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IL-1Ra 及其传递策略:关联视角下的探讨。

IL-1Ra and its delivery strategies: inserting the association in perspective.

机构信息

Institute of Pharmacology, Toxicology and Biochemical Pharmaceutics College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China,

出版信息

Pharm Res. 2013 Nov;30(11):2951-66. doi: 10.1007/s11095-013-1118-0. Epub 2013 Jun 22.

Abstract

Interleukin-1 receptor antagonist (IL-1Ra) is a naturally occurring anti-inflammatory antagonist of interleukin-1 family of pro-inflammatory cytokines. The broad spectrum anti-inflammatory effects of IL-1Ra have been investigated against various auto-immune diseases such as diabetes mellitus, rheumatoid arthritis. Despite of its outstanding broad spectrum anti-inflammatory effects, IL-1Ra has short biological half-life (4-6 h) and to cope with this problem, up till now, many delivery strategies have been applied either to extend the half-life and/or prolong the steady-state sustained release of IL-1Ra from its target site. Here in our present paper, we have provided an overview of all approaches attempted to prolong the duration of therapeutic effects of IL-1Ra either by fusing IL-1Ra using fusion protein technology to extend the half-life and/or development of new dosage forms using various biodegradable polymers to prolong its steady-state sustained release at the site of administration. These approaches have been characterized by their intended impact on either in vitro release characteristics and/or pharmacokinetic and pharmacodynamic parameters of IL-1Ra. We have also compared these delivery strategies with each other on the basis of bioactivity of IL-1Ra after fusion with fusion protein partner and/or encapsulation with biodegradable polymer.

摘要

白细胞介素-1 受体拮抗剂(IL-1Ra)是一种天然存在的抗炎拮抗剂,可对抗白细胞介素-1 家族的促炎细胞因子。IL-1Ra 的广谱抗炎作用已针对各种自身免疫性疾病(如糖尿病、类风湿关节炎)进行了研究。尽管其具有出色的广谱抗炎作用,但 IL-1Ra 的生物半衰期较短(4-6 小时),为了解决这个问题,迄今为止,已经应用了许多给药策略来延长半衰期和/或从靶部位延长 IL-1Ra 的稳态持续释放。在我们目前的论文中,我们全面概述了所有尝试延长 IL-1Ra 治疗效果持续时间的方法,这些方法要么通过融合蛋白技术融合 IL-1Ra 来延长半衰期,要么通过使用各种可生物降解聚合物开发新剂型来延长其在给药部位的稳态持续释放。这些方法的特点是根据 IL-1Ra 的体外释放特性和/或药代动力学和药效学参数对其进行了预期的影响。我们还根据与融合蛋白伴侣融合后或与可生物降解聚合物包封后 IL-1Ra 的生物活性,将这些给药策略相互进行了比较。

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