Table 2.
Pros and cons of the modified electrospinning techniques.
Technique | Pros | Cons | References |
---|---|---|---|
Combination of nanofibers and microfibers | Controllable fiber diameter and pore size. | Small pores defined by the nanofibers in the scaffold still hinder cell infiltration. | [19], [20], [21] |
Electrospinning with salt leaching | Controllable pore size. | Modifications of electrospinning setup need to disperse the salt particles into nanofibrous mats. | [22], [23] |
Cryogenic electrospinning | Open 3D structure with super large pores. | Correct balance between crystal formation and fiber deposition is difficult to be achieved. Difficult to form a thick scaffold with homogeneous porous structure. |
[24], [25], [26], [27] |
Sacrificial fibers to induce large pores | Adjustable porosity. Homogeneous porous structure. |
Difficult to increase scaffold pore size. | [28], [29], [30] |
Electrospinning using a liquid bath collector | Dispersion effect of the liquid bath results in homogeneous pores with the scaffolds. | Difficult to scale up. | [31], [32], [33], [34], [35], [36], [37], [38], [39], [40], [41] |
Ultrasonication | Feasible process. | Difficult to obtain desirable shape of scaffold. | [42], [43], [44], [45] |
Electrospinning with gas foaming | Homogeneous porous structure. | Chemical agent has a negative effect on electrospinning process. | [47], [48], [49], [50] |
Electrospinning/electrospraying | Minimize the loss of bioactivity by separating natural component from highly volatile organic solution. Allow rapid formation of hybrid tissue engineered constructs with uniform cell distribution. |
Difficult to scale up. | [56], [57], [58], [59], [60], [61] |