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Enhanced Osteogenic Potential of Phosphonated-Siloxane Hydrogel Scaffolds
Biomacromolecules ( IF 5.5 ) Pub Date : 2020-11-02 , DOI: 10.1021/acs.biomac.0c01293
Michael T Frassica 1 , Sarah K Jones 1 , Jakkrit Suriboot 1 , Ahmad S Arabiyat 2 , Esteban M Ramirez 1 , Robert A Culibrk 2 , Mariah S Hahn 2 , Melissa A Grunlan 1, 3, 4
Affiliation  

In a material-guided approach, instructive scaffolds that leverage potent chemistries may efficiently promote bone regeneration. A siloxane macromer has been previously shown to impart osteoinductivity and bioactivity when included in poly(ethylene glycol) diacrylate (PEG-DA) hydrogel scaffolds. Herein, phosphonated-siloxane macromers were evaluated for enhancing the osteogenic potential of siloxane-containing PEG-DA scaffolds. Two macromers were prepared with different phosphonate pendant group concentrations, poly(diethyl(2-(propylthio)ethyl)phosphonate methylsiloxane) diacrylate (PPMS-DA) and 25%-phosphonated analogue (PPMS-DA 25%). Macroporous, templated scaffolds were prepared by cross-linking these macromers with PEG-DA at varying mol % (15:85, 30:70, and 45:55 PPMS-DA to PEG-DA; 30:70 PPMS-DA 25% to PEG-DA). Other scaffolds were also prepared by combining PEG-DA with PDMS-MA (i.e., no phosphonate) or with vinyl phosphonate (i.e., no siloxane). Scaffold material properties were thoroughly assessed, including pore morphology, hydrophobicity, swelling, modulus, and bioactivity. Scaffolds were cultured with human bone marrow-derived mesenchymal stem cells (normal media) and calcium deposition and protein expression were assessed at 14 and 28 days.

中文翻译:

膦酸硅氧烷水凝胶支架的成骨潜能增强。

在材料指导的方法中,利用有效化学作用的指导性支架可以有效地促进骨再生。先前已证明,硅氧烷大分子单体包含在聚(乙二醇)二丙烯酸酯(PEG-DA)水凝胶支架中时具有骨诱导性和生物活性。在本文中,评估了膦酸酯化的硅氧烷大分子单体以增强含硅氧烷的PEG-DA支架的成骨潜力。制备具有不同膦酸酯侧基浓度的两个大分子单体,聚(二乙基(2-(丙硫基乙基)膦酸酯甲基硅氧烷)二丙烯酸酯(PPMS-DA)和25%的膦酸酯类似物(PPMS-DA 25%)。通过将这些大分子单体与PEG-DA以不同摩尔%(15:85、30:70和45:55 PPMS-DA与PEG-DA; 30:70 PPMS-DA 25%至PEG-DA)。还通过将PEG-DA与PDMS-MA(即,没有膦酸酯)或与乙烯基膦酸酯(即,没有硅氧烷)结合来制备其他支架。对支架材料的性能进行了全面评估,包括孔的形态,疏水性,溶胀,模量和生物活性。将支架与人骨髓源间充质干细胞(正常培养基)一起培养,并在第14天和第28天评估钙的沉积和蛋白质表达。
更新日期:2020-12-14
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