Activated polyurethane modified with latent thiol groups

被引:21
作者
Alferiev, IS [1 ]
Fishbein, I [1 ]
机构
[1] Childrens Hosp Philadelphia, Abramson Res Ctr, Div Cardiol, Philadelphia, PA 19104 USA
关键词
polyurethane; thiols; immobilization; biomaterials;
D O I
10.1016/S0142-9612(02)00224-7
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A novel type of modified polyurethane with pendant acetylthio groups (as a latent form of thiol groups) has been proposed for the use in surface modifications with various biomolecules. The polymer was prepared via a modified variant of low-temperature bromoalkylation of urethane hard segments followed by the reaction of pendant bromoalkyl groups with thiolacetic acid in mild conditions. The extent of modification with acetylthio groups can be made as high as 0.45 mmol/g. After deprotection of acetylthio groups and reaction of the resulting thiol groups with an excess of Ellman's reagent, 0.1 nmol/cm(2) of thiol-reactive 3-carboxy-4-nitrophenyidithio groups were detected on the surface of films cast from the modified polymer. A sensitive fluorescent probe-dansyl-L-cysteine was used for the quantification of thiol-reactive groups bound to the surface. The acetylthio-modified polyurethane is sufficiently stable to withstand conditions typical for the high-temperature processing (molding, extrusion) of polyurethanes. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:4753 / 4758
页数:6
相关论文
共 8 条
[1]  
Alferiev IS, 2001, J POLYM SCI POL CHEM, V39, P105, DOI 10.1002/1099-0518(20010101)39:1<105::AID-POLA120>3.3.CO
[2]  
2-#
[3]  
Castro J, 1997, SYNTHESIS-STUTTGART, P518
[4]   POLYETHYLENE GLYCOLS AS SOLVENTS FOR ANIONIC ACTIVATION - SYNTHESIS OF THIOACETATES BY MEANS OF POTASSIUM THIOACETATE IN POLYETHYLENE GLYCOL-400 [J].
FERRABOSCHI, P ;
FIECCHI, A ;
GRISENTI, P ;
SANTANIELLO, E ;
TRAVE, S .
SYNTHETIC COMMUNICATIONS, 1987, 17 (13) :1569-1575
[5]   NUCLEOPHILIC-SUBSTITUTION OF S(N)1-ACTIVE HALIDES USING ZINC SALTS - PREPARATION OF THIOLACETATES [J].
GURUDUTT, KN ;
RAO, S ;
SRINIVAS, P ;
SRINIVAS, S .
TETRAHEDRON, 1995, 51 (10) :3045-3050
[6]  
Huang LLH, 1998, J BIOMED MATER RES, V39, P630, DOI 10.1002/(SICI)1097-4636(19980315)39:4<630::AID-JBM18>3.3.CO
[7]  
2-U
[8]   Covalent linkage of recombinant hirudin to a novel ionic poly(carbonate) urethane polymer with protein binding sites: Determination of surface antithrombin activity [J].
Phaneuf, MD ;
Szycher, M ;
Berceli, SA ;
Dempsey, DJ ;
Quist, WC ;
LoGerfo, FW .
ARTIFICIAL ORGANS, 1998, 22 (08) :657-665