Chun Yong Yao, Tan William Wei Ren, Vos Marcus Ivan Gerard, Chan Wen Kiat, Tey Hong Liang, Tan Nguan Soon, Tan Timothy Thatt Yang
School of Chemical and Biomedical Engineering, Nanyang Technological University, 62 Nanyang Dr, Singapore 637459.
Lee Kong Chian School of Medicine, Nanyang Technological University, 11 Mandalay Road, Singapore 308232.
Biomater Sci. 2022 Jul 12;10(14):3963-3971. doi: 10.1039/d2bm00572g.
Currently, there is no effective method to prevent the formation of hypertrophic scars and keloids, which can cause severe physical and psychological burdens to patients. Secreted protein acidic and cysteine-rich (SPARC) is involved in wound fibrosis by modulating fibroblast functions, causing excessive collagen deposition during wound healing. Thus, the reduction in SPARC gene expression after wounding can contribute to the downstream reduction in collagen production at the wound site and prevent scar formation. In this study, a dissolvable and biocompatible hyaluronic acid (HA) microneedle patch loaded with nanoplexes containing tyramine-modified gelatin and siRNA for SPARC (siSPARC/Gtn-Tyr) was investigated for topical scar prevention. Tyramine-modified gelatin (Gtn-Tyr) provides electrostatic protection and enhances cell internalization for siSPARC. studies using human dermal fibroblasts showed that both siSPARC/Gtn-Tyr nanoplexes and siSPARC/Gtn-Tyr-loaded microneedle patches can significantly reduce SPARC gene expression ( < 0.05) and do not cause discernable cytotoxic effects. Further studies using a mouse wound model demonstrate that the siSPARC/Gtn-Tyr-loaded microneedle patch can reduce collagen production during wound healing without triggering an immune response. When Gtn-Tyr-siSPARC is administered transdermally at the wound site, effective collagen reduction is achieved through silencing of the matricellular SPARC protein, thus promising the reduction of scar formation. Overall, the siSPARC/Gtn-Tyr loaded microneedle patch can potentially provide an effective transdermal anti-fibrotic treatment.
目前,尚无有效的方法来预防增生性瘢痕和瘢痕疙瘩的形成,这些瘢痕会给患者带来严重的身心负担。富含酸性和半胱氨酸的分泌蛋白(SPARC)通过调节成纤维细胞功能参与伤口纤维化,在伤口愈合过程中导致胶原蛋白过度沉积。因此,受伤后SPARC基因表达的降低有助于减少伤口部位胶原蛋白的下游生成,并预防瘢痕形成。在本研究中,研究了一种可溶解且具有生物相容性的透明质酸(HA)微针贴片,其负载了含有酪胺修饰明胶和针对SPARC的小干扰RNA(siSPARC/Gtn-Tyr)的纳米复合物,用于局部瘢痕预防。酪胺修饰明胶(Gtn-Tyr)提供静电保护并增强siSPARC的细胞内化。使用人皮肤成纤维细胞的研究表明,siSPARC/Gtn-Tyr纳米复合物和负载siSPARC/Gtn-Tyr的微针贴片均可显著降低SPARC基因表达(<0.05),且不会引起明显的细胞毒性作用。使用小鼠伤口模型的进一步研究表明,负载siSPARC/Gtn-Tyr的微针贴片可减少伤口愈合过程中的胶原蛋白生成,而不会引发免疫反应。当在伤口部位经皮施用Gtn-Tyr-siSPARC时,通过沉默基质细胞SPARC蛋白可有效减少胶原蛋白,从而有望减少瘢痕形成。总体而言,负载siSPARC/Gtn-Tyr的微针贴片可能提供一种有效的经皮抗纤维化治疗方法。