Injectable hydrogels have been recognized as an important class of soft materials for many enticing applications, yet it remains a challenge to program functions in one hydrogel substrate. Here, we report on dynamic hydrogels bearing injectable capacity and modular functionalities enabled by hydrazone formation. The hydrogel is generated by (cis, cis)-cyclohexane-1, 3, 5-tricarbohydrazide (H) and aldehyde-decorated hyaluronic acid (HA-A) through hydrazone formation. Due to the intrinsic dynamic feature of hydrazone bonds, the hydrogels are capable of rapidly recovering against mechanical damage, which makes the hydrogels injectable. Importantly, the residual hydrazide groups in the hydrogel network allow for the incorporation of various molecular modules through hydrazone formation, enabling the hydrogels to have a variety of chemical functions. Moreover, relying on a hydrazone formation-based self-assembly system, we are even able to incorporate supramolecular nanofibers into the hydrogel network. The incorporation of supramolecular nanofibers increasing the plateau storage modulus from approximately 200 to 20 000 Pa and the yield strain from 180% to 360%, while preserving the injectable behavior. This work offers a simple approach for the development of injectable hydrogels with tunable functions for diverse applications such as drug delivery, tissue regeneration, and machine-human interfaces.
Hydrogels are high water content networks used across many applications. Stimuli-responsive hydrogels exhibit changes in properties or break down in response to stimuli, leading to new functions and applications, with self-immolative polymer hydrogels enabling amplified responses to stimuli through end-to-end depolym...
Chuan-Feng Li, Burak Tavsanli, Elizabeth R. Gillies· Macromolecules· 0 citations
Hydrogels with high mechanical strength at equilibrium swelling are crucial for load-bearing applications. However, despite significant progress in the development of strong hydrogels, their in vivo applications remain limited by the need for invasive surgical removal after use. Bioorthogonal click chemistry is intro...
Kai-Ming Zhang, Jia-Kui Ren, H. Nosrati et al.· Journal of the American Chem...· 0 citations
Hydrogels have emerged as promising materials across various fields, including biomedical, electronic, and robotic applications, due to their intrinsic softness and biocompatibility. Despite these advantages, the development of hydrogel‐based functional materials and devices remains limited by the narrow range of mat...
Hyeonjin Kim, Hyeseoung Lim, Ji Min Lee et al.· Advanced Functional Material...· 0 citations
An approach for creating self-assembling, supramolecular hydrogels based on a peptide-polymer conjugate (PPC) as a three-dimensional (3D) cell culture platform is established and a method for the encapsulation and culture of human wound healing cells, fibroblasts, within the PPC hydrogels is developed.
Breanna M. Huntington, J. Dresel, Maren Schweitzer et al.· bioRxiv· 0 citations
This study presents a robust and scalable HA-based platform, available as either an injectable hydrogel or an in situ cross-linkable solution, with broad potential in drug delivery, regenerative medicine, and aesthetic applications.
An injectable, self-healing hyaluronic acid/poly(ethylene glycol) composite hydrogel system may function as an EV-protective depot responsive to microenvironmental changes for localized therapeutic delivery.
Filippo Calascibetta, Annalisa Martorana, G. Amico et al.· International journal of pha...· 0 citations
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