Effect of microfluidization parameters on the physical properties of PEG-PLGA nanoparticles prepared using high pressure microfluidization

被引:11
|
作者
Sani, Shabnam N. [2 ,3 ]
Das, Nandita G. [1 ]
Das, Sudip K. [1 ]
机构
[1] Butler Univ, Dept Pharmaceut Sci, Indianapolis, IN 46208 USA
[2] Idaho State Univ, Dept Pharmaceut Sci, Pocatello, ID 83209 USA
[3] Coll Pharm & Hlth Sci, Dept Pharmaceut Sci, Boston, MA USA
关键词
Nanoparticle; microfluidization; poly(ethylene glycol) grafted poly(lactide-co-glycolide) (PEG-PLGA); ethyl acetate; SOLVENT EVAPORATION METHOD; POLY(LACTIDE-CO-GLYCOLIDE) NANOSPHERES; ETHYL-ACETATE; MICROSPHERES; RELEASE; HOMOGENIZATION; MICROPARTICLES; PACLITAXEL;
D O I
10.1080/02652040802500655
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The objective of this work was to develop uniformly distributed poly(ethylene glycol) grafted poly(lactide-co-glycolide) (PEG-PLGA) nanoparticles of mean size range similar to 100-200nm using ethyl acetate as the solvent. In the multiple emulsion solvent evaporation method a high pressure microfluidization process was adopted to produce the W/O/W multiple emulsion. Non-toxic ethyl acetate was used to solubilize PEG-PLGA. The mean size of nanoparticles obtained was less than 180 nm. The particle size and size distribution were dependent on the microfluidization conditions applied. Mean particle size steadily increased from 121nm at three passes to 172nm at 20 passes of the microfluidizer, indicating that over-processing may be detrimental to PEG-PLGA nanoparticles prepared using this technique. There was no significant alteration of the PEG-PLGA matrix, as evidenced from the differential scanning calorimetric studies.
引用
收藏
页码:556 / 561
页数:6
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