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浙江大学化学工程与生物工程学系,杭州,310027
纸质出版日期:2012-2-20,
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缪世锋, 余金鹏, 关怡新, 姚善泾. T型微通道装置制备单分散PLGA微球[J]. 高分子学报, 2012,(2):154-159.
MIAO Shifeng, YU Jinpeng, GUAN Yixin, YAO Shanjing. PREPARATION OF MONODISPERSE POLY(LACTIC-co-GLYCOLIC ACID) MICROPARTICLES IN A T-SHAPED MICROCHANNEL JUNCTION[J]. Acta Polymerica Sinica, 2012,(2):154-159.
缪世锋, 余金鹏, 关怡新, 姚善泾. T型微通道装置制备单分散PLGA微球[J]. 高分子学报, 2012,(2):154-159. DOI: 10.3724/SP.J.1105.2012.11091.
MIAO Shifeng, YU Jinpeng, GUAN Yixin, YAO Shanjing. PREPARATION OF MONODISPERSE POLY(LACTIC-co-GLYCOLIC ACID) MICROPARTICLES IN A T-SHAPED MICROCHANNEL JUNCTION[J]. Acta Polymerica Sinica, 2012,(2):154-159. DOI: 10.3724/SP.J.1105.2012.11091.
利用微通道法乳化技术原理
研制了一个可拆卸T型玻璃微通道装置
以聚乙烯醇水溶液为连续相
聚(乳酸-co-羟基乙酸)(PLGA)的二氯甲烷溶液为分散相
制备了单分散的PLGA微球.考察了乳化剂用量、连续相和分散相流速以及PLGA浓度对形成的液滴平均粒径和变异系数(CV值)的影响.结果表明
增大乳化剂用量
提高连续相流速或降低分散相流速
制备得到的PLGA微球直径减小;分散相浓度在5~20 g/L之间变化时
其对微球直径的影响有限.PLGA微球表面光滑无孔
且内部是实心的.用本装置制备得到的PLGA微球
其粒径范围在30~200 m之间
CV值在15%以下
最低可至3%.该方法可使用挥发性有机溶剂作为分散相而且能避免微球制备时易堵塞等问题
可应用于药物缓控释领域中微米级单分散微球的制备.
Based on the principle of microchannel emulsification
a simple device with a detachable T-shaped microchannel junction was fabricated to prepare poly(lactic-co-glycolic acid) (PLGA) microparticles where aqueous solution of polyvinyl alcohol (PVA) was used as the continuous phase and PLGA dissolved in dichloromethane solution as the disperse phase.The effects of some important parameters such as the amount of emulsifier used in the continuous phase
the PLGA concentration
the disperse phase flow rate and the continuous phase flow rate on the average diameter of PLGA microparticles and the coefficient of variation (CV value) were examined in detail.The experimental results indicated that a decrease of the disperse phase flow rate
an increase of the continuous phase flow rate and increasing the amount of emulsifier used in the continuous phase led to the decrease of the average diameter of PLGA microparticles.When the PLGA concentration was between 5 g/L and 20 g/L
the average diameter of PLGA microparticles kept nearly constant.The uniform spherical PLGA microparticles with smooth surface were successfully prepared and no pores in the interior.By adjusting operating conditions
the average diameters of particles obtained ranged from 30 m to 200 m
and CV value of all the microparticles prepared under different operating conditions was below 15% while the lowest CV value was about 3%.This improved method can use organic solvents as disperse phase and avoid the easily blocking in the traditional method
which can be applied in the preparation of micrometer drug/polymer complex spheres with monodispersity and has great potential to be used in control-released drug delivery systems.
微通道单分散PLGA微球
MicrochannelMonodispersePoly(lactic-co-glycolic acid)Microparticles
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