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. 2015 Oct 26;5(4):647–663. doi: 10.3390/bios5040647

Table 2.

Summary of hydrogels compatible for high-throughput cell printing and encapsulation.

Hydrogel Gelation Mechanism Compatible Cell Lines Advantages Limitations
Alginate Crosslinking via divalent ions Human adipose derived stem cells [61], human brain cancer cells [9] Good printability, applicable to stem cell growth [61], easy chemical modification [52] Non-supportive to viral transduction [26]
Matrigel® Temperature dependent Human umbilical vein endothelial cells, colorectal cancer cells [63], rat cardiomyocytes [64] Applicable to differentiation, xenografts, spheroidal cell growth, 3D co-cultures [63] Clogging tips and solenoid valves due to temperature sensitive gelation
Fibrin Thrombin catalyzed polymerization Chondrocytes [57], rat myoblast [68] Applicable to tissue engineering, vascular grafts, gene delivery [35,47] Unstable due to degradation via MMPs [67]
Collagen (type 1) Temperature induced Endothelial progenitor cells, mesenchymal progenitor cells [69] Applicable to tissue engineering [73] Unstable due to degradation via collagenases, clogging tips and valves [83]
Hyaluronin Thermal or photo dependent gelation [52] Mesenchymal stem cell [35], endothelial cells [37] Applicable to tissue engineering, regenerative medicine, stem cell differentiation, wound healing, angiogenesis [76] Poor mechanical strength
PuraMatrix Self-assembling when exposed to salts Primary rat hepatocytes, adult liver progenitor cells, chondrocytes [79] Embryonic stem cell cultures [79] Poor cyto-compatibility due to low pH
PEG UV crosslinking, simple redox crosslinking Human mesenchymal stem cells [54] High mechanical strength No cell-matrix interaction