LyP-1 peptide-functionalized gold nanoprisms for SERRS imaging and tumor growth suppressing by PTT induced-hyperthermia

被引:31
|
作者
Huang, Xi [1 ,2 ,3 ,4 ]
Yin, Yanlong [1 ]
Wu, Min [1 ]
Zan, Wang [1 ]
Yang, Qian [1 ]
机构
[1] Chengdu Med Coll, Sch Pharm, Coll Key Lab Sichuan Prov Specif Struct Small Mol, Chengdu 610500, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Ophthalm Lab, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Ophthalmol, State Key Lab, Chengdu 610041, Sichuan, Peoples R China
[4] Sichuan Univ, West China Hosp, Collaborat Innovat Ctr Biotherapy, Chengdu 610041, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Gold nanoprisms; SERRS imaging; LyP-1; peptide; Tumor targeting; Photothermal therapy; IN-VITRO; PHOTOTHERMAL THERAPY; NANOPARTICLES; VIVO; NANOSTARS; P32/GC1QR; NANORODS;
D O I
10.1016/j.cclet.2019.02.019
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Gold-based nanomaterials with plasmonic properties exhibit various potentials for biomedical applications. In this work, gold nanoprisms (GNPs) was synthesized and then modified with LyP-1, a tumor-homing peptide, to improve the affinity of the GNPs to tumor cells, thus, to improve the efficacy of tumor-targeted photothermal therapy. The introduction of NIR dye 1R780 not only enabled the GNPs-based nanosystem with the surface-enhanced resonant Raman scattering (SERRS) property, but also enhanced the plasmonic photothermal property which delivering therapeutic heating by 660 nm laser irradiation. The obtained GNPs/IR780-LyP-1 presented significantly increased of photothermal conversion in vitro and in vivo, which resulted in enhanced tumor-targeting photothermal therapeutic efficacy after laser irradiation. Hence, the GNPs/IR780-LyP-1 prepared in this study can be served as a Raman-encoded molecular imaging candidate and photothermal therapy agents for future cancer treatment. (C) 2019 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1335 / 1340
页数:6
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