Enhancing the osteogenic potential of 3D-printed polycaprolactone/hydroxyapatite composite scaffolds via in-situ ZIF-8 surface modification.

IF 4.5 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Saba Moslemi, Ghasem Dini, Fatemeh Ejeian, Aliakbar Najafinezhad, Sayede Tayebe Mousavi Mourkani
{"title":"Enhancing the osteogenic potential of 3D-printed polycaprolactone/hydroxyapatite composite scaffolds via in-situ ZIF-8 surface modification.","authors":"Saba Moslemi, Ghasem Dini, Fatemeh Ejeian, Aliakbar Najafinezhad, Sayede Tayebe Mousavi Mourkani","doi":"10.1007/s10856-026-07029-y","DOIUrl":null,"url":null,"abstract":"<p><p>Bone defects remain a major clinical challenge, necessitating advanced scaffolds that combine suitable mechanics, bioactivity, and osteoinductive cues for effective regeneration. This study developed 3D-printed polycaprolactone/hydroxyapatite (PCL/HA) composite scaffolds via fused deposition modeling and enhanced their surface with in-situ zeolitic imidazolate framework-8 (ZIF-8) modification to promote osteogenic performance. Hydrothermally synthesized HA nanoparticles exhibited high crystallinity, <100 nm size, and ~23 m²/g specific surface area. The optimal PCL + 25 wt.% HA composition achieved a compressive modulus of ~0.36 GPa and strength of ~17 MPa, within the range reported for human trabecular bone. The scaffolds demonstrated controlled biodegradation ( ~ 15% weight loss after 28 days in PBS) and strong bioactivity, with progressive apatite mineralization confirmed by SEM, XRD, and ion concentration changes in simulated body fluid over 28 days. ZIF-8 surface functionalization enabled sustained, non-burst Zn²⁺ release (0.18-1.66 ppm over 28 days) within safe biological limits. In vitro assays using MG-63 cells showed significantly improved cell adhesion, proliferation (MTS assay), and osteogenic differentiation on ZIF-8-modified scaffolds compared to unmodified controls, evidenced by 2.1-fold higher alkaline phosphatase (ALP) and 2.5-fold higher BMP2 gene expression after 21 days of induction. These results demonstrate that the synergistic combination of HA reinforcement and controlled Zn²⁺ release from ZIF-8 provides a multifunctional scaffold platform for bone regeneration.</p>","PeriodicalId":647,"journal":{"name":"Journal of Materials Science: Materials in Medicine","volume":" ","pages":""},"PeriodicalIF":4.5000,"publicationDate":"2026-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Science: Materials in Medicine","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1007/s10856-026-07029-y","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Bone defects remain a major clinical challenge, necessitating advanced scaffolds that combine suitable mechanics, bioactivity, and osteoinductive cues for effective regeneration. This study developed 3D-printed polycaprolactone/hydroxyapatite (PCL/HA) composite scaffolds via fused deposition modeling and enhanced their surface with in-situ zeolitic imidazolate framework-8 (ZIF-8) modification to promote osteogenic performance. Hydrothermally synthesized HA nanoparticles exhibited high crystallinity, <100 nm size, and ~23 m²/g specific surface area. The optimal PCL + 25 wt.% HA composition achieved a compressive modulus of ~0.36 GPa and strength of ~17 MPa, within the range reported for human trabecular bone. The scaffolds demonstrated controlled biodegradation ( ~ 15% weight loss after 28 days in PBS) and strong bioactivity, with progressive apatite mineralization confirmed by SEM, XRD, and ion concentration changes in simulated body fluid over 28 days. ZIF-8 surface functionalization enabled sustained, non-burst Zn²⁺ release (0.18-1.66 ppm over 28 days) within safe biological limits. In vitro assays using MG-63 cells showed significantly improved cell adhesion, proliferation (MTS assay), and osteogenic differentiation on ZIF-8-modified scaffolds compared to unmodified controls, evidenced by 2.1-fold higher alkaline phosphatase (ALP) and 2.5-fold higher BMP2 gene expression after 21 days of induction. These results demonstrate that the synergistic combination of HA reinforcement and controlled Zn²⁺ release from ZIF-8 provides a multifunctional scaffold platform for bone regeneration.

原位ZIF-8表面改性增强3d打印聚己内酯/羟基磷灰石复合支架的成骨潜能。
骨缺损仍然是主要的临床挑战,需要结合合适的力学、生物活性和骨诱导线索的先进支架来实现有效的再生。本研究通过熔融沉积建模,开发3d打印聚己内酯/羟基磷灰石(PCL/HA)复合支架,并通过原位沸石咪唑酸框架-8 (ZIF-8)改性增强其表面,以提高成骨性能。水热合成的透明质酸纳米颗粒具有高结晶度;
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Materials Science: Materials in Medicine
Journal of Materials Science: Materials in Medicine 工程技术-材料科学:生物材料
CiteScore
8.00
自引率
0.00%
发文量
73
审稿时长
3.5 months
期刊介绍: The Journal of Materials Science: Materials in Medicine publishes refereed papers providing significant progress in the application of biomaterials and tissue engineering constructs as medical or dental implants, prostheses and devices. Coverage spans a wide range of topics from basic science to clinical applications, around the theme of materials in medicine and dentistry. The central element is the development of synthetic and natural materials used in orthopaedic, maxillofacial, cardiovascular, neurological, ophthalmic and dental applications. Special biomedical topics include biomaterial synthesis and characterisation, biocompatibility studies, nanomedicine, tissue engineering constructs and cell substrates, regenerative medicine, computer modelling and other advanced experimental methodologies.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书