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Magnetic Nanoparticles and Thermally Responsive Polymer for Targeted Hyperthermia and Sustained Anti-Cancer Drug Delivery
被引:13
|作者:
Wang, Sarah Y.
[1
,2
]
Liu, Michelle C.
[1
,2
]
Kang, Kyung A.
[2
]
机构:
[1] DuPont Manual High Sch, Louisville, KY USA
[2] Univ Louisville, Dept Chem Engn, Louisville, KY 40292 USA
来源:
OXYGEN TRANSPORT TO TISSUE XXXIV
|
2013年
/
765卷
关键词:
Nanoparticles;
Anti-cancer drug delivery;
IN-VITRO;
RELEASE;
GEL;
COPOLYMER;
SYSTEM;
D O I:
10.1007/978-1-4614-4989-8_44
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
A novel cancer treatment method is being designed using a combination of iron oxide (Fe3O4) nanoparticles (IONPs) and Pluronic F-127 (PF127). IONPs have been used for heating tumors via an alternating electromagnetic (AEM) field. PF127 is a polymer possessing thermo-reversible and concentration-dependent gelation properties in aqueous solutions. PF127, as a gel, is an attractive drug delivery vehicle due to its zero-order drug release property. The combination of IONPs and PF127 would allow both short-term, tumor-specific, hyperthermic treatment, and long-term sustained drug delivery. As a preliminary study, the gelling and heating properties of IONPs/PF127 mixtures were investigated: 18% (w/w) PF127 was found to be ideal for our purpose because it gels at 28.0 degrees C, i.e., it would be injectable at room temperature (20-25 degrees C) and forms gel upon injection into the body (37 degrees C). IONPs in PF127 showed little effect on gelation temperatures. The heating performance of IONPs in PF127 slightly, but linearly decreased with PF127. In the IONP concentration range of 0.01-0.05% (w/v) mixed with PF127 at 18% (w/w), the heating performance increased linearly with the increase in IONP concentration.
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页码:315 / 321
页数:7
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