Synthesis of uniform poly(D,L-lactide) and poly(D,L-lactide-co-glycolide) microspheres using a microfluidic chip for comparison

被引:17
|
作者
Yang, Chih-Hui [1 ]
Huang, Keng-Shiang [2 ]
Grumezescu, Alexandru Mihai [3 ]
Wang, Chih-Yu [4 ]
Tzeng, Shian-Chiuan [1 ]
Chen, Szu-Yu [1 ]
Lin, Yu-Hsin [5 ]
Lin, Yung-Sheng [6 ,7 ]
机构
[1] I Shou Univ, Dept Biol Sci & Technol, Kaohsiung, Taiwan
[2] I Shou Univ, Sch Chinese Med Postbaccalaureate, Kaohsiung, Taiwan
[3] Univ Politehn Bucuresti, Fac Appl Chem & Mat Sci, Dept Sci & Engn Oxid Mat & Nanomat, Bucharest, Romania
[4] I Shou Univ, Dept Biomed Engn, Kaohsiung, Taiwan
[5] Natl Appl Res Labs, Instrument Technol Res Ctr, Hsinchu, Taiwan
[6] Hungkuang Univ, Dept Appl Cosmetol, Taichung, Taiwan
[7] Hungkuang Univ, Master Program Cosmet Sci, Taichung, Taiwan
关键词
Microfluidic chip; Microsphere; Phenol formaldehyde resin; Poly(l-lactide) (PLA); Poly(d; l-lactide-co-glycolide) (PLGA); POLYSTYRENE PARTICLES; SURFACE MODIFICATION; MICROPARTICLES; MONODISPERSE; DELIVERY; FABRICATION; POLYMERS; RELEASE; DEVICE; FLOWS;
D O I
10.1002/elps.201300185
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Applications of poly(l-lactide) (PLA) and poly(d,l-lactide-co-glycolide) (PLGA) microspheres are widely used in the biomedical and pharmaceutical fields. The effects of PLA/PLGA on microsphere properties when using conventional particulate preparation methods are not easily defined due to the uncontrollable particle size and size distribution. This study was aimed to synthesize uniform PLA and PLGA microspheres using a phenol formaldehyde resin-based microfluidic chip, which has the advantage of being solvent-resistant, flexible, and is readily disassembled for cleaning. The proposed chip can rapidly fabricate reproducible PLA and PLGA microspheres. Uniform emulsion droplets can be achieved by hydrodynamic flow focusing. After solvent evaporation, the free-flowing PLA and PLGA microspheres have a high level of morphological uniformity and size, allowing for a clear comparison of material effects. The results indicate that the sizes of the PLA and PLGA microspheres for the various flow rates of dispersed/continuous phases are very similar. The PLA/PLGA materials do not have a significant effect on particle size, but the particle surface indicates a different morphology. The result of the cytotoxicity evaluation shows no difference between PLA and PLGA and ensures the biocompatibility of both prepared PLA and PLGA microspheres for biomedical and pharmaceutical applications in the future.
引用
收藏
页码:316 / 322
页数:7
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