Thiol-ene and photo-cleavage chemistry for controlled presentation of biomolecules in hydrogels

被引:94
|
作者
Grim, Joseph C. [1 ]
Marozas, Ian A. [2 ,3 ]
Anseth, Kristi S. [1 ,2 ,3 ]
机构
[1] Univ Colorado, Howard Hughes Med Inst, Boulder, CO 80309 USA
[2] Univ Colorado, Dept Chem & Biol Engn, Boulder, CO 80309 USA
[3] Univ Colorado, BioFrontiers Inst, Boulder, CO 80309 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Thiol-ene; Hydrogel; Patterning; Regenerative medicine; Photo-cage; Immobilization; GROWTH-FACTOR-BETA; STEM-CELL FATE; EXTRACELLULAR-MATRIX; CLICK HYDROGELS; ENDOTHELIAL-CELLS; PROTECTING GROUPS; PEG HYDROGELS; IN-VITRO; PEPTIDE; DIFFERENTIATION;
D O I
10.1016/j.jconrel.2015.08.040
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrogels have emerged as promising scaffolds in regenerative medicine for the delivery of biomolecules to promote healing. However, increasing evidence suggests that the context that biomolecules are presented to cells (e.g., as soluble verses tethered signals) can influence their bioactivity. A common approach to deliver biomolecules in hydrogels involves physically entrapping them within the network, such that they diffuse out over time to the surrounding tissues. While simple and versatile, the release profiles in such system are highly dependent on the molecular weight of the entrapped molecule relative to the network structure, and it can be difficult to control the release of two different signals at independent rates. In some cases, supraphysiologically high loadings are used to achieve therapeutic local concentrations, but uncontrolled release can then cause deleterious off-target side effects. In vivo, many growth factors and cytokines are stored in the extracellular matrix (ECM) and released on demand as needed during development, growth, and wound healing. Thus, emerging strategies in biomaterial chemistry have focused on ways to tether or sequester biological signals and engineer these bioactive scaffolds to signal to delivered cells or endogenous cells. While many strategies exist to achieve tethering of peptides, protein, and small molecules, this review focuses on photochemical methods, and their usefulness as a mild reaction that proceeds with fast kinetics in aqueous solutions and at physiological conditions. Photo-click and photo-caging methods are particularly useful because one can direct light to specific regions of the hydrogel to achieve spatial patterning. Recent methods have even demonstrated reversible introduction of biomolecules to mimic the dynamic changes of native ECM, enabling researchers to explore how the spatial and dynamic context of biomolecular signals influences important cell functions. This review will highlight how two photochemical methods have led to important advances in the tissue regeneration community, namely the thiol-ene photo-click reaction for bioconjugation and photocleavage reactions that allow for the removal of protecting groups. Specific examples will be highlighted where these methodologies have been used to engineer hydrogels that control and direct cell function with the aim of inspiring their use in regenerative medicine. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:95 / 106
页数:12
相关论文
共 50 条
  • [1] Gelatin hydrogels via thiol-ene chemistry
    Laura Russo
    Antonella Sgambato
    Roberta Visone
    Paola Occhetta
    Matteo Moretti
    Marco Rasponi
    Francesco Nicotra
    Laura Cipolla
    [J]. Monatshefte für Chemie - Chemical Monthly, 2016, 147 : 587 - 592
  • [2] Gelatin hydrogels via thiol-ene chemistry
    Russo, Laura
    Sgambato, Antonella
    Visone, Roberta
    Occhetta, Paola
    Moretti, Matteo
    Rasponi, Marco
    Nicotra, Francesco
    Cipolla, Laura
    [J]. MONATSHEFTE FUR CHEMIE, 2016, 147 (03): : 587 - 592
  • [3] Development of a reversible and repeatable thiol-ene reaction for controlled presentation of signaling proteins in hydrogels
    Grim, Joseph
    Aguado, Brian
    Brown, Tobin
    Anseth, Kristi
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2019, 258
  • [4] The Power of Thiol-ene Chemistry
    Kade, Matthew J.
    Burke, Daniel J.
    Hawker, Craig J.
    [J]. JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2010, 48 (04) : 743 - 750
  • [5] Thiol-Ene Click Chemistry
    Xu Yuanhong
    Xiong Xingquan
    Cai Lei
    Tang Zhongke
    Ye Zhangji
    [J]. PROGRESS IN CHEMISTRY, 2012, 24 (2-3) : 385 - 394
  • [6] Thiol-ene chemistry of vinylsilanes
    Rissing, Christiana
    Son, David Y.
    [J]. MAIN GROUP CHEMISTRY, 2009, 8 (04) : 251 - 262
  • [7] Thiol-Ene Click Chemistry
    Hoyle, Charles E.
    Bowman, Christopher N.
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (09) : 1540 - 1573
  • [8] Fully biodegradable antibacterial hydrogels via thiol-ene "click" chemistry
    Du, Hong
    Zha, Guangyu
    Gao, Lilong
    Wang, Huan
    Li, Xiaodong
    Shen, Zhiquan
    Zhu, Weipu
    [J]. POLYMER CHEMISTRY, 2014, 5 (13) : 4002 - 4008
  • [9] Surface Functionalization Achieved by Photo-Initiated Thiol-Ene Chemistry
    Devin G. Barrett
    [J]. MRS Bulletin, 2010, 35 : 113 - 113
  • [10] Mechanical characterization of sequentially layered photo-clickable thiol-ene hydrogels
    Aziz, Aaron H.
    Wahlquist, Joseph
    Soliner, Aaron
    Ferguson, Virginia
    DelRio, Frank W.
    Bryant, Stephanie J.
    [J]. JOURNAL OF THE MECHANICAL BEHAVIOR OF BIOMEDICAL MATERIALS, 2017, 65 : 454 - 465