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Zoledronic Acid Implant Coating Results in Local Medullary Bone Growth

[Image: see text] Osteoarthritis (OA) can necessitate surgical interventions to restore the function of the joint in severe cases. Joint replacement surgery is one of the procedures implemented to replace the damaged joint with prosthetic implants in severe cases of OA. However, after successful imp...

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Autores principales: Quarterman, Juliana C., Phruttiwanichakun, Pornpoj, Fredericks, Douglas C., Salem, Aliasger K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727731/
https://www.ncbi.nlm.nih.gov/pubmed/36378992
http://dx.doi.org/10.1021/acs.molpharmaceut.2c00644
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author Quarterman, Juliana C.
Phruttiwanichakun, Pornpoj
Fredericks, Douglas C.
Salem, Aliasger K.
author_facet Quarterman, Juliana C.
Phruttiwanichakun, Pornpoj
Fredericks, Douglas C.
Salem, Aliasger K.
author_sort Quarterman, Juliana C.
collection PubMed
description [Image: see text] Osteoarthritis (OA) can necessitate surgical interventions to restore the function of the joint in severe cases. Joint replacement surgery is one of the procedures implemented to replace the damaged joint with prosthetic implants in severe cases of OA. However, after successful implantation, a fraction of OA patients still require revision surgery due to aseptic prosthetic loosening. Insufficient osseointegration is one of the factors that contribute to such loosening of the bone implant, which is commonly made from titanium-based materials. Zoledronic acid (ZA), a potent bisphosphonate agent, has been previously shown to enhance osseointegration of titanium implants. Herein, we fabricated ZA/Ca composites using a reverse microemulsion method and coated them with 1,2-dioleoyl-sn-glycero-3-phosphate monosodium salt (DOPA) to form ZA/Ca/DOPA composites. Titanium alloy screws were subsequently dip-coated with a suspension of the ZA/Ca/DOPA composites and poly(lactic-co-glycolic) acid (PLGA) in chloroform to yield Za/PLGA-coated screws. The coated screws exhibited a biphasic in vitro release profile with an initial burst release within 48 h, followed by a sustained release over 1 month. To assess their performance in vivo, the Za/PLGA screws were then implanted into the tibiae of Sprague–Dawley rats. After 8 weeks, microCT imaging showed new bone growth along the medullary cavity around the implant site, supporting the local release of ZA to enhance bone growth around the implant. Histological staining further confirmed the presence of new mineralized medullary bone growth resembling the cortical bone. Such local medullary growth represents an opportunity for future studies with alternative coating methods to fine-tune the local release of ZA from the coating and enhance complete osseointegration of the implant.
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spelling pubmed-97277312022-12-08 Zoledronic Acid Implant Coating Results in Local Medullary Bone Growth Quarterman, Juliana C. Phruttiwanichakun, Pornpoj Fredericks, Douglas C. Salem, Aliasger K. Mol Pharm [Image: see text] Osteoarthritis (OA) can necessitate surgical interventions to restore the function of the joint in severe cases. Joint replacement surgery is one of the procedures implemented to replace the damaged joint with prosthetic implants in severe cases of OA. However, after successful implantation, a fraction of OA patients still require revision surgery due to aseptic prosthetic loosening. Insufficient osseointegration is one of the factors that contribute to such loosening of the bone implant, which is commonly made from titanium-based materials. Zoledronic acid (ZA), a potent bisphosphonate agent, has been previously shown to enhance osseointegration of titanium implants. Herein, we fabricated ZA/Ca composites using a reverse microemulsion method and coated them with 1,2-dioleoyl-sn-glycero-3-phosphate monosodium salt (DOPA) to form ZA/Ca/DOPA composites. Titanium alloy screws were subsequently dip-coated with a suspension of the ZA/Ca/DOPA composites and poly(lactic-co-glycolic) acid (PLGA) in chloroform to yield Za/PLGA-coated screws. The coated screws exhibited a biphasic in vitro release profile with an initial burst release within 48 h, followed by a sustained release over 1 month. To assess their performance in vivo, the Za/PLGA screws were then implanted into the tibiae of Sprague–Dawley rats. After 8 weeks, microCT imaging showed new bone growth along the medullary cavity around the implant site, supporting the local release of ZA to enhance bone growth around the implant. Histological staining further confirmed the presence of new mineralized medullary bone growth resembling the cortical bone. Such local medullary growth represents an opportunity for future studies with alternative coating methods to fine-tune the local release of ZA from the coating and enhance complete osseointegration of the implant. American Chemical Society 2022-11-15 2022-12-05 /pmc/articles/PMC9727731/ /pubmed/36378992 http://dx.doi.org/10.1021/acs.molpharmaceut.2c00644 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Quarterman, Juliana C.
Phruttiwanichakun, Pornpoj
Fredericks, Douglas C.
Salem, Aliasger K.
Zoledronic Acid Implant Coating Results in Local Medullary Bone Growth
title Zoledronic Acid Implant Coating Results in Local Medullary Bone Growth
title_full Zoledronic Acid Implant Coating Results in Local Medullary Bone Growth
title_fullStr Zoledronic Acid Implant Coating Results in Local Medullary Bone Growth
title_full_unstemmed Zoledronic Acid Implant Coating Results in Local Medullary Bone Growth
title_short Zoledronic Acid Implant Coating Results in Local Medullary Bone Growth
title_sort zoledronic acid implant coating results in local medullary bone growth
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727731/
https://www.ncbi.nlm.nih.gov/pubmed/36378992
http://dx.doi.org/10.1021/acs.molpharmaceut.2c00644
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