Self-assembled polymeric nanoparticles of poly(ethylene glycol) grafted pullulan acetate as a novel drug carrier

被引:43
作者
Jung, SW
Jeong, YI
Kim, YH
Kim, SH
机构
[1] Chosun Univ, Coll Pharm, Kwangju 501759, South Korea
[2] Chonnam Natl Univ, Sch Med, Res Inst Med Sci, Kwangju 501746, South Korea
[3] Univ Massachusetts, Dept Chem, Lowell, MA 01854 USA
关键词
pullulan; poly(ethylene glycol); polysaccharide; self-assembly; stealth properties;
D O I
10.1007/BF02980132
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Self-assembling nanospheres of hydrophobized pullulan have been developed. Pullulan acetate (PA), as hydrophobized pullulan, was synthesized by acetylation. Carboxymethylated poly(ethylene-glycol) (CMPEG) was introduced into pullulan acetate (PA) through a coupling reaction using N,N'-dicyclohexyl carbodiimide (DCC). A synthesized PA-PEG-PA (abbreviated as PEP) conjugate was confirmed by Fourier transform-infrared (FT-IR) spectroscopy. Since PEP conjugates have amphiphilic characteristics in aqueous solution, polymeric nanoparticles of PEP conjugates were prepared using a simple dialysis method in water. From the analysis of fluorescence excitation spectra primarily, the critical association concentration (CAC) of this conjugate was found to be 0.0063 g/L. Observations by scanning electron microscopy (SEM) showed the spherical morphologies of the PEP nanoparticles. The particle size distribution of the PEP conjugates was determined using photon correlation spectroscopy (PCS) and the intensity-average particle size was 193.3 +/- 13.53 nm with a unimodal distribution. Clonazepam (CNZ), as a model drug, was easy to entrap into polymeric nanoparticles of the PEP conjugates. The drug release behavior was mainly diffusion controlled from the core portion.
引用
收藏
页码:562 / 569
页数:8
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