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Biocompatible PLGA-Mesoporous Silicon Microspheres for the Controlled Release of BMP-2 for Bone Augmentation

Bone morphogenetic protein-2 (BMP-2) has been demonstrated to be one of the most vital osteogenic factors for bone augmentation. However, its uncontrolled administration has been associated with catastrophic side effects, which compromised its clinical use. To overcome these limitations, we aimed at...

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Autores principales: Minardi, Silvia, Fernandez-Moure, Joseph S., Fan, Dongmei, Murphy, Matthew B., Yazdi, Iman K., Liu, Xuewu, Weiner, Bradley K., Tasciotti, Ennio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076394/
https://www.ncbi.nlm.nih.gov/pubmed/32024134
http://dx.doi.org/10.3390/pharmaceutics12020118
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author Minardi, Silvia
Fernandez-Moure, Joseph S.
Fan, Dongmei
Murphy, Matthew B.
Yazdi, Iman K.
Liu, Xuewu
Weiner, Bradley K.
Tasciotti, Ennio
author_facet Minardi, Silvia
Fernandez-Moure, Joseph S.
Fan, Dongmei
Murphy, Matthew B.
Yazdi, Iman K.
Liu, Xuewu
Weiner, Bradley K.
Tasciotti, Ennio
author_sort Minardi, Silvia
collection PubMed
description Bone morphogenetic protein-2 (BMP-2) has been demonstrated to be one of the most vital osteogenic factors for bone augmentation. However, its uncontrolled administration has been associated with catastrophic side effects, which compromised its clinical use. To overcome these limitations, we aimed at developing a safer controlled and sustained release of BMP-2, utilizing poly(lactic-co-glycolic acid)-multistage vector composite microspheres (PLGA-MSV). The loading and release of BMP-2 from PLGA-MSV and its osteogenic potential in vitro and in vivo was evaluated. BMP-2 in vitro release kinetics was assessed by ELISA assay. It was found that PLGA-MSV achieved a longer and sustained release of BMP-2. Cell cytotoxicity and differentiation were evaluated in vitro by MTT and alkaline phosphatase (ALP) activity assays, respectively, with rat mesenchymal stem cells. The MTT results confirmed that PLGA-MSVs were not toxic to cells. ALP test demonstrated that the bioactivity of BMP-2 released from the PLGA-MSV was preserved, as it allowed for the osteogenic differentiation of rat mesenchymal stem cells, in vitro. The biocompatible, biodegradable, and osteogenic PLGA-MSVs system could be an ideal candidate for the safe use of BMP-2 in orthopedic tissue engineering applications.
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spelling pubmed-70763942020-03-24 Biocompatible PLGA-Mesoporous Silicon Microspheres for the Controlled Release of BMP-2 for Bone Augmentation Minardi, Silvia Fernandez-Moure, Joseph S. Fan, Dongmei Murphy, Matthew B. Yazdi, Iman K. Liu, Xuewu Weiner, Bradley K. Tasciotti, Ennio Pharmaceutics Article Bone morphogenetic protein-2 (BMP-2) has been demonstrated to be one of the most vital osteogenic factors for bone augmentation. However, its uncontrolled administration has been associated with catastrophic side effects, which compromised its clinical use. To overcome these limitations, we aimed at developing a safer controlled and sustained release of BMP-2, utilizing poly(lactic-co-glycolic acid)-multistage vector composite microspheres (PLGA-MSV). The loading and release of BMP-2 from PLGA-MSV and its osteogenic potential in vitro and in vivo was evaluated. BMP-2 in vitro release kinetics was assessed by ELISA assay. It was found that PLGA-MSV achieved a longer and sustained release of BMP-2. Cell cytotoxicity and differentiation were evaluated in vitro by MTT and alkaline phosphatase (ALP) activity assays, respectively, with rat mesenchymal stem cells. The MTT results confirmed that PLGA-MSVs were not toxic to cells. ALP test demonstrated that the bioactivity of BMP-2 released from the PLGA-MSV was preserved, as it allowed for the osteogenic differentiation of rat mesenchymal stem cells, in vitro. The biocompatible, biodegradable, and osteogenic PLGA-MSVs system could be an ideal candidate for the safe use of BMP-2 in orthopedic tissue engineering applications. MDPI 2020-02-01 /pmc/articles/PMC7076394/ /pubmed/32024134 http://dx.doi.org/10.3390/pharmaceutics12020118 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Minardi, Silvia
Fernandez-Moure, Joseph S.
Fan, Dongmei
Murphy, Matthew B.
Yazdi, Iman K.
Liu, Xuewu
Weiner, Bradley K.
Tasciotti, Ennio
Biocompatible PLGA-Mesoporous Silicon Microspheres for the Controlled Release of BMP-2 for Bone Augmentation
title Biocompatible PLGA-Mesoporous Silicon Microspheres for the Controlled Release of BMP-2 for Bone Augmentation
title_full Biocompatible PLGA-Mesoporous Silicon Microspheres for the Controlled Release of BMP-2 for Bone Augmentation
title_fullStr Biocompatible PLGA-Mesoporous Silicon Microspheres for the Controlled Release of BMP-2 for Bone Augmentation
title_full_unstemmed Biocompatible PLGA-Mesoporous Silicon Microspheres for the Controlled Release of BMP-2 for Bone Augmentation
title_short Biocompatible PLGA-Mesoporous Silicon Microspheres for the Controlled Release of BMP-2 for Bone Augmentation
title_sort biocompatible plga-mesoporous silicon microspheres for the controlled release of bmp-2 for bone augmentation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076394/
https://www.ncbi.nlm.nih.gov/pubmed/32024134
http://dx.doi.org/10.3390/pharmaceutics12020118
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