Chen Yong-Ji, Cheng Hung-Wei, Yen Wan-Yu, Tsai Jen-Hao, Yeh Chin-Yi, Chen Ching-Jung, Liu Jen Tsai, Chen San-Yuan, Chang Shwu-Jen
Department of Biomedical Engineering, I-Shou University, Kaohsiung 82445, Taiwan.
Department of Materials Science and Engineering, National Yang Ming Chiao Tung University, Hsinchu 30010, Taiwan.
Polymers (Basel). 2022 Oct 20;14(20):4436. doi: 10.3390/polym14204436.
Keloid scarring is an abnormal scar disease characterised by excessive proliferation of fibroblasts and over-deposition of collagen during wound healing. Although various treatments for keloid scars have been developed, preventive medicine is believed to be a promising strategy. The skin barrier limits the gentle topical administration of medicaments such as creams and hydrogel dressings, resulting in reduced therapeutic efficacy. In recent years, microneedles (MNs) have been regarded as an appreciable device for topical administration without inducing side effects, and they are painless and do not cause bleeding. In this study, an MN patch with controlled transdermal dual-drug release was developed to achieve combinatory treatment of keloid scars using a heterogeneous gelatin-structured composite MN. Gelatin hydrogel was used as a substrate to load gallic acid (GA) and quercetin-loaded amphiphilic gelatin nanoparticles to fabricate dual-drug heterogeneous composite MNs. The results of the insertion test and mechanical properties of the MNs showed that the heterogeneous composite MN patches could be self-pressed into the stratum corneum and control dual-drug release at different time periods. GA was released at an earlier stage to retard the proliferation of fibroblasts, and quercetin was released at a later stage as a strong antioxidant to erase the generation of reactive oxygen species. Furthermore, real-time quantitative polymerase chain reaction data indicated that the gene expression of fibroblasts (such as Col I and III) was downregulated in the dual-drug system. The above results demonstrate that using heterogeneous composite MNs with the combination of dual-drug pharmacology is beneficial for preventing keloid scar formation.
瘢痕疙瘩是一种异常瘢痕疾病,其特征是在伤口愈合过程中成纤维细胞过度增殖和胶原蛋白过度沉积。尽管已经开发出多种治疗瘢痕疙瘩的方法,但预防医学被认为是一种有前景的策略。皮肤屏障限制了乳膏和水凝胶敷料等药物的温和局部给药,导致治疗效果降低。近年来,微针(MNs)被认为是一种可观的局部给药装置,不会引起副作用,而且无痛且不出血。在本研究中,开发了一种具有可控透皮双药释放功能的MN贴片,以使用异质明胶结构复合MN实现瘢痕疙瘩的联合治疗。明胶水凝胶用作负载没食子酸(GA)和载有槲皮素的两亲性明胶纳米颗粒的基质,以制备双药异质复合MNs。MNs的插入测试结果和力学性能表明,异质复合MN贴片可以自压入角质层并在不同时间段控制双药释放。GA在早期释放以抑制成纤维细胞的增殖,槲皮素在后期作为强抗氧化剂释放以消除活性氧的产生。此外,实时定量聚合酶链反应数据表明,双药系统中成纤维细胞的基因表达(如Col I和III)下调。上述结果表明,使用具有双药药理学组合的异质复合MNs有利于预防瘢痕疙瘩的形成。