Sustained release of hydrophobic drugs by the microfluidic assembly of multistage microgel/poly (lactic-co-glycolic acid) nanoparticle composites

被引:39
|
作者
Hsu, Myat Noe [1 ,2 ]
Luo, Rongcong [1 ]
Kwek, Kerwin Zeming [1 ]
Por, Yong Chen [3 ]
Zhang, Yong [1 ,2 ,4 ]
Chen, Chia-Hung [1 ,5 ]
机构
[1] Natl Univ Singapore, Dept Biomed Engn, Singapore 117575, Singapore
[2] Natl Univ Singapore, NUS Grad Sch Integrated Sci & Engn, Singapore 117456, Singapore
[3] KK Womens & Childrens Hosp, Dept Plast Reconstruct & Aesthet Surg, Singapore 229899, Singapore
[4] Natl Univ Singapore, Nanosci & Nanotechnol Initiat, Singapore 117581, Singapore
[5] Singapore Inst Neurotechnol, Singapore 117456, Singapore
来源
BIOMICROFLUIDICS | 2015年 / 9卷 / 05期
关键词
LOADED PLGA NANOPARTICLES; BEHAVIOR IN-VITRO; POROUS SILICON; DELIVERY; MICROCAPSULES; ENCAPSULATION; MONODISPERSE; MECHANISMS; PARTICLES; ESTRADIOL;
D O I
10.1063/1.4916230
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The poor solubility of many newly discovered drugs has resulted in numerous challenges for the time-controlled release of therapeutics. In this study, an advanced drug delivery platform to encapsulate and deliver hydrophobic drugs, consisting of poly (lactic-co-glycolic acid) (PLGA) nanoparticles incorporated within poly (ethylene glycol) (PEG) microgels, was developed. PLGA nanoparticles were used as the hydrophobic drug carrier, while the PEG matrix functioned to slow down the drug release. Encapsulation of the hydrophobic agents was characterized by fluorescence detection of the hydrophobic dye Nile Red within the microgels. In addition, the microcomposites prepared via the droplet-based microfluidic technology showed size tunability and a monodisperse size distribution, along with improved release kinetics of the loaded cargo compared with bare PLGA nanoparticles. This composite system has potential as a universal delivery platform for a variety of hydrophobic molecules. (C) 2015 AIP Publishing LLC.
引用
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页数:7
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