Formulation and Characterization of Novel Temperature Sensitive Polymer-Coated Magnetic Nanoparticles

被引:5
|
作者
Rahimi, Maham [1 ,2 ]
Meletis, Efstathios I. [3 ]
You, Shaoxin [3 ]
Nguyen, Kytai [1 ,2 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Biomed Engn Programs, Arlington, TX 76019 USA
[2] Univ Texas Arlington, Dept Bioengn, Arlington, TX 76019 USA
[3] Univ Texas Arlington, Dept Mat Sci & Engn, Arlington, TX 76019 USA
关键词
Temperature Sensitive Polymers; Magnetic Nanoparticles; Drug Delivery; IRON-OXIDE NANOPARTICLES; THERMALLY RESPONSIVE POLYMERS; TARGETED DRUG-DELIVERY; SUPERPARAMAGNETIC NANOPARTICLES; HYPERTHERMIA; CANCER; RELEASE; COPOLYMERS; HYDROGELS; MICELLES;
D O I
10.1166/jnn.2010.2596
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The objective of this research was to develop novel polymer coated magnetic nanoparticles for controlled drug delivery applications. To form these novel nanoparticles, silane-coated magnetic nanoparticles (MNPs) were used as a template for a free radial polymerization of three monomers, N-isopropylacrylamide, acrylamide, and allylamine (NIPA-AAm-AH), on the surface of MNPs. Transmission electron microscope results indicated that the size of the NIPA-AAm-AH coated MNPs was approximately 100 nm. To investigate the chemical composition and chemical state of our nanoparticles, FTIR and XPS were used. Results from chemical analysis illustrated the presence of the constituent functional groups of the NIPA-AAm-AH coated MNPs. In addition, the magnetic properties of different layers on the MNPs, analyzed by SQUID, indicated a decrease in saturation magnetization after each layer of coating. The nanoparticles were successfully conjugated to fluorescent PEG to prolong their circulating half life. Furthermore, bovine serum albumin (BSA) was used in order to investigate the protein release profile of the nanoparticles as a function of the temperature. The protein release profile indicated that the NIPA-AAm-AH coated MNPs have a significantly higher percent release at 41 degrees C compared to those of 4 degrees C and 37 degrees C, which demonstrates their temperature sensitivity. In the future, the release profile of therapeutic drugs from nanoparticles at various temperatures and pHs as well as targeted capability of the synthesized nanoparticles for possible applications in controlled and targeted delivery will be investigated.
引用
收藏
页码:6072 / 6081
页数:10
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