Peculiarities of the effect of manganese and cadmium ions on the properties of liposomes from lecithin

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The features of the influence of divalent cadmium and manganese ions on the ability of lecithin to form aggregates in water medium, its ζ-potential, and the state of the lipid peroxidation processes have been studied. The methods used were TLC, dynamic light scattering, and processing of UV spectra using the Gauss method. It was revealed that cadmium ions accelerate the processes of lipid oxidation in liposomes, and manganese ions inhibit them. At the same time, cadmium ions, as opposed to manganese ions, require more period to interact with the membrane structure of liposomes. The data obtained and the analysis of the literature allow us to conclude that the cadmium and manganese ions present in the solution influence the spontaneous aggregation of lecithin and participate at different stages of the oxidation process in accordance with their biological activity when entering the body.

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作者简介

P. Beletskaya

Emanuel Institute of Biochemical Physics of the Russian Academy of Sciences

Email: shishkina@sky.chph.ras.ru
俄罗斯联邦, Moscow

A. Dubovik

Emanuel Institute of Biochemical Physics of the Russian Academy of Sciences; Nesmeyanov Institute of Organoelement compounds, Russian Academy of Sciences

Email: shishkina@sky.chph.ras.ru
俄罗斯联邦, Moscow; Moscow

V. Shvydkiy

Emanuel Institute of Biochemical Physics of the Russian Academy of Sciences

Email: shishkina@sky.chph.ras.ru
俄罗斯联邦, Moscow

L. Shishkina

Emanuel Institute of Biochemical Physics of the Russian Academy of Sciences

编辑信件的主要联系方式.
Email: shishkina@sky.chph.ras.ru
俄罗斯联邦, Moscow

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2. Fig. 1. Distribution of the light scattering intensity of the size (d) of lecithin aggregates in distilled water (1) and in the presence of cadmium (2) and manganese (3) ions. [Lecithin] = 4.3 10–5 M, [M+] = 10–4 M.

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3. Fig. 2. Change in size (d) of the main fraction of lecithin particles depending on the concentration of cadmium ions in the solution at a solution exposure time of 0.5 (1) and 2.5 h (2). The dashed lines indicate the accuracy range for determining the diameter of lecithin liposomes.

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4. Fig. 3. Effect of cadmium ion concentration (exposure time – 2.3 h) and manganese (exposure time – 0.5 h) on the diameter of the main fraction of lecithin liposomes in distilled water. The dashed lines indicate the accuracy range of determining the diameter of lecithin liposomes.

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5. Fig. 4. Typical UV spectrum of lecithin in the presence of manganese ions in solution ([Mn2+] = 10–4 M) and its Gaussians: 1 and 6 – initial and calculated spectra, 2 – 197.5 nm, 3 – 231 nm, 4 – 257 nm, 5 – 330 nm.

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6. Fig. 5. Typical UV spectrum of lecithin in the presence of cadmium ions in solution ([Cd2+] = 10–4 M) and its Gaussians: 1 and 7 – initial and calculated spectra, 2 – 197.5 nm, 3 – 229.5 nm, 4 – 273 nm, 5 – 335 nm, 6 – 395 nm.

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7. Fig. 6. Changes in the ratio of ketodienes and diene conjugates [KD]/[DK] in liposome lipids depending on the concentration of manganese and cadmium ions in the solution.

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