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Yixiao Dong

Researcher at Stanford University

Publications -  45
Citations -  1830

Yixiao Dong is an academic researcher from Stanford University. The author has contributed to research in topics: Self-healing hydrogels & Ethylene glycol. The author has an hindex of 23, co-authored 40 publications receiving 1330 citations. Previous affiliations of Yixiao Dong include National University of Ireland, Galway & ShanghaiTech University.

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Injectable and Tunable Gelatin Hydrogels Enhance Stem Cell Retention and Improve Cutaneous Wound Healing

TL;DR: The data suggest that injectable PEG–gelatin hydrogel can be used for regulating stem cell behaviors in 3D culture, delivering cells for wound healing and other tissue regeneration applications.
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A hybrid injectable hydrogel from hyperbranched PEG macromer as a stem cell delivery and retention platform for diabetic wound healing.

TL;DR: A new injectable hydrogel system was fabricated from hyperbranched multi-acrylated poly(ethylene glycol) macromers (HP-PEGs) and thiolated hyaluronic acid (HA-SH) and used as a stem cell delivery and retention platform and may be a promising candidate for diabetic wound treatment.
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Encapsulation and 3D culture of human adipose-derived stem cells in an in-situ crosslinked hybrid hydrogel composed of PEG-based hyperbranched copolymer and hyaluronic acid

TL;DR: This study indicates that hADSCs can be maintained in a P-SH-HA hydrogel, and secrete pro-angiogenic growth factors with low cytotoxicity, and with the potential to add more functionality for further structural modifications, this stem cell hydrogels system can be an ideal living dressing system for wound healing applications.
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Performance of an in situ formed bioactive hydrogel dressing from a PEG-based hyperbranched multifunctional copolymer

TL;DR: An injectable hybrid hydrogel dressing system was prepared from a polyethylene glycol (PEG)-based thermoresponsive hyperbranched multiacrylate functional copolymer and thiol-modified hyaluronic acid in combination with adipose-derived stem cells (ADSCs) and found that long-term cell viability could be achieved for both in vitro (21days) and in vivo studies.