Surface-modified gemcitabine with mucoadhesive polymer for oral delivery

被引:8
|
作者
Lim, Ji-Ho [1 ,2 ]
You, Sung-Kyun [1 ,2 ,3 ]
Baek, Jong-Suep [1 ,2 ]
Hwang, Chan-Ju [1 ,2 ]
Na, Young-Guk [1 ,2 ]
Shin, Sang-Chul [4 ]
Cho, Cheong-Weon [1 ,2 ]
机构
[1] Chungnam Natl Univ, Coll Pharm, Taejon 305764, South Korea
[2] Chungnam Natl Univ, Inst Drug Res & Dev, Taejon 305764, South Korea
[3] Jeil Pharmaceut Co Ltd, R&D Inst, Yongin 449861, Kyunggi Do, South Korea
[4] Chonnam Natl Univ, Coll Pharm, Kwangju 500757, South Korea
基金
新加坡国家研究基金会;
关键词
gemcitabine; microparticles; mucoadhesive polymer; caco-2; cells; oral absorption; ANTITUMOR-ACTIVITY; PANCREATIC-CANCER; SELF-POTENTIATION; IN-VITRO; MICROSPHERES; PHARMACOKINETICS; NANOPARTICLES; ENCAPSULATION; PHARMACOLOGY; FORMULATION;
D O I
10.3109/02652048.2012.665086
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Gemcitabine microparticles were prepared using chitosan, polyethylene oxide or carbopol as the mucoadhesive polymer and eudragit L100-55 as the enteric polymer by a double emulsion method. The particle size and zeta potential changed from 1338.3 +/- 254.1 nm to 2459.4 +/- 103.6 nm and -5.16 +/- 1.62 mV to 2.84 +/- 0.65 mV, respectively, with increasing chitosan to gemcitabine weight ratio from 0.25 to 1. The gemcitabine-loaded microparticles without mucoadhesive polymer (F50) showed the particle size and zeta potential of 671.3 +/- 58.3 nm and - 16.7 +/- 1.82 mV, respectively. The cellular uptake of gemcitabine into Caco-2 cells from gemcitabine-loaded microparticles with chitosan increased with increasing incubation time in Caco-2 cells compared to that of gemcitabine-loaded microparticles with polyethylene oxide or carbopol, suggesting that chitosan might be the optimal mucoadhesive polymer. Gemcitabine microparticles will be tested to identify whether the oral absorption could be increased in the future.
引用
收藏
页码:487 / 496
页数:10
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