Composite microparticles of halloysite clay nanotubes bound by calcium carbonate

被引:15
|
作者
Jin, Yi [1 ,2 ]
Yendluri, Raghuvara [2 ]
Chen, Bin [1 ]
Wang, Jingbo [1 ]
Lvov, Yuri [2 ,3 ]
机构
[1] Ningbo Univ Technol, Inst Chem Engn, Ningbo 315016, Zhejiang, Peoples R China
[2] Louisiana Tech Univ, Inst Micromfg, Ruston, LA 71272 USA
[3] Ural Fed Univ, Ekaterinburg 620002, Russia
基金
俄罗斯科学基金会;
关键词
Halloysite; LbL self-assembly; Calcium carbonate; Drug sustained release; SUSTAINED-RELEASE; POLYELECTROLYTE MICROCAPSULES; PROTEIN PARTICLES; CACO3; PARTICLES; VATERITE; ENCAPSULATION; MICROSPHERES; FABRICATION; ADSORPTION; EFFICIENCY;
D O I
10.1016/j.jcis.2015.12.031
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Natural halloysite clay nanotubes with 15 nm inner and 75 nm outer diameters have been used as vehicles for sustained release of drugs in composite hollow microparticles "glued" with CaCO3. We used a layer-by layer assembly accomplished alginate binding with Ca2+ followed by CO2 bubbling to prepare the composite microspheres of CaCO3 and polyelectrolytes (PE) modified halloysite nanotubes (HNTs-PE2/CaCO3) with the diameter of about 5-10 mu m. These microparticles have empty spherical structure and abundant pore distributions with maxima at 2.5, 3.9, 6.0 and 13.3 nm, and higher surface area of 82.3 m(2) g(-1) as characterized by SEM and BET test. We loaded drugs in these micro-nano carriers of tight piles of halloysite nanotube with end clogged with CaCO3. The sustained release of Nifedipine drug from HNTs-PE2/CaCO3 composite microspheres was slower than for pristine halloysite nanotubes. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:254 / 260
页数:7
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