Novel core-shell structured Paclitaxel-loaded PLGA@Ag-Au nanoparticles

被引:19
|
作者
Li, Si-Yue [1 ]
Wang, Min [1 ]
机构
[1] Univ Hong Kong, Dept Mech Engn, Hong Kong, Hong Kong, Peoples R China
关键词
Bimetallic Ag-Au; Nanoshell; SERS; PLGA; Nanoparticle; Paclitaxel; SILVER; NANOSHELLS; CANCER; SERS; ACID;
D O I
10.1016/j.matlet.2012.10.129
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Novel core-shell structured anti-cancer drug-loaded poly(lactide-co-glycolide) @Ag-Au nanoparticles (NPs) for medical applications were synthesized and characterized. Monodispersed, Paclitaxel (PTX)-loaded PLGA NPs, which were fabricated using a stabilizer-free method, served as the device core and facilitated Ag NP nucleation on their surface. A shell of Ag NPs was formed in situ on PLGA NPs through the controlled reduction of AgNO3 by polyvinylpyrrolidone (PVP). The intermediate PLGA@Ag NPs were used to grow Ag-Au nanoshells on PLGA core in a replacement reaction. The bimetallic Ag-Au nanoshell could serve as an optimal metal enhancer for surface enhanced Raman spectroscopy (SEAS). SERS experiments using 4-MBA as the Raman reporter showed that the PTX-loaded PLGA@Ag-Au hybrid NPs provided enormously amplified SERS signals, which would make them as highly desirable SERS optical tags in biomedical imaging. With a combination of functions of high SERS activity, controlled anti-cancer drug release and hyperthermal effect, the PTX-loaded PLGA@Ag-Au NPs have the potential as new theranostics for effective cancer detection and treatment. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:350 / 353
页数:4
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