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Adjustable delivery of pro-angiogenic FGF-2 by alginate:collagen microspheres

机译:海藻酸盐:胶原微球可调节递送促血管生成的FGF-2

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Therapeutic induction of blood vessel growth (angiogenesis) in ischemic tissues holds great potential for treatment of myocardial infarction and stroke. Achieving sustained angiogenesis and vascular maturation has, however, been highly challenging. Here, we demonstrate that alginate:collagen hydrogels containing therapeutic, pro-angiogenic FGF-2, and formulated as microspheres, is a promising and clinically relevant vehicle for therapeutic angiogenesis. By titrating the amount of readily dissolvable and degradable collagen with more slowly degradable alginate in the hydrogel mixture, the degradation rates of the biomaterial controlling the release kinetics of embedded pro-angiogenic FGF-2 can be adjusted. Furthermore, we elaborate a microsphere synthesis protocol allowing accurate control over sphere size, also a critical determinant of degradation/release rate. As expected, alginate:collagen microspheres were completely biocompatible and did not cause any adverse reactions when injected in mice. Importantly, the amount of pro-angiogenic FGF-2 released from such microspheres led to robust induction of angiogenesis in zebrafish embryos similar to that achieved by injecting FGF-2-releasing cells. These findings highlight the use of microspheres constructed from alginate:collagen hydrogels as a promising and clinically relevant delivery system for pro-angiogenic therapy.
机译:缺血性组织中血管生长(血管生成)的治疗诱导在治疗心肌梗塞和中风方面具有巨大潜力。然而,实现持续的血管生成和血管成熟一直是极富挑战性的。在这里,我们证明了藻酸盐:胶原蛋白水凝胶含有治疗性促血管生成的FGF-2,并配制成微球,是治疗性血管生成的有前途且与临床相关的载体。通过在水凝胶混合物中用较缓慢降解的藻酸盐滴定易于溶解和降解的胶原蛋白的量,可以控制控制包埋的促血管生成性FGF-2释放动力学的生物材料的降解速率。此外,我们精心设计了一种微球合成方案,可以精确控制球的大小,这也是降解/释放速率的关键决定因素。正如预期的那样,海藻酸盐:胶原微球具有完全的生物相容性,并且在小鼠体内注射时不会引起任何不良反应。重要的是,从此类微球中释放的促血管生成性FGF-2的量导致了斑马鱼胚胎中血管生成的强烈诱导,类似于通过注射FGF-2释放细胞所实现的诱导。这些发现强调了由藻酸盐:胶原水凝胶构建的微球作为促血管生成治疗的有希望且与临床相关的递送系统的用途。

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