کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1427880 1509152 2016 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Mussel-inspired alginate gel promoting the osteogenic differentiation of mesenchymal stem cells and anti-infection
ترجمه فارسی عنوان
ژل آلژینات الهام گرفته از میسول، ترویج تمایز استئوژنیک سلول های بنیادی مزانشیمی و ضد عفونت
کلمات کلیدی
دوپامین الهام گرفته از میسول، هیدروژل، انعقاد سلول، ضد باکتری
موضوعات مرتبط
مهندسی و علوم پایه مهندسی مواد بیومتریال
چکیده انگلیسی


• Dopamine modified alginate bead and fiber promote cell viability and proliferation.
• Alginate-dopamine gel promotes osteogenic differentiation of MSCs.
• Dopamine reduced nanosilver for anti-infection.
• Alginate-dopamine bead and fiber for delivery of mesenchymal stem cells (MSCs)

Alginate hydrogels have been used in cell encapsulation for many years but a prevalent issue with pure alginates is that they are unable to provide enough bioactive properties to interact with mammalian cells. This paper discusses the modification of alginate with mussel-inspired dopamine for cell loading and anti-infection. Mouse bone marrow stem cells were immobilized into alginate and alginate-dopamine beads and fibers. Through live-dead and MTT assay, alginates modified by dopamine promoted cell viability and proliferation. In vitro cell differentiation results showed that such an alginate-dopamine gel can promote the osteogenic differentiation of mesenchymal stem cell after PCR and ALP assays. In addition to that, the adhesive prosperities of dopamine allowed for coating the surface of alginate-dopamine gel with silver nanoparticles, which provided the gel with significant antibacterial characteristics. Overall, these results demonstrate that a dopamine-modified alginate gel can be a great tool for cell encapsulation to promote cell proliferation and can be applied to bone regeneration, especially in contaminated bone defects.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Materials Science and Engineering: C - Volume 69, 1 December 2016, Pages 496–504
نویسندگان
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