interaction with biological macromolecules DNA. The use of layers of self-assembly, the potential deposition technology preparation of the modified electrode was investigated media type and concentration, pH, scanning speed of the electrochemical behavior of anti-cancer drugs. By cyclic voltammetry, linear scanning, differential pulse method, timing electricity and other electrochemical techniques to obtain the kinetic parameters of anti-cancer drugs. Way of interaction of anti-cancer drugs and DNA, the calculated binding constant and the number of binding sites. And verified by spectrometry. Research glassy carbon electrode electrochemical behavior of Magnolol in 0.1 M PBS (pH 7.0) solution Magnolol the 0.449V at oxidation peak, the electrochemical oxidation of an electron and a proton is completely irreversible The process of electron transfer coefficient (alpha) was 0.441 ± 0.001. The honokiol 100-450 mV / s scan speed range of the electrochemical reaction at the electrode surface by surface control electrode reaction is a diffusion controlled process at high scan rate of 600-950 mV / s, the corresponding electrochemical rate constant (ks) 0.0760 ± 0.0001 s -1 sup>. The diffusion coefficient (D) and the surface of the adsorbed amount (Γ) is (3.76 ± 0.01) × 10 -7 sup> cm 2 sup> / s, and (2.98 ± 0.01) x 10 < sup> -10 sup> mol / cm 2 sup>. Electrochemical methods and spectroscopy study Magnolol and DNA interactions, Magnolol DNA in the manner combined binding constant and the number of binding sites were 1.14 × 10 5 sup> M - 1 sup> and 0.973. By optimizing the conditions established honokiol the method of measuring the linear range was 4.50 × 10 -8 sup> -1.70 × 10 -7 sup> M and 3.00 × 10 - 6 sup> M-1.80 × 10 -5 sup> M, limit of detection (S / N = 3) of 1.50 × 10 -9 sup> M. 2 layers prepared by electrostatic self-assembly (DNA / CS) 6 / PGE electrode as an electrochemical probe of methylene blue modified electrode using cyclic voltammetry and electrochemical impedance method characterized. Methotrexate electrochemical behavior studies have shown that, in the range of 40-200mV / s scan rate, the electrode reaction is a surface-controlled process, while increasing the scanning speed, methotrexate for the diffusion-controlled electrochemical reaction on the electrode surface process. Proton transfer and the ratio of the number of electrons transferred for the m / n = 0.483. Methotrexate interaction with DNA studies show that methotrexate and DNA molecules in insert mode, combined with constant and number of binding sites were 6.31 × 10 5 sup> M -1 sup> and 1.86. The results obtained by UV spectroscopy and fluorescence spectroscopy and electrochemical methods. Determination of methotrexate, and its detection limit is 5.0 × 10 -9 sup> M. Prepared mesoporous materials SBA15 modified carbon paste electrode, cyclic voltammetry modified electrodes were characterized. The aminoglutethimide electrochemical behavior of studies have shown that aminoglutethimide a pair of redox peaks at 0.791V, 0.078V and 0.257V at a separate oxidation peak. Aminoglutethimide electrochemical behavior of a multimodal irreversible process. Within the scan range of 20 to 150 mV / s, aminoglutethimide electrochemical reaction at the electrode surface is a surface control was within the range of 200-600 mV / s scan rate, the electrode reaction is a diffusion controlled process, the corresponding electrical chemical rate constant of 2.41 ± 0.01 s -1 sup>, the electrode surface diffusion coefficient D for the 2.12 × 10 -3 sup> cm 2 sup> / s, surface concentration (5.87 ± 0.01) × 10 -11 sup> mol / cm 2 sup>. Aminoglutethimide and DNA interaction studies have shown that aminoglutethimide with DNA insert mode, the binding constant and the number of binding sites for β = 2.41 × 10 5 sup> M -1 sup> and m = 1.69. By optimizing the conditions established the aminoglutethimide method of measuring the linear range was 4.30 × 10 -7 sup> M-8.60 × 10 -6 sup> M and 9.60 × 10 -6 sup> M-1.08 × 10 -4 sup> M, the limit of detection (S / N = 3) to 4.62 × 10 -9 sup> M. (4) prepared using electrodeposition method of Nafion / Au / GCE electrode modified electrodes were characterized by cyclic voltammetry. The electrochemical behavior of leucovorin, leucovorin, an oxidation peak at 0.570V, the electrochemical oxidation is a completely irreversible process, the number of electron transfer and proton transfer ratio of n: m = 2:3. Low scanning speed range of 20-180 mV / s, leucovorin electrochemical reaction by the apparent control of the electrochemical rate constant ks = 0.516 ± 0.001 the s -1 sup>. In the range of 200-600 mV / s scan speed, the electrochemical reaction is diffusion controlled. Leucovorin, in Nafion / Au / GCE surface of the diffusion coefficient and the electrode surface adsorption capacity (2.44 ± 0.01) × 10 -5 sup> cm 2 sup> / s (3.03 ± 0.01) × 10 -10 sup> mol / cm 2 sup>. The leucovorin, DNA Interactions, leucovorin, and DNA by electrostatic force, combined with the constant beta and the number of binding sites m sup> M-1 and 1.83 to 4.89 × 10 5. Establish a method for determination of leucovorin, optimum conditions, the linear range is 6.42 × 10 -6 sup> M-1.18 × 10 -5 sup> M, the detection limit to 2.04 × 10 < sup> -8 sup> M.
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CLC: > Medicine, health > Pharmacy > Pharmacology
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