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首页> 外文期刊>Pharmaceutical research >Co-delivery of vascular endothelial growth factor and angiopoietin-1 using injectable microsphere/hydrogel hybrid systems for therapeutic angiogenesis
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Co-delivery of vascular endothelial growth factor and angiopoietin-1 using injectable microsphere/hydrogel hybrid systems for therapeutic angiogenesis

机译:血管内皮生长因子和血管生成素-1使用可注射微球/水凝胶杂交系统进行治疗血管生成的共聚

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Purpose: We hypothesized that combined delivery of vascular endothelial growth factor (VEGF) and angiopoietin-1 (Ang-1) using microsphere/hydrogel hybrid systems could enhance mature vessel formation compared with administration of each factor alone. Methods: Hybrid delivery systems composed of alginate hydrogels and poly(D,L-lactic-co-glycolic acid) (PLGA) microspheres containing angiogenic factors were prepared. The release behavior of angiogenic factors from hybrid systems was monitored in vitro. The hybrid systems were injected into an ischemic rodent model, and blood vessel formation at the ischemic site was evaluated. Results: The sustained release over 4 weeks of both VEGF and Ang-1 from hybrid systems was achieved in vitro. Co-delivery of VEGF and Ang-1 was advantageous to retain muscle tissues and significantly induced vessel enlargement at the ischemic site, compared to mice treated with either VEGF or Ang-1 alone. Conclusions: Sustained and combined delivery of VEGF and Ang-1 significantly enhances vessel enlargement at the ischemic site, compared with sustained delivery of either factor alone. Microsphere/hydrogel hybrid systems may be a promising vehicle for delivery of multiple drugs for many therapeutic applications.
机译:目的:我们假设使用微球/水凝胶杂交系统的血管内皮生长因子(VEGF)和血管生成素-1(Ang-1)的组合递送可以增强与单独的每个因子的给药相比的成熟血管形成。方法:制备由藻酸盐水凝胶和聚(D,L-乳酸共乙醇酸)(PLGA)含有血管生成因子的微球组成的杂化输送系统。在体外监测来自杂化系统的血管生成因子的释放行为。将杂交系统注射到缺血性啮齿动物模型中,评估缺血部位的血管形成。结果:在体外实现了来自混合系统的VEGF和Ang-1的4周超过4周的持续释放。与单独用VEGF或Ang-1处理的小鼠相比,VEGF和Ang-1的共同递送是有利的,在缺血部位上保持肌肉组织和显着诱导的血管扩大。结论:VEGF和Ang-1的持续和组合递送显着增强了缺血部位的血管增大,而单独的任何一个因素持续递送。微球/水凝胶混合系统可以是用于在许多治疗应用中递送多种药物的有希望的车辆。

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