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脂质体阿仑膦酸盐治疗再狭窄。

Liposomal alendronate for the treatment of restenosis.

机构信息

Institute for Drug Research, School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Israel.

出版信息

J Control Release. 2012 Jul 20;161(2):619-27. doi: 10.1016/j.jconrel.2011.11.037. Epub 2011 Dec 8.

Abstract

The current treatment for coronary restenosis following balloon angioplasty involves the use of a mechanical or drug eluting stent (DES). The advent of DES systems has effectively allayed much of the challenge of restenosis that has plagued the success of percutaneous coronary interventions (PCI). However, there are certain limitations to DES use, among which is late stent thrombosis. Innate immunity and inflammation are of major importance in the overreaction of the wound healing response to PCI-induced vascular injury, which leads to restenosis. Liposomes containing alendronate have been shown to deplete circulating monocytes and reduce experimental restenosis. This review presents a unique systemic approach for treating restenosis with alendronate liposomal nano-carriers and reports on its formulation development, formulation variables affecting monocyte/macrophage targeting, pharmacokinetics (PK) and biodistribution, in vitro and in vivo anti-inflammatory effect, and the recent results of the phase II clinical trial.

摘要

目前,经球囊血管成形术后再狭窄的治疗方法包括使用机械或药物洗脱支架(DES)。DES 系统的出现有效地缓解了困扰经皮冠状动脉介入治疗(PCI)成功的再狭窄的许多挑战。然而,DES 的使用存在某些限制,其中之一是晚期支架血栓形成。固有免疫和炎症在 PCI 诱导的血管损伤引起的伤口愈合反应过度反应中非常重要,这会导致再狭窄。含有阿仑膦酸钠的脂质体已被证明可耗尽循环中的单核细胞并减少实验性再狭窄。这篇综述提出了一种用阿仑膦酸钠脂质体纳米载体治疗再狭窄的独特系统方法,并报告了其制剂开发、影响单核细胞/巨噬细胞靶向的制剂变量、药代动力学(PK)和生物分布、体外和体内抗炎作用,以及最近的 II 期临床试验结果。

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