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Oxidized-Alginate Microbead Encapsulated Osteoclasts as a Cell-based Therapy to Reverse Vascular #Calcification

机译:氧化藻酸盐微珠封装破骨细胞作为基于细胞的逆向血管钙化治疗。

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Conclusion: We were able to properly form microbeads with the 1% oxidized and non-oxidized alginate solutions, but no beads materialized from the 2% oxidized alginate. This suggests that the alginate is strongly sensitive to oxidation via sodium periodate. A degradation study (not shown) revealed the 1% oxidized alginate microbeads to be . the preferred scaffold choice because of the fast degradation exhibited. The 1% oxidized alginate microbeads significantly degraded throughout the 72-hour study. The non-oxidized microbeads however, showed virtually no significant degradation under identical conditions. A fast-releasing delivery vehicle is preferred because it will help alleviate problems that could occur during in vivo applications regarding cell viability and injection attachment stability at target locations. Taken together, the results suggest that the oxidized alginate microbeads could potentially serve as delivery vehicle for cell-based therapies. We will continue to optimize our alginate oxidation protocol to adjust microbead degradability as needed. Our next steps will involve cell encapsulations with the oxidized alginate microbeads towards testing proliferation and viability in normal culture media, and ultimately in vivo applications of the osteoclast-based therapy.
机译:结论:我们能够用1%氧化和未氧化藻酸盐溶液正确形成微珠,但2%氧化藻酸盐不会形成珠。这表明藻酸盐对通过高碘酸钠的氧化非常敏感。降解研究(未显示)显示1%的氧化藻酸盐微珠为。由于显示出快速降解,因此是优选的支架选择。在整个72小时的研究中,1%氧化的藻酸盐微珠显着降解。然而,在相同条件下,未氧化的微珠实际上没有显示出明显的降解。优选快速释放的运载工具,因为它将帮助减轻在体内应用过程中可能发生的与目标位置处的细胞生存力和注射附着稳定性有关的问题。两者合计,结果表明,氧化的藻酸盐微珠可以潜在地充当基于细胞的疗法的传递载体。我们将继续优化藻酸盐氧化方案,以根据需要调整微珠的降解性。我们的下一步将涉及用氧化的藻酸盐微珠进行细胞封装,以测试正常培养基中的增殖和活力,并最终在体内应用破骨细胞疗法。

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