Real-time in vivo imaging of surface-modified liposomes to evaluate their behavior after pulmonary administration

被引:38
作者
Murata, Mitsutaka [1 ]
Tahara, Kohei [1 ]
Takeuchi, Hirofumi [1 ]
机构
[1] Gifu Pharmaceut Univ, Lab Pharmaceut Engn, Gifu 5011196, Japan
关键词
In vivo imaging; Indocyanine green; Liposomal surface modification; PVA; Pulmonary drug delivery; IVIS (R); MODIFIED POLYVINYL-ALCOHOL; INDOCYANINE GREEN; DELIVERY; INSULIN; AEROSOL; RATS;
D O I
10.1016/j.ejpb.2013.09.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Our previous study demonstrated that surface modification of liposomes using polyvinyl alcohol with a hydrophobic anchor (PVA-R) achieved sustained absorption from the lung after pulmonary administration and prolonged the pharmacological effects of the model peptide drug. In the present study, the behavior of PVA-R-modified liposomes in the lung and whole body was monitored using a real-time in vivo imaging system. Subsequently, the influence of surface modification with PVA-R on liposomal behavior in lung tissue was examined. Indocyanine green (ICG) was used as a near-infrared label of PVA-R-modified liposomes and was used to observe their dynamic behavior using non-invasive in vivo imaging (IVIS (R) imaging system) after pulmonary administration to rats. PVA-R-modified submicronsized liposomes (ssLips) induced long-term retention in the lung compared with unmodified liposomes. Moreover, liposome association with alveolar macrophages (NR8383) was decreased by PVA-R modification in vitro. Therefore, PVA-R modification may prevent rapid elimination of ssLips by macrophages, thereby increasing retention in the lung. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 119
页数:5
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