Fabrication of drug-loaded polymer microparticles with arbitrary geometries using a piezoelectric inkjet printing system

被引:108
作者
Lee, Byung Kook [1 ,2 ]
Yun, Yeon Hee [1 ,2 ]
Choi, Ji Suk [1 ,2 ]
Choi, Young Chan [1 ,2 ]
Kim, Jae Dong [1 ,2 ]
Cho, Yong Woo [1 ,2 ]
机构
[1] Hanyang Univ, Dept Chem Engn, Ansan 426791, Gyeonggi Do, South Korea
[2] Hanyang Univ, Dept Bionanotechnol, Ansan 426791, Gyeonggi Do, South Korea
关键词
Inkjet printing; Microparticles; Geometry; Drug release; In vitro cytotoxicity; DELIVERY; RELEASE; MICROSPHERES; PARTICLES; DEVICES; DESIGN; SHAPE; FLOW; LITHOGRAPHY; MICROSCALE;
D O I
10.1016/j.ijpharm.2012.02.011
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Carrier geometry is a key parameter of drug delivery systems and has significant impact on the drug release rate and interaction with cells and tissues. Here we present a piezoelectric inkjet printing system as a simple and convenient approach for fabrication of drug-loaded polymer microparticles with well-defined and controlled shapes. The physical properties of paclitaxel (PTX)-loaded poly(lactic-co-glycolic acid) (PLGA) inks, such as volatility, viscosity and surface tension, were optimized for piezoelectric inkjet printing, and PTX-loaded PLGA microparticles were fabricated with various geometries, such as circles, grids, honeycombs, and rings. The resulting microparticles with 10% (w/w) PTX exhibited a fairly homogeneous shape and size. The microparticle fabrication by piezoelectric inkjet printing was precise, reproducible, and highly favorable for mass production. The microparticles exhibited a biphasic release profile with an initial burst due to diffusion and a subsequent, slow second phase due to degradation of PLGA. The release rate was dependent on the geometry, mainly the surface area, with a descending rate order of honeycomb > grid, ring > circle. The PTX-loaded microparticles showed a comparable activity in inhibiting the growth of HeLa cells. Our results demonstrate that a piezoelectric inkjet printing system would provide a new approach for large-scale manufacturing of drug carriers with a desired geometry. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:305 / 310
页数:6
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