Self-assembling peptide-polysaccharide hybrid hydrogel as a potential carrier for drug delivery

被引:173
作者
Huang, Renliang [1 ]
Qi, Wei [1 ]
Feng, Libin [1 ]
Su, Rongxin [1 ]
He, Zhimin [1 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, State Key Lab Chem Engn, Tianjin 300072, Peoples R China
关键词
RELEASE;
D O I
10.1039/c1sm05375b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Here we report a novel peptide-polysaccharide hybrid hydrogel as a potential carrier for sustained delivery of hydrophobic drugs. The hybrid hydrogel composed of Fmoc-diphenylalanine (Fmoc-FF) peptide and konjac glucomannan (KGM) was prepared through molecular self-assembly of Fmoc-FF in the KGM solution. The physicchemical properties of the Fmoc-FF-KGM hybrid hydrogel were further evaluated. This hybrid hydrogel exhibited a highly hydrated, rigid and nanofibrous gel network in which self-assembled peptide nanofibers were interwoven with the KGM chains. The results of a stability test and rheology study showed that the hybrid hydrogel has much higher stability and mechanical strength compared to Fmoc-FF hydrogel alone. Both CD and FTIR analysis indicated an anti-parallel beta-sheet arrangement of Fmoc-FF peptide in self-assembled nanofibers, regardless the presence of KGM. Moreover, docetaxel was chosen as a model of hydrophobic drugs and incorporated into hydrogels to study the in vitro release behavior. The sustained and controlled drug release from this hybrid hydrogel was achieved by varying the KGM concentration, molecular weight, aging time or beta-mannanase concentration. Our results not only provide a new strategy for fabricating Fmoc-FF-KGM hybrid hydrogel as a sustained-release drug carrier but also open an avenue for the design of new self-assembling peptide-polysaccharide hybrid hydrogels.
引用
收藏
页码:6222 / 6230
页数:9
相关论文
共 37 条
[1]  
Alberts B., 2002, The shape and structure of proteins, Vfourth, DOI 10.1093/aob/mcg023
[2]  
Annabi N, 2010, TISSUE ENG PART B-RE, V16, P371, DOI [10.1089/ten.teb.2009.0639, 10.1089/ten.TEB.2009.0639]
[3]  
[Anonymous], 1997, Circular Dichroism and Linear Dichroism
[4]   Pronounced hydrogel formation by the self-assembled aggregates of N-alkyl disaccharide amphiphiles [J].
Bhattacharya, S ;
Acharya, SNG .
CHEMISTRY OF MATERIALS, 1999, 11 (12) :3504-3511
[5]   Controlled drug release from multilayered phospholipid polymer hydrogel on titanium alloy surface [J].
Choi, Jiyeon ;
Konno, Tomohiro ;
Takai, Madoka ;
Ishihara, Kazuhiko .
BIOMATERIALS, 2009, 30 (28) :5201-5208
[6]   Enzymatic modification of self-assembled peptide structures with tissue transglutaminase [J].
Collier, JH ;
Messersmith, PB .
BIOCONJUGATE CHEMISTRY, 2003, 14 (04) :748-755
[7]   Self-Assembly of Peptide Amphiphiles: From Molecules to Nanostructures to Biomaterials [J].
Cui, Honggang ;
Webber, Matthew J. ;
Stupp, Samuel I. .
BIOPOLYMERS, 2010, 94 (01) :1-18
[8]   Hydrogels for tissue engineering: scaffold design variables and applications [J].
Drury, JL ;
Mooney, DJ .
BIOMATERIALS, 2003, 24 (24) :4337-4351
[9]   Slow and sustained release of active cytokines from self-assembling peptide scaffolds [J].
Gelain, Fabrizio ;
Unsworth, Larry D. ;
Zhang, Shuguang .
JOURNAL OF CONTROLLED RELEASE, 2010, 145 (03) :231-239
[10]   Electroconductive hydrogels: Synthesis, characterization and biomedical applications [J].
Guiseppi-Elie, Anthony .
BIOMATERIALS, 2010, 31 (10) :2701-2716