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. 2023 Feb 11;19:100579. doi: 10.1016/j.mtbio.2023.100579

Table 2.

MNs for corneal regeneration.

Materials Structure Bioactive substances Mechanisms Ref.
Frozen glycerin Arrays: 3 ​× ​3
Height: 400–440 ​μm Shape: pyramidal
Strength: 00.3–0.4 ​N/neelde
Bdellovibrio bacteriovorus Bacterial activity exceeded 80% after 14 ​d of storage. [85]
Needle: outer MeHA shell and internal HA
Base: HA
Arrays: 3 ​× ​3
Height: 500 ​μm Shape: pyramidal
Strength: 0.4 ​N/neelde
Anti-angiogenic monoclonal antibody (DC101), diclofenac Rapid dissolution of the outer layer of the needle tip, releasing >80% of the drug within 5 ​min;
Slow release of the inner hydrogel layer (over 3 ​d).
[90]
Needle: silicon
Base: PVA
Arrays:
Height: 60 ​μm Shape: Circular
Strength:
Bevacizumab Painless and long-term sustained delivery of ocular drugs over the course of months. [137]
PLGA, SU8 resin Arrays: 1 needle
Height: 150 ​μm Shape: Tapered
Strength: 00.3–0.4 ​N/neelde
Antibiotics The drug-tip is separated from base and released drugs after the hydrolysis of PLGA occurred in cornea. [143]
Poly(D,l-lactide), HA Arrays: 20 ​× ​20
Height: 390 ​μm Shape: pyramidal
Strength:
Fluconazole Penetrating the corneal epithelial layer reversibly; Increasing the residence time of drug in the conjunctival sac [144]