Liposomes surface conjugated with human hemoglobin target delivery to macrophages

被引:28
|
作者
Zhang, Ning [1 ,2 ]
Palmer, Andre F. [1 ]
机构
[1] Ohio State Univ, William G Lowrie Dept Chem & Biomol Engn, Columbus, OH 43210 USA
[2] Ohio State Univ, Ohio State Biochem Program, Columbus, OH 43210 USA
基金
美国国家卫生研究院;
关键词
hemoglobin; liposome; Hb-liposome; targeted drug delivery; macrophage; CD-163; receptor; DRUG-DELIVERY; CANCER; PEGYLATION; FILTRATION; CARRIERS; THERAPY; SYSTEMS; PROTEIN; MP4;
D O I
10.1002/bit.24340
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 HbHp 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. Biotechnol. Bioeng. 2012; 109:823829. (C) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:823 / 829
页数:7
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