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Synthesis of Biocompatible Silver-Doped Carbonate Hydroxyapatite Nanoparticles Using Microwave-Assisted Precipitation and In Vitro Studies for the Prevention of Peri-Implantitis

A carbonate-hydroxyapatite-based antibacterial implant material with low cytotoxicity was synthesized. The silver ion (Ag(+)) was incorporated into CHA material, resulting in silver-doped carbonate hydroxyapatite (CHA-Ag). The microwave-assisted precipitation method was used to synthesize the CHA-Ag...

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Autores principales: Aziz, Saifuddin, Ana, Ika Dewi, Yusuf, Yusril, Pranowo, Harno Dwi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10382064/
https://www.ncbi.nlm.nih.gov/pubmed/37504880
http://dx.doi.org/10.3390/jfb14070385
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author Aziz, Saifuddin
Ana, Ika Dewi
Yusuf, Yusril
Pranowo, Harno Dwi
author_facet Aziz, Saifuddin
Ana, Ika Dewi
Yusuf, Yusril
Pranowo, Harno Dwi
author_sort Aziz, Saifuddin
collection PubMed
description A carbonate-hydroxyapatite-based antibacterial implant material with low cytotoxicity was synthesized. The silver ion (Ag(+)) was incorporated into CHA material, resulting in silver-doped carbonate hydroxyapatite (CHA-Ag). The microwave-assisted precipitation method was used to synthesize the CHA-Ag material. The amount of Ag(+) was varied at 0.005, 0.010, and 0.015 mol fractions ([Formula: see text]). The XRD results showed that the diffractograms corresponded with hydroxyapatite (ICSD 98-05-1414), without any additional phase. The presence of carbonate ions was indicated by vibrations at wavenumber of 871, 1411, and 1466 cm(−1) in the infrared spectra. The CHA-Ag materials were agglomerates of nanosized particles with low crystallinity. The particle size and crystallinity of the materials decreased due to the incorporation of CO(3)(2−) and Ag(+). The incorporated Ag(+) successfully inhibited peri-implant-associated bacterial growth. The antibacterial ability increased alongside the increase in the Ag(+) amount. The pre-osteoblast MC3T3E1 cell could grow up to >70% in the MTT assay, despite the use of Ag(+) as a dopant. The cell viability was higher in the CHA-Ag-containing media than in the CHA-containing media. The MTT assay also revealed that the CHA-Ag cytotoxicity decreased even though the Ag(+) amount increased. The CHA-Ag-15 had the lowest cytotoxicity and highest antibacterial activity. Therefore, the optimal amount of Ag(+) in the CHA-Ag formulation was [Formula: see text] = 0.015.
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spelling pubmed-103820642023-07-29 Synthesis of Biocompatible Silver-Doped Carbonate Hydroxyapatite Nanoparticles Using Microwave-Assisted Precipitation and In Vitro Studies for the Prevention of Peri-Implantitis Aziz, Saifuddin Ana, Ika Dewi Yusuf, Yusril Pranowo, Harno Dwi J Funct Biomater Article A carbonate-hydroxyapatite-based antibacterial implant material with low cytotoxicity was synthesized. The silver ion (Ag(+)) was incorporated into CHA material, resulting in silver-doped carbonate hydroxyapatite (CHA-Ag). The microwave-assisted precipitation method was used to synthesize the CHA-Ag material. The amount of Ag(+) was varied at 0.005, 0.010, and 0.015 mol fractions ([Formula: see text]). The XRD results showed that the diffractograms corresponded with hydroxyapatite (ICSD 98-05-1414), without any additional phase. The presence of carbonate ions was indicated by vibrations at wavenumber of 871, 1411, and 1466 cm(−1) in the infrared spectra. The CHA-Ag materials were agglomerates of nanosized particles with low crystallinity. The particle size and crystallinity of the materials decreased due to the incorporation of CO(3)(2−) and Ag(+). The incorporated Ag(+) successfully inhibited peri-implant-associated bacterial growth. The antibacterial ability increased alongside the increase in the Ag(+) amount. The pre-osteoblast MC3T3E1 cell could grow up to >70% in the MTT assay, despite the use of Ag(+) as a dopant. The cell viability was higher in the CHA-Ag-containing media than in the CHA-containing media. The MTT assay also revealed that the CHA-Ag cytotoxicity decreased even though the Ag(+) amount increased. The CHA-Ag-15 had the lowest cytotoxicity and highest antibacterial activity. Therefore, the optimal amount of Ag(+) in the CHA-Ag formulation was [Formula: see text] = 0.015. MDPI 2023-07-21 /pmc/articles/PMC10382064/ /pubmed/37504880 http://dx.doi.org/10.3390/jfb14070385 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Aziz, Saifuddin
Ana, Ika Dewi
Yusuf, Yusril
Pranowo, Harno Dwi
Synthesis of Biocompatible Silver-Doped Carbonate Hydroxyapatite Nanoparticles Using Microwave-Assisted Precipitation and In Vitro Studies for the Prevention of Peri-Implantitis
title Synthesis of Biocompatible Silver-Doped Carbonate Hydroxyapatite Nanoparticles Using Microwave-Assisted Precipitation and In Vitro Studies for the Prevention of Peri-Implantitis
title_full Synthesis of Biocompatible Silver-Doped Carbonate Hydroxyapatite Nanoparticles Using Microwave-Assisted Precipitation and In Vitro Studies for the Prevention of Peri-Implantitis
title_fullStr Synthesis of Biocompatible Silver-Doped Carbonate Hydroxyapatite Nanoparticles Using Microwave-Assisted Precipitation and In Vitro Studies for the Prevention of Peri-Implantitis
title_full_unstemmed Synthesis of Biocompatible Silver-Doped Carbonate Hydroxyapatite Nanoparticles Using Microwave-Assisted Precipitation and In Vitro Studies for the Prevention of Peri-Implantitis
title_short Synthesis of Biocompatible Silver-Doped Carbonate Hydroxyapatite Nanoparticles Using Microwave-Assisted Precipitation and In Vitro Studies for the Prevention of Peri-Implantitis
title_sort synthesis of biocompatible silver-doped carbonate hydroxyapatite nanoparticles using microwave-assisted precipitation and in vitro studies for the prevention of peri-implantitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10382064/
https://www.ncbi.nlm.nih.gov/pubmed/37504880
http://dx.doi.org/10.3390/jfb14070385
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