首页> 美国卫生研究院文献>Nanoscale Research Letters >Biocompatible 5-Aminolevulinic Acid/Au Nanoparticle-Loaded Ethosomal Vesicles for In Vitro Transdermal Synergistic Photodynamic/Photothermal Therapy of Hypertrophic Scars
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Biocompatible 5-Aminolevulinic Acid/Au Nanoparticle-Loaded Ethosomal Vesicles for In Vitro Transdermal Synergistic Photodynamic/Photothermal Therapy of Hypertrophic Scars

机译:生物相容性5-氨基乙酰丙酸/金纳米颗粒负载的囊泡用于增生性瘢痕的体外透皮协同光动力/光热疗法

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摘要

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.Electronic supplementary materialThe online version of this article (10.1186/s11671-017-2389-x) contains supplementary material, which is available to authorized users.
机译:通过超声制备生物相容的5-氨基乙酰丙酸/金纳米颗粒负载的核糖体囊泡(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,合成了Au纳米颗粒(AuNPs),并同时将其负载在没有任何有毒物质的核糖体囊泡(ES)中; 5-氨基乙酰丙酸(ALA)也以20%的包封率(EE)负载在ES中。由于相同A / A-ES中相邻AuNP之间的等离子体耦合效应,制得的A / A-ES在600-650 nm处显示出强吸收性,这可以同时刺激A / A-ES产生热量并提高A / A-ES的量子产率使用632 nm激光产生活性氧(ROS)体外透皮渗透性研究表明,A / A-ES可以作为一种高效的药物载体来增强ALA和AuNPs渗透到HS组织中。以人肥厚性瘢痕成纤维细胞(HSF)为治疗靶点,HS的PDT / PTT协同作用表明A / A-ES可以通过光热效应和AuNPs的局部表面等离振子共振(LSPR)来提高ROS的量子产量,从而导致高水平凋亡或坏死。简而言之,所制备的A / A-ES对HSF的PDT / PTT协同效果优于单个PDT和PTT,这为HS的治疗提供了前景。电子补充材料本文的在线版本(10.1186 / s11671-017- 2389-x)包含补充材料,授权用户可以使用。

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