Solvent-Resistant Perfluoropolyether Microfluidic Devices with Microfibrous Channels for the Production of Poly(ε-caprolactone) Microspheres Containing Dexamethasone

被引:0
|
作者
Oh, Do-Hyun [1 ]
Choi, Inseong [1 ]
Ryu, Young-Hyun [1 ]
Ahn, Guk-Young [1 ]
Ryu, Tae-Kyung [2 ]
Choi, Sung-Wook [1 ]
机构
[1] Catholic Univ Korea, Dept Biotechnol, Biomed & Chem Engn, Bucheon Si 14662, Gyeonggi Do, South Korea
[2] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Dept Neurol, Baltimore, MD 21205 USA
基金
新加坡国家研究基金会;
关键词
microfiber; microfluidics; perfluoropolyether; solvent-resistance; drug carrier; SIMPLE FLUIDIC DEVICE; DRUG-RELEASE; PDMS; ZIDOVUDINE; DROPLETS; DELIVERY; PLA;
D O I
10.1021/acsapm.2c02093
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A microfluidic device with microfibrous channels was prepared using perfluoropolyether (PFPE) and poly(ethylene glycol) diacrylate (PEG-DA). PFPE was chosen as a major material for the device due to its excellent solvent resistance. PEG-DA was used in the device to improve its hydrophilicity. Microfibrous channels with different diameters (approximately 12 and 17 mu m) were developed using an electrospun disc as a template. Compared to a polydimethylsiloxane microfluidic device, the PFPE micro fluidic device exhibited a significantly lower swelling ratio. The continuous production of poly(epsilon-caprolactone) (PCL) micro spheres with dexamethasone was achieved using the oil-in-water (O/W) emulsification and solvent evaporation methods. The microsphere size was decreased with the use of smaller microfibrous channels at a higher flow rate of the continuous phase. PCL microspheres prepared by the PFPE microfluidic device showed higher encapsulation efficiency than conventional homogenization. The addition of poly(ethylene glycol) (PEG, 5 wt %) in the discontinuous phase enhanced the encapsulation efficiency to 39.4%. PCL microspheres with PEG showed more sustained release profiles than PCL microspheres without PEG. These results indicate that the PFPE microfluidic device with microfibrous channels can be used as a platform for the continuous production of drug carriers.
引用
收藏
页码:2062 / 2069
页数:8
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