Obtaining Polyvinylpyrrolidone Fibers Using the Electroforming Method with the Inclusion of Microcrystalline High-Temperature Phosphates

Author:

Papezhuk Marina Vladimirovna1,Ivanin Sergei Nikolaevich12ORCID,Yakupov Roman Pavlovich12,Buz’ko Vladimir Yurievich12,Sukhno Igor Vladimirovich2,Gneush Anna Nikolaevna2,Petriev Iliya Sergeevich13ORCID

Affiliation:

1. Faculty of Chemistry and High Technologies, Kuban State University, 350040 Krasnodar, Russia

2. Laboratory of Advanced Nanobiotechnologies, Kuban State Agricultural University, 350044 Krasnodar, Russia

3. Laboratory of Problems of Stable Isotope Spreading in Living Systems, Southern Scientific Centre of the Russian Academy of Sciences, 344006 Rostov-on-Don, Russia

Abstract

The results of the synthesis of microcrystalline calcium phosphates such as hydroxoapatite, pyrophosphate, and tricalcium phosphate are presented herein. The influence of the addition of polyvinylpyrrolidone (PVP) on the phase characteristics of the resulting high-temperature ceramic sample is considered. The X-ray results show that hydroxyapatite (HAp) consists of a Ca5(PO4)3(OH) phase, while the sample with the addition of polyvinylpyrrolidone contains β-Ca3(PO4)2 (65.5%) and β-Ca2P2O7 (34.5%) phases calcium phosphates (CPs). IR spectroscopy was used to characterize the compositions of the samples. An important characteristic of the obtained samples is the elemental Ca/P ratio, which was determined via energy-dispersive analysis. The data obtained are consistent with the composition of dental enamel apatites, namely, in the CPs (1.27) and HAp (1.40). SEM was used to study the morphology of the surfaces of hydroxyapatite particles. Polyvinylpyrrolidone polymer fibers were obtained using the electroforming method with the inclusion of CPs in the composition. The fibers were oriented randomly, and nanoscale hydroxyapatite particles were incorporated into the fiber structure. Solubility data of the HAp, CPs, and Fibers in a physiological solution at room temperature and human body temperature were obtained. The solubility of the resulting HAp turned out to be higher than the solubility of the CPs. In turn, the concentration of Ca2+ in a physiological solution of PVP composite fibers with the inclusion of CPs was lower than that in powdered CPs.

Funder

Ministry of Science and Higher Education of the Russian Federation

Publisher

MDPI AG

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