TABLE 3.
Overview of polymeric MN manufacturing processes.
| Manufacturing process | Advantages | Disadvantages | Ref. | |
|---|---|---|---|---|
| Micro-moulding | Centrifugation-filling | Cost-effective | Excess formula solution needs to be removed from the mould surface and wasted | [130, 131] |
| Short centrifugal cycle | Risk of variation in each batch | |||
| More suitable for laboratory research | ||||
| Vacuum-filling | Filling and drying steps can be combined | Excess formula solution also needs to be removed from the mould surface and disposed of | [132, 133] | |
| Cost-effective | Drug loading capacity | |||
| Easy to scale batch output | ||||
| Lithography | 3D printing | Reduce waste and rapid prototyping | Layer-by-layer printing may affect mechanical strength | [134, 135] |
| Very precise geometries | High-resolution instruments are expensive | |||
| Centrifugal lithography | Reproducibly produced | Available materials and API are limited | [136, 137] | |
| Suitable for fabricating MNs loaded with fragile biological drugs | Not ideal for industrial production | |||