William G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, Ohio 43210, USA.
Biotechnol Bioeng. 2012 Mar;109(3):823-9. doi: 10.1002/bit.24340. Epub 2011 Nov 6.
Current strategies to deliver therapeutic molecules to specific cell and tissue types rely on conjugation of antibodies and other targeting ligands directly to the therapeutic molecule itself or its carrier. This work describes a novel strategy to deliver therapeutic molecules into macrophages that takes advantage of the native hemoglobin (Hb) scavenging activity of plasma haptoglobin (Hp) and the subsequent uptake of the Hb-Hp complex into macrophages via CD163 receptor-mediated endocytosis. The drug delivery system described in this work consists of Hb decorated liposomes that can encapsulate any therapeutic molecule of interest, in this case the model fluorescent dye calcein was used in this study. The results of this study clearly demonstrate that this delivery system is specific towards macrophages and demonstrates the feasibility of using this approach in targeted drug delivery.
目前将治疗分子递送到特定细胞和组织类型的策略依赖于将抗体和其他靶向配体直接缀合到治疗分子本身或其载体上。本工作描述了一种将治疗分子递送到巨噬细胞中的新策略,该策略利用了血浆触珠蛋白(Hp)对天然血红蛋白(Hb)的清除活性,以及随后通过 CD163 受体介导的内吞作用将 Hb-Hp 复合物摄取到巨噬细胞中。本工作中描述的药物递送系统由 Hb 修饰的脂质体组成,该脂质体可以包封任何感兴趣的治疗分子,在本研究中使用了模型荧光染料 calcein。本研究的结果清楚地表明,该递药系统对巨噬细胞具有特异性,并证明了在靶向药物递送中使用这种方法的可行性。