Nanoparticle uptake by circulating leukocytes: A major barrier to tumor delivery

被引:37
作者
Betker, Jamie L. [1 ]
Jones, Dallas [2 ]
Childs, Christine R. [3 ]
Helm, Karen M. [3 ]
Terrell, Kristina [3 ]
Nagel, Maria A. [2 ]
Anchordoquy, Thomas J. [1 ]
机构
[1] Univ Colorado, Skaggs Sch Pharm & Pharmaceut Sci, Anschutz Med Campus,12850 E Montview Blvd, Aurora, CO 80045 USA
[2] Univ Colorado, Dept Neurol, Anschutz Med Campus, Aurora, CO USA
[3] Univ Colorado, Flow Cytometry Core Facil, Anschutz Med Campus, Aurora, CO USA
基金
美国国家卫生研究院;
关键词
Lipoplexes; Leukocyte uptake; Gene delivery; PEGylation; MEDIATED GENE DELIVERY; CATIONIC LIPID/DNA COMPLEXES; IN-VITRO; CHOLESTEROL DOMAINS; DRUG-DELIVERY; SERUM STABILITY; DYNAMIC CHANGES; DNA COMPLEXES; CHARGE RATIO; PLASMID DNA;
D O I
10.1016/j.jconrel.2018.07.031
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Decades of research into improving drug delivery to tumors has documented uptake of particulate delivery systems by resident macrophages in the lung, liver, and spleen, and correlated short circulation times with reduced tumor accumulation. An implicit assumption in these studies is that nanoparticles present in the blood are available for distribution to the tumor. This study documents significant levels of lipoplex uptake by circulating leukocytes, and its effect on distribution to the tumor and other organs. In agreement with previous studies, PEGylation dramatically extends circulation times and enhances tumor delivery. However, our studies suggest that this relationship is not straightforward, and that particle sequestration by leukocytes can significantly alter biodistribution, especially with non-PEGylated nanoparticle formulations. We conclude that leukocyte uptake should be considered in biodistribution studies, and that delivery to these circulating cells may present opportunities for treating viral infections and leukemia.
引用
收藏
页码:85 / 93
页数:9
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