Reimaging biological barriers affecting distribution and extravasation of PEG/peptide-modified liposomes in xenograft SMMC7721 tumor

被引:13
作者
Tang, Hailing [1 ,2 ]
Rui, Mengjie [3 ]
Mai, Junhua [4 ]
Guo, Wei [5 ]
Xu, Yuhong [2 ]
机构
[1] Shanghai Jiao Tong Univ, Renji Hosp, Inst Mol Med, Sch Med, Shanghai 200127, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Pharm, Shanghai 200240, Peoples R China
[3] Jiangsu Univ, Sch Pharm, Zhenjiang 212001, Jiangsu, Peoples R China
[4] Methodist Hosp Res Inst, Dept Nanomed, Houston, TX 77030 USA
[5] Dalian Med Univ, Inst Canc Stem Cell, Dalian 116044, Peoples R China
基金
美国国家科学基金会;
关键词
GE11; Liposome; Target delivery; Biology barrier; EGFR; SMMC7721; GROWTH-FACTOR RECEPTOR; DRUG-DELIVERY SYSTEMS; ENHANCED PERMEABILITY; PEPTIDE LIGAND; NANOPARTICLES; OPSONIZATION; DOXORUBICIN; EFFICACY;
D O I
10.1016/j.apsb.2019.06.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Liposomes, as one of the most successful nanotherapeutics, have a major impact on many biomedical areas. In this study, we performed laser scanning confocal microscope (LSCM) and immunohistochemistry (IHC) assays to investigate the intra-tumor transport and antitumor mechanismof GE11 peptide-conjugated active targeting liposomes (GE11-TLs) in SMMC7721 xenograft model. According to classification of individual cell types in high resolution images, biodistribution of macrophages, tumor cells, cells with high epidermal growth factor receptor (EGFR) expression and interstitial matrix in tumor microenvironment, in addition, their impacts on intra-tumor penetration of GE11-TLs were estimated. Type I collagen fibers and macrophage flooded in the whole SMMC7721 tumor xenografts. Tumor angiogenesis was of great heterogeneity from the periphery to the center region. However, the receptor-binding site barriers were supposed to be the leading cause of poor penetration of GE11-TLs. We anticipate these images can give a deep reconsideration for rational design of target nanoparticles for overcoming biological barriers to drug delivery. (C) 2020 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.
引用
收藏
页码:546 / 556
页数:11
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