Department of Plastic and Reconstructive Surgery, Shanghai Ninth People's Hospital, School of Medicine , Shanghai Jiao Tong University , 639 Zhizaoju Road , Shanghai 200011 , P.R. China.
Cosmetic Laser Center, Shanghai Ninth People's Hospital, School of Medicine , Shanghai Jiao Tong University , 639 Zhizaoju Roadd , Shanghai 200011 , P.R. China.
ACS Appl Mater Interfaces. 2019 Jan 30;11(4):3704-3714. doi: 10.1021/acsami.8b17498. Epub 2019 Jan 14.
5-Aminolevulinic acid (ALA)-loaded nanoethosome (ALA-ES) gels are successfully prepared to realize a transdermal delivery of ALA, and they provide a feasible approach for the photodynamic therapy (PDT) of hypertrophic scars (HS). Herein, the morphological and physicochemical features indicate that ALA-ES is stable in gel matrix. In vitro transdermal penetration studies suggest ALA-ES gels can overcome the compact dermal barrier and deliver more ALA into human HS tissue. In vivo delivery studies further reveal that ALA-ES gels can penetrate into rabbit HS tissue to facilitate ALA accumulating in hypertrophic scar fibroblast (HSF) and converting into protoporphyrin IX in the cytoplasm. Utilizing transmission electron microscopy, the visual in vivo penetration process indicates ALA-ES penetrate into HS tissue utilizing its deformable membrane, enters HSF by a pinocytotic-like mechanism, and then releases ALA in the cytoplasm. Subsequently, PDT efficacy is assessed using rabbit HS models. The morphological and histological analysis reveal that ALA-ES gels can improve HS by promoting HSF apoptosis, remodelling collagen fibers and increasing MMP3 expression. The results demonstrate that ALA-ES gels are suitable in clinical treatment of HS and make a substantial progress within the field.
5-氨基酮戊酸(ALA)负载的纳米囊泡(ALA-ES)凝胶成功制备,实现了 ALA 的经皮递药,为增生性瘢痕(HS)的光动力疗法(PDT)提供了一种可行的方法。在此,形态和物理化学特征表明 ALA-ES 在凝胶基质中稳定。体外透皮渗透研究表明,ALA-ES 凝胶可以克服致密的皮肤屏障,将更多的 ALA 递送到人 HS 组织中。体内递药研究进一步表明,ALA-ES 凝胶可以穿透到兔 HS 组织中,促进 ALA 在增生性瘢痕成纤维细胞(HSF)中积累,并在细胞质中转化为原卟啉 IX。利用透射电子显微镜,直观的体内渗透过程表明,ALA-ES 利用其可变形的膜穿透 HS 组织,通过胞饮样机制进入 HSF,并在细胞质中释放 ALA。随后,利用兔 HS 模型评估 PDT 疗效。形态学和组织学分析表明,ALA-ES 凝胶可通过促进 HSF 凋亡、重塑胶原纤维和增加 MMP3 表达来改善 HS。结果表明,ALA-ES 凝胶适合 HS 的临床治疗,并在该领域取得了实质性进展。