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Autologous Red Blood Cell Delivery of Betamethasone Phosphate Sodium for Long Anti-Inflammation

机译:倍他米松磷酸钠的自体红细胞递送可长期抗炎

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摘要

Although glucocorticoids are highly effective in treating various types of inflammation such as skin disease, rheumatic disease, and allergic disease, their application have been seriously limited for their high incidence of side effects, particularly in long term treatment. To improve efficacy and reduce side effects, we encapsulated betamethasone phosphate (BSP) into biocompatible red blood cells (RBCs) and explored its long acting-effect. BSP was loaded into rat autologous erythrocytes by hypotonic preswelling method, and the loading amount was about 2.5 mg/mL cells. In vitro, BSP loaded RBCs (BSP-RBCs) presented similar morphology, osmotic fragility to native RBCs (NRBCs). After the loading process, the loaded cells can maintain around 70% of Na+/K+-ATPase activity of natural cells. In vivo, a series of tests including survival, pharmacokinetics, and anti-inflammatory effect were carried out to examine the long-acting effect of BSP-RBCs. The results shown that the loaded cells could circulate in plasma for over nine days, the release of BSP can last for over seven days and the anti-inflammatory effect can still be observed on day 5 after injection. Totally, BSP-loaded autologous erythrocytes seem to be a promising sustained releasing delivery system with long anti-inflammatory effect.
机译:尽管糖皮质激素在治疗各种类型的炎症如皮肤病,风湿病和过敏性疾病方面非常有效,但是由于其副作用高发生率,特别是在长期治疗中,糖皮质激素的应用受到了严重限制。为了提高疗效并减少副作用,我们将磷酸倍他米松(BSP)封装到生物相容性红细胞(RBC)中,并探索了其长效作用。通过低渗预溶胀法将BSP加载到大鼠自体红细胞中,加载量约为2.5 mg / mL细胞。在体外,负载BSP的RBC(BSP-RBC)具有与天然RBC(NRBC)类似的形态,渗透脆性。加载过程后,加载的细胞可以维持天然细胞的Na + / K + -ATPase活性约70%。在体内,进行了一系列测试,包括存活率,药代动力学和抗炎作用,以检查BSP-RBC的长效作用。结果表明,加载的细胞可以在血浆中循环超过9天,BSP的释放可以持续超过7天,并且在注射后第5天仍可以观察到抗炎作用。总体而言,加载BSP的自体红细胞似乎是一种有希望的持续释放递送系统,具有长的抗炎作用。

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