Thermoresponsive polysaccharides and their thermoreversible physical hydrogel networks

被引:151
作者
Graham, Sarah [1 ]
Marina, Paula Facal [1 ,2 ]
Blencowe, Anton [1 ,2 ]
机构
[1] Univ South Australia, Sch Pharm & Med Sci, Adelaide, SA 5000, Australia
[2] Univ South Australia, Future Ind Inst, Mawson Lakes, SA 5095, Australia
关键词
Thermoresponsive; Polysaccharides; Hydrogel; Sol-gel; Polymers; Biomaterials; CHITOSAN-BASED HYDROGEL; MESENCHYMAL STEM-CELLS; THERMOSENSITIVE HYDROGEL; GRAFT-COPOLYMERS; HYDROXYBUTYL CHITOSAN; GUAR GUM; ISOPROPYLACRYLAMIDE COPOLYMER; N-ISOPROPYLACRYLAMIDE; INJECTABLE HYDROGEL; CARBOXYMETHYL GUAR;
D O I
10.1016/j.carbpol.2018.11.053
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Thermoresponsive polymers have been used extensively for various applications including food additives, pharmaceutical formulations, therapeutic delivery, cosmetics and environmental remediation, to mention a few. Many thermoresponsive polymers have the ability to form physical hydrogel networks in response to temperature changes, which are particularly useful for emerging biomedical applications, including cell therapies, drug delivery systems, tissue engineering, wound healing and 3D bioprinting. In particular, the use of polysaccharides with thermoresponsive properties has been of interest due to their wide availability, versatile functionality, biodegradability, and in many cases, inherent biocompatibility. Naturally thermoresponsive polysaccharides include agarose, carrageenans and gellan gum, which exhibit upper critical solution temperatures, transitioning from a solution to a gel state upon cooling. Arguably, this limits their use in biomedical applications, particularly for cell encapsulation as they require raised temperatures to maintain a solution state that may be detrimental to living systems. Conversely, significant progress has been made over recent years to develop synthetically modified polysaccharides, which tend to exhibit lower critical solution temperatures, transitioning from a solution to a gel state upon warming. Of particular interest are thermoresponsive polysaccharides with a lower critical solution temperature in between room temperature and physiological temperature, as their solutions can conveniently be manipulated at room temperature before gelling upon warming to physiological temperature, which makes them ideal candidates for many biological applications. Therefore, this review provides an introduction to the different types of thermoresponsive polysaccharides that have been developed, their resulting hydrogels and properties, and the exciting applications that have emerged as a result of these properties.
引用
收藏
页码:143 / 159
页数:17
相关论文
共 133 条
  • [11] AGAROSE DOUBLE HELIX AND ITS FUNCTION IN AGAROSE-GEL STRUCTURE
    ARNOTT, S
    FULMER, A
    SCOTT, WE
    DEA, ICM
    MOORHOUSE, R
    REES, DA
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1974, 90 (02) : 269 - &
  • [12] Tunable Aggregation and Gelation of Thermoresponsive Suspensions of Polymer-Grafted Cellulose Nanocrystals
    Azzam, Firas
    Siqueira, Eder
    Fort, Sebastien
    Hassaini, Roumaissa
    Pignon, Frederic
    Travelet, Christophe
    Putaux, Jean-Luc
    Jean, Bruno
    [J]. BIOMACROMOLECULES, 2016, 17 (06) : 2112 - 2119
  • [13] A thermosensitive hydroxybutyl chitosan hydrogel as a potential co-delivery matrix for drugs on keloid inhibition
    Bao, Zixian
    Gao, Ping
    Xia, Guixue
    Wang, Zhiguo
    Kong, Ming
    Feng, Chao
    Cheng, Xiaojie
    Liu, Ya
    Chen, Xiguang
    [J]. JOURNAL OF MATERIALS CHEMISTRY B, 2016, 4 (22) : 3936 - 3944
  • [14] PEG-grafted chitosan as an injectable thermoreversible hydrogel
    Bhattarai, N
    Matsen, FA
    Zhang, M
    [J]. MACROMOLECULAR BIOSCIENCE, 2005, 5 (02) : 107 - 111
  • [15] Synthesis and aqueous solution properties of novel thermoresponsive graft copolymers based on a carboxymethylcellulose backbone
    Bokias, G
    Mylonas, Y
    Staikos, G
    Bumbu, GG
    Vasile, C
    [J]. MACROMOLECULES, 2001, 34 (14) : 4958 - 4964
  • [16] Versatile grafting of polysaccharides in homogeneous mild conditions by using atom transfer radical polymerization
    Bontempo, Debora
    Masci, Giancarlo
    De Leonardis, Piero
    Mannina, Luisa
    Capitani, Donatella
    Crescenzi, Vittorio
    [J]. BIOMACROMOLECULES, 2006, 7 (07) : 2154 - 2161
  • [17] The effect of concentration, thermal history and cell seeding density on the initial mechanical properties of agarose hydrogels
    Buckley, Conor T.
    Thorpe, Stephen D.
    O'Brien, Fergal J.
    Robinson, Anthony J.
    Kelly, Daniel J.
    [J]. JOURNAL OF THE MECHANICAL BEHAVIOR OF BIOMEDICAL MATERIALS, 2009, 2 (05) : 512 - 521
  • [18] Photoimmobilization of biomolecules within a 3-dimensional hydrogel matrix
    Cao, X
    Shoichet, MS
    [J]. JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2002, 13 (06) : 623 - 636
  • [19] Thermoreversible gelation of hydroxypropylcellulose aqueous solutions
    Carotenuto, Claudia
    Grizzuti, Nino
    [J]. RHEOLOGICA ACTA, 2006, 45 (04) : 468 - 473
  • [20] Thermoresponsive sodium alginate-g-poly(N-isopropylacrylamide) copolymers III. Solution properties
    Cheaburu, Catalina Natalia
    Ciocoiu, Oana-Nicoleta
    Staikos, Georgios
    Vasile, Cornelia
    [J]. JOURNAL OF APPLIED POLYMER SCIENCE, 2013, 127 (05) : 3340 - 3348