微载波
超顺磁性
材料科学
聚合物
纳米颗粒
纳米复合材料
化学工程
微流控
有孔小珠
原位
磁性纳米粒子
组织工程
氧化铁纳米粒子
流变学
自愈水凝胶
傅里叶变换红外光谱
纳米技术
磁性纳米颗粒
生物高聚物
动力学
化学
聚二甲基硅氧烷
生物相容性
扫描电子显微镜
表征(材料科学)
作者
Sayan Ganguly,Fatemeh Parniani,Li Yan Wong,Xiaowu Shirley Tang
标识
DOI:10.1021/acsabm.5c01848
摘要
This study presents an approach to the synthesis of nanocomposite magnetic hydrogel microbeads using a microfluidic-assisted droplet method followed by in situ gelation in a heated oil column. The beads were fabricated from a semi-interpenetrating polymer network (semi-IPN) comprising gelatin, and vinylic monomers, with incorporation of iron oxide nanoparticles (Fe 3 O 4 ) synthesized via coprecipitation. The unique combination of pressure-mediated bead formation and controlled gelation kinetics enabled tunable porosity, as validated through SEM and pore size distribution analysis, where increased oil column height yielded narrower pore distributions due to enhanced gelation. Magnetic characterization confirmed strong superparamagnetic behavior, while FTIR and XRD analyses verified successful chemical integration of the polymeric and nanoparticle components. Rheological studies revealed enhanced elasticity and network strength in nanoparticle-loaded hydrogels, and swelling/deswelling tests, fitted with first-order and exponential decay models, demonstrated reversible, magnetically tunable water uptake. Furthermore, in vitro cell culture studies showed excellent cell attachment and proliferation on the bead surface, facilitated by the porous, wrinkled morphology. Collectively, these multifunctional beads exhibit significant promise for applications in cell delivery, magnetically guided therapies, and responsive tissue engineering platforms.
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