E-jet printed polycaprolactone with strontium-substituted mesoporous bioactive glass nanoparticles for bone tissue engineering

被引:1
作者
Kong, Chee Hoe [1 ]
Steffi, Chris [2 ]
Cai, Yanli [3 ]
Wang, Wilson [1 ]
机构
[1] Natl Univ Singapore, Dept Orthopaed Surg, NUHS Tower Block,Level 11,1E Kent Ridge Rd, Singapore 119228, Singapore
[2] Swiss Fed Inst Technol, Inst Biomech, GLC H 20-2,Gloriastr 37-39, CH-8092 Zurich, Switzerland
[3] Natl Univ Singapore, NUS Ctr Addit Mfg AM NUS, Singapore 117597, Singapore
来源
BIOMATERIALS ADVANCES | 2025年 / 169卷
关键词
Mesoporous bioactive glass; Osteoblasts; Osteoclasts; Strontium; 3D printing; Tissue engineering; Polycaprolactone; Icariin; COLONY-STIMULATING FACTOR; OSTEOGENIC DIFFERENTIATION; POSTMENOPAUSAL WOMEN; DRUG-DELIVERY; OSTEOCLAST FORMATION; CONTROLLED-RELEASE; STEM-CELLS; ICARIIN; RANELATE; OSTEOPOROSIS;
D O I
10.1016/j.bioadv.2024.214173
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Osteoporosis, characterized by reduced bone mineral density and increased fracture risk, poses a significant health challenge, particularly for aging populations. Systemic treatments often lead to adverse side effects, emphasizing the need for localized solutions. This study introduces a 3D-printed polycaprolactone (PCL) scaffold embedded with strontium-substituted mesoporous bioactive glass nanoparticles (Sr-MBGNPs) and icariin (ICN) for the targeted regeneration of osteoporotic bone. The scaffold was characterized using scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), ion release studies, and cellular assays, which confirmed its dual functionality in both enhancing osteoblast proliferation and differentiation and inhibiting osteoclastogenesis. The optimized Sr-MBGNP concentration ensured sustained ion release, superior hydrophilicity, and bioactivity without compromising scaffold integrity. Additionally, e-jet printing provided high precision and uniform pore sizes conducive to cellular activity. This novel scaffold platform demonstrates a promising localized treatment strategy, reducing systemic side effects while improving fixation stability. The innovative integration of Sr-MBGNPs and ICN highlights its potential to revolutionize osteoporosis therapy by promoting bone regeneration and mitigating bone resorption.
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页数:13
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