Seo Dong-Hyuk, Jeong Young-Il, Kim Don-Gon, Jang Min-Ja, Jang Mi-Kyeong, Nah Jae-Woon
Department of Polymer Science and Engineering, Sunchon National University, Republic of Korea.
Colloids Surf B Biointerfaces. 2009 Mar 1;69(2):157-63. doi: 10.1016/j.colsurfb.2008.10.020. Epub 2008 Nov 12.
We prepared methotrexate (MTX)-encapsulated polymeric nanoparticles using methoxy poly(ethylene glycol) (MPEG)-grafted chitosan (ChitoPEG) copolymer. MTX-encapsulated polymeric nanoparticles of ChitoPEG copolymer has around 50-300nm in particle size and showed spherical shape when observed by transmission electron microscope (TEM). In (1)H nuclear magnetic resonance (NMR) study, the specific peaks of MTX and chitosan as a drug carrying inner-core disappeared at D(2)O and only the specific peak of MPEG was observed, while specific peaks of MPEG, MTX, and chitosan appeared in DCl/D(2)O mixtures. These results indicated that MTX was complexed with chitosan and then core-shell type nanoparticles had formed in aqueous environment, i.e., MTX/chitosan complexes composed of inner-core and MPEG composed of outer-shell of the nanoparticles. Loading efficiency of MTX in the polymeric nanoparticles was 94% (w/w) of ChitoPEG-1, 91.1% (w/w) of ChitoPEG-2, 90.1% (w/w) of ChitoPEG-3 and 65.2% (w/w) of ChitoPEG-4, expectively. The higher the drug feeding ratio, the higher the drug content and the lower the loading efficiency. The higher the MPEG graft ratio in the copolymer, the lower the drug content and loading efficiency. Drug contents evaluated by (1)H NMR were the same as found by UV spectrophotometer.
我们使用甲氧基聚(乙二醇)(MPEG)接枝的壳聚糖(ChitoPEG)共聚物制备了甲氨蝶呤(MTX)包封的聚合物纳米颗粒。ChitoPEG共聚物的MTX包封聚合物纳米颗粒粒径约为50 - 300nm,通过透射电子显微镜(TEM)观察呈球形。在氢核磁共振(NMR)研究中,MTX和作为载药内核的壳聚糖的特定峰在重水(D₂O)中消失,仅观察到MPEG的特定峰,而在氘代盐酸/重水(DCl/D₂O)混合物中出现了MPEG、MTX和壳聚糖的特定峰。这些结果表明MTX与壳聚糖复合,然后在水性环境中形成了核壳型纳米颗粒,即纳米颗粒由内核的MTX/壳聚糖复合物和外壳的MPEG组成。MTX在聚合物纳米颗粒中的负载效率分别为ChitoPEG - 1的94%(w/w)、ChitoPEG - 2的91.1%(w/w)、ChitoPEG - 3的90.1%(w/w)和ChitoPEG - 4的65.2%(w/w)。药物投料比越高,药物含量越高,负载效率越低。共聚物中MPEG接枝率越高,药物含量和负载效率越低。通过氢核磁共振评估的药物含量与紫外分光光度计测定的结果相同。