Synthesis and characterization of biodegradable TPP/genipin co-crosslinked chitosan gel beads

被引:239
作者
Mi, FL
Sung, HW
Shyu, SS
Su, CC
Peng, CK
机构
[1] Chinese Naval Acad, Div Appl Chem, Dept Appl Chem, Kaohsiung 813, Taiwan
[2] Natl Tsing Hua Univ, Dept Chem Engn, Hsinchu 300, Taiwan
[3] Van Nung Inst Technol, Dept Chem Engn, Chungli 320, Taiwan
[4] Natl Cent Univ, Dept Chem & Mat Engn, Katsuta, Ibaraki 312, Japan
关键词
chitosan; tripolyphosphate; genipin;
D O I
10.1016/S0032-3861(03)00620-7
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Novel chitosan gel beads were synthesized by a coupled ionic and chemical co-crosslinking mechanism. Tripolyphosphate (TPP) and a naturally occurring crosslinking reagent, genipin, which has been used in herbal medicine, were employed, respectively, as an ionic and a chemical crosslinkers to prepare the chitosan-based networks of gel beads. The competitive crosslinking of chitosan with ionic crosslinker (TPP) and chemical crosslinker (genipin) was characterized by FTIR, UV and EDAX spectroscopy (X-ray energy dispersion) spectroscopy. The variation of characteristic peak of genipin observed from UV spectroscopy and the characteristic peak of tripolyphosphate in crosslinked chitosan-based networks observed from FTIR spectroscopy suggests that the co-crosslinking mechanism is dependent on the pH of TPP/genipin co-crosslinker. The energy profiles of carbon and phosphorus estimated from confirms that chemical crosslinking dominates the co-crosslinking reaction at higher pH condition (pH 7.0 and 9.0) and ionic crosslinking dominates the co-crosslinking reaction at lower pH condition (pH 1.0, 3.0 and 5.0). The pH-dependent ionic/chemical co-crosslinking mechanism shows an obvious effect on the swelling property and enzymatic degradation behavior of prepared chitosan networks. These results reveal that the ionic/chemical co-crosslinked chitosan networks may be suitable for biomedical applications. (C) 2003 Published by Elsevier Ltd.
引用
收藏
页码:6521 / 6530
页数:10
相关论文
共 41 条
[1]  
AIEA S, 1992, INT J BIOL MACROMOL, V14, P225
[2]   5-fluorouracil-loaded chitosan microspheres: Preparation and release characteristics [J].
Akbuga, J ;
Bergisadi, N .
JOURNAL OF MICROENCAPSULATION, 1996, 13 (02) :161-168
[3]  
Andrady AL, 1997, J POLYM SCI POL PHYS, V35, P517, DOI 10.1002/(SICI)1099-0488(199702)35:3<517::AID-POLB10>3.0.CO
[4]  
2-K
[5]  
Angelis A.A.D., 1998, MACROMOLECULES, V31, P1595
[6]  
Cha SY, 2001, J POLYM SCI POL CHEM, V39, P880, DOI 10.1002/1099-0518(20010315)39:6<880::AID-POLA1062>3.0.CO
[7]  
2-K
[8]   Vascular cell responses to polysaccharide materials: in vitro and in vivo evaluations [J].
Chupa, JM ;
Foster, AM ;
Sumner, SR ;
Madihally, SV ;
Matthew, HWT .
BIOMATERIALS, 2000, 21 (22) :2315-2322
[9]   THE CONTINUOUS HYDROLYSIS OF GENIPOSIDE TO GENIPIN USING IMMOBILIZED BETA-GLUCOSIDASE ON CALCIUM ALGINATE GEL [J].
FUJIKAWA, S ;
YOKOTA, T ;
KOGA, K ;
KUMADA, J .
BIOTECHNOLOGY LETTERS, 1987, 9 (10) :697-702
[10]   CROSS-LINKED CHITOSAN MICROSPHERES AS CARRIERS FOR PROLONGED DELIVERY OF MACROMOLECULAR [J].
JAMEELA, SR ;
MISRA, A ;
JAYAKRISHNAN, A .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 1994, 6 (07) :621-632