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Sustained release of 5-FU from Poloxamer gels interpenetrated by crosslinking chitosan network
被引:28
作者:
Chung, Tze-Wen
[1
]
Lin, Shyr-Yi
[4
]
Liu, Der-Zen
[2
]
Tyan, Yu-Chang
[3
]
Yang, Juin-Sen
[1
]
机构:
[1] Natl Yunlin Univ Sci & Technol, Dept Chem & Mat Engn, Dou Liu, Yunlin, Taiwan
[2] Taipei Med Univ, Grad Inst Biomed Mat & Engn, Taipei, Taiwan
[3] Kaohsiung Med Univ, Dept Med Imaging & Radiol Sci, Kaohsiung, Taiwan
[4] Taipei Med Univ, Dept Internal Med & Primary Care Med, Sch Med, Taipei, Taiwan
关键词:
Hydrogels;
Poloxamer;
Interpenetrating CS network;
Drug delivery;
5-FU;
DRUG-RELEASE;
5-FLUOROURACIL;
MICROSPHERES;
DIFFUSION;
COPOLYMER;
HYDROGELS;
PH;
D O I:
10.1016/j.ijpharm.2009.07.035
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
This study investigates in vitro the drug delivery characteristics of new thermo-sensitive gels, P-CS/GA gels, in which a chitosan (CS) network is crosslinked with various concentrations of glutaraldehyde (GA) that interpenetrates Poloxamer (P) gels. The results indicate that the swelling ratios of all P-CS/GA gels are markedly superior to those of non-swelling P and P-CS gels. For example, P-CS/GA (0.1 wt.%) gels have swelling ratios of 13.2 +/- 1.0, which are maintained for approximately 18 h in water at 37 degrees C. In vitro releases of 5-FU from P-CS/GA (0.1 wt.%) gels had significantly lower initial burst release (P < 0.01) and lasted much longer than those from gels without a CS network. For example, the duration of release of 5-FU was in a significantly sustained manner for up to 52 h, which was about 10 times or longer than the period of delivery using P or P-CS gels. The release of drugs from gels with an interpenetrating CS network could be modeled by Fickian diffusion; the characteristic constant 'k' of drug-gel systems decreased as increasing CA concentrations in the P-CS/GA gels, and increasing the viscosities of the P, P-CS and P-CS/GA solutions. (C) 2009 Elsevier B.V. All rights reserved.
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页码:39 / 44
页数:6
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