Combining Mg–Zn–Ca Bulk Metallic Glass with a Mesoporous Silica Nanocomposite for Bone Tissue Engineering

Mg–Zn–Ca bulk metallic glass (BMG) is a promising orthopedic fixation implant because of its biodegradable and biocompatible properties. Structural supporting bone implants with osteoinduction properties for effective bone regeneration have been highly desired in recent years. Osteogenic growth pept...

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Main Authors: Yun Shin Chu, Pei-Chun Wong, Jason Shian-Ching Jang, Chih-Hwa Chen, Si-Han Wu
Format: Article
Language:English
Published: MDPI AG 2022-05-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/14/5/1078
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author Yun Shin Chu
Pei-Chun Wong
Jason Shian-Ching Jang
Chih-Hwa Chen
Si-Han Wu
author_facet Yun Shin Chu
Pei-Chun Wong
Jason Shian-Ching Jang
Chih-Hwa Chen
Si-Han Wu
author_sort Yun Shin Chu
collection DOAJ
description Mg–Zn–Ca bulk metallic glass (BMG) is a promising orthopedic fixation implant because of its biodegradable and biocompatible properties. Structural supporting bone implants with osteoinduction properties for effective bone regeneration have been highly desired in recent years. Osteogenic growth peptide (OGP) can increase the proliferation and differentiation of mesenchymal stem cells and enhance the mineralization of osteoblast cells. However, the short half-life and non-specificity to target areas limit applications of OGP. Mesoporous silica nanoparticles (MSNs) as nanocarriers possess excellent properties, such as easy surface modification, superior targeting efficiency, and high loading capacity of drugs or proteins. Accordingly, we propose a system of combining the OGP-containing MSNs with Mg–Zn–Ca BMG materials to promote bone regeneration. In this work, we conjugated cysteine-containing OGP (cgOGP, 16 a.a.) to interior walls of channels in MSNs and maintained the dispersity of MSNs via PEGylation. An in vitro study showed that metal ions released from Mg–Zn–Ca BMG promoted cell proliferation and migration and elevated alkaline phosphatase (ALP) activity and mineralization. On treating cells with both BMG ion-containing Minimum Essential Medium Eagle-alpha modification (α-MEM) and OGP-conjugated MSNs, enhanced focal adhesion turnover and promoted differentiation were observed. Hematological analyses showed the biocompatible nature of this BMG/nanocomposite system. In addition, in vivo micro-computed tomographic and histological observations revealed that our system stimulated osteogenesis and new bone formation around the implant site.
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spelling doaj.art-2d967c47e172496dbbd6ed72f36757852023-11-23T12:39:15ZengMDPI AGPharmaceutics1999-49232022-05-01145107810.3390/pharmaceutics14051078Combining Mg–Zn–Ca Bulk Metallic Glass with a Mesoporous Silica Nanocomposite for Bone Tissue EngineeringYun Shin Chu0Pei-Chun Wong1Jason Shian-Ching Jang2Chih-Hwa Chen3Si-Han Wu4Graduate Institute of Biomedical Materials and Tissue Engineering, Taipei Medical University, Taipei 11031, TaiwanDepartment of Orthopedics, Taipei Medical University Hospital, Taipei 11031, TaiwanGraduate Institute of Materials Science and Engineering, National Central University, Taoyuan 32001, TaiwanSchool of Biomedical Engineering, College of Biomedical Engineering, Taipei Medical University, Taipei 11031, TaiwanGraduate Institute of Nanomedicine and Medical Engineering, Taipei Medical University, Taipei 11031, TaiwanMg–Zn–Ca bulk metallic glass (BMG) is a promising orthopedic fixation implant because of its biodegradable and biocompatible properties. Structural supporting bone implants with osteoinduction properties for effective bone regeneration have been highly desired in recent years. Osteogenic growth peptide (OGP) can increase the proliferation and differentiation of mesenchymal stem cells and enhance the mineralization of osteoblast cells. However, the short half-life and non-specificity to target areas limit applications of OGP. Mesoporous silica nanoparticles (MSNs) as nanocarriers possess excellent properties, such as easy surface modification, superior targeting efficiency, and high loading capacity of drugs or proteins. Accordingly, we propose a system of combining the OGP-containing MSNs with Mg–Zn–Ca BMG materials to promote bone regeneration. In this work, we conjugated cysteine-containing OGP (cgOGP, 16 a.a.) to interior walls of channels in MSNs and maintained the dispersity of MSNs via PEGylation. An in vitro study showed that metal ions released from Mg–Zn–Ca BMG promoted cell proliferation and migration and elevated alkaline phosphatase (ALP) activity and mineralization. On treating cells with both BMG ion-containing Minimum Essential Medium Eagle-alpha modification (α-MEM) and OGP-conjugated MSNs, enhanced focal adhesion turnover and promoted differentiation were observed. Hematological analyses showed the biocompatible nature of this BMG/nanocomposite system. In addition, in vivo micro-computed tomographic and histological observations revealed that our system stimulated osteogenesis and new bone formation around the implant site.https://www.mdpi.com/1999-4923/14/5/1078mesoporous silica nanoparticlesMg–Zn–Ca bulk metallic glassbone tissue engineeringosteogenic growth peptideosteogenic differentiationosteoinduction
spellingShingle Yun Shin Chu
Pei-Chun Wong
Jason Shian-Ching Jang
Chih-Hwa Chen
Si-Han Wu
Combining Mg–Zn–Ca Bulk Metallic Glass with a Mesoporous Silica Nanocomposite for Bone Tissue Engineering
Pharmaceutics
mesoporous silica nanoparticles
Mg–Zn–Ca bulk metallic glass
bone tissue engineering
osteogenic growth peptide
osteogenic differentiation
osteoinduction
title Combining Mg–Zn–Ca Bulk Metallic Glass with a Mesoporous Silica Nanocomposite for Bone Tissue Engineering
title_full Combining Mg–Zn–Ca Bulk Metallic Glass with a Mesoporous Silica Nanocomposite for Bone Tissue Engineering
title_fullStr Combining Mg–Zn–Ca Bulk Metallic Glass with a Mesoporous Silica Nanocomposite for Bone Tissue Engineering
title_full_unstemmed Combining Mg–Zn–Ca Bulk Metallic Glass with a Mesoporous Silica Nanocomposite for Bone Tissue Engineering
title_short Combining Mg–Zn–Ca Bulk Metallic Glass with a Mesoporous Silica Nanocomposite for Bone Tissue Engineering
title_sort combining mg zn ca bulk metallic glass with a mesoporous silica nanocomposite for bone tissue engineering
topic mesoporous silica nanoparticles
Mg–Zn–Ca bulk metallic glass
bone tissue engineering
osteogenic growth peptide
osteogenic differentiation
osteoinduction
url https://www.mdpi.com/1999-4923/14/5/1078
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