β-Cyclodextrin derivatives hybrid Fe3O4 magnetic nanoparticles as the drug delivery for ketoprofen

被引:19
|
作者
Huang, Lizhen [1 ,2 ]
Wang, Haixia [1 ,2 ]
Li, Bo [1 ,2 ]
Li, Erdong [1 ,2 ]
Zhou, Yehong [1 ,2 ]
Yang, Yonggang [1 ,2 ]
Dong, Chuan [1 ,2 ]
Shuang, Shaomin [1 ,2 ]
机构
[1] Shanxi Univ, Sch Chem & Chem Engn, Res Ctr Environm Sci & Engn, Taiyuan 030006, Peoples R China
[2] Shanxi Univ, Inst Loess Plateau, Taiyuan 030006, Peoples R China
关键词
beta-Cyclodextrin derivatives; Fe3O4 magnetic nanoparticles; Drug delivery; Ketoprofen; IRON-OXIDE NANOPARTICLES; NANO-COMPOSITE; SHELL; CORE; ADSORPTION; SEPARATION;
D O I
10.1007/s10847-013-0378-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
beta-Cyclodextrin (beta-CD) and its derivatives carboxymethyl-beta-CD (CM-beta-CD) and 2,6-dimethyl-beta-CD (DM-beta-CD) modified magnetic nanoparticles (CD-MNPs) were synthesized via layer-by-layer method. CDs grafted onto Fe3O4 MNPs were demonstrated by transmission electron microscopy, Fourier transform infrared and Zeta potential. Magnetic properties of CM-beta-CD-MNPs, DM-beta-CD-MNPs and beta-CD-MNPs were characterized by vibrating sample magnetometer and the magnetic saturation values were 47, 46 and 44 emu g(-1), respectively. CD-MNPs as drug carriers were investigated by inclusion behavior and in vitro release using ketoprofen (KP) as a model drug. The maximum adsorption quantities of CM-beta-CD-MNPs, DM-beta-CD-MNPs and beta-CD-MNPs for KP were 37.03, 7.63 and 25.12 mg g(-1), respectively, and the loading behaviors followed the Langmuir adsorption isotherm model with monolayer adsorption. The release profiles of KP released from KP-loaded CD-MNPs were rapid in initial 60 min and then gradually tend to level off, the release efficiency order was CM-beta-CD-MNPs[beta-CD-MNPs > DM-beta-CD-MNPs, which was consistent with the order of inclusion capability. Therefore, the CD-MNPs were promising candidates for drug delivery.
引用
收藏
页码:209 / 215
页数:7
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