Identifying glioblastoma margins using dual-targeted organic nanoparticles for efficient in vivo fluorescence image-guided photothermal therapy

被引:57
作者
Cai, Xiaolei [1 ]
Bandla, Aishwarya [2 ]
Chuan, Chan Kim [2 ]
Magarajah, Gayathiri [2 ]
Liao, Lun-De [2 ,3 ]
Teh, Daniel Boon Loong [4 ,5 ]
Kennedy, Brian K. [4 ,5 ]
Thakor, Nitish V. [2 ]
Liu, Bin [1 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, 4 Engn Dr 4, Singapore 117585, Singapore
[2] Natl Univ Singapore, Singapore Inst Neurotechnol SINAPSE, 28 Med Dr, Singapore 117456, Singapore
[3] Natl Hlth Res Inst, Inst Biomed Engn & Nanomed, 35 Keyan Rd, Zhunan Town 35053, Miaoli County, Taiwan
[4] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, 8 Med Dr, Singapore 117456, Singapore
[5] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Physiol, 8 Med Dr, Singapore 117456, Singapore
基金
新加坡国家研究基金会;
关键词
BLOOD-BRAIN-BARRIER; MULTIFORME; SURVIVAL; TEMOZOLOMIDE; GRAPHENE;
D O I
10.1039/c8mh00946e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Current therapeutics for glioblastoma multiforme (GBM) treatment are unsatisfactory due to their limited ability to control the progression from tumour margins. In this work, organic nanoparticles (NPs) are synthesized by co-encapsulating a fluorogen with aggregation-induced emission to generate a bright red emission for imaging and a semiconducting polymer to offer NIR absorption for photothermal therapy. The NPs are further modified with different ratios of two targeting ligands, folate and cRGD peptide. The best ratio that performs specific and efficient GBM targeting is screened out through in vitro and ex vivo fluorescence imaging analysis. The NPs with an FA to cRGD ratio of 25:75 exhibit superior ability to target GBM cells in vitro and also show efficient accumulation at the GBM margin and in the tumour interior after in vivo administration. The progression of GBM can be greatly suppressed through photothermal therapy, which provides a simple but promising strategy for GBM treatment.
引用
收藏
页码:311 / 317
页数:7
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