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Gold Nanoparticle-Mediated Delivery of Molecules into Primary Human Gingival Fibroblasts Using ns-Laser Pulses: A Pilot Study

机译:金纳米颗粒介导的使用ns激光脉冲将分子输送到主要人类牙龈成纤维细胞中的初步研究

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摘要

Interaction of gold nanoparticles (AuNPs) in the vicinity of cells’ membrane with a pulsed laser (λ = 532 nm, τ = 1 ns) leads to perforation of the cell membrane, thereby allowing extracellular molecules to diffuse into the cell. The objective of this study was to develop an experimental setting to deliver molecules into primary human gingival fibroblasts (pHFIB-G) by using ns-laser pulses interacting with AuNPs (study group). To compare the parameters required for manipulation of pHFIB-G with those needed for cell lines, a canine pleomorphic adenoma cell line (ZMTH3) was used (control group). Non-laser-treated cells incubated with AuNPs and the delivery molecules served as negative control. Laser irradiation (up to 35 mJ/cm2) resulted in a significant proportion of manipulated fibroblasts (up to 85%, compared to non-irradiated cells: p < 0.05), while cell viability (97%) was not reduced significantly. pHFIB-G were perforated as efficiently as ZMTH3. No significant decrease of metabolic cell activity was observed up to 72 h after laser treatment. The fibroblasts took up dextrans with molecular weights up to 500 kDa. Interaction of AuNPs and a pulsed laser beam yields a spatially selective technique for manipulation of even primary cells such as pHFIB-G in high throughput.
机译:细胞膜附近的金纳米颗粒(AuNPs)与脉冲激光(λ= 532 nm,τ= 1 ns)相互作用导致细胞膜穿孔,从而使细胞外分子扩散到细胞中。这项研究的目的是通过使用与AuNPs相互作用的ns激光脉冲,开发出一种将分子递送到主要人类牙龈成纤维细胞(pHFIB-G)中的实验装置。为了将操纵pHFIB-G所需的参数与细胞系所需的参数进行比较,使用犬多形性腺瘤细胞系(ZMTH3)(对照组)。与AuNPs孵育的未经激光处理的细胞和递送分子用作阴性对照。激光辐照(高达35 mJ / cm 2 )导致可操纵的成纤维细胞比例显着(与未辐照细胞相比,高达85%:p <0.05),而细胞活力(97%) )没有明显减少。 pHFIB-G的穿孔效率与ZMTH3一样高。激光处理后直至72小时,未观察到代谢细胞活性的显着降低。成纤维细胞吸收了分子量高达500 kDa的葡聚糖。 AuNP和脉冲激光束的相互作用产生了一种空间选择性技术,可用于以高通量操作甚至pHFIB-G等原代细胞。

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