Department of Plastic and Reconstructive Surgery, Ninth People's Hospital Affiliated to Medical School of Shanghai Jiao Tong University, 639 Zhi Zao Ju Road, Shanghai 200011, PR China.
School of Biomedical Engineering and Med-X Research Institute, Shanghai Jiao Tong University, Shanghai, PR China.
Colloids Surf B Biointerfaces. 2014 Mar 1;115:61-70. doi: 10.1016/j.colsurfb.2013.11.030. Epub 2013 Nov 24.
Prevention of hypertrophic scar formation of the skin requires a complex treatment process, which mainly includes promoting skin regeneration in an early stage while inhibiting hypertrophic formation in a later stage. Electrospinning PLGA with the three-dimensional micro/nano-fibrous structure and as drugs carrier, could be used as an excellent skin repair scaffold. However, it is difficult to combine the advantage of nanofibrous membranes and drug carriers to achieve early and late treatment. In this study, Ginsenoside-Rg3 (Rg3) loaded hydrophilic poly(D,L-lactide-co-glycolide) (PLGA) electrospun fibrous membranes coated with chitosan (CS) were fabricated by combining electrospinning and pressure-driven permeation (PDP) technology. The PDP method was able to significantly improve the hydrophilicity of electrospun fibrous membranes through surface coating of the hydrophilic fibers with CS, while maintaining the Rg3 releasing rate of PLGA electrospun fibrous membranes. Experimental wounds of animal covered with PDP treated fibrous membranes completely re-epithelialized and healed 3-4 days earlier than the wounds in control groups. Scar elevation index (SEI) measurements and histologic characteristics revealed that Rg3 significantly inhibited scar formation 28 days post-surgery. Moreover, RT-PCR assays and western blot analysis revealed that at day 28 after wound induction the expression of VEGF, mRNA and Collagen Type I in the scars treated with Rg3 was decreased compared to control groups. Taken together PLGA-Rg3/CS electrospun fibrous membranes induced repair of tissue damage in the early stage and inhibited scar formation in the late stage of wound healing. These dual-functional membranes present a combined therapeutic approach for inhibiting hypertrophic scars of the skin.
预防皮肤的增生性瘢痕形成需要一个复杂的治疗过程,主要包括在早期促进皮肤再生,同时在后期抑制增生性形成。具有三维微/纳米纤维结构的电纺 PLGA 及其作为药物载体,可以用作出色的皮肤修复支架。然而,将纳米纤维膜和药物载体的优势结合起来以实现早期和晚期治疗具有一定的难度。在这项研究中,通过结合静电纺丝和压力驱动渗透(PDP)技术,制备了负载人参皂苷 Rg3(Rg3)的亲水性聚(D,L-乳酸-共-乙醇酸)(PLGA)电纺纤维膜,其表面涂覆有壳聚糖(CS)。PDP 方法能够通过 CS 对亲水性纤维进行表面涂覆,显著提高电纺纤维膜的亲水性,同时保持 PLGA 电纺纤维膜的 Rg3 释放速率。用 PDP 处理的纤维膜覆盖的动物实验性伤口完全再上皮化,比对照组的伤口提前 3-4 天愈合。瘢痕隆起指数(SEI)测量和组织学特征表明,Rg3 可显著抑制术后 28 天的瘢痕形成。此外,RT-PCR 测定和 Western blot 分析表明,与对照组相比,在诱导伤口后第 28 天,Rg3 处理的瘢痕中 VEGF、mRNA 和胶原 I 的表达减少。总之,PLGA-Rg3/CS 电纺纤维膜在组织损伤的早期诱导修复,并在伤口愈合的后期抑制瘢痕形成。这些双重功能的膜为抑制皮肤的增生性瘢痕提供了一种联合治疗方法。