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一种温敏性壳聚糖凝胶的研制,该凝胶与人骨髓间充质干细胞和去铁胺结合,作为一种多模式促血管生成治疗药物,用于治疗严重肢体缺血。

Development of a thermoresponsive chitosan gel combined with human mesenchymal stem cells and desferrioxamine as a multimodal pro-angiogenic therapeutic for the treatment of critical limb ischaemia.

机构信息

Dept. of Anatomy, The Royal College of Surgeons in Ireland, Dublin 2, Ireland.

出版信息

J Control Release. 2012 Jul 10;161(1):73-80. doi: 10.1016/j.jconrel.2012.04.033. Epub 2012 Apr 27.

DOI:10.1016/j.jconrel.2012.04.033
PMID:22562065
Abstract

Critical limb ischaemia (CLI) is a debilitating ischaemic disease caused by vascular occlusion. Pro-angiogenic therapeutics have the potential to produce collateral vasculature, delaying or negating the need for amputation or invasive revascularisation. Thermoresponsive hydrogels can provide an in situ depot for the sustained release of drugs and provide protection and cohesion for encapsulated cells. Human mesenchymal stem cells (hMSCs) have demonstrated strong angiogenic potential in vitro and angiogenic efficacy in vivo. Desferrioxamine (DFO), a pharmacological activator of the pro-angiogenic hypoxia inducible factor-1α pathway, has shown pro-angiogenic efficacy in vivo. This study combined hMSCs and DFO with a thermoresponsive chitosan/β-glycerophosphate (β-GP) gel, to function as an injectable, multimodal, pro-angiogenic therapeutic for the treatment of CLI. This gel underwent a thermogelation beginning at 33°C, and provided a sustained, biologically active release of DFO over the space of seven days, whilst permitting the survival, proliferation and migration of encapsulated hMSCs. hMSCs encapsulated in gel containing a 100μM concentration of DFO displayed an upregulation in VEGF expression. The combination of hMSCs and DFO within the gel resulted in a synergistic enhancement in bioactivity, as measured by increased VEGF expression in gel-exposed human umbilical vein endothelial cells. This formulation displays significant potential as an injectable pro-angiogenic therapeutic for the treatment of CLI.

摘要

严重肢体缺血(CLI)是一种由血管阻塞引起的使人虚弱的缺血性疾病。促血管生成治疗剂有可能产生侧支血管,从而延迟或避免截肢或侵入性血管重建的需要。温敏水凝胶可为药物的持续释放提供原位储存库,并为包封的细胞提供保护和凝聚力。人骨髓间充质干细胞(hMSCs)在体外表现出很强的血管生成潜力,在体内具有血管生成功效。去铁胺(DFO)是一种促血管生成缺氧诱导因子-1α通路的药理学激活剂,在体内显示出促血管生成功效。本研究将 hMSCs 和 DFO 与温敏壳聚糖/β-甘油磷酸酯(β-GP)凝胶结合,作为一种可注射的、多模式的促血管生成治疗剂,用于治疗 CLI。这种凝胶在 33°C 时开始形成温凝胶,在七天的时间内持续、生物活性地释放 DFO,同时允许包封的 hMSCs 存活、增殖和迁移。在含有 100μM DFO 的凝胶中包封的 hMSCs 显示出 VEGF 表达的上调。凝胶中 hMSCs 和 DFO 的组合导致生物活性协同增强,这可以通过凝胶暴露的人脐静脉内皮细胞中 VEGF 表达的增加来衡量。该制剂具有作为 CLI 治疗的可注射促血管生成治疗剂的巨大潜力。

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