Zhang Zheng, Chen Yunsheng, Ding Jiayue, Zhang Chunlei, Zhang Amin, He Dannong, Zhang Yixin
Department of Plastic and Reconstructive Surgery, Shanghai Ninth People's Hospital, School of Medicine, Shanghai Jiao Tong University, 639 Zhizaoju Rd, Shanghai, 200011, People's Republic of China.
Institute of Nano Biomedicine and Engineering, Shanghai Engineering Research Center for Intelligent Instrument for Diagnosis and Therapy, School of Biomedicine Engineering, Shanghai Jiao Tong University, 800 Dongchuan Rd, Shanghai, 200240, People's Republic of China.
Nanoscale Res Lett. 2017 Dec 15;12(1):622. doi: 10.1186/s11671-017-2389-x.
Biocompatible 5-aminolevulinic acid/Au nanoparticle-loaded ethosomal vesicle (A/A-ES) is prepared via ultrasonication for synergistic transdermal photodynamic/photothermal therapy (PDT/PTT) of hypertrophic scar (HS). Utilizing ultrasonication, Au nanoparticles (AuNPs) are synthesized and simultaneously loaded in ethosomal vesicles (ES) without any toxic agents, and 5-aminolevulinic acid (ALA) is also loaded in ES with 20% of the entrapment efficiency (EE). The prepared A/A-ES displays strong absorbance in 600-650 nm due to the plasmonic coupling effect between neighboring AuNPs in the same A/A-ES, which can simultaneously stimulate A/A-ES to produce heat and enhance quantum yields of reactive oxygen species (ROS) by using 632 nm laser. In vitro transdermal penetrability study demonstrates that A/A-ES acts as a highly efficient drug carrier to enhance both ALA and AuNPs penetration into HS tissue. Taking human hypertrophic scar fibroblasts (HSF) as therapeutic targets, synergistic PDT/PTT of HS indicates that A/A-ES could enhance quantum yields of ROS by photothermal effect and localized surface plasmon resonance (LSPR) of AuNPs, resulting in a high level of apoptosis or necrosis. In a word, the prepared A/A-ES shows a better synergistic PDT/PTT efficiency for HSF than the individual PDT and PTT, encouraging perspective for treatment of HS.
通过超声处理制备了生物相容性的负载5-氨基乙酰丙酸/金纳米颗粒的乙醇脂质体(A/A-ES),用于增生性瘢痕(HS)的协同经皮光动力/光热疗法(PDT/PTT)。利用超声处理合成金纳米颗粒(AuNPs)并将其同时负载到乙醇脂质体(ES)中,且不使用任何有毒试剂,5-氨基乙酰丙酸(ALA)也以20%的包封率(EE)负载到ES中。所制备的A/A-ES由于同一A/A-ES中相邻AuNPs之间的等离子体耦合效应,在600-650nm处显示出强吸收,这可以在使用632nm激光时同时刺激A/A-ES产生热量并提高活性氧(ROS)的量子产率。体外透皮渗透性研究表明,A/A-ES作为一种高效的药物载体,可增强ALA和AuNPs向HS组织的渗透。以人增生性瘢痕成纤维细胞(HSF)作为治疗靶点,HS的协同PDT/PTT表明,A/A-ES可通过AuNPs的光热效应和局域表面等离子体共振(LSPR)提高ROS的量子产率,从而导致高水平的细胞凋亡或坏死。总之,所制备的A/A-ES对HSF的协同PDT/PTT效率优于单独的PDT和PTT,为HS的治疗带来了令人鼓舞的前景。