Electron Spin Resonance Method Research Articles

Shelf-Life Optimisation of Plasma Polymerised (2,2,6,6-Tetramethylpiperidin-1-yl)oxyl (TEMPOpp) Coatings; A New Possible Approach to Tackle Infections in Chronic Wounds.

Chronic wounds fail to heal and are accompanied by an ongoing infection. They cause suffering, shorten lifespans, and their prevalence is increasing. Unfortunately, the medical treatment of chronic wounds has remained unchanged for decades. A novel approach to break the biological vicious cycle is the long-lived radical (2,2,6,6-Tetramethylpiperidin-1-yl)oxyl (TEMPO). TEMPO can be plasma polymerised (TEMPOpp) into thin coatings that have antimicrobial properties. However, due to its radical nature, quenching causes it to lose effectiveness over time. Our aim in this study was to extend the shelf-life of TEMPOpp coatings using various storage conditions: Namely, room temperature (RT), room temperature & vacuum sealed (RTV), freezer temperature & vacuum sealed (FTV). We have analysed the coatings’ quality via the surface analytical methods of X-Ray Photoelectron spectroscopy (XPS) and electron paramagnetic resonance (EPR); finding marked differences among the three storage conditions. Furthermore, we have compared the antimicrobial efficacy of the stored coatings against two major bacterial pathogens, Staphylococcus aureus and Staphylococcus epidermidis, commonly found in chronic wounds. We did so both qualitatively via live/dead staining, as well as quantitatively via (2-methoxy-4-nitro-5-sulfophenyl)-5-[(phenylamino) carbonyl]-2H-tetrazolium (XTT) viability assay for up to 15 weeks in 5 weeks increments. Taken all together, we demonstrate that samples stored under FTV conditions retain the highest antimicrobial activity after 15 weeks and that this finding correlates with the retained concentration of nitroxides.

Differences in the properties of porcine cortical and nuclear fiber cell plasma membranes revealed by saturation recovery EPR spin labeling measurements

Eye lens membranes are complex biological samples. They consist of a variety of lipids that form the lipid bilayer matrix, integral proteins embedded into the lipid bilayer, and peripheral proteins. This molecular diversity in membrane composition induces formation of lipid domains with particular physical properties that are responsible for the maintenance of proper membrane functions. These domains can be, and have been, effectively described in terms of the rotational diffusion of lipid spin labels and oxygen collision with spin labels using the saturation recovery (SR) electron paramagnetic resonance method and, now, using stretched exponential function for the analysis of SR signals. Here, we report the application of the stretched exponential function analysis of SR electron paramagnetic resonance signals coming from cholesterol analog, androstane spin label (ASL) in the lipid bilayer portion of intact fiber cell plasma membranes (IMs) isolated from the cortex and nucleus of porcine eye lenses. Further, we compare the properties of these IMs with model lens lipid membranes (LLMs) derived from the total lipids extracted from cortical and nuclear IMs. With this approach, the IM can be characterized by the continuous probability density distribution of the spin-lattice relaxation rates associated with the rotational diffusion of a spin label, and by the distribution of the oxygen transport parameter within the IM (i.e., the collision rate of molecular oxygen with the spin label). We found that the cortical and nuclear LLMs possess very different, albeit homogenous, spin lattice relaxation rates due to the rotational diffusion of ASL, indicating that the local rigidity around the spin label in nuclear LLMs is considerably greater than that in cortical LLMs. However, the oxygen transport parameter around the spin label is very similar and slightly heterogenous for LLMs from both sources. This heterogeneity was previously missed when distinct exponential analysis was used. The spin lattice relaxation rates due to either the rotational diffusion of ASL or the oxygen collision with the spin label in nuclear IMs have slower values and wider distributions compared with those of cortical IMs. From this evidence, we conclude that lipids in nuclear IMs are less fluid and more heterogeneous than those in cortical membranes. Additionally, a comparison of properties of IMs with corresponding LLMs, and lipid and protein composition analysis, allow us to conclude that the decreased lipid-to-protein ratio not only induces greater rigidity of nuclear IMs, but also creates domains with the considerably decreased and variable oxygen accessibility. The advantages and disadvantages of this method, as well as its use for the cluster analysis, are discussed.

Spin Dynamics of the Radicals Produced from Methane Sulfonic Acid and Acetic Acid by Hydroxyl Radicals in Aqueous Solution Studied by Means of Time-Resolved Electron Spin Resonance Spectroscopy.

Fundamental information on the reactions of ·OH radical with alkyl sulfonic acid and carboxylic acid is important for understanding the degradation of the polymer electrolytes for fuel cells. In the present research, the spin dynamics of the organic radicals generated by the ·OH radical was investigated by means of a time-resolved electron spin resonance (TR-ESR) method with the pulsed laser irradiation on H2O2 in aqueous solution. The time profiles of the ESR signals of ·SO3-, ·CH2SO3-, ·CH2COOH, and ·CH2COO- have been analyzed along with the evaluation of characteristics of electron spins such as the g factor, hyperfine coupling constant A, lifetime of radicals, and electron spin relaxation time T1. The effects of the laser repetition frequency on the TR-ESR spectra, the pH dependence on the kinetic parameters, and the mechanism of chemically induced dynamic electron polarization (CIDEP) were discussed. The radical pair mechanism was suggested for the CIDEP, where the electron spins of these radicals are polarized by forming a free radical pair with another radical or the·OH radical, which have remained in the vicinity of photon absorption.

Study of the Effect of External Factors on the Structural and Dynamic Parameters of Film Materials Based on Poly(3-Hydroxybutyrate) and Polyactide

The structure of film and fibrous materials based on poly(3-hydroxybutyrate)–polylactide blends has been studied. Ultrafine fibers have been spun by the electrospinning of a polymer solution; the films have been prepared by casting onto a glass substrate. Using optical microscopy, it has been shown that, depending on the fiber composition, the fibers have different diameters and geometries. The features of the crystalline and amorphous structures of the composites have been studied by the spin-probe electron paramagnetic resonance method and differential scanning calorimetry. The addition of 10 and 30% of polylactide to the composite leads to a slowdown of the molecular mobility in the film and fibrous materials and an increase in the enthalpy of melting of the ultrafine fibers. At a polylactide content in the blend of 30%, a kink in the dependences of the enthalpy of melting, correlation time, and radical concentration is observed. Annealing at a temperature of 140°C and exposure to an aqueous medium at 25 and 70°C for 3 h have a significant effect on the polymer structure: the enthalpy of melting and molecular dynamics increase, while the radical concentration in the ultrafine fibers and the film material decreases. Ozonolysis has a complex effect on the structure of the ultrafine fibers.

Discovery of Bisulfite and an Uncharacterized Carbon-Centered Radical Systems in Non-Dry-Hopped and Dry-Hopped Beers Using a Different Spin Trap, 5, 5-Dimethyl-1-Pyrroline-N-Oxide, and a New Electron Paramagnetic Resonance Method

The amount of bisulfite (HSO3 −, hydrated SO2) needed in beer to extend flavor stability is controversial with results that show elevated HSO3 − levels in beer improves beer shelf-life analytically, yet decreases sensory flavor and flavor stability. Electron paramagnetic resonance (EPR) beer methods, using the N-tert-Butyl-α-phenylnitrone (PBN) spin trap, can detect the hydroxyl and ethoxy radicals from ethanol (•OH/CH3C • HOH). Water soluble 5, 5-Dimethyl-1-Pyrroline-N-Oxide (DMPO) trapped bisulfite (•SO3 -) and uncharacterized C-centered radicals in vastly different dry-hopped (DH) and non-dry-hopped (NDH-a and NDH-b) beers and can also trap radicals of nitrogen and oxygen. A new DMPO capillary tube method detected •SO3 - and C-centered radicals in cold stored and forced aged DH and NDH beers, dosed with 3 mM and 5 mM of sodium sulfite (Na2SO3), and displayed substantially higher •SO3 - radical signals from the 5 mM versus 3 mM Na2SO3 dosage. The lowest SO2 DH beer had greater polyphenols (antioxidants) and significantly less •SO3 - radical activity than the lower polyphenols NDH beers, indicating higher polyphenols in the DH beer quench more •SO3 - and uncharacterized C-centered radicals by way of H2O2 reduction. Increasing polyphenols and reducing beer SO2 levels can potentially improve beer flavor stability and reduce bisulfite allergies in humans.

Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(dppf)Fe(CO) 3]+/0.

Here we explore the electronic structure of the diiron complex [(dppf)Fe(CO)3]0/+ [10/+; dppf = 1,1'-bis(diphenylphosphino)ferrocene] in two oxidation states by an advanced multitechnique experimental approach. A combination of magnetic circular dichroism, X-ray absorption and emission, high-frequency electron paramagnetic resonance (EPR), and Mössbauer spectroscopies is used to establish that oxidation of 10 occurs on the carbonyl iron ion, resulting in a low-spin iron(I) ion. It is shown that an unequivocal result is obtained by combining several methods. Compound 1+ displays slow spin dynamics, which is used here to study its geometric structure by means of pulsed EPR methods. Surprisingly, these data show an association of the tetrakis[3,5-bis(trifluoromethylphenyl)]borate counterion with 1+.

Performance and mechanism of nickel hydroxide catalyzed reduction of N-nitrosodimethylamine by iron

Since iron (Fe) was first proven to have a strong reduction ability, it has been successfully applied to remove pollutants from water. In this study, nickel hydroxide (Ni(OH)2), a catalyst commonly used in hydrogen evolution reactions, was added to improve the activity of Fe to remove N-nitrosodimethylamine (NDMA). The results showed that with the increasing Ni(OH)2 dosages, the reactions accelerated. The NDMA removal rates increased when the pH value was 6 or 7. Further, when the dissolved oxygen concentration was in the range of 0–12.0 mg∙L−1, it had little effect on the Fe/Ni(OH)2 system, and all the reactions obeyed pseudo-first-order kinetics. 1,1-dimethylhydrazine and dimethylamine were formed during NDMA degradation. The capture of active substances and electron spin resonance method confirmed that the main active species were active hydrogen atoms, which participated in the removal of NDMA. Ni(OH)2 acting as a catalyst was confirmed using wide-angle X-ray diffraction, X-ray photoelectron spectroscopy and Ni2+ dissolution. Further, catalytic hydrogenation was proposed as the main removal mechanism as Ni(OH)2 promotes the corrosion of Fe and dissociation of water, thereby generating more active hydrogen atoms. In addition, Ni(OH)2 may activate both Fe and NDMA. This technique could be employed as an alternative for NDMA reduction and expand the application field of Ni(OH)2.

Study Of Fossil Coals In The Kuznetsk Basin By Epr Spectroscopy

Fossil coals of the Kuznetsk Basin of varying degrees of metamorphism were studied by the method of electron paramagnetic resonance. It is shown that in the series from brown coal to anthracite, the g-factor of the EPR signal decreases, due to the aromatization of the carbon framework and a decrease in oxygen-containing and hydrogen-containing fragments in the coals. The maximum width of the EPR spectrum is observed for coals of the middle stage of metamorphism, which indicates the presence of both aliphatic and aromatic paramagnetic centers (PCs) in their structure. Also, in the series of coal metamorphism, the concentration of PCs increases. Thus, it has been shown that in the process of coal metamorphism, a change in the electronic structure occurs, associated with the rearrangement of the carbon skeleton of the organic mass of coal (OMC) and a decrease in the amount of oxygen-containing and hydrogen-containing radicals.

A magnetoactive metamaterial based on a structured ferrite

Subject and Purpose. The use of spatially structured ferromagnets is promising for designing materials with unique predetermined electromagnetic properties welcome to the development of magnetically controlled microwave and optical devices. The paper addresses the electromagnetic properties of structured ferrite samples of a different shape (spatial geometry) and is devoted to their research by the method of electron spin resonance (ESR). Methods and methodology. The research into magnetic properties of structured ferrite samples was performed by the ESR method. The measurements of transmission coefficient spectra were carried out inside a rectangular waveguide with an external magnetic field applied. Results. We have experimentally shown that over a range of external magnetic field strengths, the frequency of the ferromagnetic resonance (FMR) of grooved ferrite samples (groove type spatial geometry) increases with the groove depth. The FMR frequency depends also on the groove orientation relative to the long side of the sample. We have shown that as the external static magnetic field approaches the saturation field of the ferrite, the FMR frequency dependence on the external static magnetic field demonstrates "jump-like" behavior. And as the magnetic field exceeds the ferrite saturation field, the FMR frequency dependence on the groove depth gets a monotonic character and rises with the further growth of the field strength. Conclusion. We have shown that the use of structured ferrites as microwave electronics components becomes reasonable at magnetic field strengths exceeding the saturation field of the ferrite. At these fields, such a ferrite offers a monotonically increasing dependence of the resonant frequency on the external magnetic field and on the depth of grooves on the ferrite surface. Structured ferrites are promising in the microwave range as components of controlled filters, polarizers, anisotropic ferrite resonators since they can provide predetermined effective permeability and anisotropy

ESR Chronology of Bedrock Fault Activity in Carbonate Area: Preliminary Results from the Study of the Lijiang-Xiaojinhe Fault, Southeastern Tibet, China

Carbonated rocks constitute one of the main lithologies of the southeastern Tibet area, China, a tectonically very active zone. However, due to the lack of suitable dating materials, it is difficult to carry out chronological studies of the local tectonic evolution in such carbonate areas. In the present study, electron spin resonance (ESR) method had been applied on the dating of carbonates heated during fault activity of the Lijiang-Xiaojinhe (LX) Fault, an important active fault located in the northwest of Yunnan Province. Clear displaced landforms show that the fault has undergone strong late-Quaternary activity. During the fault activity, the heat produced by friction lead to the melting of the frictional surface of the rocks, and the melting can attenuate or zero the ESR dating signal of carbonate. The aim of the present paper was to check the ability of carbonate use to chronologically identify fault activity using electron spin resonance (ESR) method. The results showed the last fault activity of the LX fault was dated by ESR about 2.0±0.2 ka ago, in agreement with historical and radiocarbon data. Hence ESR can be if necessary a practicable dating alternative method for the study of fault activity chronology in carbonate rock area.

Study of Translocation of Stabilized NO Forms through Rat Skin using Electron Paramagnetic Resonance Method

We studied the effect of dinitrosyl-iron complexes with N-acetyl-L-cysteine as a thiol-containing ligand (DNIC-Acc) after transdermal administration to rats. Electron paramagnetic resonance spectroscopy with a lipophilic NO spin trap (a complex of iron and diethyldithiocarbamate ions) showed that DNIC-Acc administration significantly increased the total level of NO in the lung and liver tissues of the animal, which was accompanied by a slight decrease in the mean BP (<10%).

Changes in the Relative Nitric Oxide Content in the Cortex of a Rat Brain in the Acute Ischemia Model

This study uses the electron paramagnetic resonance (EPR) method to study changes in the relative nitric oxygen content in the cortex of a rat brain in conditions of acute ischemia. Laser-induced vascular thrombosis is used as the model of ischemia. Rose bengal is administered into the bloodstream beforehand. In response to laser beaming, it generates reactive oxygen species, which induces protein coagulation, vascular wall damage, and, as a consequence, the formation of thrombus. It is shown histologically that the acute ischemic process ends a day after the laser surgery, and active remission, with the corresponding morphological changes in the area of the lesion, starts within three days. The relative nitric oxide content is determined 1 and 3 days after the brain vascular photothrombosis using the NO–Fe–DETC paramagnetic complex as a spin trap. The nitric oxide content is estimated by the extreme lower field of the EPR spectrum of this complex. It is shown that a significant increase in the relative nitric oxide (NO) content occurs on the third day after laser surgery and coincides with the beginning of remission after the acute ischemia. A possible role of nitric oxide in the remission is discussed in the study.

Dipolar coupling-based electron paramagnetic resonance method for protease enzymatic characterization and inhibitor screening.

Herein, we report an EPR-based method for protease enzymatic characterization and inhibitor screening. This method utilizes dual paramagnetically-labeled probes consisting of a nitroxide spin probe and a Gd3+ ion flanking a peptide that could be specifically cleaved by protease caspase-3. Distance-dependent dipolar coupling between the two paramagnetic centers can be modulated by the protease cleavage activity, thus providing a straightforward and convenient method for protease activity detection using EPR spectroscopy under ambient conditions. Moreover, time-course monitoring of the protease-catalyzed cleavage reaction demonstrated that this EPR-based method could not only allow a direct quantitative enzymatic kinetic assessment, but also could be used for protease inhibitor screening, thus holding great potential in drug discovery studies.

Reversible Dimerization of Human Serum Albumin.

Pulsed Dipolar Spectroscopy (PDS) methods of Electron Paramagnetic Resonance (EPR) were used to detect and characterize reversible non-covalent dimers of Human Serum Albumin (HSA), the most abundant protein in human plasma. The spin labels, MTSL and OX063, were attached to Cys-34 and these chemical modifications of Cys-34 did affect the dimerization of HSA, indicating that other post-translational modifications can modulate dimer formation. At physiologically relevant concentrations, HSA does form weak, non-covalent dimers with a well-defined structure. Dimer formation is readily reversible into monomers. Dimerization is very relevant to the role of HSA in the transport, binding, and other physiological processes.

Determination of Optimal Modulation Amplitude for Electron Spin Resonance (ESR) Dating and Dosimetry Studies of Tooth Enamel

Fossil remains, which provide important information about past life and ecology, are especially important in natural history and life evolution. Recently, many interdisciplinary dating studies have been conducted and many different techniques have been used to investigate the data obtained in this field. Electron Spin Resonance (ESR) (or alternatively, Electron Paramagnetic Resonance, EPR) is one of the methods used in absolute dating and dosimetry studies. It is based on determination of the radiation-centered radicals obtained from the radiation dose absorbed by irradiated materials. One of the important problems in dosimetry and dating studies performed with ESR method is the dependence of experimental parameters on the accumulated dose. The accumulated dose value is effective in determining the actual result of the dating and dosimetric samples. This value is influenced from the stability of the ESR centers, experimental stages, sample preparation or measurement processes. In this study, how the modulation amplitude parameter affects ESR signal intensity in ESR dating and dosimetry studies of tooth enamel investigated. The selective archaeological animal tooth enamel sample was used from the archaeological site of Köşk Höyük, in Turkey for experimental studies. This sample was prepared with combined processes of mechanical and chemical treatment of tooth in laboratory. Tooth enamel sample was irradiated by 60Co gamma-ray source in dose of 1000 Gy at Çekmece Nuclear Research and Training Center (ÇNAEM), Turkey. After irradiation, ESR spectra were recorded at different modulation amplitude values at room temperature using X-band ESR Spectrometer. According to the results obtained, the most suitable modulation amplitude values for ESR measurements of tooth enamel sample examined in the study was found between 0.25G and 2G.

Chemical and spectroscopic characteristics of humic acid from a clay loam soil in Ontario after 52 years of consistent fertilization and crop rotation

Long-term fertilization and crop rotation can influence both organic C sequestration as well as the C composition of soils and the more resistant organic C compounds contained in humic acid (HA). This study examined the effects of fertilization and cropping type (monoculture corn (MC) and Kentucky bluegrass sod (KBS) and corn-oat-alfalfa-alfalfa rotation (RC)) on the HA composition of soil from a 52-year field study in southern Ontario, Canada. Humic acid samples were extracted from soil, and elemental analysis, infrared spectroscopy, solid state 13 C nuclear magnetic resonance spectra, and electron paramagnetic resonance methods were used to determine the influence of the cropping type on the characteristics of HA. Both fertilization and cropping type affected the chemical characteristics of HA. Fertilization led to a 5.9% increase in C, a 7.6% decrease in O, and lower O/C and (N + O)/C ratios in HA as compared to the corresponding non-fertilized treatments. Rotation resulted in a lower proportion of C (48.1%) and a greater (N + O)/C ratio (0.7) relative to monoculture cropping. Infrared spectroscopy analysis showed that HA contained more C-O groups in fertilized soil than in non-fertilized soil under MC and KBS. Fertilization increased the O-alkyl-C, phenolic-C, and free radical contents of HA relative to non-fertilization treatments. Rotation decreased the aliphatic and carboxyl groups and increased the O-alkyl, carbohydrate, aryl, and phenolic groups and free radicals, relative to MC and KBS. Both long-term crop rotation and fertilization dramatically modified the soil HA composition. Significant relationships were observed between the molecular composition of HA and soil organic C. Hence, humic acid characterization could be used as an indicator of the long-term sustainability of crop management practices.

Investigation of lanthanum substitution effects in yttrium aluminium garnet: importance of solid state NMR and EPR methods

In this study, yttrium aluminium garnet (YAG) specimens in which yttrium was partially substituted by lanthanum Y3-xLaxAl5O12 (YLaAG) were prepared by an aqueous sol-gel method. YLaAG samples were analyzed by X-ray diffraction (XRD), solid state nuclear magnetic resonance (NMR) and electron paramagnetic resonance (EPR) methods. The presence of Ce3+ ions as an impurity originating from starting material was determined, therefore, luminescence measurements of YLaAG samples were also recorded. It was demonstrated that luminescent properties are strongly dependent on the phase composition of synthesized species. The XRD analysis results showed that only low substitution of yttrium by lanthanum is possible in Y3-xLaxAl5O12 without destroying garnet crystal structure. It was also demonstrated, that solid state NMR and EPR methods are indispensable tools for the explanation of processes and properties observed in the newly synthesized Y3-xLaxAl5O12 compounds.

Rate constant measurements for radical addition reactions with C60 by means of time-resolved EPR and spin-echo detected pulsed EPR spectroscopy

C60 fullerene shows high reactivity with free radicals and is considered as a radical trapping agent. Addition reaction of radicals to C60 was investigated by time-resolved Electron Paramagnetic Resonance (TR-EPR) and pulsed EPR methods. The structures of adduct radicals were determined by TR-EPR, and the reaction mechanism was clarified. Addition rate constants, k's of radicals to C60 were measured by the electron spin echo detection method utilizing pulsed EPR. The measured k values were remarkably high and the reactions are diffusion-controlled. We discussed activation energy on the basis of the charge transfer effect and enthalpy change.

Interaction of alpha-crystallin with four major phospholipids of eye lens membranes

It is well-studied that the significant factor in cataract formation is the association of α-crystallin, a major eye lens protein, with the fiber cell plasma membrane of the eye lens. The fiber cell plasma membrane of the eye lens consists of four major phospholipids (PLs), i.e., phosphatidylcholine (PC), phosphatidylethanolamine (PE), phosphatidylserine (PS), and sphingomyelin (SM). Despite several attempts to study the interaction of α-crystallin with PLs of the eye lens membrane, the role of individual PL for the binding with α-crystallin is still unclear. We recently developed the electron paramagnetic resonance (EPR) spin-labeling method to study the binding of α-crystallin to the PC membrane (Mainali et al., 2020a). Here, we use the recently developed EPR method to explicitly measure the binding affinity (Ka) of α-crystallin to the individual (PE*, PS, and SM) and two-component mixtures (SM/PE, SM/PS, and SM/PC in 70:30 and 50:50 mol%) of PL membranes as well as the physical properties (mobility parameter and maximum splitting) of these membranes upon binding with α-crystallin. One of the key findings of this study was that the Ka of α-crystallin binding to individual PL membranes followed the trends: Ka(PC) > Ka(SM) > Ka(PS) > Ka(PE*), indicating PE* inhibits binding the most whereas PC inhibits binding the least. Also, the Ka of α-crystallin binding to two-component mixtures of PL membranes followed the trends: Ka(SM/PE) > Ka(SM/PS) > Ka(SM/PC), indicating SM/PC inhibits binding the most whereas SM/PE inhibits binding the least. Except for the PE* membrane, for which there was no binding of α-crystallin, the mobility parameter for all other membranes decreased with an increase in α-crystallin concentration. It represents that the membranes become more immobilized near the headgroup regions of the PLs when more and more α-crystallin binds to them. The maximum splitting increased only for the SM and the SM/PE (70:30 mol%) membranes, with an increase in the binding of α-crystallin. It represents that the PL headgroup regions of these membranes become more ordered after binding of α-crystallin to these membranes. Our results showed that α-crystallin binds to PL membranes in a saturable manner. Also, our data suggest that the binding of α-crystallin to PL membranes likely occurs through hydrophobic interaction between α-crystallin and the hydrophobic fatty acid core of the membranes, and such interaction is modulated by the PL headgroup's size and charge, hydrogen bonding between headgroups, and PL curvature. Thus, this study provides an in-depth understanding of α-crystallin interaction with the PL membranes made of individual and two-component mixtures of the four major PLs of the eye lens membranes.

In Vitro Properties of Manganese-Substituted Tricalcium Phosphate Coatings for Titanium Biomedical Implants Deposited by Arc Plasma.

Bioactive manganese (Mn)-doped ceramic coatings for intraosseous titanium (Ti) implants are developed. Arc plasma deposition procedure is used for coatings preparation. X-ray Diffraction, Scanning Electron Microscopy-Energy Dispersive X-ray Spectroscopy, and Electron Paramagnetic Resonance (EPR) methods are applied for coatings characterization. The coatings are homogeneous, composed of the main phase α-tricalcium phosphate (α-TCP) (about 67%) and the minor phase hydroxyapatite (about 33%), and the Mn content is 2.3 wt%. EPR spectroscopy demonstrates that the Mn ions are incorporated in the TCP structure and are present in the coating in Mn2+ and Mn3+ oxidation states, being aggregated in clusters. The wetting contact angle of the deposited coatings is suitable for cells’ adhesion and proliferation. In vitro soaking in physiological solution for 90 days leads to a drastic change in phase composition; the transformation into calcium carbonate and octacalcium phosphate takes place, and no more Mn is present. The absence of antibacterial activity against Escherichia coli, Enterococcus faecalis, and Pseudomonas aeruginosa bacteria strains is observed. A study of the metabolic activity of mouse fibroblasts of the NCTC L929 cell line on the coatings using the MTT (dye compound 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) test demonstrates that there is no toxic effect on the cell culture. Moreover, the coating material supports the adhesion and proliferation of the cells. A good adhesion, spreading, and proliferative activity of the human tooth postnatal dental pulp stem cells (DPSC) is demonstrated. The developed coatings are promising for implant application in orthopedics and dentistry.