Solid-state photocrosslinking of hyaluronan microfibres

被引:21
作者
Bobula, Tomas [1 ]
Bet'ak, Jiri [1 ]
Buffa, Radovan [1 ]
Moravcova, Martina [1 ]
Klein, Pavel [1 ]
Zidek, Ondrej [1 ]
Chadimova, Veronika [1 ]
Pospisil, Robert [1 ]
Velebny, Vladimir [1 ]
机构
[1] Contipro Biotech Ltd, Dolni Dobrouc 56102, Czech Republic
关键词
Cinnamic acid; Fibres; Hyaluronan; Photocrosslinking; Wet-spinning; ACID; DERIVATIVES;
D O I
10.1016/j.carbpol.2015.02.027
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Hyaluronan (HA) was chemically modified to a photocurable derivative by the acylation with a mixed anhydride of trans-cinnamic acid and characterized by UV, IR and 2D NMR spectroscopy. Photocurable HA was processed to a microfibrous structure by wet-spinning technology. Water solubility of otherwise water-soluble HA microfibres was reduced significantly by the solid-state photocrosslinking. We also investigated that the nature of polymer structure had a great impact to a final crosslink ratio. The analysis of the mechanical properties showed higher ultimate tensile strength and increased rigidity of the photocrosslinked fibres in comparison to the untreated ones. Moreover all tested materials are regarded as biocompatible according to the tests of cell viability, phototoxicity and enzymatic degradability, which make them suitable candidates for numerous biomedical applications. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:153 / 160
页数:8
相关论文
共 24 条
[1]   The photodimerisation of the α- and β-forms of trans-cinnamic acid:: a study of single crystals by vibrational microspectroscopy [J].
Atkinson, SDM ;
Almond, MJ ;
Hollins, P ;
Jenkins, SL .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2003, 59 (03) :629-635
[2]  
Bellini D., 2003, Hyaluronic acid esters, threads and biomaterials containing them, and their use in surgery, Patent No. [US/6632802, 6632802]
[3]  
Betak J., 2014, Endless fibres based on hyaluronate selectively oxidized in position 6 N-acetyl-D- glucosamine portion, their preparation, use, threads, yarns, fabrics and process for preparing thereof, Patent No. [W02014082610, 2014085610]
[4]   Hyaluronic acid: a unique topical vehicle for the localized delivery of drugs to the skin [J].
Brown, MB ;
Jones, SA .
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2005, 19 (03) :308-318
[5]  
Bulpitt P, 1999, J BIOMED MATER RES, V47, P152
[6]   Hyaluronic Acid Hydrogels for Biomedical Applications [J].
Burdick, Jason A. ;
Prestwich, Glenn D. .
ADVANCED MATERIALS, 2011, 23 (12) :H41-H56
[7]   Prevention of tissue injury and postsurgical adhesions by precoating tissues with hyaluronic acid solutions [J].
Burns, JM ;
Skinner, K ;
Colt, J ;
Sheidlin, A ;
Bronson, R ;
Yaacobi, Y ;
Goldberg, EP .
JOURNAL OF SURGICAL RESEARCH, 1995, 59 (06) :644-652
[8]   Hyaluronic acid based scaffolds for tissue engineering-A review [J].
Collins, Maurice N. ;
Birkinshaw, Colin .
CARBOHYDRATE POLYMERS, 2013, 92 (02) :1262-1279
[9]  
Griffiths B., 2007, Wound dressing material, Patent No. [W0/2007/003905, 2007003905]
[10]   Novel crosslinking methods to design hydrogels [J].
Hennink, W. E. ;
van Nostrum, C. F. .
ADVANCED DRUG DELIVERY REVIEWS, 2012, 64 :223-236