Water, solute, and segmental dynamics in polysaccharide hydrogels

被引:28
作者
Cavalieri, Francesca
Chiessi, Ester
Finelli, Ivana
Natali, Francesca
Paradossi, Gaio
Telling, Mark F.
机构
[1] Univ Roma Tor Vergata, Dipartimento Chim, I-00173 Rome, Italy
[2] INFM, OGG, ILL, F-38042 Grenoble, France
[3] Rutherford Appleton Lab, Chilton OX11 0QZ, Didcot, England
关键词
diffusion; FRAP; hydrogels; polysaccharides; QENS;
D O I
10.1002/mabi.200600077
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polysaccharide hydrogels have found several applications in the food industry, in biomedicine, and cosmetics. The study of polysaccharide hydrogels offers a challenging scenario of intrinsic heterogeneities in the crosslinking density and large time and space ranges that characterize a number of dynamic processes entailing segmental motions, water diffusion, and small-molecule diffusion. The understanding of such complex features is essential because of the extensive use of polysaccharidic moieties in the food industry, biomedical devices, and cosmetics. The study of phenomena occurring at the nanoscale to the mesoscale requires the combination of investigative tools to probe different time and distance scales and the structural characterization of the networks by established methodologies such as swelling and elastic modulus measurements. Elastic and quasielastic neutron scattering, and fluorescence recovery after photobleaching are emerging methodologies in this field. In this feature article we focus, somewhat arbitrarily, on these new approaches because other techniques, such as low-resolution proton NMR relaxometry and rheology, have been already described thoroughly in the literature. Case examples of polysaccharide hydrogels studied by neutron scattering and fluorescence recovery are presented here as contributions to the comprehension of the dynamic behavior of physical and chemical hydrogels based on polysaccharides.
引用
收藏
页码:579 / 589
页数:11
相关论文
共 31 条
[1]  
BEE M, 1988, QUASIELASTIC NEUTRON, P67
[2]   Three-dimensional fluorescence recovery after photobleaching with the confocal scanning laser microscope [J].
Braeckmans, K ;
Peeters, L ;
Sanders, NN ;
De Smedt, SC ;
Demeester, J .
BIOPHYSICAL JOURNAL, 2003, 85 (04) :2240-2252
[3]   NEUTRON SCATTERING FROM A LIQUID ON A JUMP DIFFUSION MODEL [J].
CHUDLEY, CT ;
ELLIOTT, RJ .
PROCEEDINGS OF THE PHYSICAL SOCIETY OF LONDON, 1961, 77 (494) :353-&
[4]   A crosslinked system from Scleroglucan derivative: preparation and characterization [J].
Coviello, T ;
Grassi, M ;
Rambone, G ;
Alhaique, F .
BIOMATERIALS, 2001, 22 (13) :1899-1909
[5]  
De Gennes PG., 1979, SCALING CONCEPTS POL
[6]   Diffusion of macromolecules in dextran methacrylate solutions and gels as studied by confocal scanning laser microscopy [J].
De Smedt, SC ;
Meyvis, TKL ;
Demeester, J ;
VanOostveldt, P ;
Blonk, JCG ;
Hennink, WE .
MACROMOLECULES, 1997, 30 (17) :4863-4870
[7]   CHARACTERIZATION OF THE NETWORK STRUCTURE OF DEXTRAN GLYCIDYL METHACRYLATE HYDROGELS BY STUDYING THE RHEOLOGICAL AND SWELLING BEHAVIOR [J].
DE SMEDT, SC ;
LAUWERS, A ;
DEMEESTER, J ;
VANSTEENBERGEN, MJ ;
HENNINK, WE ;
ROEFS, SPFM .
MACROMOLECULES, 1995, 28 (14) :5082-5088
[8]   Dynamics of hydrated starch saccharides [J].
Di Bari, M ;
Deriu, A ;
Albanese, G ;
Cavatorta, F .
CHEMICAL PHYSICS, 2003, 292 (2-3) :333-339
[9]   Statistical mechanics of cross-linked polymer networks II Swelling [J].
Flory, PJ ;
Rehner, J .
JOURNAL OF CHEMICAL PHYSICS, 1943, 11 (11) :521-526
[10]   THEORY OF ELASTICITY OF POLYMER NETWORKS .3. [J].
FLORY, PJ ;
ERMAN, B .
MACROMOLECULES, 1982, 15 (03) :800-806