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. 2021 Jan 13;8:606982. doi: 10.3389/fbioe.2020.606982

TABLE 4.

Summary of studies based on AM hydrogels.

Author, year Therapeutic goal Experimental settings (target tissue/cells) Secondary biomaterial Conclusion References
Hussin, 2011 Cartilage TE In vitro (primary chondrocytes) Fibrinogen The hydrogel-based on AM and fibrin not only secretes cartilage-specific ECM and has significant amounts of GAGs but also preserves cellular phenotype and has a reasonable biodegradation rate Hussin et al., 2011
Ryzhuka, 2017 Cell delivery and TE In vitro and in vivo (PMSCs, Sprague Dawley rat) AM hydrogel supports cellular growth and maintains the normal morphology and physiology of the embedded cells and does not induce any inflammation Ryzhuk et al., 2018
Murphy, 2017 Wound healing In vitro and in vivo (human dermal fibroblast and keratinocyte, mice) HA HA-AME hydrogel accelerates wound closure through increasing epithelialization and decreasing contraction and results in smaller average vessel areas Murphy et al., 2017
Lee, 2018 Fetal membrane healing In vivo (pregnant miniature swine) PCL framework AM gel successfully seals the defect site in the fetal membrane and stop AF leakage Lee et al., 2018
Murphy, 2019 Wound healing In vivo (pig) HA HA-AME and AM powder both better stabilize the wound in comparison with other treatments Tseng, 2016
Toniato, 2019 Articular cartilage TE In vitro Chitosan Hybrid hydrogel based on dAM and Ch has the high swelling capacity and elastic modulus Toniato et al., 2019
Rahman, 2019 Burn wound healing In vitro and in vivo (HaCaT, HFF1, Wistar rats) Aloe vera Wound dressing based on AM and AV accelerated wound closure with minimum scar formation Rahman et al., 2019
Henry, 2019 Post-MI tissue repair In vitro and in vivo (BAECs, rat) Injectable and thermoresponsive AM hydrogel improves cardiac contractility and decreases fibrosis Henry et al., 2020
Rana, 2020 Burn healing In vitro and in vivo (RBC, Wistar rat) Collagen Hydrogel based on AM and collagen increases the rate of wound healing mainly when it is utilized with a wound dressing membrane Rana et al., 2020
Lei, 2020 Vascular graft In vitro and in vivo (HUVEC, RBC, New Zealand rabbit) AlgSr/PAM This graft is resistance to enzymatic degradation and possesses anti-calcification effect, activates platelet and hemolysis, and enhances vascular remodeling and repair Lei et al., 2020
Peng, 2020 Vascular graft In vitro and in vivo (HUVECs, HASMCs, New Zealand rabbits ADA/REDV This graft has enhanced mechanical strength and resistance to enzymic degradation. It accelerates endothelialization, and the addition of REDV to this structure stimulates natural anticoagulant substances on naturally derived blood vessels. Peng et al., 2020