scholarly journals Transiently malleable multi-healable hydrogel nanocomposites based on responsive boronic acid copolymers

2018 ◽  
Vol 9 (4) ◽  
pp. 525-537 ◽  
Author(s):  
Adérito J. R. Amaral ◽  
Mina Emamzadeh ◽  
George Pasparakis

Dynamic multi-responsive gel nanocomposites with rapid self-healing and cell encapsulation properties are presented.

Polymers ◽  
2021 ◽  
Vol 13 (21) ◽  
pp. 3782
Author(s):  
Anupama Devi V. K. ◽  
Rohin Shyam ◽  
Arunkumar Palaniappan ◽  
Amit Kumar Jaiswal ◽  
Tae-Hwan Oh ◽  
...  

Polymeric hydrogels are widely explored materials for biomedical applications. However, they have inherent limitations like poor resistance to stimuli and low mechanical strength. This drawback of hydrogels gave rise to ‘’smart self-healing hydrogels’’ which autonomously repair themselves when ruptured or traumatized. It is superior in terms of durability and stability due to its capacity to reform its shape, injectability, and stretchability thereby regaining back the original mechanical property. This review focuses on various self-healing mechanisms (covalent and non-covalent interactions) of these hydrogels, methods used to evaluate their self-healing properties, and their applications in wound healing, drug delivery, cell encapsulation, and tissue engineering systems. Furthermore, composite materials are used to enhance the hydrogel’s mechanical properties. Hence, findings of research with various composite materials are briefly discussed in order to emphasize the healing capacity of such hydrogels. Additionally, various methods to evaluate the self-healing properties of hydrogels and their recent advancements towards 3D bioprinting are also reviewed. The review is concluded by proposing several pertinent challenges encountered at present as well as some prominent future perspectives.


2015 ◽  
Vol 4 (2) ◽  
pp. 220-224 ◽  
Author(s):  
Christopher C. Deng ◽  
William L.A. Brooks ◽  
Khalil A. Abboud ◽  
Brent S. Sumerlin
Keyword(s):  

2021 ◽  
Vol 22 (8) ◽  
pp. 4104
Author(s):  
Yusuke Sugioka ◽  
Jin Nakamura ◽  
Chikara Ohtsuki ◽  
Ayae Sugawara-Narutaki

Physically crosslinked hydrogels with thixotropic properties attract considerable attention in the biomedical research field because their self-healing nature is useful in cell encapsulation, as injectable gels, and as bioinks for three-dimensional (3D) bioprinting. Here, we report the formation of thixotropic hydrogels containing nanofibers of double-hydrophobic elastin-like polypeptides (ELPs). The hydrogels are obtained with the double-hydrophobic ELPs at 0.5 wt%, the concentration of which is an order of magnitude lower than those for previously reported ELP hydrogels. Although the kinetics of hydrogel formation is slower for the double-hydrophobic ELP with a cell-binding sequence, the storage moduli G′ of mature hydrogels are similar regardless of the presence of a cell-binding sequence. Reversible gel–sol transitions are demonstrated in step-strain rheological measurements. The degree of recovery of the storage modulus G′ after the removal of high shear stress is improved by chemical crosslinking of nanofibers when intermolecular crosslinking is successful. This work would provide deeper insight into the structure–property relationships of the self-assembling polypeptides and a better design strategy for hydrogels with desired viscoelastic properties.


2018 ◽  
Vol 7 (8) ◽  
pp. 904-908 ◽  
Author(s):  
Yangjun Chen ◽  
Diana Diaz-Dussan ◽  
Di Wu ◽  
Wenda Wang ◽  
Yi-Yang Peng ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (73) ◽  
pp. 69156-69166 ◽  
Author(s):  
Ana Gantar ◽  
Nataša Drnovšek ◽  
Pablo Casuso ◽  
Adrián Pérez-San Vicente ◽  
Javier Rodriguez ◽  
...  

Combination of Au-based dynamic hydrogel with 100 nm bioactive glass nanoparticles resulted in the formation of an injectable, self-healing and biocompatible hydrogel nanocomposites with osteoinductive properties and potential for bone regeneration.


2020 ◽  
Vol 52 (8) ◽  
pp. 997-1006 ◽  
Author(s):  
Adérito J. R. Amaral ◽  
Vítor M. Gaspar ◽  
João F. Mano

2017 ◽  
Vol 53 (23) ◽  
pp. 3350-3353 ◽  
Author(s):  
Asja Pettignano ◽  
Santiago Grijalvo ◽  
Marleen Häring ◽  
Ramon Eritja ◽  
Nathalie Tanchoux ◽  
...  

Boronic acid-modified alginate allows the direct formation of biocompatible hydrogels under basic conditions with remarkable injectable, self-healing and multistimuli-responsive properties.


2021 ◽  
Author(s):  
Beverly Miller ◽  
Audrey Hansrisuk ◽  
Christopher B Highley ◽  
Steven R Caliari

The fibrous architecture of the extracellular matrix (ECM) is recognized as an integral regulator of cell function. However, there is an unmet need to develop mechanically robust biomaterials mimicking nanofibrous tissue topography that are also injectable to enable minimally invasive delivery. In this study we have developed a fibrous hydrogel composed of supramolecularly-assembled hyaluronic acid (HA) nanofibers that exhibits mechanical integrity, shear-thinning, rapid self-healing, and cytocompatibility. HA was modified with methacrylates to permit fiber photocrosslinking following electrospinning and either guest adamantane or host β-cyclodextrin groups to guide supramolecular fibrous hydrogel assembly. Analysis of fibrous hydrogel rheological properties showed that the mixed guest-host fibrous hydrogel was more mechanically robust (6.6 ± 2.0 kPa, storage modulus (G')) than unmixed guest hydrogel fibers (1.0 ± 0.1 kPa, G') or host hydrogel fibers (1.1 ± 0.1 kPa, G') separately. The reversible nature of the guest-host supramolecular interactions also allowed for shear-thinning and self-healing behavior as demonstrated by cyclic deformation testing. Human mesenchymal stromal cells (hMSCs) encapsulated in fibrous hydrogels demonstrated satisfactory viability following injection and after seven days of culture (> 85%). Encapsulated hMSCs were more spread and elongated when cultured in viscoelastic guest-host hydrogels compared to non-fibrous elastic controls, with hMSCs also showing significantly decreased circularity in fibrous guest-host hydrogels compared to non-fibrous guest-host hydrogels. Together, these data highlight the potential of this injectable fibrous hydrogel platform for cell and tissue engineering applications requiring minimally invasive delivery.


2018 ◽  
Vol 6 (11) ◽  
pp. 2932-2937 ◽  
Author(s):  
Laura J. Macdougall ◽  
Maria M. Pérez-Madrigal ◽  
Joshua E. Shaw ◽  
Maria Inam ◽  
Judith A. Hoyland ◽  
...  

A self-healable, mechanically strong and stretchable hydrogel network that supports cell encapsulation is reported to be achieved by creation of an interpenetrating network approach between PEG and natural polymers.


Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1133
Author(s):  
Yeonsun Choi ◽  
Kyuha Park ◽  
Heewon Choi ◽  
Donghee Son ◽  
Mikyung Shin

Implantable electronics have recently been attracting attention because of the promising advances in personalized healthcare. They can be used to diagnose and treat chronic diseases by monitoring and applying bioelectrical signals to various organs. However, there are challenges regarding the rigidity and hardness of typical electronic devices that can trigger inflammatory reactions in tissues. In an effort to improve the physicochemical properties of conventional implantable electronics, soft hydrogel-based platforms have emerged as components of implantable electronics. It is important that they meet functional criteria, such as stretchability, biocompatibility, and self-healing. Herein, plant-inspired conductive alginate hydrogels composed of “boronic acid modified alginate” and “oligomerized epigallocatechin gallate,” which are extracted from plant compounds, are proposed. The conductive hydrogels show great stretchability up to 500% and self-healing properties because of the boronic acid-cis-diol dynamic covalent bonds. In addition, as a simple strategy to increase the electrical conductivity of the hydrogels, ionically crosslinked shells with cations (e.g., sodium) were generated on the hydrogel under physiological salt conditions. This decreased the resistance of the conductive hydrogel down to 900 ohm without trading off the original properties of stretchability and self-healing. The hydrogels were used for “electrophysiological bridging” to transfer electromyographic signals in an ex vivo muscle defect model, showing a great bridging effect comparable to that of a muscle-to-muscle contact model. The use of plant-inspired ionically conductive hydrogels is a promising strategy for designing implantable and self-healable bioelectronics.


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