Initial bone tissue reactions of hydroxyapatite/collagen–(3‐glycidoxypropyl)trimethoxysilane injectable bone paste

We have previously reported that a novel bioresorbable self‐setting injectable bone paste composed of hydroxyapatite/collagen bone‐like nanocomposite (HAp/Col) and (3‐glycidoxypropyl)trimethoxysilane (GPTMS) was successfully prepared and was replaced with new bone within 3 months of implantation in...

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Veröffentlicht in:Journal of biomedical materials research. Part B, Applied biomaterials Applied biomaterials, 2024-08, Vol.112 (8), p.e35451-n/a
Hauptverfasser: Sato, Taira, Shirosaki, Yuki, Oshima, Sho, Tsuru, Kanji, Koyama, Yoshihisa, Aizawa, Mamoru, Kikuchi, Masanori
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container_issue 8
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container_title Journal of biomedical materials research. Part B, Applied biomaterials
container_volume 112
creator Sato, Taira
Shirosaki, Yuki
Oshima, Sho
Tsuru, Kanji
Koyama, Yoshihisa
Aizawa, Mamoru
Kikuchi, Masanori
description We have previously reported that a novel bioresorbable self‐setting injectable bone paste composed of hydroxyapatite/collagen bone‐like nanocomposite (HAp/Col) and (3‐glycidoxypropyl)trimethoxysilane (GPTMS) was successfully prepared and was replaced with new bone within 3 months of implantation in defects created in porcine tibia. In this study, the HAp/Col‐GPTMS paste was implanted into bone defects in rat tibiae to investigate the initial kinetics and bone tissue response. Even though more than 35% of GPTMS molecules should be eluted rapidly from directly injected pastes according to previously reported cell culture tests, in this study, energy‐dispersive X‐ray spectrometry did not detect Si (GPTMS) deposition in tissues surrounding the paste at 1 day postimplantation. Further, no abnormal inflammatory responses were observed in the surrounding tissues over the test period for both directly injected and prehardened pastes. Companying these observations with the results of the previous animal test (in which the paste was fully resorbed and was substituted with new bone), the eluted GPTMS resolved in no harm in vivo from the initial to final (completely resorbed) stages. Material resorption rates calculated from X‐ray microcomputed tomography (μ‐CT) images decreased with increasing in GPTMS concentration. Histological observations indicated that tartrate‐resistant acid phosphatase (TRAP) active cells, (assumed to be osteoclasts), exist on the periphery of pastes. This result suggested that the paste was resorbed by osteoclasts in the same way as the HAp/Col. Since a good correlation was observed between TRAP active areas in histological sections and material resorption rate calculated from μ‐CT, the TRAP activity coverage ratio offers the possibility to estimate the osteoclastic resorption ratio of materials, which are replaced with bone via bone remodeling process.
doi_str_mv 10.1002/jbm.b.35451
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Part B, Applied biomaterials</jtitle><addtitle>J Biomed Mater Res B Appl Biomater</addtitle><date>2024-08</date><risdate>2024</risdate><volume>112</volume><issue>8</issue><spage>e35451</spage><epage>n/a</epage><pages>e35451-n/a</pages><issn>1552-4973</issn><issn>1552-4981</issn><eissn>1552-4981</eissn><abstract>We have previously reported that a novel bioresorbable self‐setting injectable bone paste composed of hydroxyapatite/collagen bone‐like nanocomposite (HAp/Col) and (3‐glycidoxypropyl)trimethoxysilane (GPTMS) was successfully prepared and was replaced with new bone within 3 months of implantation in defects created in porcine tibia. In this study, the HAp/Col‐GPTMS paste was implanted into bone defects in rat tibiae to investigate the initial kinetics and bone tissue response. Even though more than 35% of GPTMS molecules should be eluted rapidly from directly injected pastes according to previously reported cell culture tests, in this study, energy‐dispersive X‐ray spectrometry did not detect Si (GPTMS) deposition in tissues surrounding the paste at 1 day postimplantation. Further, no abnormal inflammatory responses were observed in the surrounding tissues over the test period for both directly injected and prehardened pastes. Companying these observations with the results of the previous animal test (in which the paste was fully resorbed and was substituted with new bone), the eluted GPTMS resolved in no harm in vivo from the initial to final (completely resorbed) stages. Material resorption rates calculated from X‐ray microcomputed tomography (μ‐CT) images decreased with increasing in GPTMS concentration. Histological observations indicated that tartrate‐resistant acid phosphatase (TRAP) active cells, (assumed to be osteoclasts), exist on the periphery of pastes. This result suggested that the paste was resorbed by osteoclasts in the same way as the HAp/Col. Since a good correlation was observed between TRAP active areas in histological sections and material resorption rate calculated from μ‐CT, the TRAP activity coverage ratio offers the possibility to estimate the osteoclastic resorption ratio of materials, which are replaced with bone via bone remodeling process.</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>39052003</pmid><doi>10.1002/jbm.b.35451</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-9451-8147</orcidid><oa>free_for_read</oa></addata></record>
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subjects (3‐glycidoxypropyl)trimethoxysilane
Acid phosphatase
Acid phosphatase (tartrate-resistant)
Acid resistance
Animals
Biocompatibility
Biomedical materials
bioresorbability evaluation
Bone remodeling
Bone resorption
Bone Substitutes - chemistry
Bone Substitutes - pharmacology
bone tissue reaction
Bones
Cell culture
Collagen
Collagen - chemistry
Computed tomography
Defects
Durapatite - chemistry
Durapatite - pharmacology
Hydroxyapatite
hydroxyapatite/collagen
In vivo methods and tests
injectable bone paste
Male
Materials Testing
Nanocomposites
Nanocomposites - chemistry
Osteoclasts
Pastes
Rats
Rats, Sprague-Dawley
Silanes - chemistry
Silanes - pharmacology
Spectrometry
Swine
Tibia
Tibia - metabolism
Tissue culture
title Initial bone tissue reactions of hydroxyapatite/collagen–(3‐glycidoxypropyl)trimethoxysilane injectable bone paste
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