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

机译:氧化 - 藻酸盐微珠包封骨细胞作为基于细胞的疗法以反向血管#calcification

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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%氧化和非氧化的藻酸盐溶液正确形成微珠,但不从2%氧化藻酸盐物质化的珠子。这表明海藻酸盐通过钠周期性对氧化非常敏感。降解研究(未示出)显示出1%氧化的藻酸盐微珠。由于表现出快速降解,优选的支架选择。在整个72小时的研究中,1%的氧化藻酸盐微珠显着降低。然而,未氧化的微珠在相同的条件下显着降解显着降解。优选快速释放的递送车辆,因为它将有助于缓解在体内应用期间可能发生的关于靶位置的细胞活力和注射附着稳定性的问题。结果表明,氧化的藻酸盐微珠可能用作基于细胞疗法的递送载体。我们将继续优化我们的藻酸盐氧化方案,根据需要调整微珠可降解性。我们的下一步将涉及细胞包封与氧化的藻酸盐微珠朝向正常培养基中的氧化藻酸盐微珠,最终在骨酸骨醛治疗的体内应用中。

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