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Dual‐Targeting Heparin‐Based Nanoparticles that Re‐Assemble in Blood for Glioma Therapy through Both Anti‐Proliferation and Anti‐Angiogenesis
Author(s) -
Wang Jihui,
Yang Yuantao,
Zhang Yonghong,
Huang Min,
Zhou Zhenjun,
Luo Wanxian,
Tang Jiao,
Wang Jianguo,
Xiao Qian,
Chen Huajian,
Cai Yingqian,
Sun Xinlin,
Wang Ying,
Ke Yiquan
Publication year - 2016
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.201602810
Subject(s) - vasculogenic mimicry , glioma , in vivo , angiogenesis , drug delivery , materials science , in vitro , blood–brain barrier , heparin , zeta potential , cancer research , pharmacology , biomedical engineering , biophysics , nanoparticle , nanotechnology , medicine , biology , cancer , biochemistry , metastasis , central nervous system , microbiology and biotechnology
The efficient and specific delivery of nanoparticles (NPs) to brain tumors is crucial for successful glioma treatment. Heparin‐based polymers decorated with two peptides self‐assemble into multi‐functional NPs that specifically target glioma cells. These NPs re‐self‐assemble to a smaller size in blood, which is beneficial for in‐vivo brain drug delivery. The hydrodynamic size of one type of these NPs is 63 ± 11 nm under blood‐mimic conditions (10% fetal bovine serum), but it is 164 ± 16 nm in water. Additionally their zeta potential is more neutral in the blood‐mimic conditions. Transmission electron microscopy reveals the morphology of the spherical NPs. In vitro experiments demonstrate that the NPs exhibit a high cellular uptake and the ability to efficiently discourage proliferation, endothelial‐lined vessels, and vasculogenic mimicry. In vivo studies demonstrate that the NPs can by‐pass the normal blood–brain and blood–(brain tumor) barriers and specifically accumulate in glioma tissues; moreover, they present an excellent anti‐glioma effect in subcutaneous/intracranial glioma‐bearing mice. Their superiority is due to their appropriate size in blood and the synergic effect arising from their targeting of two different receptors. The data suggests that these NPs are ideal for anti‐glioma therapy.