Composites based on calcium phosphates in the matrix of biopolymer (citrated plasma and fibrin) were synthesized in neutral and alkaline medium. At pH 7 brushite composites were obtained, whereas at pH 11 amorphized hydroxyapatite was precipitated. Disruption of precipitation conditions led to the formation of tricalcium phosphate impurity, which was detected by XRD after thermal treatment of composites at 800 °C. Composition and morphology of calcium phosphates did not depend on biopolymer nature. To determine bioactivity degree, composites were incubated in model Simulated Body Fluid (SBF) for 75 days. It was found that composites based on amorphized hydroxyapatite incorporated in biopolymer matrix have maximum growth of biomimetic layer of apatite.

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Bovine pericardium samples modified with ethylene glycol diglycidyl ether, designed for surgical correction of congenital heart defects and large blood vessels, were studied by scanning electron microscopy, X-ray diffraction, IR spectroscopy, and differential thermal analysis. It was found that the initial samples of pericardium, before implantation, contain sites of disorganization of the collagen matrix, fragile fracture of collagen fibrils and destruction of the interstitial membranes promoting the penetration of immunocytes into the deep layers of the pericardium. Ossifying calcification with amorphized hydroxyapatite deposition and bone tissue formation as well as multiple erosions and hypertrophic proliferation in the endothelial membrane were detected in the implantation pericardium samples.

Получена многофазная кальцийфосфатная пенокерамика, представленная Д -трикальцийфосфатом (65 %) и Д -пирофосфатом кальция (25 %), включающая гидроксиапатит ( 5 %) и а -трикальцийфосфат ( 5 %), пористостью 60 - 64 % со сквозной архитектурой пенополиуретана. Нанесение слоя гидроксиапатита приводило к увеличению содержания гидроксиапатита до 25 %, а -трикальцийфосфата до 40 %, и повышению статической прочности до 0,03 МПа при снижении пористости до 49 %. Нанесение второго слоя гидроксиапатита способствовало повышению содержания гидроксиапатита до 40 %, статическая прочность достигала 0,05 МПа при пористости 40%. Формирование биоапатита в виде слоя «пеносфер» размером от 2 до 10 мкм происходило в процессе модифицирования всех видов пенокерамики в растворе SBF в течение 21 - 28 суток. Модифицированная кальцийфосфатная пенокерамика, обогащенная а -трикальцийфосфатом и гидроксиапатитом, характеризовалась максимальной статической прочностью 0,08 МПа при пористости 38%. The multiphase calcium phosphate foam ceramics, represented by р -tricalcium phosphate (65 %) and р -calcium pyrophosphate (25 %), including hydroxyapatite (5 %) and а -tricalcium phosphate (5%), with 60 - 64% porosity and a through architecture of polyurethane foam was obtained. The application of a layer of hydroxyapatite led to an increase in the content of hydroxyapatite to 25 %, а -tricalcium phosphate to 40%, and an increase in static strength to 0,03 MPa with a decrease in porosity to 49%. The application of the second layer of hydroxyapatite promoted an increase in the content of hydroxyapatite to 40%, the static strength reached 0,05 MPa at a porosity 40 %. The bioapatite formation in the shape of «foam spheres» with a size from 2 to 10 pm occurred in the process of modifying all types of foam ceramics in a SBF solution during 21 - 28 days. The modified calcium phosphate foam ceramics enriched with а -tricalcium phosphate and hydroxyapatite, was characterized by the maximum static strength 0,08 MPa at a porosity 38 %.

Изучена зависимость фазового состава наноразмерных фосфатов магния (MgNHPO·6HO, Mg(HPO), MgHPO·3HO, Mg(PO)•22HO) с размером кристаллитов 13-54 нм от условий осаждения из водных растворов в присутствии поливинилового спирта и его смеси с поливинилпирролидоном. В полимерной матрице дополнительно образуется примесная фаза MgOHCl. Наличие средних и двузамещенных фосфатов магния в пленках поливинилового спирта и поливинилового спирта/поливинилпирролида ингибируют их термическую деструкцию. The dependence of the phase composition of nanoscale magnesium phosphates (MgNHPO·6HO, Mg(HPO), MgHPO·3HO, Mg(PO)•22HO) with 13-54 nm crystallite size on the conditions of precipitation from aqueous solutions in the presence of the polyvinyl alcohol and its mixture with polyvinylpyrrolidone was studied. In the polymer matrix an additional impurity phase MgOHCl is formed. The presence of medium and disubstituted magnesium phosphates in polymer films of polyvinyl alcohol and polyvinyl alcohol/polyvinylpyrrolidone inhibit their thermal destruction.