Prospects for Using a Binding Agent to Improve the Adhesion of a Bioactive Coating on Surfaces with Different Structures

Author(s):  
E. A. Bogdanova ◽  
V. M. Skachkov ◽  
K. V. Nefedova
Author(s):  
Екатерина Анатольевна Богданова ◽  
Владимир Михайлович Скачков

Порошки наноразмерных гидроксиапатита и фторапатита синтезированы методом осаждения из растворов. В качестве связующего вещества использован пищевой желатин. Такая композиция имеет высокую адгезию на материалах различной природы и пористости. Получены также пористые пленки и гранулы с развитой удельной поверхностью. Рассмотрены их микроструктуры. Изучена возможность использования коллоидной суспензии и водной суспензии кристаллического апатита в сочетании с раствором желатина в качестве биоактивного материала, как для создания покрытий, так и получения гранул. Установлено, что использование порошка апатита совместно с желатином позволяет существенно сократить сроки формирования биоактивного покрытия и значительно повысить его адгезионную прочность. Сопоставлены получаемые гранулы апатита по размерам в зависимости от концентрации желатина в водном растворе. На разработанные биоактивные покрытия и гранулированный материал на основе наноразмерного апатита со связующим агентом поданы заявки на патент. Nanoscale hydroxyapatite and fluorapatite powders were synthesized by precipitation from solutions. Food gelatin is used as a binder. This composition has a high adhesion on materials of different nature and porosity. Porous films and granules with a developed specific surface area were also obtained. Their microstructures are considered. The possibility of using a colloidal suspension and an aqueous suspension of crystalline apatite in combination with a gelatin solution as a bioactive material, both for creating coatings and obtaining granules, has been studied. It is established that the use of apatite powder together with gelatin can significantly reduce the time of formation of a bioactive coating and significantly increase its adhesive strength. The obtained apatite granules are compared in size depending on the concentration of gelatin in an aqueous solution. Patent applications have been filed for the developed bioactive coatings and granular material based on nanoscale apatite with a binding agent.


Author(s):  
T. R. Davydova ◽  
А. I. Shaikhaliev ◽  
D. A. Usatov ◽  
G. A. Gasanov ◽  
R. S. Korgoloev

The aim of this study was to study the effect of surface branching of titanium endoprostheses on the efficiency of fibrointegration. The object of the study was samples of titanium alloy Ti6Al4V in the form of disks with a diameter of 5 mm and a thickness of 1 mm with various surface treatments: 1) samples with a rough surface after sandblasting; 2) samples with a rough surface after sandblasting with a bioactive coating of titanium dioxide TiO2 with anatase structure. The study of surface roughness was carried out by profilometry. Evaluation of the spreading and proliferation of cells on the surface of test samples, as well as evaluation of the effectiveness of fibrointegration was carried out according to standard methods using scanning electron microscopy. During the experiments, mesinchymal stem cells were sown on test samples and the test samples were introduced into the soft tissues of experimental animals. Based on the results obtained, it was concluded that the technology of forming rough surfaces by sandblasting does not provide high uniformity and reproducibility in the nanometer range and, apparently, another method for obtaining a rough surface should be chosen. The application of a bioactive coating of titanium dioxide TiO2 with the anatase structure to the surface of titanium endoprostheses increases the efficiency of fibrointegration, however, primarily the fibrointegration of titanium endoprostheses depends on their surface roughness, which determines the concentration of cell structures, the intensity of their adhesion and the ability to fibrointegrative process.


2020 ◽  
Vol 16 (9) ◽  
pp. 1404-1410
Author(s):  
Rishabha Malviya

Background: In the previous study, investigators have synthesized acrylamide grafted and carboxymethylated derivatives of neem gum and evaluated their potential in the formulation of nanoparticles. In continuation of previous work, authors have evaluated neem gum polysaccharide (NGP), acrylamide grafted neem gum polysaccharide (NGP-g-Am) and carboxymethylated neem gum polysaccharide (CMNGP) as binding agent in the tablet dosage form. Methods: Diclofenac sodium was used as a model drug while microcrystalline cellulose and talc were used as excipient in the preparation of granules employing wet granulation technique. NGP, NGP-g-Am and CMNGP were utilized as binding agent in the preparation of granules. Prepared granules were characterized for various pre-compression and post-compression parameters. Results and Discussion: Binding agents were used in the concentration of 4-24%w/w. NGP incorporated granules showed more bulk density and lower values of tapped density, Carr’s index, bulkiness, Hausner’s ratio and angle of repose as compared to NGP-g-Am consisting granules. NGP-g-Am consisting tablets showed more hardness and zero friability as compared to NGP based tablets. Drug content was found lower for the tablets having grafted polymer in place of NGP. CMNGP were also utilized to prepare granules but granules were not be able to compress keeping all the compacting parameters same as used in the case of NGP and NGP-g-Am consisting granules. NGP and NGP-g-Am were able to sustain drug release up to 6 and 8 h, respectively. Conclusion: It can be concluded that NGP-g-Am induces better properties when used as a binder in the tablet formulation than native polymer, while CMNGP cannot be utilized as a binding agent in the preparation of a tablet.


2020 ◽  
Vol 11 (1) ◽  
pp. 220
Author(s):  
Svetlana A. Kulikova ◽  
Sergey E. Vinokurov ◽  
Ruslan K. Khamizov ◽  
Natal’ya S. Vlasovskikh ◽  
Kseniya Y. Belova ◽  
...  

Magnesium oxide is a necessary binding agent for the synthesis of a magnesium potassium phosphate (MPP) matrix based on MgKPO4 × 6H2O, which is promising for the solidification of radioactive waste (RW) on an industrial scale. The performed research is devoted to finding a cost-effective approach to the synthesis of MPP matrix by using MgO with an optimal ratio of the quality of the binding agent and the cost of its production. A method for obtaining MgO from the widely available natural mineral serpentinite was proposed. The phase composition, particle morphology, and granulometric composition of MgO were studied. It was found that the obtained MgO sample, in addition to the target periclase phase, also contains impurities of brucite and hydromagnesite; however, after calcining at 1300 °C for 3 h, MgO transforms into a monophase state with a periclase structure with an average crystallite size of 62 nm. The aggregate size of the calcined MgO powder in an aqueous medium was about 55 μm (about 30 μm after ultrasonic dispersion), and the specific surface area was 5.4 m2/g. This powder was used to prepare samples of the MPP matrix, the compressive strength of which was about 6 MPa. The high hydrolytic stability of the MPP matrix was shown: the differential leaching rate of magnesium, potassium, and phosphorus from the sample on the 91st day of its contact with water does not exceed 1.6 × 10−5, 4.7 × 10−4 и 8.9 × 10−5 g/(cm2·day), respectively. Thus, it was confirmed that the obtained MPP matrix possesses the necessary quality indicators for RW immobilization.


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