A novel magnetic fluid based on starch-coated magnetite nanoparticles functionalized with homing peptide

被引:69
作者
Jiang, Ji-Sen [1 ]
Gan, Zhi-Feng [1 ]
Yang, Yong [1 ]
Du, Bing [2 ]
Qian, Min [2 ]
Zhang, Ping [2 ]
机构
[1] E China Normal Univ, Dept Phys, Ctr Funct Nanomat & Devices, Shanghai 200062, Peoples R China
[2] E China Normal Univ, Sch Life Sci, Shanghai 200062, Peoples R China
关键词
Magnetic fluid; Dual function; Homing peptide; Nanoparticles coupling; Nanomedicine; SURFACE MODIFICATION;
D O I
10.1007/s11051-008-9534-5
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Preparation and characterization in vitro and in vivo of a novel magnetic fluid based on starch-coated magnetite nanoparticles functionalized with homing peptide is reported in this paper. Precursory magnetic fluids stabilized with starch were prepared, in a polymeric starch matrix, by controlled chemical coprecipitation of magnetite phase from aqueous solutions. The average hydrodynamic diameter of starch-coated iron oxide nanoparticles (SIONs) was 46 nm. As a homing peptide, A54 is the most effective peptide specific to the human hepatocellular carcinoma cell line BEL-7402. Final magnetic fluids were obtained through chemical coupling of homing peptide labeled with 5-carboxyl-fluorescein (FAM-A54) and SIONs. Magnetic measurements showed the saturation magnetization value of SIONs amounted to 45 emu/g and the FAM-A54-coupled SIONs showed a good magnetic response in magnetic field. The results of experiments in vitro and in vivo showed that SIONs were endowed with specific affinity to corresponding tumor cells after coupling with FAM-A54 and the FAM-A54-coupled SIONs could be accumulated in the tumor tissue with more efficiency than individual magnetic targeting or biomolecular targeting. This novel magnetic fluid with dual function has great potential applications in diagnostics and therapeutics of human tumor such as drug targeting, magnetic hyperthermia, and magnetic resonance imaging.
引用
收藏
页码:1321 / 1330
页数:10
相关论文
共 24 条
[1]   Therapeutic cancer targeting peptides [J].
Aina, OH ;
Sroka, TC ;
Chen, ML ;
Lam, KS .
BIOPOLYMERS, 2002, 66 (03) :184-199
[2]   Nanocrystal targeting in vivo [J].
Åkerman, ME ;
Chan, WCW ;
Laakkonen, P ;
Bhatia, SN ;
Ruoslahti, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :12617-12621
[3]  
Alexiou C, 2000, CANCER RES, V60, P6641
[4]   Synthesis, characterization and targeting of biodegradable magnetic nanocomposite particles by external magnetic fields [J].
Asmatulu, R ;
Zalich, MA ;
Claus, RO ;
Riffle, JS .
JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS, 2005, 292 :108-119
[5]   Functionalisation of magnetic nanoparticles for applications in biomedicine [J].
Berry, CC ;
Curtis, ASG .
JOURNAL OF PHYSICS D-APPLIED PHYSICS, 2003, 36 (13) :R198-R206
[6]   Neurotransplantation of magnetically labeled oligodendrocyte progenitors: Magnetic resonance tracking of cell migration and myelination [J].
Bulte, JWM ;
Zhang, SC ;
van Gelderen, P ;
Herynek, V ;
Jordan, EK ;
Duncan, ID ;
Frank, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (26) :15256-15261
[7]   A note on the optimal L2-estimate of the finite volume element method [J].
Chen, ZY ;
Li, RH ;
Zhou, AH .
ADVANCES IN COMPUTATIONAL MATHEMATICS, 2002, 16 (04) :291-303
[8]  
Gan ZF, 2005, PROG CHEM, V17, P978
[9]   Immobilization of homing peptide on magnetite nanoparticles and its specificity in vitro [J].
Gan, Zhi-Feng ;
Jiang, Ji-Sen ;
Yang, Yong ;
Du, Bing ;
Qian, Min ;
Zhang, Ping .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2008, 84A (01) :10-18
[10]   Synthesis and surface engineering of iron oxide nanoparticles for biomedical applications [J].
Gupta, AK ;
Gupta, M .
BIOMATERIALS, 2005, 26 (18) :3995-4021