Study of Fe3O4-PLLA-PEG-PLLA magnetic microspheres based on supercritical CO2: Preparation, physicochemical characterization, and drug loading investigation

被引:19
|
作者
Chen, Ai-Zheng [1 ,2 ]
Li, Li [1 ]
Wang, Shi-Bin [1 ,2 ]
Lin, Xiao-Fen [1 ]
Liu, Yuan-Gang [1 ,2 ]
Zhao, Chen [1 ]
Wang, Guang-Ya [1 ]
Zhao, Zheng [3 ]
机构
[1] Huaqiao Univ, Coll Chem Engn, Xiamen 361021, Peoples R China
[2] Huaqiao Univ, Inst Biomat & Tissue Engn, Inst Pharmaceut Engn, Xiamen 361021, Peoples R China
[3] Hong Kong Polytech Univ, Inst Text & Clothing, Kowloon, Hong Kong, Peoples R China
来源
JOURNAL OF SUPERCRITICAL FLUIDS | 2012年 / 67卷
基金
中国国家自然科学基金;
关键词
Fe3O4; nanoparticles; PLLA-PEG-PLLA; Methotrexate; Supercritical CO2; SOLUTION-ENHANCED DISPERSION; BETA-CAROTENE; NANOPARTICLES; POLYMER; MICROPARTICLES; PRECIPITATION; NANOCOMPOSITES; PARTICLES; CARRIERS; COPRECIPITATION;
D O I
10.1016/j.supflu.2012.04.009
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
The Fe3O4-poly(L-lactide)-poly(ethylene glycol)-poly(L-lactide) magnetic microspheres (Fe3O4-PLLA-PEG-PLLA MMPs) were successfully developed in a process of suspension-enhanced dispersion by supercritical CO2 (SpEDS), and their physicochemical properties were characterized. Methotrexate (MM-loaded Fe3O4-PLIA-PEG-PLLA MMPs were produced by co-precipitation and microencapsulation processes, and their drug loads, encapsulation efficiencies and drug release profiles were investigated. The resulting Fe3O4-PLLA-PEG-PLLA MMPs have a spherical shape, with a good magnetic response, which is dominated by the Fe3O4 content. With an increase in the Fe3O4 nanoparticle content (5.6%, 13.2%, 19.6%, 23.7%, and 42.8%), the particle size of the resulting MMPs decreased (mean diameters: 666, 629, 583, 578, and 566 nm, respectively); their corresponding saturation magnetizations increased dramatically (5.0, 16.3, 35.6, 3.1 x 10(3), and 1.3 x 10(5) emu/g, respectively). Compared with the parallel study of co-precipitation, the microencapsulation process produced MTX-loaded MMPs with a smaller mean particle size (564 rim versus 677 nm), a higher drug load (8.9% versus 7.2%), a higher encapsulation efficiency (60.8% versus 29.4%), and a much longer sustained-release effect without a burst release (12.6% in 0.5 h and 98.9% in 144 h versus 52.8% in 0.5 h and 96.1% in Oh). The results also indicate that the SpEDS process is a physical process to produce a magnetic drug carrier, with a very low organic solvent residue of 20 ppm, which would have potential as a sustained and targeted drug delivery system when combined with the microencapsulation process. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:139 / 148
页数:10
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