Hypertrophic
scar (HS) is an unfavorable skin disorder that typically
develops after trauma, burn injury, or surgical procedures and causes
numerous physical and psychological issues in patients. Currently,
intralesional multi-injection of corticosteroid, particularly compound
betamethasone (CB), is one of the most prevalent treatments for HS.
However, injection administration could result in severe pain and
dose-related side effects. Additionally, the vacuum therapeutic efficacy
of this treatment relies on the level of expertise of the healthcare
professional. To overcome the limitations of conventional injections,
a new method that is convenient, painless, and self-administrable
is urgently required. In this study, we developed a methacrylate gelatin
(GelMA)/polyethylene glycol diacrylate (PEGDA) double-network hydrogel
microneedle patch loaded with CB (CB-HMNP) as an intradermal delivery
system for HS treatment. The double-network structure conferred the
CB-HMNP with sufficient mechanical properties to successfully penetrate
scar tissue while also helping to regulate the drug’s sustained
release rate. Subsequently, we confirmed that the CB-HMNP had a pronounced
inhibitory effect on human HS fibroblasts (hHSFs), whereas drug-free
HMNPs had no effect on hHSFs, indicating its high biocompatibility.
In order to assess the therapeutic efficacy of CB-HMNPs, HS models
of New Zealand rabbit ears were developed. The administration of CB-HMNP
three times significantly decreased the scar elevation index (SEI),
collagen I/III, and transforming growth factor-β1 (TGF-β1)
protein. Therefore, the CB-HMNP may offer an administration pathway
for the treatment of HS that is less painful, more convenient, less
invasive, and sustain-released.