| Alginate–PVA–hydroxyapatite |
Mouse calvaria (MC) 3T3-E1 |
14 days |
In vitro, viability = ∼77% (after incubation), >∼22% for only alginate, could maintain structure for at least 14 days. Alginate hydroxyapatite had optimum mechanical, rheological and biological characteristics. PVA–hydroxyapatite modulates viscosity and thus enhanced osteoconduction and viscosity |
32
|
| Alginate–polylactic acid short fibers |
Human chondrocytes |
14 days |
In vitro, ∼80% viability |
33
|
| Alginate–PVA–hydroxyapatite–collagen |
Mouse calvaria (MC) 3T3-E1 |
10 days |
In vitro, initial viability >98%, collagen increases cell adhesion and activity |
34
|
| Na alginate–collagen or Na alginate–agarose |
Chondrocytes from the articular cartilage of rats |
14–21 days |
Na alginate–collagen possessed better mechanical strength and bioactivity than other combinations |
35
|
| Alginate–polycaprolactone |
Human nasal septum cartilage chondrocytes |
7 days |
Osteogenic tissue engineering, viability = ∼94% (chondrocytes) ∼96% (osteoblast), no observable proliferation in chondrocytes |
36
|
| Alginate–alginate sulfate |
Bone morphogenetic protein-2, MC3T3-E1 |
7 days |
In vitro, 80% proliferation, improved retention of proteins, alginate–alginate sulfate tightly bound BMP-2, which aids adhesion and cell viability, Ca presence and porosity favorable for bone tissue engineering |
37
|
| Alginate–gelatin–fibrinogen |
Glioma cells/stem cells |
21 days |
3rd week showed accelerated growth mimicking the tumor spreading and growth, cell viability = 86.92% |
38
|
| Sodium alginate–gelatin |
Rat Schwann cell line (RSC96) |
14 days |
Viability = ∼93% (post 14 days), printed structures start degrading after 14 days |
39
|
| Alginate–polycaprolactone |
Chondrogenic cell ATDC5 |
21 days |
In vivo, ∼70 viable cells, maintained integrity of the PCL scaffold even after 21 days, composite mimics the natural characteristics of cartilage |
40
|
| Oxidized alginate–gelatin–NCDs |
Osteosarcoma cell line MG63 |
1–3 days |
Viability = 97% after 3 days, adding NCDs increases cell viability, cell attachment, and storage modulus |
This work |