Formation of the first injectable poly(vinyl alcohol) hydrogel by mixing of functional PVA precursors

被引:54
作者
Ossipov, Dmitri A. [1 ]
Brannvall, Karin
Forsberg-Nilsson, Karin
Hilborn, Jons
机构
[1] Uppsala Univ, Dept Chem Mat, S-75121 Uppsala, Sweden
[2] Uppsala Univ, Dept Med Biochem & Microbiol, S-75123 Uppsala, Sweden
关键词
poly(vinyl alcohol); injectable hydrogels; hydrazone crosslinking; cell encapsulation;
D O I
10.1002/app.26455
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this study we describe the development of an injectable, in situ chemical hydrogel forming system. The gelation occurs under neutral pH and at room temperature immediately upon mixing of the two aqueous poly (vinyl alcohol) components specifically derivatized through carbamate linkages with aldehyde (PVA-AL) and hydrazide (PVA-HY) functional groups, respectively. Aldehyde and hydrazide pendant groups were incorporated with a low degree of substitution (DS) into the PVA backbone to keep PVA structural homogeneity minimally altered. As a result, the hydrazone crosslinks are formed rapidly between aldehyde and hydrazide pendant groups when the correspondingly modified PVA components are brought in contact as water solutions. To assess in situ hydrazone crosslinks formation for in vitro cytocompatibility, murine neuroblastoma N2a cells were suspended in cell culture medium with the dissolved PVA-HY prior to addition to the PVA-AL aqueous solution. Thus, the cells were chemically encapsulated in a polymer network that was formed by mixing of the corresponding aqueous solutions of PVA functional precursors. Biochemical analysis revealed that cells survived chemical crosslinking and remained viable in the hydrogel for 4 days of culture. (c) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:60 / 70
页数:11
相关论文
共 31 条
[1]   In situ forming degradable networks and their application in tissue engineering and drug delivery [J].
Anseth, KS ;
Metters, AT ;
Bryant, SJ ;
Martens, PJ ;
Elisseeff, JH ;
Bowman, CN .
JOURNAL OF CONTROLLED RELEASE, 2002, 78 (1-3) :199-209
[2]  
Bulpitt P, 1999, J BIOMED MATER RES, V47, P152
[3]   Photoencapsulation of osteoblasts in injectable RGD-modified PEG hydrogels for bone tissue engineering [J].
Burdick, JA ;
Anseth, KS .
BIOMATERIALS, 2002, 23 (22) :4315-4323
[4]  
Cousins GRL, 2001, ANGEW CHEM INT EDIT, V40, P423, DOI 10.1002/1521-3773(20010119)40:2<423::AID-ANIE423>3.0.CO
[5]  
2-6
[6]   Protein delivery from materials formed by self-selective conjugate addition reactions [J].
Elbert, DL ;
Pratt, AB ;
Lutolf, MP ;
Halstenberg, S ;
Hubbell, JA .
JOURNAL OF CONTROLLED RELEASE, 2001, 76 (1-2) :11-25
[7]   Injectable gels for tissue engineering [J].
Gutowska, A ;
Jeong, B ;
Jasionowski, M .
ANATOMICAL RECORD, 2001, 263 (04) :342-349
[8]   Synthesis and characterization of in situ cross-linkable hyaluronic acid-based hydrogels with potential application for vocal fold regeneration [J].
Jia, XQ ;
Burdick, JA ;
Kobler, J ;
Clifton, RJ ;
Rosowski, JJ ;
Zeitels, SM ;
Langer, R .
MACROMOLECULES, 2004, 37 (09) :3239-3248
[9]   Prolongation of sciatic nerve blockade by in situ cross-linked hyaluronic acid [J].
Jia, XQ ;
Colombo, G ;
Padera, R ;
Langer, R ;
Kohane, DS .
BIOMATERIALS, 2004, 25 (19) :4797-4804
[10]   Tissue engineering [J].
Langer, R .
MOLECULAR THERAPY, 2000, 1 (01) :12-15